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1q31.3

A chromosome band present on 1q.
National Institutes of Health

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3 relations
ChromosomesMIR181A1 wt AlleleMIR181B1 wt Allele

Papers overview

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2015
2015
DENND1B gene variants associate with elevated exhaled nitric oxide in healthy high‐risk neonates
Increased neonatal fraction of exhaled nitric oxide (FeNO) is associated with lung symptoms early in life, while predictors of… Expand
2013
2013
Mutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplex.
Hypotrichosis simplex (HS) comprises a group of hereditary isolated alopecias that are characterized by a diffuse and progressive… Expand
2012
2012
SNP array analysis of acute promyelocytic leukemia may be of prognostic relevance and identifies a potential high risk group with recurrent deletions on chromosomal subband 1q31.3
To search for new copy number alterations (CNAs) in acute promyelocytic leukemia (APL), we analyzed DNA from leukemic blasts of… Expand
Review
2011
Review
2011
The genetics of eating disorders.
The eating disorders anorexia nervosa (AN), bulimia nervosa (BN), binge eating disorder and allied diagnoses such as eating… Expand
Highly Cited
2010
Highly Cited
2010
Variants of DENND1B associated with asthma in children.
BACKGROUND Asthma is a complex disease that has genetic and environmental causes. The genetic factors associated with… Expand
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2009
2009
Structural Variation in the Human Genome
The study of variation found in DNA is fundamental in human genetic studies. Single nucleotide polymorphisms (SNPs) are simple to… Expand
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Highly Cited
2008
Highly Cited
2008
In vivo differentiation and genomic evolution in adult male germ cell tumors
Germ cell tumors (GCTs) are the most common solid malignancy in young adult men, but the genes and genomic regions involved in… Expand
Highly Cited
2006
Highly Cited
2006
KIF14 mRNA expression is a predictor of grade and outcome in breast cancer
Gain of chromosome 1q is a hallmark of breast cancer, and likely reflects oncogene amplification. We previously identified… Expand
Highly Cited
2004
Highly Cited
2004
Localization of the coagulation factor XIII B subunit gene (F13B) to chromosome bands 1q31–32.1 and restriction fragment length polymorphism at the locus
SummaryIn situ hybridization of tritiated cDNA probes for the gene for the B subunit of coagulation factor XIII localized the… Expand
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1997
1997
Fine mapping of five human skeletal muscle genes: alpha-tropomyosin, beta-tropomyosin, troponin-I slow-twitch, troponin-I fast-twitch, and troponin-C fast.
In this paper the chromosomal localization of the human skeletal muscle genes Troponin-I slow-twitch (TNNI1), Troponin-I fast… Expand
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