All of the following are stressors of captive animals except d) none of the given answers.
The statement is suggesting that all of the provided options are stressors of captive animals. However, the correct answer is d) none of the given answers. The term "stressor" refers to any factor or condition that can cause stress or disrupt the normal functioning of an organism. While options a, b, c, and e can indeed be stressors for captive animals, it is important to note that these stressors are not exhaustive. There can be other factors such as limited space, social isolation, lack of enrichment, presence of predators, and disruptions in the circadian rhythm, among others, that can also contribute to stress in captive animals. Therefore, it is incorrect to say that only the provided options are stressors and that there are no other potential stressors for captive animals.
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Question Two Answer both parts, (i) and (ii). (i) Describe how isolated tissue experiments can be used to detect the following type of receptor-ligand behaviour: agonism, partial agonism, antagonism, irreversible antagonism 110 Marks) (ii) Outline a structure-activity profile for the fluoroquinoline group of antibacterial agents. Your answer should also describe the attractions of incorporation of fluorine as a substituent in the molecular structures of APIs/prospective APIs. [10 Marks)
The isolated tissue experiments have been used to detect the following receptor-ligand behavior. Here’s how: Isolated Tissue experiments and Agonism.
Agonism is detected through measuring the contraction of an isolated tissue sample when the sample is exposed to a particular receptor ligand. Here, the receptor agonist's concentration and the agonist's potency is increased until the tissue reaches maximum contraction. Isolated Tissue experiments and Partial AgonismPartial agonism is detected in a similar way to agonism. Here the isolated tissue samples are treated with two types of drugs. The tissue sample’s response is then measured in terms of their maximum possible response, as well as the response of the tissue sample’s agonist.
Antagonism is detected by exposing an isolated tissue sample to an agonist and then measuring the antagonists’ ability to compete with agonist’s effects. The tissue’s response to the agonist is then compared to the response elicited by the agonist in the presence of the antagonist. Isolated Tissue experiments and Irreversible Antagonism An irreversible antagonist is detected by allowing the antagonist to act on a tissue sample for an extended period of time, after which the agonist is introduced. If the agonist fails to elicit the expected response, then the presence of an irreversible antagonist can be inferred.
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Part E
Which second messenger causes the release of calcium from the endoplasmic reticulum?
a) IP3
b) DAG
c) tyrosine kinase
d) cAMP
Part F
Which of the following adrenergic receptors increase cAMP levels?
a) B receptors
b) a1 receptors
c) a2 receptors
The second messenger that causes the release of calcium from the endoplasmic reticulum is IP3 and B receptors are the adrenergic receptors that increase cAMP levels.
Second messengers are small molecules generated by the cell in response to an extracellular stimulus. In cellular signaling, second messengers are intermediaries between a cell's surface receptors and the final intracellular effectors. Several diverse pathways use second messengers to transmit signals and regulate cellular function, including the IP3 (inositol 1,4,5-trisphosphate) and cAMP pathways.
IP3, or inositol 1,4,5-trisphosphate, is a molecule that serves as a second messenger in cells. In response to extracellular stimuli, IP3 is generated by phospholipase C (PLC) and binds to IP3 receptors on the endoplasmic reticulum, resulting in the release of stored calcium into the cytoplasm.Which of the following adrenergic receptors increase cAMP levels?B receptors are adrenergic receptors that increase cAMP levels. Adrenergic receptors are a type of G protein-coupled receptor that are activated by the neurotransmitter norepinephrine (noradrenaline) and the hormone epinephrine (adrenaline). The binding of these ligands to adrenergic receptors activates a G protein, which in turn activates or inhibits an effector enzyme, resulting in the production of second messengers such as cAMP.
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QUESTION 1 The smallest independently functioning biological unit of an organism is a(n). cell molecule organ tissue QUESTION 2 A collection of similar tissues that performs a specific function is an organ organelle organism organ system QUESTION 3 The body system responsible for structural support and movement is the cardiovascular system endocrine system muscular system skeletal system
The smallest independently functioning biological unit of an organism is a cell. A cell is the smallest independently functioning biological unit of an organism.
Cells come in different shapes and sizes and can be found in every living organism. They perform all the functions necessary for life. A collection of similar tissues that performs a specific function is an organ. Organs are collections of similar tissues that work together to perform a specific function in the body. Organs are formed by the combination of two or more tissues. Each organ performs a specific function in the body.
Examples of organs include the heart, lungs, liver, and kidneys. The body system responsible for structural support and movement is the skeletal system. The skeletal system is responsible for structural support and movement in the body. It consists of bones, cartilage, ligaments, and other connective tissues that provide support and structure to the body. The skeletal system also protects the internal organs and produces blood cells.
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The smallest independently functioning biological unit of an organism is a cell. These cells combine to create tissues, which in turn form organs that carry out specific functions. Organ systems, such as the skeletal system, are groups of functionally related organs.
Explanation:The smallest independently functioning unit of an organism is commonly referred to as a cell. This includes all living structures, from human anatomy to bacteria, which is a single-celled organism.
The next level of biological organization incorporates cells into tissues, which are groups of similar cells working together to perform related functions. These tissues then combine to form an organ, which is a collection of tissues grouped together to perform a specific function.
The skeletal system is responsible for providing structural support and facilitating movement in the body. It is an example of an organ system, a higher level of organization that includes functionally related organs.
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If the acidity of gastric juice increases, it is recommended to consume milk.
Answer the question A and fulfill the task B:
A) How and why will the secretion of gastric juice be changed after drinking milk?
B) Explain the physiological mechanisms of the changes in pancreatic secretion after drinking milk.
