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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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2013
2013
A novel homozygous R764H mutation in crumbs homolog 1 causes autosomal recessive retinitis pigmentosa
Purpose Retinitis pigmentosa (RP; MIM 268000) is a hereditary disease characterized by poor night vision and progressive loss of… 
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… 
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… 
2011
2011
ACUTE LEUKEMIAS XIII
1 A TRISPECIFIC ANTIBODY DERIVATIVE DIRECTED AGAINST CD123 AND CD33 MEDIATES EFFECTIVE ELIMINATION OF AML CELLS BY DUAL TARGETING… 
2011
2011
Identification of Recurrent Submicroscopic Deletions of chromosome1q31.3 As Possible Molecular Prognostic Markers in Acute Promyelocytic Leukemia (APL)
Abstract 420 Introduction: The characteristic hallmark of acute promyelocytic leukemia (APL) is a balanced reciprocal chromosomal… 
2009
2009
Refined mapping of loss of heterzygosity on 1q31. 1-32. 1 in sporadic colorectal carcinoma
Objective To explore preeise loss of heterzygosity (LOH) regions on 1 q31.1-32.1 in Chinese patients with coloreetal cancer… 
2005
2005
Chromosome 1q loss of heterozygosity frequently occurs in sporadic insulinomas and is associated with tumor malignancy
The pathogenesis of sporadic insulinomas is not clear, and there are no reliable genetic determinants that are useful to… 
2001
2001
Linkage studies of SOX13, the ICA12 autoantigen gene, in families with type 1 diabetes.
SOX13 is a member of the SOX family of transcription factors that encodes the type 1 diabetes autoantigen, ICA12. The SOX13 gene… 
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… 
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