What is fragile X-syndrome? What are the molecular events that
underlie it?

Answers

Answer 1

Fragile X syndrome is a genetic disorder that causes intellectual disability.

The underlying molecular events in fragile X syndrome is caused by a mutation in the FMR1 gene.

What is Fragile X syndrome?

Intellectual disability and other behavioral or developmental difficulties are common effects from fragile x syndrome's genetic disorder. It tends to affect both genders equally, although males may display more severe symptoms overall than females do.

Fragile x mental retαrdation 1 (FMR1) gene holds its primary responsibility for molecular conditions behind this syndrome.

The gene is found located on the X chromosome, carrying specific DNA sequences that experience repeat expansion where CGG trinucleotide enlargement frequently occurs across those with diagnosis of this condition.

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Related Questions

Given the value proposition "A device for managing
insects in rice farms without the use of toxic chemicals", who are
the implied customers and what are the implied benefits?

Answers

the implied customers would benefit from adopting this device through sustainable and environmentally conscious farming practices, enhanced crop quality and yield, safer food production, potential cost savings, and improved worker health and safety.

The implied customers for the device for managing insects in rice farms without the use of toxic chemicals are likely rice farmers or agricultural professionals involved in rice farming. The device targets individuals or organizations involved in rice production and pest management.

The implied benefits of the device can include:

1. Environmentally Friendly: The device offers an alternative to the use of toxic chemicals, indicating that it promotes environmentally friendly practices in rice farming. It helps reduce the negative impact of chemical pesticides on the ecosystem, including soil, water, and non-target organisms.

2. Sustainable Farming: By eliminating the need for toxic chemicals, the device aligns with sustainable farming practices. It enables farmers to adopt pest management strategies that are less harmful to the environment, maintaining the long-term health of the rice fields.

3. Safe Food Production: Using the device helps ensure the production of safer, chemical-free rice. It addresses concerns related to pesticide residues on rice grains, promoting food safety for consumers.

4. Cost-Effective: The device may offer cost savings by reducing the reliance on expensive chemical pesticides. By providing an alternative method for insect management, it can help farmers optimize their expenses and potentially improve profitability.

5. Improved Crop Quality and Yield: Effective insect management can contribute to better crop quality and yield. By using this device, farmers can mitigate the damage caused by insects, leading to healthier rice plants and increased productivity.

6. Reduced Health Risks: The device's focus on non-toxic insect management implies a reduced risk to the health of farmers and workers involved in rice farming. It helps create a safer working environment by minimizing exposure to harmful chemicals.

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Can you simplify and summarize the meaning of shortsighted
evolution hypothesis with examples. Please help me understand this
topic hope you can explain it clearly.

Answers

The shortsighted evolution hypothesis, also known as the "Red Queen hypothesis," suggests that in a changing environment, organisms must constantly adapt and evolve in order to survive and reproduce.

This hypothesis is based on the idea that species must continuously evolve just to maintain their current fitness levels relative to other species they interact with. It implies that evolutionary changes are driven by interactions and competition between species, rather than simply adapting to the environment.

For example, in the predator-prey relationship between cheetahs and gazelles, as cheetahs evolve to become faster and more efficient hunters, gazelles must also evolve to become faster and more agile to avoid predation. This constant adaptation and counter-adaptation create a "evolutionary arms race" between the two species.

Another example is the coevolution between parasites and their hosts. Parasites evolve strategies to exploit their hosts, such as developing drug resistance, while hosts evolve defenses to combat the parasites, like immune system adaptations.

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All the following about telomerase and telomeres are true except: there is no telomerase activity in somatic cells. the telomerase enzyme carries an RNA template. telomerase adds RNA nucleotides to the lagging strand. O telomere length and age-at-death appear to be correlated. human telomeres are repeats of 6 nucleotides. Question 10 1 pts Which of the following statements about DNA replication is correct? Does not require a primer to replicate the leading strand. The lagging strand is synthesised discontinuously in the 5' to 3' direction. Proceeds in one direction from the origin of replication. Topoisomerase unwinds and separates the parental DNA strands. O Uses DNA ligase to form the H-bonds holding the two complementary strands together.

Answers

All the following about telomerase and telomeres are true except there is no telomerase activity in somatic cells.The statement, “there is no telomerase activity in somatic cells” is false as somatic cells, due to the constant cell division they undergo, need telomerase to prevent shortening of telomeres. The rest of the given statements are true regarding telomerase and telomeres:Telomerase carries an RNA template.Telomerase adds RNA nucleotides to the lagging strand.Telomere length and age-at-death appear to be correlated.Human telomeres are repeats of 6 nucleotides.The correct statement about DNA replication is - Proceeds in one direction from the origin of replication.DNA replication is a process by which a cell duplicates its DNA and replicates it. This is an important process during the cell division as each daughter cell needs to have an exact copy of the genetic material of the parent cell. During DNA replication, DNA polymerase moves along the parental DNA and creates a new strand of DNA that is complementary to the parental DNA molecule. It proceeds in one direction from the origin of replication.Topoisomerase unwinds and separates the parental DNA strands, and Uses DNA ligase to form the H-bonds holding the two complementary strands together. DNA polymerase can only add nucleotides in the 5' to 3' direction, so it replicates the leading strand continuously but has to replicate the lagging strand discontinuously in the 5' to 3' direction and then uses DNA ligase to seal the gaps to form a continuous strand. It requires a primer to replicate the leading strand.

Help
2. What is the advantage of using Sabouraud agar?

Answers

The advantage of using Sabouraud agar is it relatively easy to prepare, has higher yield rate than other fungal growth media, will change colour as the pH changes, and can differentiate between fungal species.