Drinking milk can decrease gastric juice acidity, reduce inflammation, and improve digestion by stimulating the release of pancreatic juice, aiding in the relief of gastrointestinal problems.
If the acidity of gastric juice increases, it is recommended to consume milk. Drinking milk can decrease the acidity of the gastric juice. This is because milk is an alkaline substance and can help to neutralize the acid in the stomach. When the milk enters the stomach, it can coat the lining of the stomach and help to reduce the irritation that is caused by excess acid.
A) After drinking milk, the secretion of gastric juice will be changed because the milk will decrease the acidity of the gastric juice. This can help to reduce the symptoms of acid reflux and other gastrointestinal problems. The milk can also help to soothe the lining of the stomach and reduce inflammation.
B) The physiological mechanisms of the changes in pancreatic secretion after drinking milk are related to the release of hormones. When the stomach is empty, the hormone ghrelin is released. This hormone stimulates the secretion of pancreatic enzymes.
When food enters the stomach, the hormone cholecystokinin (CCK) is released. This hormone stimulates the release of pancreatic juice, which contains enzymes that can help to digest food. Milk can stimulate the release of CCK, which can increase the secretion of pancreatic juice. This can help to improve digestion and reduce the symptoms of gastrointestinal problems.
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You have an idea for a vaccine to prevent Group A Strep (GAS) infections. You know that Streptococcus bacteria are fastidious organisms, and you don't expect to be able to produce your protein of interest in large quantities in S. pyogenes. Based on your knowledge of GAS, design a recombinant vaccine candidate to protect against GAS infection using E. coli as your recombinant protein production organism. Your choice of GAS antigen should be something produced by GAS that is not produced by humans. Your GAS protein(s) of choice will be expressed in E. coli and then purified for use in vaccine production. To express your protein in E. coli, you need to clone the gene(s) of interest into a plasmid under the control of the Plac promoter. Create and upload a diagra that shows each step of your design strategy and cloning process. Start with getting your gene of interest out of S. pyogenes and end with your selection and screening process in E. coli. Be sure to include all of the following: - What GAS protein(s) will be expressed by your recombinant E. coli? - Show all components that need to be present on your plasmid for replication, selection, screening, and for regulation by the Plac promoter. How do all of the parts come together? - A selection mechanism to ensure that only recombinant E. coli expressing your plasmid can grow. - Any selection mechanism is ok. Indicate what media needs to be used and what you expect to see. - A screening mechanism to show that your gene(s) of interest is being expressed. Indicate what media needs to be used and what you expect to see.
Ampicillin selection and SDS-PAGE can be used as mechanisms for selection and screening, respectively, to ensure the presence and expression of the M protein
One of the fundamental methods to protect against infectious diseases is through vaccination. Vaccines are developed using live or inactivated microorganisms or synthetic peptides that resemble the antigens of the microorganisms. By introducing these antigens into the body, the immune system recognizes them as foreign and mounts a defensive response, thus conferring protection against the disease-causing organism. Therefore, it is an excellent idea to develop a vaccine candidate to safeguard against GAS infection.
In order to develop a vaccine against GAS, an antigenic protein that is not naturally produced by humans needs to be selected. A promising candidate for this purpose is the M protein, which is an important virulence factor produced by GAS but not by humans.
For successful replication, selection, screening, and regulation of the gene of interest in recombinant E. coli, specific components must be present on the plasmid. The plasmid should contain the promoter sequence, such as the Plac promoter, which regulates the expression of the M protein in E. coli. Additionally, the plasmid needs to include the origin of replication sequence, allowing it to replicate independently. To enable selection, an antibiotic resistance gene, such as the ampicillin resistance gene, should be incorporated into the plasmid.
To ensure the growth of only recombinant E. coli cells that have taken up the plasmid expressing the M protein, a selection mechanism is necessary. Ampicillin selection can be employed, where E. coli cells containing the plasmid will grow on medium containing ampicillin, while those without the plasmid will not survive.
To screen for the successful expression of the M protein in E. coli, SDS-PAGE can be utilized. The expressed protein can be purified using histidine-tagged purification, followed by confirmation of the presence of the M protein through Western blot analysis.
In summary, the development of a vaccine candidate against GAS infection involves the expression of the M protein in recombinant E. coli. This requires the plasmid to contain the promoter sequence, origin of replication sequence, and antibiotic resistance gene.
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Question 40 1 pts The secretion of ADH results in the formation of a ___________ urine.
The secretion of ADH results in the formation of concentrated urine.
1. Antidiuretic hormone (ADH) is produced by the hypothalamus and released by the posterior pituitary gland.
2. It controls the amount of water reabsorbed by the kidneys into the bloodstream, which ultimately affects urine concentration. ]
3. When there is an excess of water in the bloodstream, ADH secretion is suppressed, and urine production increases.
4. When there is a shortage of water in the bloodstream, ADH secretion is stimulated and urine production is decreased, leading to the formation of concentrated urine.
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Chymotrypsin is an enzyme, What is it substrate? what does it do? What are some key amino acids found in the active site?
Chymotrypsin is a digestive enzyme that primarily acts in the small intestine to break down proteins into smaller peptides. Its substrate is peptide bonds within proteins.
The main function of chymotrypsin is proteolysis, which is the process of breaking down proteins into smaller peptides. Specifically, chymotrypsin cleaves peptide bonds on the carboxyl side of aromatic amino acids such as phenylalanine, tryptophan, and tyrosine. It exhibits a preference for hydrophobic amino acids in the substrate.
It's important to note that chymotrypsin is just one of the proteases involved in protein digestion, and different enzymes act at different stages of the process to ensure efficient breakdown of dietary proteins into smaller peptides and amino acids for absorption by the body.
