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What do you do if a testicle is damaged?
Hospital, or destroy both and help the gene pool get better
What is the main role of the AT gene?
to induce several cellular responses to DNA damage, such as preventing damaged DNA from being reproduced. When the AT gene is mutated into ATM, the signaling networks are affected and the cell no longer responds correctly to minimize the damage
Which mechanism might have affected the gene pools of the organism populations that remained in the areas damaged by the Exxon Valdez oil spill?
Genetic Drift
I am looking for a children's book about a baker with a pet mouse and the baker bakes a cake for the King but it get's damaged and the mouse helps the baker out?
"The Sugar Mouse Cake" by Gene Zion, published 1964.
Which is the worse a serious error in mRNA processing for a gene or a serious mutation in the gene for transfer rna?
a serious mutation in ribosomal RNA gene is worse. the mutated ribosomes may lose their abilty to bind to messenger RNAs through Shine Dalgarno Sequences. they may also present wrongly placed E,P and A sites to the messenger RNA. this will lead to lethal results ranging from abnormal polypeptide formation to no formation at all.
Which of the following can cause a mutation in a gene?
An error in the repair of damaged DNA-Apex
What nicknames does Gene Snisky go by?
Gene Snisky goes by Mean Gene, Gene Sinisky, Gene Snitsky, and The Foot Freak.
When was Gene Gene the Dancing Machine born?
Gene Gene the Dancing Machine was born in 1932.
What nicknames does Gene Patton go by?
Gene Patton goes by Gene Gene The Dancing Machine.
What gene controls the expression of the D1x gene in vertebrates?
The HOX gene or the master gene of D1x
When one gene expresses itself over another the former gene is said to be the DNA?
The gene that expresses itself over the other is Dominant. The former gene is recessive.
Is gene therapy bad?
During the last several years, we have witnessed "the best of times and the worst of times" in the embryonic field of gene therapy. Rapid advances in human genomic sciences, the development of novel mouse models of human diseases, and the construction and characterization of new vector systems for in vivo gene transduction have significantly expanded the potential feasibility of human gene therapy. On the other hand, the tragic events surrounding the gene therapy-related death of Jessie Gelsinger and subsequent revelations about additional unreported gene therapy-related complications have seriously damaged both the scientific credibility and public confidence in gene therapy. Given these recent events, this would seem to be an opportune time to pause and carefully reassess where we are and, more importantly, where we should be going in this promising but controversial field.
