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9q32

A chromosome band present on 9q
National Institutes of Health

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ChromosomesDEC1 wt AlleleORM1 wt AllelePTBP3 wt Allele

Papers overview

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2008
2008
Loss of heterozygosity at 9q32–33 (DBC1 locus) in primary non‐invasive papillary urothelial neoplasm of low malignant potential and low‐grade urothelial carcinoma of the bladder and their associated…
Tumour recurrence has a major impact on patients with non‐invasive papillary urothelial tumours of the bladder. To explore the… 
2002
2002
DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34
We report the identification of a novel locus responsible for an autosomal recessive form of hearing loss (DFNB) segregating in a… 
Highly Cited
2001
Highly Cited
2001
Hypermethylation at 9q32-33 tumour suppressor region is age-related in normal urothelium and an early and frequent alteration in bladder cancer
Transcriptional silencing by CpG island hypermethylation of gene regulatory regions is one mechanism for inactivation of tumour… 
2001
2001
Frequently deleted loci on chromosome 9 may harbor several tumor suppressor genes in human renal cell carcinoma.
2000
2000
Isolation and mutational analysis of a novel human cDNA, DEC1 (deleted in esophageal cancer 1), derived from the tumor suppressor locus in 9q32
The long arm of chromosome 9 is thought to contain one or more putative tumor suppressor genes that are mutated in squamous cell… 
2000
2000
Initiation-development modelling of allelic losses on chromosome 9 in multifocal bladder cancer.
1991
1991
Dinucleotide repeat polymorphism at the GSN locus (9q32-34).
Source/Description: A human genomic 2.0 kb EcoRI fragment from the intron between exons la and 2 in the c-abl gene' (provided by… 
1991
1991
Identification of a highly polymorphic microsatellite VNTR within the argininosuccinate synthetase locus: exclusion of the dystonia gene on 9q32-34 as the cause of dopa-responsive dystonia in a large…
Dopa-responsive dystonia is a clinical variant of idiopathic torsion dystonia that is distinguished from other forms of dystonia… 
Highly Cited
1988
Highly Cited
1988
Molecular analysis of human complement component C5: localization of the structural gene to chromosome 9.
A human C5 clone (pC5HG2) was isolated from a cDNA library constructed from Hep G2 mRNA. The DNA sequence showed that the pC5HG2… 
Highly Cited
1985
Highly Cited
1985
The phenotypic and cytogenetic spectrum of partial trisomy 9.
A new patient with trisomy for the chromosome segment 9pter----q22 is compared to 19 previously reported cases of partial trisomy… 
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