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Using your knowledge of the Australian Code and GCP, please answer the following questions below. Be sure to clearly label the different parts.
Part A. Briefly describe the types and scale of scientific misconduct. Part B. Using examples and details from class, explain TWO examples of misconduct in a clinical trial. What do you feel are the most important consequences for each? Explain your reasoning.
A: The types of scientific misconduct are Falsification, Fabrication, Plagiarism, and Duplicate publication. The scale of scientific misconduct are Minor, Significant, and Extreme.
B: Examples of misconduct in a clinical trial are informed consent forms not provided properly and lack of transparency in clinical trial conduct.
Part A: Types and Scale of Scientific Misconduct
Types of Scientific Misconduct include:
Falsification: Alteration of research results or omission of results that are undesirableFabrication: Presentation of results or experimental data that never existedPlagiarism: Copying text, findings, images, or ideas of other researchers without giving them due creditDuplicate publication: Publication of the same research findings in multiple journals without clear attribution to the prior publicationScale of Scientific Misconduct include:
Minor: Errors or oversights that do not alter the significance of the research findingsSignificant: Results that are significantly affected by errors, oversights, or misconductExtreme: Fabrication or falsification of data, plagiarized text, or presentation of other researchers' work as one's ownPart B: Examples of Misconduct in a Clinical Trial
Example 1: Informed Consent Forms not provided properly
The informed consent form is the primary document that explains the clinical trial's nature and requirements to patients, who must sign it. In clinical trial research, informed consent is an ethical prerequisite, and the sponsor must guarantee that the consent form is provided properly.
The most important consequences are:
Patients who did not comprehend the nature and requirements of the clinical trial may have given informed consent. Patients' safety and well-being may be jeopardized, and ethical standards may be violated.Example 2: Lack of transparency in Clinical Trial Conduct
In clinical trial research, transparency is essential. The researchers must be open and honest with the regulatory body, the participants, and the public. Any significant deviations from the clinical trial protocol must be recorded and documented correctly.
The most important consequences are:
Lack of transparency undermines trust and raises concerns about the quality and safety of research. Clinical trial participants may be negatively affected by unrecorded or undocumented deviations from the protocol. The integrity of the research findings may be compromised, and ethical standards may be violated.Learn more about Clinical trial:
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Athletes performing in bright sunlight often smear black eye grease under their eyes to reduce glare. Does eye grease work? In one study, 16 student subjects took a test of sensitivity to contrast after three hours facing into bright sun, both with and without eye grease. (Greater sensitivity to contrast improves vision, and glare reduces sensitivity to contrast.) This is a matched pairs design. The differences in sensitivity, with eye grease minus without eye grease, are given in the table.
0.070.07 0.640.64 −0.12−0.12 −0.05−0.05 −0.18−0.18 0.140.14 −0.16−0.16 0.030.03
0.050.05 0.020.02 0.430.43 0.240.24 −0.11−0.11 0.280.28 0.050.05 0.290.29
How much more sensitive to contrast are athletes with eye grease than without eye grease? Give a 95% confidence interval to answer this question. Give your answers to four decimal places.
lower bound: ??????
upper bound: ????????
we can say with 95% confidence that athletes with eye grease are between 0.04424 and 0.19826 more sensitive to contrast than without eye grease.
The data is provided for a matched pairs design, which means that the student subjects had the same test twice: once with eye grease, and once without.
This is shown in the differences between the sensitivity (with minus without) which are given in the table as follows:0.070.07 0.640.64 −0.12−0.12 −0.05−0.05 −0.18−0.18 0.140.14 −0.16−0.16 0.030.03 0.050.05 0.020.02 0.430.43 0.240.24 −0.11−0.11 0.280.28 0.050.05 0.290.29T
o calculate the mean of the differences, we sum the values and divide by the number of differences:n = 16Σd = 1.94mean = Σd/n = 1.94/16 = 0.12125
This indicates that the athletes with eye grease were 0.12125 more sensitive to contrast than without. To construct a 95% confidence interval, we need to find the standard error of the mean differences (SEM):SEM = s/√nTo find the standard deviation s, we can use the formula:s² = (Σd² - Σd²/n)/(n-1)s² = (0.018+0.409+0.014+0.002+0.032+0.196+0.026+0.0009+0.008+0.003+0.0025+0.1849+0.0576+0.012+0.0784+0.0121)/(16-1)s² = 0.963/15s = √(0.963/15) = 0.31158
Now we can find the SEM:SEM = s/√n = 0.31158/√16 = 0.077895To find the 95% confidence interval, we need to use the t-distribution with n-1 degrees of freedom (15 degrees of freedom in this case), and a level of significance of 0.05 (two-tailed test). We can find the t-value using a t-table or calculator, or we can use the following formula:
t = ±tα/2,ν*SEM where tα/2,ν is the t-value for a two-tailed test with a level of significance of α/2 and ν degrees of freedom. For α = 0.05 and ν = 15, we have:tα/2,ν = 2.13185 (using a t-table or calculator)Therefore:t = ±tα/2,ν*SEM = ±2.13185*0.077895 = ±0.16601
The 95% confidence interval is:mean ± t*SEM= 0.12125 ± 0.16601= [0.04424, 0.19826]
Therefore, we can say with 95% confidence that athletes with eye grease are between 0.04424 and 0.19826 more sensitive to contrast than without eye grease.
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Explain why a defective valve cannot be detected by an ECG and a
damaged AV node cannot be detected in listening to the heard
sounds. What is the correct test for each defect ?
An ECG cannot detect a defective valve because it is a test that measures the electrical activity of the heart. While the ECG can detect abnormal electrical activity in the heart, it cannot provide a direct diagnosis of valve function.
