突变英语怎么说
Evidence of abrupt change — on a geological time scale — wrought by human hands would seem to be overwhelming.
In a bacterial population exposed to a killer drug, a few lucky individuals might have a genetic mutation that kept them alive.
To find out, they studied mice that were naturally obese because of a rare genetic mutation.
In some of the families, they found large chunks of missing DNA regions that followed that recessive rule.
The five key mutations could not be reversed first, because the receptor would be rendered useless.
They're not exactly antibiotic resistant, so they don't have any special drug-destroying mutations.
A disease caused by the presence of two recessive mutant genes on an autosome.
They just need to carry the recessive mutation. So it's not uncommon for white bears to be born to black parents.
It is also recessive and is more commonly exhibited in males, causing it to go undetected in many carriers, who may pass it on to future generations.
While most disease-causing mutated are found in humans at a rate of one in a few thousand to one in a few million people, founder mutation can occur at much higher rates.
Heritable mutations of ALAS2 gene are responsible for the human X-linked sideroblastic anemia.
Virus from one of the patients shows mutations at the receptor-binding site.
They discovered five additional mutations that were crucial to the transition.
Had a few, fateful mutations changed an innocuous chimp virus into a human killer?
That's because they aren't under selection, so they tend to accumulate mutations.
Variations of viruses are also similar to mutations, another factor in genetic algorithms.
Yet, sometimes, I like to think of myself as belonging to a kind of fellowship of mutations.
They did this by genetically modifying mice to make them prone to passing on genetic mutations.
Blood samples taken from the patient before taking entecavir had no M184V mutations in the HIV.
There are many different forms of the disorder, each caused by mutations in a different gene.
Mutations in genes governing cell growth and death can affect the anatomy of a region of cortex.
Founder mutations are a class of disease-causing genetic mutations, each derived from its own ancestral "founder" in whom the mutation originated.
Two of the encode mutations involved are also known to cause a rare disease called mucolipidosis.
Two of the mutations involved are also known to cause a rare disease called mucolipidosis.
The objective is to analyse the mutation of K17 gene in a pedigree with steatocystoma multiplex.