Sabouraud agar is a selective and differential medium used for fungal growth, it has a distinct composition with lowered pH that inhibits bacterial growth and improves fungal growth. One of the advantages of using Sabouraud agar is that it's relatively easy to prepare and relatively inexpensive. Secondly, it has a higher yield rate than other fungal growth media, which is why it is commonly used for clinical specimen cultures. Sabouraud agar can also be used for the isolation and identification of fungi from food, water, soil and other materials, this is due to the fact that it has a high degree of sensitivity and specificity.

Another advantage is that the pH indicator of Sabouraud agar will change colour as the pH changes, which makes it easier for the detection of fungal colonies. Lastly, it can differentiate between fungal species by the color and texture of their growth, which helps identify the type of fungal infection a patient has. So therefore the advantage of using Sabouraud agar is it relatively easy to prepare has higher yield rate than other fungal growth media, will change colour as the pH changes, and can differentiate between fungal species.

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which of the two if any does Digestion of food not occur? explain stomach or mouth?

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The digestion of food occurs in the stomach and mouth. Digestion is the process of breaking down large molecules of food into smaller molecules that can be absorbed and used by the body.

Digestion begins in the mouth, where the food is physically broken down by chewing and mixed with saliva, which contains enzymes that begin the chemical breakdown of carbohydrates.The stomach is the next stop in the digestive process. It is a muscular sac that mixes the food with stomach acid and enzymes to further break down the food into a liquid called chyme. The stomach also releases the hormone gastrin, which triggers the release of more digestive juices in the small intestine, where the majority of digestion and absorption take place.In conclusion, both the mouth and stomach are involved in the digestion of food. The mouth is where the process begins, with the mechanical and chemical breakdown of food, while the stomach continues the process by mixing the food with digestive juices to break it down further.

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Do we have to add a chemical to see the results for the urea
tubes? protein test
Yes
No

Answers

The urea tubes protein test is used to measure the concentration of protein in a patient's urine. There are two tubes: the protein test tube and the urea test tube.

The urea tube contains a chemical that reacts with urea, resulting in a color change. The protein test tube, on the other hand, contains a reagent that reacts with protein, resulting in a color change.The presence of protein in urine may be an indication of a variety of medical problems. These tests are used to detect and monitor these issues. As a result, it is essential to follow all of the test's instructions to achieve the desired outcome.

The chemical in the urea tube is used to make sure that the urea in the patient's urine is broken down so that the protein level can be determined accurately. In conclusion, we need to add a chemical to see the results for the urea tubes protein test. It is a critical part of the test, and if omitted, the results may not be accurate. a chemical is necessary to obtain the desired outcome.

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The vertical gaze center contains premotor neurons that project to lower motor neurons and interneurons in the abducens nucleus. True False

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The statement is false. The vertical gaze center does not contain premotor neurons that project to lower motor neurons and interneurons in the abducens nucleus.

The vertical gaze center, which is responsible for controlling eye movements in the vertical direction, does not directly contain premotor neurons that project to lower motor neurons and interneurons in the abducens nucleus. Instead, the vertical gaze center involves the integration of multiple brain regions and neural pathways.

The primary brain structure involved in vertical eye movements is the rostral interstitial nucleus of the medial longitudinal fasciculus (riMLF). The riMLF receives input from the superior colliculus, a midbrain structure involved in eye movements, and it projects to the oculomotor nucleus, which controls the extraocular muscles responsible for vertical eye movements. The abducens nucleus, on the other hand, primarily controls horizontal eye movements. Thus, there is no direct connection between the premotor neurons of the vertical gaze center and the lower motor neurons and interneurons in the abducens nucleus.

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Targeting an Antibiotic Resistance Gene using CRISPR-Cas9
The rise and spread of antibiotic resistance in bacteria are alarming because of the impact on the cost, complications, and outcomes of treatment. Of particular concern are resistant bacteria that cause hospital-acquired infections (HAIs). Enterococcus faecalis, a member of the intestinal normal microbiota, is now a leading cause these infections. This organism is an opportunist, meaning that if the normal microbiota population is disturbed (for example by antibiotic treatment), it proliferates and becomes pathogenic. The pathogenic strains usually exhibit larger than normal genomes, having acquired mobile genetic elements such as plasmids, transposons, or phages (viruses that infect bacteria). Some of these elements contain antibiotic resistance genes.
Now a collaborative research team from the University of Texas at Dallas and the University of Colorado is investigating the use of CRISPR-Cas9 for overcoming antibiotic resistance in E. faecalis. Recall that bacteria use the CRISPR-Cas system as a defense mechanism, protecting them against the foreign DNA of mobile gene elements. CRISPR-Cas9 consists of an endonuclease (Cas9) that uses a guide RNA (gRNA) to locate and cleave foreign double stranded DNA at a specific site. For example, if a phage injects its DNA into a bacterial cell, that cell uses its CRISPR-Cas9 system to identify and destroy that phage DNA. The system also creates "memory" so that the bacterial cell is protected against future encounters with that same type of phage. Scientists can manipulate the CRISPR-Cas9 system by inserting specific gRNAs to target the Cas9 endonuclease to exactly where they want it to go in a genome, a potential tool for gene silencing or editing.
The research team previously showed that drug resistant E. faecalis does not have an intact CRISPR-Cas system; it lacks the Cas9 component and is thus susceptible to the uptake of foreign DNA. Now the team has developed a novel way of getting a functional CRISPR-Cas9 into those organisms in an effort to rid them of their antibiotic resistance genes. They engineered a plasmid, inserting genes for CRISPR-Cas9 along with gRNA sequences that are homologous to a resistance gene for the antibiotic erythromycin. The engineered plasmid was then introduced into a donor strain of E. faecalis that has conjugation ability. The presence of the CRISPR-Cas9 in the donor strain makes it immune to acquiring foreign DNA. When the donor strain conjugated with the drug resistant E. faecalis strain, the resistant strain gained a copy of the engineered plasmid containing the modified CRISPR-Cas9 system. The CRISPR-Cas9 in that cell then targeted its erthromycin resistance gene.
The team was able to show that the introduced plasmid significantly reduced the resistance of the resistant E. faecalis to erythromycin, making it sensitive to this drug. The work indicates that it may be possible in the future to use conjugation delivery of CRISPR-Cas9 antimicrobials.
Rodrigues, M. et. al. 2019. Conjugative Delivery of CRISPR-Cas9 for the Selective Depletion of Antibiotic-Resistant Enterococci. Antimicrob Agents Chemother. 63(11). pii: e01454-19.
Why is the genome of pathogenic Entercoccus aerogenes slightly larger than that of their nonpathogenic counterparts?
a. Pathogenic strains of Enterococcus have a CRISPR-Cas9 cassette and this makes them larger.
b. Pathogenic Entercoccus strains make the enzyme Dicer, so have an additional gene for this enzyme.
c. Pathogenic strains have acquired extra DNA in the form of a mobile genetic element (MGE).
d. Pathogenic strains do not have a larger genome; they have a double copy of their single chromosome.
e. Pathogenic strains of any bacterium are larger than nonpathogenic strains, and have larger genomes.

