Sentence examples for mutation share from inspiring English sources

Variant late-infantile neuronal ceroid lipofuscinosis (vLINCL), caused by CLN6 mutation, and juvenile neuronal ceroid lipofuscinosis (JNCL), caused by CLN3 mutation, share clinical and pathological features, including lysosomal accumulation of mitochondrial ATP synthase subunit c, but the unrelated CLN6 and CLN3 genes may initiate disease via similar or distinct cellular processes.

Patients with GLUD1 or HADH mutation share further similarities in terms of being leucine sensitive.

Rescue models in both fields separating the contributions of SGV and de novo mutation share a number of common assumptions.

Genotypes that differ in a single mutation share, on average, more than 93% of their alternative phenotypes (C1 > 0.93).

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.

The first lesion exhibited 2 mutations where as the second one exhibited 3 with one identical mutation shared with M1 (A10995C, Fig. 2A B, matched color).

The lens cataract and myopathic muscle in mutant mice and humans with the αB-crystallin R120G mutation shared common pathological features and molecular mechanisms.

We found no mutation shared between tarsier and either New World monkeys or catarrhine primates; again, it is not possible to determine whether GC-D function was lost before these species diverged, or lost independently in all three lineages.

We did not observe any inactivating mutation shared between New World monkeys and catarrhine primates, and thus cannot determine whether GC-D was already non-functional in the simian ancestor, or whether function was lost independently in the two lineages.

The R273H mutation shared serine hydrolase pathway with R282W, but R175H did not show significant similarity with other mutations.