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To date, over 200 known KCNH2 mutations have been described causing a variant of long QT syndrome, known as LQT2.
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Measles has been described as causing a suppression in cell mediated immunity (although this is contested [ 20, 21]) and potentially this may aid the colonization process with H. pylori[ 22].
In breast, head and neck and lung cancer, the inhibitory effects of VEGF on DC differentiation have been described to cause a decrease of PB DCs closely associated with accumulation of immature myeloid cells lacking markers of mature haematopoietic cells (Almand et al, 2000).
Vomiting can be caused as a direct effect of the AA solution which has been described to cause a delay in gastric emptying and lowers the esophageal spincter tone [36].
In addition to hydrogen peroxide, dopamine has been described to cause a conformational change of human parkin.
S. enterica, as well as other Gram negative and Gram positive pathogens, has been described to cause a persistent infection, leading to distension of the C. elegans intestinal lumen [7].
The E79K mutation has previously been described to cause a decreased autoactivation [ 11].
The effect of a single gene on behaviour has been described as small causing a slight bias towards one end of a continuum [ 4, 24].
Alternatively-spliced transcripts of HYAL1 and HYAL3 have been described that cause an in-frame deletion of the putative catalytic site and abolish hyaluronidase function [ 33].
An autosomal dominant form of AID deficiency has been described as caused by a missense mutation in the C terminal domain of the molecule, which is the domain involved in nuclear egress.
The identified DKPs were described to cause a bitter taste in these foods.
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