Sentence examples for determined deficiency from inspiring English sources

Most common of these is lactose intolerance, which is a genetically determined deficiency of the enzyme lactase that is needed to digest the milk sugar, lactose.

We wanted to know, if a genetically determined deficiency in sensing meningococcal LPS increases risk of disease.

Dogs with a genetically determined deficiency of complement C3 more often develop renal and infectious diseases [ 18].

A genetically or epigenetically determined deficiency of GGFs is compatible with the limited regeneration of motor neurons observed in schizophrenia [ 104, 105] and with the incomplete remission of the disorder, which is the foundation of Kraepelin's schizophrenia (dementia praecox) concept.

Such a gene-environmental exposure interaction was recently demonstrated for passive smoking and asthma in children: a genetically determined deficiency of glutathione S transferase (GST) enzymes involved in the detoxification of environmental tobacco smoke (ETS) accounted for a massive increase in the risk for current asthma and asthma symptoms such as wheeze and shortness of breath [ 29].

Although C3 and C4 (Table  1, proteins 19 and 20 and Table  2, proteins 1 and 23) play a significant role in the innate immune system [ 15] a mouse model demonstrated that deficiency in C3 can be compensated by thrombin [ 41] and a genetically determined deficiency of C4 increases the risk for developing systemic lupus erythematosus [ 42].

As with selenium, there is a lack of published information on choline status in dogs and, in particular, methods of determining deficiency.

Although there is no global consensus on the biochemical definition of vitamin D deficiency, a cut-off point of ≤ 37.5 nmol/L (≤ 15 ng/mL) 25(OH D is typically used to determine deficiency [ 13].

Further, a risk-based framework is used to determine deficiencies in the safety management systems.

Blood tests can determine deficiencies.

Of 62 people with enzymatically determined G6PD deficiency, we were unable to identify a deficiency-causing variant in ∼25% (16/62) after assessing the three common G6PD A- variants found in African populations.