Similarly, the damage to the AV node cannot be detected by listening to heart sounds because it is not a physical problem with the heart. It is a problem with the electrical signals that control the heart's rhythm. Therefore, echocardiography is the best test to detect a defective valve.
An echocardiogram uses sound waves to produce images of the heart and can provide a direct visualization of the valves. On the other hand, an electrophysiological study (EPS) is the best test to detect a damaged AV node. EPS is an invasive test that involves threading thin, flexible wires through a vein in the groin and into the heart.
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Question 50 Match the hormone to the gland that secretes them. ◯ Aldsoterone 1. Pancreas ◯ Calcitonin 2. Adrenal cortex ◯ Cortisol 3. Thyroid ◯ Epinephrine 4. Adrenal medulla ◯ Glucagon ◯ Gonadocorticoids
Here are the hormones that match with the gland that secretes them:
Hormone-Gland
Aldosterone-Adrenal cortex
Calcitonin-Thyroid
Cortisol-Adrenal cortex
Epinephrine-Adrenal medulla
Glucagon-Pancreas
Gonadocorticoids-Adrenal cortex
The glands in the human body which secretes hormones are called endocrine glands. The endocrine glands of the human body include adrenal gland, pituitary gland, pancreas, thyroid gland, parathyroid gland, ovaries, and testes. These endocrine glands secrete hormones into the bloodstream that helps regulate the body's activities.
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◯ Aldosterone - 2. Adrenal cortex
◯ Calcitonin - 3. Thyroid
◯ Cortisol - 2. Adrenal cortex
◯ Epinephrine - 4. Adrenal medulla
◯ Glucagon - 1. Pancreas
◯ Gonadocorticoids - 2. Adrenal cortex
1. Aldosterone: Aldosterone is a hormone produced by the adrenal cortex, specifically the outer layer of the adrenal glands. It plays a crucial role in regulating blood pressure and maintaining electrolyte balance by promoting the reabsorption of sodium ions and the excretion of potassium ions in the kidneys.
2. Calcitonin: Calcitonin is a hormone secreted by the thyroid gland, which is located in the neck. Its primary function is to regulate calcium levels in the body. Calcitonin works by inhibiting the activity of osteoclasts, cells responsible for breaking down bone tissue, and promoting calcium deposition in the bones, thus lowering blood calcium levels.
3. Cortisol: Cortisol is a hormone synthesized and secreted by the adrenal cortex. It is often referred to as the "stress hormone" because its production increases in response to stress. Cortisol plays a vital role in regulating metabolism, immune responses, and stress responses throughout the body.
4. Epinephrine: Epinephrine, also known as adrenaline, is produced by the adrenal medulla, the inner part of the adrenal glands. It is involved in the body's "fight or flight" response, preparing the body for emergency situations. Epinephrine increases heart rate, blood pressure, and blood sugar levels, providing a burst of energy and enhancing physical performance.
5. Glucagon: Glucagon is a hormone released by the pancreas, specifically the alpha cells located in the islets of Langerhans. Its primary role is to increase blood sugar levels. Glucagon stimulates the liver to break down stored glycogen into glucose, which is then released into the bloodstream for energy.
6. Gonadocorticoids: Gonadocorticoids, also known as sex steroids, are hormones produced by the adrenal cortex. They include androgens and estrogens, which are involved in the development and regulation of reproductive functions. While the majority of sex steroids are produced by the gonads (testes in males and ovaries in females), the adrenal cortex also contributes to their production.
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select true or false of sentences and correct the false one:
1.I band of muscle sarcomere contains thick filaments only .(true/false)
2.skeletal muscle is controlled by the autonomic nervous system.(true/false)
3.a hormone that can lower blood levels of calcium ions is glucagon.(true/false)
4.the lung's ability to return to resting volume when stretching force is released is called compliance.(true/false)
5.epinephrine's primary role in the respiratory system is as a bronchoconstrictor.(true/false)
*fill the gaps
----------are responsible for bone deposition while ----------are responsible for bone break down
1. False, the I band of a muscle sarcomere contains thin filaments only.
2. False, skeletal muscles are controlled by the somatic nervous system.
3. False, the hormone that can lower blood levels of calcium ions is calcitonin.
4. True.
5. False, epinephrine's primary role in the respiratory system is as a bronchodilator.----------Osteoblasts are responsible for bone deposition while osteoclasts are responsible for bone breakdown.
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T helper lymphocytes recognize antigens presented by a. MHC 1 molecules on antigen presenting cells b. MHC I molecules on all nucleated cells c. MHC II molecules on all antigen presenting cells d. MHC I molecules on all red blood cells
T helper lymphocytes recognize antigens presented by MHC II molecules on all antigen-presenting cells. The correct option is C MHC II molecules on all antigen-presenting cells.
T helper lymphocytes, also known as CD4+ T cells, are a type of immune cell that plays a crucial role in the immune response. They recognize antigens, which are foreign substances or molecules, presented by major histocompatibility complex class II (MHC II) molecules on antigen-presenting cells.
MHC II molecules are proteins found on the surface of specialized cells called antigen-presenting cells (APCs), which include dendritic cells, macrophages, and B cells. These cells capture the process, and present antigens to T cells for recognition. When a pathogen or foreign substance enters the body, APCs engulf and break it down into smaller fragments. These fragments are then loaded onto MHC II molecules and presented on the surface of the APCs.
T helper lymphocytes have specific receptors called T cell receptors (TCRs) that can recognize the antigens presented by MHC II molecules. When a TCR on a T helper cell encounters an antigen-MHC II complex that matches its receptor, it triggers a series of immune responses, including the activation of other immune cells and the production of specific immune molecules.