Answers

Pathogenic strains have acquired extra DNA in the form of a mobile genetic element (MGE).

The correct option to the given question is option c.

The genome of pathogenic Enterococcus aerogenes is slightly larger than that of their nonpathogenic counterparts because pathogenic strains have acquired extra DNA in the form of a mobile genetic element (MGE).

In particular, some of these elements contain antibiotic resistance genes. The pathogenic strains usually exhibit larger than normal genomes, having acquired mobile genetic elements such as plasmids, transposons, or phages (viruses that infect bacteria).

The acquisition of extra DNA in pathogenic strains makes it possible for them to proliferate and become pathogenic, especially if the normal microbiota population is disturbed, for example, by antibiotic treatment.Therefore,Pathogenic strains have acquired extra DNA in the form of a mobile genetic element (MGE).

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Research one genetic disorder, either something you have
experience with or something interesting, and discuss how it is
tied to meiosis. Include your understanding of how this disorder
occurs in the

Answers

One genetic disorder that is tied to meiosis is Down syndrome, also known as trisomy 21. It is caused by the presence of an extra copy of chromosome 21, which disrupts the normal chromosomal distribution during meiosis.

During meiosis, the process of cell division that produces gametes (sperm and eggs), chromosomes undergo recombination and segregation to create genetically diverse and haploid cells. However, in individuals with Down syndrome, there is an error in meiosis called nondisjunction, where chromosome 21 fails to separate properly. This results in one of the resulting gametes having two copies of chromosome 21 instead of one.

When a fertilized egg with an extra copy of chromosome 21 (trisomy) is formed, it leads to the development of Down syndrome. Individuals with Down syndrome typically exhibit physical characteristics such as distinct facial features, intellectual disabilities, and various health issues.

The occurrence of Down syndrome is directly linked to the abnormal distribution of chromosomes during meiosis, specifically the failure of proper separation of chromosome 21, resulting in an additional copy of this chromosome in the resulting offspring.

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What is the cause of the evolution of senescence according to the two evolutionary hypotheses (Mutation Accumulation and Antagonistic Pleiotropy)? a)mutations accumulate in individuals as they grow older, leading to senescence
b)mutations that have pleiotropic fitness effects are removed by selection
c)mutations that cause deleterious fitness effects late in life are effectively neutral
d)mutations that cause deleterious fitness effects late in life experience a strong "force of natural selection"

Answers

The Antagonistic Pleiotropy theory postulates that senescence results from the presence of mutations that have advantageous early-life effects but unfavourable late-life consequences.

The two evolutionary explanations for senescence provide the following descriptions of the causes: According to the hypothesis of mutation accumulation, as people age, they accumulate harmful mutations that lead to senescence. These mutations can remain and cause a reduction in fitness and ageing because natural selection is less successful at getting rid of mutations that have late-life effects. The Antagonistic Pleiotropy theory postulates that senescence results from the presence of mutations that have advantageous early-life effects but unfavourable late-life consequences. Because the advantages of these mutations early in life outweigh the disadvantages of senescence later, they are kept in the population. Therefore, the appropriate response is: a) as people age, mutations increase, leading to senility

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1. In both the male and female cath, identify structures that hure a urogcritil function. a. Male cat b. Fernale cat QUESTIONS 2-11: Match the cat teproductive structure in columin A with the apeopeia

Answers

In the male cat the urethra and the pe.nis have a urogenital function, while in the female cat, the va.gina has a urogenital function.

What organs have a urogenital structure?

Organs have a urogenital structure if they are important for both the reproductive and the urinary systems:

The urethra, and pe.nis: These organs are important for the transportation of spermatozoids in the reproductive system but also for the transportation of urine.Va.gina:  Similar to the urethra this structure has a reproductive purpose but also allows the urine to be transported out of the body.

Note: Here is the complete question:

In both the male and female cath, identify structures that have a urogenital function.

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no explanation needed pls answer
quick.
Answer all short answer questions and the essay DQuestion 23 Crossing over occurs between..... Sister chromatids during prophase 1 of mitosis O Sater chromatics during prophase I of meiosis O Non-sist

Answers

Crossing over occurs between sister chromatids during prophase 1 of mitosis (option a).

