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2q37

A chromosome band present on 2q
National Institutes of Health

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7 relations
ALPP wt AlleleChromosomesUGT1A LocusUGT1A1 wt Allele

Papers overview

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Highly Cited
2012
Highly Cited
2012
Genome-wide linkage and association analyses implicate FASN in predisposition to Uterine Leiomyomata.
Highly Cited
2012
Highly Cited
2012
Family history of von Hippel–Lindau disease was uncommon in Chinese patients: suggesting the higher frequency of de novo mutations in VHL gene in these patients
Von Hippel–Lindau (VHL) disease is an autosomal dominant familial cancer syndrome caused by germline mutations in VHL tumor… 
Highly Cited
2007
Highly Cited
2007
A cluster of translocation breakpoints in 2q37 is associated with overexpression of NPPC in patients with a similar overgrowth phenotype
Overexpression of the C‐type natriuretic peptide, encoded by the NPPC gene in 2q37.1, was recently reported in a patient… 
Highly Cited
2005
Highly Cited
2005
Hepatic Expression of the UGT1A9 Gene Is Governed by Hepatocyte Nuclear Factor 4α
UDP-glucuronosyltransferase (UGT) enzymes catalyze the glucuronidation reaction, which is a major pathway in the catabolism and… 
Highly Cited
2004
Highly Cited
2004
Molecular cloning and characterization of NEU4, the fourth member of the human sialidase gene family.
Highly Cited
1999
Highly Cited
1999
The Monkey and Human Uridine Diphosphate-Glucuronosyltransferase UGT1A9, Expressed in Steroid Target Tissues, Are Estrogen-Conjugating Enzymes.
Considering the physiologic importance of the steroid response, which is regulated in part by steroid levels in a given tissue… 
Highly Cited
1996
Highly Cited
1996
Type VI collagen mutations in Bethlem myopathy, an autosomal dominant myopathy with contractures
Among the diverse family of collagens, the widely expressed microfibrillar type VI collagen is believed to play a role in… 
Highly Cited
1993
Highly Cited
1993
Assignment of the human UDP glucuronosyltransferase gene (UGT1A1) to chromosome region 2q37.
UDP glucuronosyltransferases (UGTs) comprise a multigene family of drug-metabolizing enzymes. The sub-family of UGTs that… 
1993
1993
Genetic heterogeneity of Crigler-Najjar syndrome type I: a study of 14 cases.
Highly Cited
1990
Highly Cited
1990
Assignment of the locus for Waardenburg syndrome type I to human chromosome 2q37 and possible homology to the Splotch mouse.
We have demonstrated close linkage between the locus for the autosomal dominant Waardenburg syndrome type I and the placental… 
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