FAQ

4q31.1

A chromosome band present on 4q
National Institutes of Health

Topic mentions per year

Topic mentions per year

1990-2015
01219902015

Related topics

Related topics

2 relations
ChromosomesNR3C2 wt Allele

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
4q31.1
Chromosomes
NR3C2 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
The genetics of alcohol dependence: Twin and SNP-based heritability, and genome-wide association study based on AUDIT scores.
Alcohol dependence (AD) is among the most common and costly public health problems contributing to morbidity and mortality… (More)
  • table I
  • table III
  • table II
  • table V
Is this relevant?
2013
2013
A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations
Congenital heart malformation (CHM) is the most common form of congenital human birth anomaly and is the leading cause of infant… (More)
  • figure 1
  • figure 2
Is this relevant?
2012
2012
Mutation in RAB33B, which encodes a regulator of retrograde Golgi transport, defines a second Dyggve--Melchior--Clausen locus.
BACKGROUND Dyggve--Melchior--Clausen syndrome (DMC) is a chondrodysplasia that bears significant phenotypic resemblance to… (More)
  • figure 1
  • table 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
2012
2012
Genomic CGH-assessed structural DNA alterations in rectal carcinoma as related to local recurrence following primary operation for cure.
Several factors determine overall outcome and possible local recurrence after curative surgery for rectal carcinoma. Surgical… (More)
  • figure 1
  • table I
  • table II
  • figure 2
  • figure 3
Is this relevant?
2011
2011
NTM and NR3C2 polymorphisms influencing intelligence: family-based association studies.
Family, twin, and adoption studies have indicated that human intelligence quotient (IQ) has significant genetic components. We… (More)
Is this relevant?
2006
2006
Mutational and LOH analyses of the chromosome 4q region in esophageal adenocarcinoma.
OBJECTIVE Mortality due to esophageal adenocarcinoma has risen markedly, but the molecular mechanisms underlying this… (More)
  • figure 1
  • table 1
  • figure 2
Is this relevant?
2003
2003
Genome-wide allelotype study of primary glioblastoma multiforme.
OBJECTIVE To investigate the molecular genetic pathogenesis of primary glioblastoma multiforme (GBM) and identify which… (More)
Is this relevant?
2002
2002
Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements.
Vitamin B(12) (cobalamin) is an essential cofactor of two enzymes, methionine synthase and methylmalonyl-CoA mutase. The… (More)
Is this relevant?
1998
1998
Cloning and mapping of SMARCA5 encoding hSNF2H, a novel human homologue of Drosophila ISWI.
We have isolated a novel cDNA encoding a peptide with 86% sequence homology to hSNF2L protein, a previously isolated human… (More)
Is this relevant?
1990
1990
Regional chromosomal assignment of the human mineralocorticoid receptor gene to 4q31.1
The gene for human mineralocorticoid receptor (hMR), previously mapped to chromosome 4, has been further localized to 4q31.1 by… (More)
  • figure 1
  • figure 3
  • figure 4
  • figure 5
  • figure 6
Is this relevant?