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1) Determine what kind of DNA mutation in a gene would result in the production of a shorter version of a protein missing amino acids in the middle of the protein, but beginning and ending with the same amino acids found int he wild type protein?a) an anticodon mutationb) an insertion that adds a number of nucleotides that is some multiple ofthreec) a deletion that removes a number of nucleotides that is some multiple ofthreed) a frameshift mutatione) a nonsense mutation2) Which of the following domains is found in the GAL80 protein?a) DNA binding domainb) transcription activation domainc) GAL4 binding domaind) two of the abovee) all of the above3) A positive result in the Ames test indicates that the tested chemical is a mutagen. A positive testresults ina) break down of a mouse liver extractb) death of the mousec) production of bacterial auxotrophic mutant strainsd) reversion of a bacterial auxotrophic mutant straine) reversion of a bacterial prototrophic mutant strain4) The Fragile X syndrome is caused by trinucleotide repeat expansion. The repeated nucleotidesare CGG, and in affected individuals the CGG repeat region is found to be methylated at CpGresidues. Knowing this, which of these best describes the likely genetic behavior of Fragile XSyndrome?a) maternal effect lethalb) autosomal recessivec) X-linked recessived) X-linked dominante) autosomal dominant5) You are engaged in the study of a gene, the transcription of which is activated in muscle cells byglucocorticoid. From cultured muscle cells, you are able to isolate mutant cells in which the geneno longer responds to glucocorticoid. What is a possible explanations for why these cells nolonger resond to hormone?a) a nonsense mutation in these cells leading to production of a truncatedversion of RNA polymerase IIb) a gain-of-function mutation in these cells leading to production of aconstitutively active glucocorticoid receptorc) a mutation in these cells that deletes the glucocorticoid response elementfrom upstream of the target gened) a loss-of-function mutation in these cells leading to production of adefective enzyme required to synthesize glucocorticoide) none of the above
What techniques might be used to characterize the structure and composition of the structure. Which of the follow will the nurse include in her teaching plan for this patient.
Defend the stem cell v/s gene therapy with regard to the current treatment projections for the ALS.Recognize the Mimoun Azzouz and explain his work in gene therapy.
When a pea plant of genotype Aa Bb produces gametes, what proportion would be Ab? (Assume that the two genes are independent)
Your assignment, if you want to accept this, is to cross two of the F1 offspring and complete Punnett square for this cross and then write the resulting genotype and phenotypes. This must be 100 percent completely done for any extra credit. Your cros..
Discuss the types of drugs which might be expected to be ordered for the patient with a localized infection such as an infected vaginal laceration.
Assume you isolate a mutant e.coli strain that is unable to grow without tryptophan supplementation at 37 degrees C but grows normally at 25 degrees C.
A woman, age 36, had suffered from anorexia nervosa for 10 years and was admitted to the hospital for treatment. Her weight was about 60 percent of the ideal for her height
What is the probability that they will have a male child who is a hemophiliac. what is the possibility that he will be colour blind.
If you cross a black fur rabbit and a white fur rabbit, the resulting offspring look gray, when examining closely the fur of gray rabbit consist of both black and white hairs. What type of non-mendelian inheritance is this.
When the children of various such two-child families are totaled, what proportion of children in these families will show the phenotype.
Modify population equation Nt = Noe^rt such that Nt includes both males and females. Be sure to list any assumptions needed by your modification and explain why this new model works.
Suppose that the long ear lobes in humans is an autosomal dominant trait that exhibits 30 percent penetrance. A person who is heterozygous for long ear lobes mates with a person who is homozygous for normal ear lobes.
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