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10q25

A chromosome band present on 10q
National Institutes of Health

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6 relations
10qCASP7 wt AlleleChromosomesDUSP5 wt Allele

Papers overview

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Highly Cited
2010
Highly Cited
2010
Genome-wide meta-analyses identify multiple loci associated with smoking behavior
Consistent but indirect evidence has implicated genetic factors in smoking behavior. We report meta-analyses of several smoking… 
Highly Cited
2006
Highly Cited
2006
Polymorphisms in the Transcription Factor 7-Like 2 (TCF7L2) Gene Are Associated With Type 2 Diabetes in the Amish
Transcription factor 7-like 2 (TCF7L2) regulates genes involved in cell proliferation and differentiation. The TCF7L2 gene is… 
Review
1999
Review
1999
Loss of chromosome 13 is the most frequent genomic imbalance in malignant fibrous histiocytomas. A comparative genomic hybridization analysis of a series of 30 cases.
Highly Cited
1998
Highly Cited
1998
A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD
We report here the identification of a new human homeobox gene, PITX3, and its involvement in anterior segment mesenchymal… 
Highly Cited
1998
Highly Cited
1998
Identification of PKD2L, a human PKD2-related gene: tissue-specific expression and mapping to chromosome 10q25.
Mutations in PKD2 cause autosomal dominant kidney disease (ADPKD). Polycystin-2, the PKD2 gene product, is an integral membrane… 
Highly Cited
1997
Highly Cited
1997
A functional neo-centromere formed through activation of a latent human centromere and consisting of non-alpha-satellite DNA
We recently described a human marker chromosome containing a functional neo-centromere that binds anti-centromere antibodies, but… 
Highly Cited
1995
Highly Cited
1995
Chromosome 10 deletion mapping in human gliomas: a common deletion region in 10q25.
The high incidence of loss of chromosome 10 alleles in glioblastoma multiforme suggests the presence on this chromosome of a… 
Highly Cited
1993
Highly Cited
1993
A functional marker centromere with no detectable alpha-satellite, satellite III, or CENP-B protein: activation of a latent centromere?
We report the investigation of an unusual human supernumerary marker chromosome 10 designated "mar del(10)." This marker is… 
Highly Cited
1993
Highly Cited
1993
A human synaptic vesicle monoamine transporter cDNA predicts posttranslational modifications, reveals chromosome 10 gene localization and identifies TaqI RFLPs
Highly Cited
1993
Highly Cited
1993
Chromosomal localization of the human vesicular amine transporter genes.
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