Significados de genetic modifier en inglés

Severity rate phenotypes were also assessed as potential phenotypes for genetic modifier studies.

Cats can be identified as fast and slow progressors, thus, could assist with genetic modifier discovery.

Maestro maps to a region of mouse chromosome 18 containing a genetic modifier of XX sex reversal.

Conclusions: Our results provide the first demonstration, to our knowledge, of a risk-conferring genetic modifier in a large LQTS cohort.

A number of genetic modifier loci of Min have been mapped, but so far most of the underlying genes have not been identified.

Interpretation: SIPA1L2 is a potential genetic modifier of CMT1A phenotypic expressions and offers a new pathway to therapeutic interventions.

We undertook a chemical genetic modifier screen to identify small molecules that suppress the ability of FK506 to inhibit yeast growth in high NaCl.

This finding suggests that RAD51 is a genetic modifier of breast cancer risk in BRCA1 carriers in the Polish population.

We investigated whether TMEM106B is also a genetic modifier of disease in carriers of chromosome 9 open reading frame 72 (C9ORF72) expansions.

Variability may be due in part to the presence of genetic modifiers.

Genotype-phenotype association studies have been used to identify novel genetic modifiers.

In addition, the background-dependent differences revealed will enable the identification of important genetic modifiers.

There are likely many more genetic modifiers of human longevity that remain to be discovered.

The wide variation in cystic presentation suggested genetic modifiers likely influence disease progression in cats.

In conclusion, the consequences of CK deficiency are highly dependent on genetic modifiers, gender and age.

These results suggest that genetic modifiers play an important role in susceptibility to severe PCD-associated hydrocephalus.