Sentence examples for mutations shared by from inspiring English sources

That makes tracing mutations through the generations easier than looking at those genes that get mixed up by sex.In a study involving 640 people from nine Taiwanese tribes, Dr Trejaut and Dr Lin found three mutations shared by Taiwanese, Polynesians and Melanesians (who also speak Austronesian) which are not found in other Asians.

To find the gene on chromosome 12 that causes PARK8, an international collaboration of scientists, led by Jordi Perez-Tur from the Institute for Biomedicine, Valencia, Spain, Nick Wood at the Institute of Neurology, London, UK, and Andrew Singleton at the National Institute on Aging, Bethesda, Maryland looked for mutations shared by several Basque families in Spain.

In other words, we considered only mutations shared by the species pairs.

We found 1386 maximal patterns of mutations shared by at least 5 samples.

Indeed, two mutations shared by haplotypes H1 and H3 were associated with vertical transmission of HIV-1.

There were 6 pairs of affected brothers, and 7 different mutations shared by 2 or more unrelated individuals in the SCH DMD IQ study group.

On the basis of 19 Y chromosome biallelic loci, Su et al. (1999) estimate an age of 18,000 to 60,000 years for the O-M122T → C mutation shared by "Asian-specific" haplotypes H6 H8.

But a new study appearing online today in Science reveals a mutation shared by housecats and cheetahs, which may explain how the cat got its stripes or in this case, its blotches.

Twenty years after he first stumbled on FOP, Economides and his colleagues report today that the gene mutation shared by 97% of people with the disease can trigger its symptoms in a manner different than had been assumed through a single molecule not previously eyed as a suspect.

Thus, the probability that a given nucleotide position has an erroneous mutation shared by more than k isolates is.

Therefore, taken together, we defined a "nodal mutation" as a mutation shared by at least five sequences comprising at least 85% of the sequences within a given branch.