Crossing over occurs during prophase 1 of meiosis. It is the exchange of genetic material between non-sister chromatids of homologous chromosomes. During meiosis, two rounds of cell division occur which produces haploid cells. During prophase 1 of meiosis, crossing over occurs between non-sister chromatids of homologous chromosomes. During this stage, the two homologous chromosomes exchange genetic material. This process leads to the creation of new combinations of genetic material and increases genetic diversity. The correct option is: Sister chromatids during prophase I of meiosis

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Examine this pedigree for a rare human disease and determine the most likely mode of inheritance. If person II-3 and person III-1 had a child, what would be the probability of that child having the disease? a) zero chance b) 1/4 c) 100 percent d) 1/2

Answers

Based on the pedigree, the most likely mode of inheritance for the rare human disease is autosomal recessive.

In an autosomal recessive inheritance pattern, individuals need to inherit two copies of the disease-causing allele (one from each parent) in order to express the disease. In this pedigree, individuals II-3 and II-4 are unaffected but both carry one copy of the disease-causing allele, making them carriers. Their child, III-1, expresses the disease, indicating that both II-3 and II-4 must have passed on their disease-causing alleles to III-1.If person II-3 and person III-1 were to have a child, the probability of that child having the disease would be 1/4 or 25 percent. This is because person II-3 is a carrier (heterozygous) and person III-1 is affected (homozygous recessive). When they have a child, there is a 25 percent chance that the child will inherit two copies of the disease-causing allele and therefore express the disease. The other possible outcomes include a 50 percent chance of the child being a carrier like II-3 or a 25 percent chance of the child being unaffected.

It's important to note that this probability assumes that both II-3 and III-1 are correctly identified as carriers and affected, respectively, based on their phenotypes and genetic testing.

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41​The site of the formation of the primary structure for protein synthesis in animal cells is the
a) mitochondrion​b) nucleus​c) SER ​d) RER​​e) vacuole
42. ​Phospholipids can form all of the following structures in water except which one?
a) cell membranes​ b) bilayers​c)nuclear membranes ​d) vesicles​e) Bones cell membranes

Answers

The site of the formation of the primary structure for protein synthesis in animal cells is the ribosome. The site of the formation of the primary structure for protein synthesis in animal cells is the ribosome.

Ribosomes, the site of protein synthesis in cells, are composed of two subunits that are unequal in size. Both ribosomal subunits contain ribosomal RNA (rRNA) molecules and a number of ribosomal proteins that help to maintain the structure and function of the ribosome.
Therefore, option D is the answer.
Phospholipids can form all of the following structures in water except bones cell membranes. Phospholipids are the main structural component of cell membranes in living organisms. When in contact with water, these amphipathic molecules spontaneously self-organize into a bilayer to form a cell membrane. The two layers of a bilayer have opposing orientations of the phospholipid molecules that create a hydrophobic interior sandwiched between two hydrophilic surfaces.
They can also form vesicles or liposomes when a bilayer spontaneously closes to create an isolated compartment. However, bones cell membranes is not a structure that can be formed by phospholipids in water.
Therefore, option E is the answer.

Ribosomes are the site of the formation of the primary structure for protein synthesis in animal cells, while phospholipids can form all of the following structures in water except bones cell membranes.

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Question 1
The difference between a nucleoside and a nucleotide is that
A. nucleotides contain a different sugar compared to nucleosides.
B. the bases in nucleotides are attached to sugars at different carbons compared to nucleosides.
C. nucleosides are used to synthesize DNA, whereas nucleotides are used to synthesize RNA.
D. nucleotides contain one or more phosphate groups, whereas nucleosides have none.
E. nucleosides contain purine bases, whereas nucleotides contain pyrimidine bases.
Question 3
Which statement is true regarding the relationship between replication and transcription of DNA?
A. Replication requires both a template and a primer, whereas transcription requires only a template.
B. The polymerases for both require a Mn2+ cofactor for activity.
C. Copies of both DNA strands are made during both processes.
D. Both have extensive processes to correct errors.
E. Both utilize the same nucleotides.
Question 5
In eukaryotes, nucleosomes are formed by binding of DNA and histone proteins. Which of the following is NOT true regarding histone proteins?
A. H1 functions as a monomer
B. Histone proteins have five major classes: H1, H2A, H2B, H3, and H4
C. Positively coiled DNA is wrapped around a histone core to form nucleosome
D. H1, H2A, H3 and H4 form the nucleosome histone core.
E. They are found in the nucleus.

Answers

Question 1:
Nucleosides are compounds composed of a nitrogenous base and a sugar, but without the phosphate group. Nucleotides, on the other hand, contain all three: nitrogenous base, sugar, and phosphate group. Hence, the difference between a nucleoside and a nucleotide is that nucleotides contain one or more phosphate groups, whereas nucleosides have none. The correct option is D.

Question 3:
Replication requires both a template and a primer, whereas transcription requires only a template. This statement is true regarding the relationship between replication and transcription of DNA.Question 5:
H1 functions as a monomer is the option that is NOT true regarding histone proteins. The histone proteins are proteins that help to package the DNA into the nucleus of the cell. They are found in the nucleus, and the DNA is wrapped around a histone core to form nucleosome. The histones are the major protein component of chromatin. Histone proteins have five major classes: H1, H2A, H2B, H3, and H4, and H1, H2A, H3 and H4 form the nucleosome histone core. The positively coiled DNA is wrapped around a histone core to form nucleosome.