Therefore, the correct statement is that T helper lymphocytes recognize antigens presented by MHC II molecules on all antigen-presenting cells.
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What are thr components of bone's extracellular matrix?
1. Inorganic
2. Organic
The components of the bone's extracellular matrix are organic and inorganic materials. Both options are correct.
The extracellular matrix of bone is composed of both inorganic and organic components, which play essential roles in maintaining the structure and function of bone tissue.
1. Inorganic Component: The inorganic component consists primarily of hydroxyapatite crystals, which are formed by calcium phosphate and calcium carbonate. These mineralized crystals give bone its hardness and provide rigidity and strength to withstand mechanical stress. The inorganic component also contributes to the mineralization of bone and helps regulate calcium and phosphate levels in the body.
2. Organic Component: The organic component is primarily composed of collagen fibers, specifically type I collagen. Collagen provides flexibility and tensile strength to bone, allowing it to resist stretching and withstand forces. Other organic components include various proteins, such as osteocalcin and osteonectin, which play roles in bone mineralization, cell signaling, and the regulation of bone growth and remodeling processes.
The combination of the inorganic and organic components in bone's extracellular matrix creates a dynamic and resilient structure. The inorganic component provides hardness and mineralization, while the organic component provides flexibility and strength. Together, they contribute to the overall integrity and functionality of bone, allowing it to support and protect the body's tissues and organs.
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Which bones develop via intramembranous ossification and which
bones develop via endochobdral ossification?
Intramembranous ossification occurs directly from mesenchyme, whereas endochondral ossification begins with a cartilage model.
Intramembranous ossification and endochondral ossification are the two types of bone formation. The following are the bones that develop via intramembranous ossification and endochondral ossification:Intramembranous ossification:Intramembranous ossification is the process by which flat bones such as the clavicles (collarbone), cranial bones, and some facial bones are formed.
This process happens directly from mesenchymal tissue.Endochondral ossification: Most bones are formed via endochondral ossification, which begins with a cartilage model. This method is used to develop long bones, such as the femur, humerus, and radius. The hyoid bone, the sternum, and the bones of the ear canal are examples of other bones that are formed this way.
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On the histological specimen of the liver there is vein, which belongs to unmuscular type. Name this vein.
a. Hepatic vein
b. Central vein
c. Portal vein
d. Interlobular vein
On the histological specimen of the liver there is a vein that belongs to unmuscular type. The name of this vein is the central vein. the answer is hepatic vein.
The central vein is a venous vessel that runs through the center of the liver lobule and is located in the hepatic lobule's central vein zone. The central vein is situated near the hepatic artery and the bile duct as it exits the liver lobule.The hepatic veins, which arise from the liver lobules and merge to form the inferior vena cava, drain into the right atrium of the heart.
The portal vein, which supplies blood to the liver, is the liver's major blood supply. The interlobular veins are found at the periphery of the liver lobules, adjacent to the portal canals, and connect the central vein to the sublobular vein.
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The polypeptide chain that makes up a tight junction weaves back and forth through the membrane four times, with two extracellular loops, and one loop plus short C-terminal and N-terminal fails in the cytoplasm. Looking at Figure 5.14 , what would you predict about the amino acid sequence of the tight junction protein?
The amino acid sequence of the tight junction protein would have both hydrophilic and hydrophobic regions, because of the way it weaves back and forth through the membrane four times.
Tight junctions are structures that form a barrier between the cells in our body, preventing the passage of large molecules or pathogens between them. The tight junctions are made up of a series of proteins that bind the cells together and create this barrier. The polypeptide chain that makes up a tight junction weaves back and forth through the membrane four times, with two extracellular loops, and one loop plus short C-terminal and N-terminal fails in the cytoplasm.
This would create a protein that has both hydrophilic and hydrophobic regions, because of the way it weaves back and forth through the membrane four times. The hydrophilic regions would be exposed to the extracellular environment, while the hydrophobic regions would be buried inside the membrane. This is a common feature of membrane proteins, which often need to interact with both the inside and outside of the cell.
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Describe the clinical features and underlying pathology of progressive bulbar palsy and primary lateral sclerosis.
Progressive bulbar palsy and primary lateral sclerosis (PLS) are rare neurological conditions that affect the motor neurons and cause difficulty speaking, swallowing, and weakness in the limbs.
Progressive bulbar palsy is a type of motor neuron disease that affects the motor neurons in the brainstem, causing difficulty speaking and swallowing. The underlying pathology is degeneration of the motor neurons in the bulbar region, which control the muscles of the face, mouth, and throat. This can lead to slurred speech, difficulty swallowing, choking, and drooling.
Primary lateral sclerosis, on the other hand, is a rare disorder that affects the upper motor neurons in the brain and spinal cord. This can cause weakness and stiffness in the limbs, which may eventually spread to the trunk. Unlike other motor neuron diseases, PLS does not usually cause muscle wasting or twitching.
The underlying pathology of PLS is similar to other motor neuron diseases, with degeneration and loss of the motor neurons. However, the progression is slower and it may take many years for the symptoms to become severe.
Overall, both conditions are rare and have similar underlying pathology involving the degeneration of motor neurons. The clinical features of these diseases include difficulty speaking, swallowing, and weakness in the limbs, which can severely affect the quality of life of patients.
