Sentence examples for mutation exhibit a from inspiring English sources

Mice heterozygous for the Brachyury T mutation exhibit a variable short-tailed phenotype [58] while other mutations such as Brachyury T137 have a kinked or bent tail [59].

Moreover, subjects bearing the R225W mutation exhibit a ∼90% increase of skeletal muscle glycogen content and a ∼30% decrease in intramuscular triglyceride (IMTG).

The gain-of-function allele hopTum-l encodes a constitutively active form of the Hopscotch (Hop) Janus kinase (JAK) and larvae carrying this mutation exhibit a melanotic tumor phenotype including extensive lamellocyte differentiation [14].

Conversely, mice heterozygous for the (PCD) mutation exhibit a slow but significant age-dependent decrease in Purkinje cell number, and importantly, without any detectable inflammation or reactive gliosis.

Consistent with the published data, embryos from females carrying any of these alleles in trans to a strong or null tube mutation exhibit a broad range of phenotypes, with a distinct phenotypic distribution for each allele.

Second, whereas patients with DDD and C3 glomerulonephritis not caused by CFHR5 mutation exhibit a wide variety of clinical features, often including nephrotic range proteinuria (Servais et al., 2007; Licht and Fremeaux-Bacchi, 2009), the clinical and histological features of CFHR5 nephropathy bear a remarkable and consistent similarity to those of IgA nephropathy.

Airway and intestinal epithelial cells from CF patients bearing the F508del-CFTR mutation exhibit an impressive derangement of cellular proteostasis, with oxidative stress, overactivation of the tissue transglutaminase (TG2), and disabled autophagy.

Mice that are homozygous for this mutation exhibit an embryonic lethal phenotype.

The proband carrying the deleterious MT1-I49N mutation exhibited a delayed sleep onset confirmed with actimetry.

For instance, negative interactions, such as synthetic lethal and sick pairs, are inferred when a double mutation exhibits a more severe phenotypic effect than expected [1], [39].

It was shown that actively contracting cardiomyocytes expressing GFP-myosin (green fluorescent protein fused to an embryonic myosin heavy chain) carrying the R403Q mutation, exhibited a significant decrease in organization of the contractile cytoskeleton of embryonic chicken cardiomyocytes [36].