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1q21-q23

A chromosome band present on 1q
National Institutes of Health

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6 relations
CD5L wt AlleleCRP wt AlleleChromosomesETV3 wt Allele

Papers overview

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2006
2006
Polymorphisms in the Glucokinase-Associated, Dual-Specificity Phosphatase 12 (DUSP12) Gene Under Chromosome 1q21 Linkage Peak Are Associated With Type 2 Diabetes
Linkage of type 2 diabetes to chromosome 1q21-q23 is well replicated across populations. In an initial 50-kb marker map (580… 
2004
2004
Contribution of Chromosome 1q21‐q23 to Familial Combined Hyperlipidemia in Mexican Families
Familial combined hyperlipidemia (FCHL) is the most common familial dyslipidemia, with a prevalence of 1‐2% in the general… 
2004
2004
The transcribed endosulfine alpha gene is located within a type 2 diabetes-linked region on 1q: sequence and expression analysis in Pima Indians.
2003
2003
Molecular screening and association studies of retinoid-related orphan receptor gamma (RORC): a positional and functional candidate for type 2 diabetes.
2003
2003
DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23
Approximately 1 in 1000 children is born with a serious permanent hearing impairment (pre-lingual deafness), and it is estimated… 
2002
2002
Cloning, expression and genomic structure of human LMX1A, and variant screening in Pima Indians.
2002
2002
Structure and expression of Strabismus 1 gene on human chromosome 1q21-q23.
Xenopus Strabismus (Stbm) is a negative regulator of the WNT - beta-catenin signaling pathway. Strabismus 1 (STB1/VangL2) and… 
1995
1995
Assignment of human G-protein-coupled inward rectifier K+ channel homolog GIRK3 gene to chromosome 1q21-q23.
More than 20 genes that encode voltage-gated and Ca{sup 2+}-dependent K{sup +} channels have been identified. These channels are… 
1994
1994
PE-1, a novel ETS oncogene family member, localizes to chromosome 1q21-q23.
The v-ets oncogene family shares a conserved peptide motif called the ETS domain that mediates sequence-specific DNA binding… 
1994
1994
Linkage and mutation analysis in an extended family with Charcot-Marie-Tooth disease type 1B.
Charcot-Marie-Tooth disease type 1 (CMT1) or hereditary motor and sensory neuropathy type I (HMSNI) is an autosomal dominant… 
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