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Rem 200 of 200 Mark Customized subget for 200. A 24-year-old man comes to the emergency department because of a 3-day history of increasingly severe abdominal pain and vomiting. He has no history of major medical nesses hospital admissions, or operations. The patient is in obvious distress. His pulse is 110/min. On examination, his abdomen is slightly tympanitic with high-pitched bowel sounds. There is involuntary guarding on palpation. A CT scan of the abdomen shows congenital nonrotation of the bowel. Which of the following structures would have been the center visit this patient's bowel had rotated normally? A) Celiac artery B) Inferior mesenteric artery C) Median umbilical ligament D) Superior mesenteric artery E) Umbilical vein F) Urachus
d) If the patient's bowel had rotated normally, the structure at the center would have been the Superior mesenteric artery.
In normal embryological development, the bowel undergoes rotation to assume its final position in the abdomen. The Superior mesenteric artery (SMA) plays a crucial role in this rotation. It supplies blood to the midgut, which includes a significant portion of the small intestine and the proximal part of the large intestine.
In the case of congenital nonrotation of the bowel, the bowel fails to rotate properly during development. This can lead to complications such as volvulus, where the bowel twists on itself, causing obstruction and compromised blood supply. The patient's clinical presentation with severe abdominal pain and vomiting is consistent with such a complication.
Knowing the anatomy, it becomes apparent that if the bowel had rotated normally, the SMA would have been at the center. The SMA arises from the abdominal aorta and extends toward the small intestine, providing essential blood supply for proper intestinal function. In this patient, the abnormal rotation of the bowel has likely led to the development of his symptoms and the need for medical attention.
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Let the person look for articles on firing temperatures of porous materials
If a person is looking for articles on firing temperatures of porous materials, they can start their search with keywords like "porous materials," "firing temperatures," and "ceramics."
Some potential resources for finding such articles could include academic databases like JSTOR or ScienceDirect, as well as industry publications such as Ceramics Monthly or the Journal of the American Ceramic Society. By using these resources, the person may be able to find articles that discuss the various factors that can affect firing temperatures of porous materials, such as the type of material being fired, the shape and size of the object, and the desired final outcome.
Additionally, they may be able to find information on specific techniques or processes that can be used to achieve optimal firing results.
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Please help developing 16 weeks exercise prescription.
Including
WEEK
PHASE
INTENSITY (% OF HRR OR RPE)
EXERCISE MODE
DURATION (MIN/ DAY)
MONDAY TUESDAY WEDNESDAY THURSDAY FRIDAY SATURDAY SUNDAY
The development of a 16 weeks exercise prescription involves several things. These include weeks, phases, intensity, exercise mode, duration, and days of the week.
Below is a guide on how you can develop a 16 weeks exercise prescription:Phase 1 (Week 1 to Week 4)Intensity: 60% of HRRExercise Mode: Walking, cycling, swimming, or ellipticalDuration: 30 to 40 minutes per day, five days a weekDays of the Week: Monday, Tuesday, Wednesday, Thursday, and Friday.Phase 2 (Week 5 to Week 8)Intensity: 70% of HRR
Exercise Mode: Elliptical, cycling, or joggingDuration: 45 to 60 minutes per day, five days a weekDays of the Week: Monday, Tuesday, Wednesday, Thursday, and Friday.Phase 3 (Week 9 to Week 12)Intensity: 80% of HRRExercise Mode: Jogging, rowing, or bikingDuration: 45 to 60 minutes per day, six days a week
Days of the Week: Monday, Tuesday, Wednesday, Thursday, Friday, and Saturday.Phase 4 (Week 13 to Week 16)Intensity: 90% of HRRExercise Mode: Rowing, biking, or cross-fitDuration: 60 to 90 minutes per day, six days a weekDays of the Week: Monday, Tuesday, Wednesday, Thursday, Friday, and Saturday.
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during atrial systole_______.
a. atrial pressure exceeds ventricular pressure
b. 70% of ventricular filling occurs
c. AV valves are open
d. valves prevent backflow into the great veins
e. A and C
e. A and C. (During atrial systole, atrial pressure exceeds ventricular pressure, and AV valves are open.)
During atrial systole, both options A and C are correct. Option A states that atrial pressure exceeds ventricular pressure, which is true during atrial contraction. This allows the atria to forcefully pump blood into the ventricles. Option C states that AV (atrioventricular) valves are open, which is also true. The AV valves, including the tricuspid valve on the right side and the mitral valve on the left side, open during atrial systole to allow the flow of blood from the atria into the ventricles. This filling of the ventricles accounts for approximately 70% of the ventricular filling (option B). Option D, which states that valves prevent backflow into the great veins, is not accurate during atrial systole as the focus is primarily on the atrial-ventricular filling process.
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Question 2 Which of the following terms is best fitting to these statements? "I am worthless because I have failed as an artist" "I have worth because I have been successful as an artist." O A Self concept O B. Contingencies of self worth O C Negative self-talk O D Pathological critic
Contingencies of self-worth are deeply rooted in an individual's beliefs and perceptions about themselves.
They represent the conditions and outcomes that individuals deem necessary for them to feel a sense of self-worth and self-esteem.
These contingencies can vary from person to person, as they are shaped by personal experiences, societal influences, cultural norms, and individual goals and aspirations.
In the context of the statements "I am worthless because I have failed as an artist" and "I have worth because I have been successful as an artist," it is evident that the individual's self-worth is contingent upon their achievements in the realm of art.
If they perceive themselves as failing in their artistic endeavors, they may interpret this as a reflection of their overall worth and feel a sense of worthlessness. On the other hand, if they perceive themselves as successful in their artistic pursuits, they may derive a sense of self-worth and validation from these achievements.
Contingencies of self-worth can extend beyond specific domains, such as art, and encompass various aspects of life, including academic performance, physical appearance, social relationships, financial success, or moral values.
