Sentence examples for a dominant condition from inspiring English sources

In those places, as on the abyssal plains, life is not a dominant condition.

The small energy gap between singlet excitons (S) and triplet excitons (T) of organic molecules is a dominant condition for high efficient thermally activated delayed fluorescence (TADF).

Some drawbacks of the scenario-axes approach [34, 60, 61] relate, for example, to the poor incorporation of discontinuities (a temporary or permanent, sometimes unexpected, break in a dominant condition caused by the interaction of events and long term processes) into studies based on the scenario-axes technique and thus hampering the scenario complexity and dynamics.

This can be done for a recessive condition, such as cystic fibrosis or spinal muscular atrophy, in which parents are healthy carriers, or for a dominant condition such as certain inherited cancers, cardiac disorders, or neurologic diseases.

In 1985, one of the authors described this entity as a dominant condition distinct from BHD, showing childhood onset, preferential localisation of lesions on the ears and distinct histology, which mimics the trichodiscomas in BHD (Starink et al, 1985).

A common feature of Huntington disease (HD), an autosomal dominant condition, is a severe loss of neurons in striatum, the main information processing unit of the basal ganglia.

FJHN is an autosomal dominant condition characterised by a hypoexcretion of urate leading to hyperuricaemia, gout and renal disease.

First, Finkel type SMA (SMA-FK) is an autosomal dominant condition caused by a dominant founder mutation (p.P56S) in the VAPB gene, encoding VAMP (vesicle-associated membrane protein -associated protein -associatedshimura et al., 2004).

Lynch syndrome (LS) (previously referred to as hereditary non-polyposis colorectal cancer; HNPCC) is an autosomal dominant condition caused by a defect in one of the mismatch repair (MMR) genes. 1 The syndrome is characterised by the development of colorectal cancer (CRC), endometrial cancer (EC) and various other cancers frequently diagnosed at an early age.

HDR (hypoparathyroidism, sensorineural deafness, renal dysplasia) syndrome, which is characterized by a variety of craniofacial defects, is an autosomal dominant condition caused by mutations in the gene encoding a human zinc finger transcription factor, GATA3.

AML occur sporadically in 80% of cases with a prevalence of 0.2%-0.4 0.2%-0.4art of an autosomal dominant condition known as tuberous sclerosis complex (TSC) and have a female predilection [63, 64].