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Deletions of chromosome 5q are associated with poor outcomes in acute myeloid leukemia (AML) suggesting the presence of tumor… Expand Atopic dermatitis (AD) is a commonly occurring chronic skin disease with high heritability. Apart from filaggrin (FLG), the genes… Expand BACKGROUND
Asthma is a heterogeneous disease that is caused by the interaction of genetic susceptibility with environmental… Expand BACKGROUND
Ineffective erythropoiesis is the hallmark of myelodysplastic syndromes. Management of the anemia caused by… Expand Atopy is generally considered to be caused by interaction of genetic and environmental factors. Recently, an association of a C… Expand BACKGROUND & AIMS
Gain-of-function trypsin mutations cause acute pancreatitis and chronic pancreatitis. Loss of trypsin inhibitor… Expand Total serum immunoglobulin (Ig)E levels are genetically regulated, but the mechanism of inheritance is not well understood… Expand Sib-pair analysis of 170 individuals from 11 Amish families revealed evidence for linkage of five markers in chromosome 5q31.1… Expand Interferon regulatory factor 1 (IRF-1) and IRF-2 are structurally similar DNA-binding factors which were originally identified as… Expand One of the most frequent cytogenetic abnormalities in human leukemia and myelodysplasia is an interstitial deletion within… Expand