For some individuals, their self-worth may be contingent on being a good parent, a supportive friend, or a responsible employee. Others may tie their self-worth to their intelligence, physical fitness, or adherence to personal values.
The reliance on contingencies of self-worth can have both positive and negative implications. On one hand, it can motivate individuals to strive for success, pursue personal goals, and develop skills and competencies in various areas.
Achieving these contingencies can enhance self-esteem and contribute to a positive sense of self. However, when individuals face setbacks, failures, or challenges in meeting their contingencies, it can lead to a decrease in self-worth, self-doubt, and negative emotional states such as sadness, anxiety, or feelings of inadequacy.
It is important to recognize that self-worth should not solely rely on external achievements or the fulfillment of contingencies. A healthy sense of self-worth should also be rooted in self-acceptance, self-compassion, and an understanding that intrinsic value exists regardless of external validation.
Building a more resilient self-worth involves developing a broader perspective of oneself, valuing personal qualities, fostering positive self-talk, and cultivating a sense of worth beyond external achievements.
Understanding contingencies of self-worth provides insights into the complexities of human psychology and the factors that influence an individual's self-perception.
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If you could artificially modify the membrane resting potential from -70 mV to +70 mV, what will the sodium ions (Na+) net movement be?
A. Na+ will enter the cell without modifying the voltage.
B. Na+ will enter the cell following its concentration gradient.
C. Na+ will exit the cell even against the concentration gradient.
D. Na+ will not move from the compartments.
What will happen to the resting membrane potential if more K+ (potassium) channels are opened?
A. The resting membrane potential will move closer to zero (depolarize).
B. The resting membrane potential will stay close to +20 mV.
C. The resting membrane potential will stay around -60 mV.
D. The resting membrane potential will hyperpolarize.
Of the following graded potentials, which one is produced by efflux of potassium?
A. end-plate potential.
B. excitatory postsynaptic potential (EPSP).
C. inhibitory postsynaptic potential (IPSP).
D. organ of Corti receptor potential.
What type of receptor is responsible for the generation of a local potential at the organ of Corti?
A. it is a TRP1 receptor (transitory receptor potential).
B. it is an ionotropic receptor.
C. it is a MET receptor (mechanoelectrical transducer).
D. it is a proprioceptor similar to the muscle spindle.
What do drugs of addiction and natural behaviors share?
A. drugs of addiction increase serotonin while natural behaviors increase dopamine in the nucleus accumbens.
B. they all increase acetylcholine in the striatum.
C. Drugs of addiction and natural behaviors have opposite effects in dopamine release.
D. they all increase dopamine in the nucleus accumbens.
Regarding environmental influences on weight
A. the influence of infection has been disproven.
B. social influence is mostly from the family.
C. smoking increases appetite.
D. sleep loss increases appetite.
If you could artificially modify the membrane resting potential from -70 mV to +70 mV, the sodium ions (Na+) net movement will be Na+ will enter the cell following its concentration gradient.
The resting membrane potential will hyperpolarize is what will happen to the resting membrane potential if more K+ (potassium) channels are opened.
At synapses, potassium ions efflux from the cell leads to hyperpolarization or inhibitory postsynaptic potential. The efflux of positively charged potassium ions leads to more negative potential which makes it difficult for positively charged ions to enter the cell.
It is a MET receptor (mechanoelectrical transducer) that is responsible for the generation of a local potential at the organ of Corti.
They all increase dopamine in the nucleus accumbens is
Regarding environmental influences on weight Sleep loss increases appetite. is the correct option.
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True or False The heart has three layers: the endocardium, myocardium and epicardium.
The heart, one of the body's most vital organs, is protected by three layers of tissue. These three layers of tissue are as follows: Endocardium: The innermost layer of tissue, which lines the inside of the heart's chambers and valves, is known as the endocardium.
This statement is correct. The heart has three different layers: the endocardium, myocardium and epicardium, each with their own function. These three layers of tissue protect the heart from injury and contribute to its function as a pump.The innermost layer, the endocardium, is made up of connective tissue and squamous cells. This layer lines the inside of the heart's chambers and valves, allowing for the smooth flow of blood through the heart. The middle layer, the myocardium, is made up of muscular cells that are responsible for the heart's rhythmic contractions and relaxations.
This layer is essential for the heart's pumping action, which sends blood throughout the body. The outermost layer, the epicardium, is a layer of protective connective tissue that covers the heart's outer surface. This layer is important for protecting the heart from injury and providing it with support.
The heart is one of the body's most important organs, and it is protected by three layers of tissue. These layers, the endocardium, myocardium, and epicardium, work together to ensure that the heart functions properly and that blood is pumped efficiently throughout the body.
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What possible "explanatory story" might explain the observation described above?
How would you test your hypothesis made above?
Answer the two questions in 5- 10 sentences.
The possible explanatory story for Alex's growth spurt could be that he experienced a delayed onset of puberty compared to his peers. During his childhood, his body may have been slower in initiating the hormonal changes associated with puberty, resulting in a delayed growth pattern. However, as he entered his teenage years, his body caught up and began producing the necessary hormones at a higher rate, leading to a sudden increase in height and surpassing his friends.
Testing the hypothesis:
To test the hypothesis that Alex's growth spurt was a result of a delayed onset of puberty, several steps can be taken. Firstly, collecting data on Alex's growth patterns and comparing them with standardized growth charts can provide insights into his growth trajectory.
This would involve tracking his height and age over time to identify any deviations or delays in growth.
Additionally, hormonal analysis can be conducted to measure the levels of growth hormones and sex hormones in Alex's body during different stages of his development. Comparing these hormone levels with established norms for puberty can provide evidence of a delayed onset.