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What are the infective stage and diagnostic stages for the following diseases?
1. Giardia Lamblia.
2. Leishmania.
3. Ascaris lumbricoides.
4. Toxoplasma Gondi.
5. african trypanosomiasis.
6. Chagas disease.
7. Trichomoniasis Vagainalis.
8. Malaria.
9. Hookworms.
10. Enterobiasis.
11. Entermba Histolatika

Answers

1. Giardia Lamblia: Infective stage - Cyst; Diagnostic stage - Trophozoite.

2. Leishmania: Infective stage - Promastigote; Diagnostic stage - Amastigote.

Certainly! Here are the infective stages and diagnostic stages for the mentioned diseases:

1. Giardia Lamblia:

  - Infective Stage: Cyst

  - Diagnostic Stage: Trophozoite

2. Leishmania:

  - Infective Stage: Promastigote

  - Diagnostic Stage: Amastigote

3. Ascaris lumbricoides:

  - Infective Stage: Eggs

  - Diagnostic Stage: Adult worm

4. Toxoplasma gondii:

  - Infective Stage: Oocyst

  - Diagnostic Stage: Tissue cyst

5. African trypanosomiasis (Sleeping sickness):

  - Infective Stage: Metacyclic trypomastigote

  - Diagnostic Stage: Bloodstream trypomastigotes, intracellular amastigotes

6. Chagas disease:

  - Infective Stage: Trypomastigote

  - Diagnostic Stage: Amastigote

7. Trichomoniasis vaginalis:

  - Infective Stage: Trophozoite

  - Diagnostic Stage: Trophozoite (observed in vaginal secretions or urine)

8. Malaria:

  - Infective Stage: Sporozoite

  - Diagnostic Stage: Merozoite

9. Hookworms:

  - Infective Stage: Infective larvae (L3)

  - Diagnostic Stage: Adult worm, eggs in stool

10. Enterobiasis:

   - Infective Stage: Infective eggs

   - Diagnostic Stage: Adult pinworm or eggs on perianal swab or tape test

11. Entamoeba histolytica:

   - Infective Stage: Cyst

   - Diagnostic Stage: Trophozoite or cyst in stool sample.

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Deep nucleotide sequencing (NGS) is now cheap enough for general application. What can the technique mainly be useful for?
a. Quickly identifying new viruses
b. O speedy vaccine development
c. giving details on virus excretion in symptomless carriers
d. establishing the reproductive number of a virus

Answers

NGS (deep nucleotide sequencing) can mainly be useful for:

a. Quickly identifying new viruses.

c. Giving details on virus excretion in symptomless carriers.

A virus is an infectious submicroscopic creature that only reproduces inside of live cells. All living things, including plants, animals, and microbes like bacteria and archaea, are susceptible to virus infection. More than 11,000 of the millions of viral species have been characterised in detail since Dmitri Ivanovsky's 1892 publication revealing a non-bacterial disease infecting tobacco plants and Martinus Beijerinck's discovery of the tobacco mosaic virus in 1898. Viruses are the most common sort of living organism and may be found in practically all ecosystems on Earth. Virology is the study of viruses; it is a branch of microbiology.

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pitenesin 6. In this lab, we reviewed numerous fossil species and their defining characteristics. To help you make compari- sons across these species and understand larger trends in our evolutionary history, complete the Australopith and Early Homo Chart on pp. 446-447. AUSTRALOPITH AND EARLY HOMO CHART Fossil Species Dates and Geographic Region Cranial and Dental Traits Postcranial Traits Suggested Behavior Australopithecus anamensis Australopithecus afarensis LAB 15 | The Australopiths and Early Members of the Australopithecus africanus Australopithecus garhi Australopithecus sediba Australopithecus (Paranthropus) aethiopicus AUSTRALOPITH AND EARLY HOMO CHART (continued) Fossil Species Dates and Geographic Region Cranial and Dental Traits Postcranial Traits Suggested Behavior Australopithecus (Paranthropus) boisei Australopithecus (Paranthropus) robustus Australopithecus deyiremeda Homo habilis (including H. rudolfensis)
Previous question

Answers

In this lab, we have examined many fossil species and their defining characteristics. To help you make comparisons across these species and understand larger trends in our evolutionary history.

let us complete the Australopith and Early Homo Chart. The Australo pith and Early Homo Chart is a tabular presentation of some Australopith and Early Homo fossils. This chart allows you to make comparisons across these fossils, to identify some of their similarities and differences.

Understand some of the significant trends in the evolution of these hominins.The following is a sample of the Australopith and Early Homo Chart that we have completed in this lab: Fossil Species Dates and Geographic Region Cranial and Dental Traits Postcranial Traits Suggested Behavior Australopithecus anamensis .

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Which of the following statements about influenza replication
and exit is TRUE? (1.5 points)
High pH is a signal to release the viral genome into the
cytoplasm
Viral transcription and translation occ

Answers

The statement that is TRUE about influenza replication and exit are that viral transcription and translation occur in the nucleus.

During the replication and exit of the influenza virus, several important processes take place. Influenza viruses have a segmented genome consisting of multiple RNA segments. After the virus enters the host cell, it needs to replicate its genome and produce viral proteins for the assembly of new viral particles.

In the case of influenza, viral transcription and translation occur in the nucleus of the host cell. The viral RNA segments are transcribed into messenger RNA (mRNA) by the viral RNA polymerase. These viral mRNAs are then transported out of the nucleus into the cytoplasm, where they undergo translation to produce viral proteins.

Once the viral proteins are synthesized, they are transported back into the nucleus, where viral genome replication takes place. The replicated viral RNA segments are then exported from the nucleus to the cytoplasm, where they associate with the newly synthesized viral proteins to form new viral particles.

Therefore, the statement that viral transcription and translation occur in the nucleus is true, highlighting an essential step in the replication and exit of the influenza virus.

