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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

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
High Complement Factor H-Related (FHR)-3 Levels Are Associated With the Atypical Hemolytic-Uremic Syndrome-Risk Allele CFHR3*B
Dysregulation of the complement alternative pathway (AP) is a major pathogenic mechanism in atypical hemolytic-uremic syndrome… 
2017
2017
Pediatric pineal germinomas: Epigenetic and genomic approach
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… 
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… 
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… 
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… 
2001
2001
Identification and assignment of the human NIMA-related protein kinase 7 gene (NEK7) to human chromosome 1q31.3
Neks (NIMA-related kinase) are a group of protein kinases sharing high amino acid sequence identity with NIMA which controls… 
2000
2000
Genomic characterisation and fine mapping of the human 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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