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17q25

A chromosome band present on 17q
National Institutes of Health

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13 relations
17qASPSCR1 wt AlleleBAIAP2 wt AlleleBIRC5 wt Allele

Papers overview

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Review
2012
Review
2012
Genetics of age-related white matter lesions from linkage to genome wide association studies
Highly Cited
2002
Highly Cited
2002
Chromosomal imbalances of primary and metastatic lung adenocarcinomas
Comparative genomic hybridization (CGH) was used to screen 83 lung adenocarcinomas of 60 patients for chromosomal imbalances. The… 
Highly Cited
2002
Highly Cited
2002
Novel immunoglobulin superfamily gene cluster, mapping to a region of human chromosome 17q25, linked to psoriasis susceptibility
Abstract. Chromosome 17q25 harbors a susceptibility locus for psoriasis (PSORS2). This locus may overlap with loci for atopic… 
2002
2002
Characterization of a 500 kb region on 17q25 and the exclusion of candidate genes as the familial Tylosis Oesophageal Cancer (TOC) locus
The locus for a syndrome of focal palmoplantar keratoderma (Tylosis) associated with squamous cell oesophageal cancer (TOC) has… 
Highly Cited
2000
Highly Cited
2000
Characterization of human retinal fascin gene (FSCN2) at 17q25: close physical linkage of fascin and cytoplasmic actin genes.
Retinal fascin is a newly identified photoreceptor-specific paralog of the actin-bundling protein fascin. Fascins crosslink f… 
Highly Cited
2000
Highly Cited
2000
A new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to 17q25.
We report the localization of DFNA20, a gene causing dominant, nonsyndromic, progressive hearing loss in a three-generation… 
2000
2000
The human inward rectifier K+ channel subunit Kir5.1 (KCNJ16) maps to chromosome 17q25 and is expressed in kidney and pancreas
A novel human Kir5.1 (inward rectifier K+ channel subunit, gene name KCNJ16) was identified through database searches. This human… 
1999
1999
An integrated physical and gene map of human distal chromosome 17q24-proximal 17q25 encompassing multiple disease loci.
Genetic mapping studies suggest that a small interval on human chromosome distal 17q24-proximal 17q25 harbors genes involved in… 
1999
1999
A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genes.
Hereditary neuralgic amyotrophy (HNA) is an autosomal dominant recurrent neuropathy mapped to a 4-cM interval on chromosome 17q25… 
1997
1997
A region of interstitial 17q25 allelic loss in ovarian tumors coincides with a defined region of loss in breast tumors
Chromosomal regions of allelic imbalance in tumors are predicted to define the general location of tumor suppressor genes. We… 
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