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Tachycardia with marked rise of blood pressure occur after administration of : Select one O a. Isoprenaline b. Noradrenaline O c. Dobutamine d. Adrenaline d e. Atropine

Answers

Tachycardia with a marked rise in blood pressure is observed when adrenaline is administered. Adrenaline is a naturally occurring hormone, also known as epinephrine.

That plays a vital role in the fight or flight response in the body.Tachycardia, an abnormally high heart rate, and hypertension, or high blood pressure, are among the possible side effects of the drug administration. Adrenaline is a medication that is often used in emergency situations.

The medication is administered by injection, and the dosage is determined by the patient's weight, the severity of their condition, and other factors. The medication stimulates beta receptors in the body, resulting in increased heart rate and constriction of blood vessels.

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list of bacteria for bacterial identification assignment Here is the the "list of suspects" for the bacterial identification assignment. Again, for the bacterial identification assignment, you will design a key that allows you to identify every bacteria on this list (i.e., they key should put EACH bacteria on the list into a group all by itself). Use the same approach you used in the "building your key" exercise that you worked on over the last 2-3 weeks and turned in last friday. Bacillus cereus Citrobacter freundii Clostridium Enterobacter aerogenes Enterococcus (Streptococcus) faecalis Escherichia (E.) coli Lactococcus (Streptococcus) lactis Mycobacterium Proteus vulgaris Proteus mirabilis Serratia marcescens Staphylococcus epidermidis

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In the list of bacteria for bacterial identification assignment, Bacillus cereus is an aerobic spore-forming bacterium that is gram-positive. They may be found in soil, air, water, and some foods. Citrobacter freundii is an opportunistic pathogen that is gram-negative and has peritrichous flagella.

Clostridium is a gram-positive bacterium that produces an endospore. Enterobacter aerogenes is a gram-negative bacterium that is opportunistic and may cause healthcare-associated infections. Enterococcus (Streptococcus) faecalis is a gram-positive bacterium that is a commensal of the gastrointestinal tract, but may also cause healthcare-associated infections.

Escherichia coli is a gram-negative bacterium that is a normal constituent of the gut flora but can also cause urinary tract infections. Lactococcus (Streptococcus) lactis is a gram-positive bacterium used in the dairy industry.

Mycobacterium is an acid-fast bacterium that is difficult to stain with the Gram method. Proteus vulgaris is a gram-negative bacterium that is rod-shaped and mobile. Proteus mirabilis is a gram-negative bacterium that is rod-shaped and mobile.

Serratia marcescens is an opportunistic bacterium that is gram-negative and has a prodigious pigment that gives it a reddish-orange hue. Staphylococcus epidermidis is a gram-positive bacterium that is a commensal of the skin, but can also cause healthcare-associated infections.

Thus, the list of bacteria for the bacterial identification assignment is as follows:

Bacillus cereus, Citrobacter freundii, Clostridium, Enterobacter aerogenes, Enterococcus (Streptococcus) faecalis, Escherichia (E.) coli, Lactococcus (Streptococcus) lactis, Mycobacterium, Proteus vulgaris, Proteus mirabilis, Serratia marcescens, and Staphylococcus epidermidis.

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Which of the following is an incorrect statement about "calories"?
a. All one needs to know to accurately calculate one's daily calorie needs is knowledge of their sex and their weight. b. Two hundred calories from an avocado (which offers healthy fats and other nutrients) can be a better choice than eating 100 calories of deli meat. c. Fiber helps to slow the absorption of sugar. d. Healthy eating and drinking choices is about more than calories.
e. A zero-calorie pop/soda, for example, might also provide zero nutrients, and come packed with artificial sweetners. f. Consuming 100 calories in the form of an apple will provide a more "full" feeling than drinking 100 calories of pop/soda/Red Bull, etc.

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An incorrect statement about "calories" is: a. All one needs to know to accurately calculate one's daily calorie needs is knowledge of their sex and their weight.

Option (a) is the incorrect statement. While sex and weight are important factors in estimating daily calorie needs, they are not the sole factors. Other variables, such as age, height, activity level, and metabolic rate, also play a significant role in determining individual calorie requirements. Therefore, relying solely on sex and weight to calculate daily calorie needs would not provide an accurate estimation.

Options (b), (c), (d), (e), and (f) are all correct statements about calories. Option (b) highlights that the nutrient content and overall health benefits of food should be considered along with calorie content. Option (c) emphasizes the role of fiber in slowing down sugar absorption, which is important for managing blood sugar levels. Option (d) acknowledges that healthy eating is not solely about calorie intake but also about nutrient quality and overall dietary choices. Option (e) points out that zero-calorie beverages may lack nutrients and contain artificial sweeteners. Option (f) highlights the difference in satiety and fullness between consuming calories from different sources, such as whole foods versus sugary beverages.

Therefore, option (a) is the incorrect statement among the given options.

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Explain the common cold and flu of viral origin.
Explain the disease caused by the varicella-zoster virus
Explain the disease measles, mumps and rubella

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Common cold and flu are respiratory illnesses caused by viral infections, with the common cold usually caused by rhinoviruses and the flu by influenza viruses. Varicella-zoster virus causes chickenpox (varicella) and later reactivates as shingles (herpes zoster).

Measles, mumps, and rubella are viral infections with distinct symptoms, with measles causing fever and a characteristic rash, mumps affecting the salivary glands, and rubella causing a rash and posing risks to pregnant women.

Common Cold and Flu:

The common cold and flu are both respiratory illnesses caused by viral infections. The common cold is usually caused by rhinoviruses, while the flu is caused by influenza viruses. These viruses are highly contagious and primarily spread through respiratory droplets when an infected person coughs, sneezes, or talks.