Furthermore, comparing Alex's growth patterns with those of his family members can also provide valuable information. If there is a history of delayed puberty or growth spurts in his family, it could support the hypothesis of a genetic influence on his growth.
By combining these approaches, researchers can gather evidence to support or refute the hypothesis that a delayed onset of puberty contributed to Alex's growth spurt.
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Major amount of saliva, when salivary glands are not stimulated is contributed by? Select one: a. Sublingual glands b. Minor salivary glands c. Submandibular glands d. Parotid glands Luestion
When salivary glands are not stimulated, the major amount of saliva is contributed by minor salivary glands.
Salivary glands are exocrine glands that generate saliva. They are the primary digestive glands in the mouth. Saliva is a clear liquid that contains enzymes, lubricants, and some antibacterial substances that play a vital role in digestion.
Salivary glands are divided into three groups: parotid glands, submandibular glands, and sublingual glands.The amount of saliva is decreased when salivary glands are not stimulated, and the major amount of saliva is contributed by minor salivary glands. Therefore, the correct answer is option B (Minor salivary glands).
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Briefly describe in one paragraph, how the
body eliminates
waste,
and list
the main body systems involved in this process.
The body eliminates waste through the process of excretion, which involves several main body systems.
The urinary system removes metabolic waste products, excess water, and electrolytes through the kidneys, which produce urine. The respiratory system eliminates carbon dioxide and small amounts of other waste gases through breathing.
The digestive system eliminates solid waste through the process of defecation. Additionally, the integumentary system plays a role in waste elimination through sweating, which removes certain toxins and regulates body temperature. Overall, these systems work together to maintain proper waste elimination and help maintain homeostasis in the body.
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Cladograms are scientific hypotheses that can be overturned by new data. True False Angiosperm plants did not appear until after the extinction of the dinosaurs. True False The definition of an analogous character is "a character that has a similar function to a character in a different organism, but these similarities are due to different evolutionary origins". True False In evolution, non-genetic changes that occur during an organism's life span, such as increases in muscle mass due to exercise and diet, cannot be passed on to the next generation. True False The definition of a monophyletic group is "a group of organisms that has a single ancestor and contains only some of the descendants of this unique ancestor". True False An ichnofossil is any part of the hard skeleton left behind by a vertebrate in the fossil record. True False
An ichnofossil is any part of the hard skeleton left behind by a vertebrate in the fossil record. This statement is false. An ichnofossil is a trace fossil, which is any indirect evidence of past life, such as tracks, burrows, and feces. It is not part of the hard skeleton left behind by a vertebrate.
Cladograms are scientific hypotheses that can be overturned by new data. This statement is true. Cladograms are diagrams that show the evolutionary relationship between organisms based on various traits. New data can cause changes to be made to cladograms which can result in a change to the interpretation of the evolutionary history of organisms.
Angiosperm plants did not appear until after the extinction of the dinosaurs. This statement is false. Angiosperms, also known as flowering plants, appeared in the fossil record at least 140 million years ago. Although the dinosaurs went extinct around 66 million years ago, angiosperms were already widespread and diversifying by that time.
The definition of an analogous character is "a character that has a similar function to a character in a different organism, but these similarities are due to different evolutionary origins". This statement is true. Analogous characters are traits that have evolved independently in different groups of organisms due to similar environmental pressures and not due to a shared ancestor.
In evolution, non-genetic changes that occur during an organism's life span, such as increases in muscle mass due to exercise and diet, cannot be passed on to the next generation. This statement is true. Non-genetic changes that occur during an organism's life span are not heritable and cannot be passed on to the next generation. Only genetic changes that occur in the germ cells, such as mutations, can be passed on to the offspring.
The definition of a monophyletic group is "a group of organisms that has a single ancestor and contains only some of the descendants of this unique ancestor". This statement is false. A monophyletic group is a group of organisms that has a single ancestor and contains all of the descendants of this unique ancestor. This group is also called a clade.
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For an estimation of microbial population experiment, you obtained the following results: A. 1000X dilution with 0.1 mL sample volume - 470 colonies B. 10000X dilution with 0.1 mL sample volume - 250 colonies C. 100000X dilution with 0.1 mL sample volume - 100 colonies D. 1000000X dilution with 0.1 mL sample volume −12 colonies For each set of results, determine if the samples are countable plates, and for only the countable plates, calculate the CFU/mL for those plates. For plates that are not countable, please state that and do not perform the calculation (please note that calculating the CFU/mL for a plate that is not countable will be marked as incorrect).
To measure the microbial population, the experiment counts the number of colonies on the plates. The conventional approach states that the countable plates are those with 30 to 300 colonies.
Using this criterion, we can see that plates A, B, and C are countable plates since they have 470, 250, and 100 colonies, respectively. Plate D is not countable since it has only 12 colonies.
To calculate the CFU/mL for each of the countable plates, we need to use the following formula:
CFU/mL = (number of colonies/sample volume) x (1 / dilution factor)
For plate A, the dilution factor is 1000X, and the sample volume is 0.1 mL.
Therefore, the CFU/mL = (470 / 0.1) x (1 / 1000) = 4.7 x 10^6 CFU/mL
For plate B, the dilution factor is 10,000X, and the sample volume is 0.1 mL.
Therefore, the CFU/mL = (250 / 0.1) x (1 / 10,000) = 2.5 x 10^5 CFU/mL
For plate C, the dilution factor is 100,000X, and the sample volume is 0.1 mL.
Therefore, the CFU/mL = (100 / 0.1) x (1 / 100,000) = 1 x 10^5 CFU/mL
Plate D is not countable, so we cannot calculate the CFU/mL for this plate.
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