Varicella-Zoster Virus (VZV) Disease:

The varicella-zoster virus causes two distinct diseases. The primary infection results in chickenpox, also known as varicella. Chickenpox is highly contagious and spreads through direct contact or respiratory droplets. It is characterized by a blister-like rash, itching, fever, and general malaise.

Measles, Mumps, and Rubella:

Measles, mumps, and rubella are all viral infections that can cause distinct diseases. Measles, caused by the measles virus, is highly contagious and spreads through respiratory droplets.

Mumps, caused by the mumps virus, is also highly contagious and spreads through respiratory droplets or direct contact with infected saliva. It affects the salivary glands, leading to swelling and pain in the cheeks and jaw.

Rubella, caused by the rubella virus, is generally a mild infection but can have severe consequences if contracted by pregnant women. It spreads through respiratory droplets and causes a rash, low-grade fever, and swollen lymph nodes.

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1. Which (TWO) of the following bones would you NOT use to kick a soccer ball?
fibula humerus metacarpals metatarsals patella phalanges tarsals tibia
2. Someone has a "cervical" injury. Is this an injury to the spine in their neck, upper back, or lower back?
3. Which of the three joints affords the most range of motion?

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1) The bones you would not use to kick a soccer ball are the humerus and metacarpals.

2) A "cervical" injury refers to an injury to the spine in the neck region.

3) The joint that affords the most range of motion is the ball-and-socket joint.

1) The bones you would not use to kick a soccer ball are the humerus and metacarpals. The humerus is the bone of the upper arm, and the metacarpals are the bones in the hand. These bones are not directly involved in the kicking motion.

2) A "cervical" injury refers to an injury to the spine in the neck region. The cervical spine consists of the vertebrae in the neck area, and an injury to this region can affect the neck and potentially extend to the upper back.

3) The joint that affords the most range of motion is the ball-and-socket joint. This type of joint allows for movement in multiple directions, including flexion, extension, abduction, adduction, and rotation. Examples of ball-and-socket joints in the human body are the shoulder joint and the hip joint. These joints provide a wide range of motion compared to pivot joints.

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Which of the following is NOT a role of the kidneys? * 1 point regulates ion balance rids the body of metabolic waste egestion of nitrogenous wastes regulates water balance secretion of hormones involved in the production of RBCs Urea is produced * * 1 point by the liver in every cell of the body when amino acids are dephosphorylated by the kidneys by birds and reptiles

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The kidneys are the pair of organs that perform a variety of important functions that are important for a healthy body. The primary roles of kidneys are the regulation of water balance, maintenance of acid-base balance, regulation of blood pressure, filtration of waste products from the body, and production of urine.

The kidney's main job is to filter the blood to remove excess waste products and fluids from the body.

The following functions are performed by the kidneys except for the secretion of hormones involved in the production of red blood cells.

Erythropoietin is a hormone that regulates the production of red blood cells in the body, and it is produced by the kidneys.

Kidneys regulate the body's ion balance by filtering the blood.

Kidneys remove metabolic waste products such as urea, uric acid, and creatinine from the body. Kidneys are involved in the egestion of nitrogenous wastes, which include excess urea, uric acid, and creatinine.

Kidneys are involved in regulating the water balance of the body by regulating the concentration of urine and maintaining blood pressure.

Urea is produced by the liver in every cell of the body when amino acids are dephosphorylated. Urea is a waste product that is filtered by the kidneys.

Birds and reptiles excrete nitrogenous waste products in the form of uric acid rather than urea, which is the case in mammals. Hence, this is not a role of the kidneys.

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Which variable rises after capillary beds?
a. Blood pressure
b. Blood vessel area
c. blood velocity
d. blood volume

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A blood velocity After capillary beds, the blood velocity of the blood rises because of the following reasons. After capillary beds, blood velocity increases. Explanation:Capillaries are the smallest and the thinnest vessels in the human body. These vessels play a vital role in the body as they help in the exchange of various substances such as nutrients, waste, and oxygen. It connects the arterial and venous systems.

The narrowing of the capillaries from tiny vessels increases the resistance of the flow of blood. This then leads to a drop in blood pressure and an increase in blood velocity.The sum of the cross-sectional area of the capillaries is bigger than the cross-sectional area of the arteries and veins; this means that the blood that flows in the capillaries moves at a much slower pace than the blood that flows in the arteries and veins.

This causes a drop in the speed of blood flow, thus leading to a rise in blood velocity.Along with blood velocity, the blood pressure and blood volume may also change after capillary beds. Blood pressure decreases after capillary beds while the blood vessel area and blood volume vary depending on the situation or condition.

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9. Which of the following sunlight classes of UV radiation has the shortest wavelength? a) UVA b) UVB c) UVC d) UVD 10. Human Papillomavirus is the main cause of _____.
a) testicular cancer b) cervical cancer c) breast cancer d) hepatocarcinoma 11. The phenomena in which the integration of viral DNA into host chromosome that cause activation or disruption of a normal gene is known as ______.
a) insertional mutagenesis b) proliferating mutagenesis c) transforming mutagenesis d) constitutive mutagenesis

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UVC has the shortest wavelength among the sunlight classes of UV radiation. Cervical cancer is mainly caused by Human Papillomavirus (HPV). The underlying mechanism is thought to be insertional mutagenesis, a process by which there is an integration of viral DNA into the host chromosome that causes activation or disruption of the normal host gene.

Among the sunlight classes of UV radiation, UVC has the shortest wavelength. UVA has the longest wavelength, followed by UVB and then UVC.

Human Papillomavirus (HPV) is the man causative agent of cervical cancer. HPV is a sexually transmitted infection that can lead to the development of abnormal cervical cells, which, if left untreated, can progress to cervical cancer. It is important for individuals, particularly females, to undergo regular screening tests, such as Pap smears and HPV testing, to detect and prevent cervical cancer.

The phenomenon in which viral DNA integrates into the host chromosome and causes activation or disruption of a normal gene is known as insertional mutagenesis. Viral DNA can insert itself into the host genome and affect the expression and function of genes.

This integration can lead to genetic changes that contribute to the development of various diseases, including certain types of cancer. Insertional mutagenesis is a mechanism through which viruses can alter the normal functioning of host cells and potentially drive cellular transformation.

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28. In Chapter 12, we discussed different tests/assays we could use to identify the microbe(s) causing an infection in a host. Please describe one of these methods (or use your own example) and report (1 sentence/term):
a) The name of the method and how it works:
b) A type of control sample (either positive or negative control) you can run with your sample:
c) A false positive or false negative result that could occur when you run each assay:

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The method described is Polymerase Chain Reaction (PCR), a molecular technique used to amplify specific DNA sequences. PCR involves a series of temperature cycles that allow DNA replication to occur in vitro.

It starts with denaturation, where the DNA strands are separated by heating. Then, primers specific to the target DNA sequence are annealed to the separated strands. Next, DNA polymerase extends the primers, synthesizing new DNA strands. This process of denaturation, annealing, and extension is repeated multiple times, resulting in the exponential amplification of the target DNA sequence if present.

A positive control sample that can be run alongside the test sample is a known sample containing the target DNA sequence of the microbe being tested. This positive control should yield a positive result, confirming that the PCR assay is working correctly and capable of detecting the target DNA sequence.

False positive results in PCR can occur if there is contamination in the laboratory. Contaminating DNA, such as stray DNA from previous experiments or reagents, can be amplified, leading to a positive signal even in the absence of the target microbe. False negatives, on the other hand, can occur if the primers used in the PCR assay do not match the DNA sequence of the microbe causing the infection. If the primers fail to bind to the target DNA, amplification will not occur, resulting in a negative result despite the presence of the microbe.

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Chain Reactions Linking Acorns to Gypsy Moth Outbreaks and Lyme Disease Risk Oak trees (Quercus spp.) produce large autumnal acorn crops every two to five years, and produce few or no acorns during intervening years. Acorns are a critical food for white-footed mice (Peromyscus leucopus). Mice are important predators of the pupal stage of the gypsy moth (Lymantria dispar). This introduced insect periodically undergoes outbreaks that defoliate millions of hectares of oak forests, decreasing tree growth, survival, and acorn crop production. An abundance of acoms provides food for white-tailed deer (Odocoileus virginianus). Mice and deer are the primary hosts of the black-legged tick (Ixodes scapularis), which carries Lyme disease.

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The chain of events linking acorns to gypsy moth outbreaks and Lyme disease risk can be summarized as follows:

1. Acorn Production: Oak trees produce large acorn crops every two to five years, with intervening years having few or no acorns.

2. White-Footed Mice: Acorns are a critical food source for white-footed mice. During years with abundant acorn production, the mouse population increases due to the availability of food.

3. Gypsy Moth Predation: White-footed mice play a crucial role in controlling gypsy moth populations. They are important predators of the pupal stage of the gypsy moth.

4. Gypsy Moth Outbreaks: The gypsy moth, an introduced insect, periodically undergoes outbreaks. During these outbreaks, the gypsy moth larvae defoliate millions of hectares of oak forests. This defoliation can have detrimental effects on tree growth, survival, and acorn crop production.

5. Deer and Acorns: An abundance of acorns provides a food source for white-tailed deer. Deer play a role in dispersing acorns and can consume large quantities when they are available.

6. Tick Hosts: Both white-footed mice and white-tailed deer are primary hosts for the black-legged tick, also known as the deer tick (Ixodes scapularis). These ticks are responsible for transmitting Lyme disease.

7. Lyme Disease Risk: The black-legged tick carries the bacterium that causes Lyme disease. When ticks feed on infected hosts, such as white-footed mice and white-tailed deer, they can acquire the bacterium. Subsequently, these ticks can transmit the bacterium to humans when they bite.

The chain reaction begins with the production of acorns by oak trees, which supports an increase in the population of white-footed mice. These mice, in turn, prey on gypsy moth pupae, helping to control gypsy moth populations. However, when gypsy moth outbreaks occur, they can defoliate oak forests and impact tree health and acorn production. Abundant acorns also attract white-tailed deer, which are hosts for black-legged ticks carrying Lyme disease. Thus, the interconnectedness of these factors contributes to the risk of Lyme disease transmission to humans.

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If crossing over occurred in one cell and not another, how would the two cells compare?
A. Crossing over would have no effect on either cell.
B. Crossing over would increase the genetic diversity in one of the cells.
C. Crossing over would increase the chromosome number in one of the cells.
D. Crossing over would decrease the chromosome number in one of the cells.
E. Crossing over would cause one of the cells to stop dividing.

Answers

If crossing over occurred in one cell and not another, the two cells would have different genetic compositions.

Option B, "Crossing over would increase the genetic diversity in one of the cells," is the correct answer. Crossing over introduces new combinations of alleles by shuffling genetic material between the homologous chromosomes. This process promotes genetic diversity in offspring, as it creates novel combinations of genes that were not present in the parent cells. Options A, C, D, and E are not accurate in this context. Crossing over does have an effect on cell genetics, it does not affect the chromosome number, it does not decrease the chromosome number, and it does not cause one of the cells to stop dividing.

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