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11p12

A chromosome band present on 11p
National Institutes of Health

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Chromosome 11 Short ArmChromosomesEHF wt Allele

Papers overview

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2013
2013
Chromosomal imbalances in successive moments of human bladder urothelial carcinoma.
2009
2009
Cloning , Expression , and Chromosomal Localization to llpl 2-13 of a Human LIM / HOMEOBOX Gene , hLim-1
We have identified a putative transcription factor, designated hLim-1, from human fetal brain using degen¬ erate polymerase chain… 
2006
2006
A novel region of amplification at 11p12‐13 in gastric cancer, revealed by representational difference analysis, is associated with overexpression of CD44v6, especially in early‐onset gastric…
Diffuse‐type gastric carcinomas (GCs) are often difficult to characterize because of contamination of tumor samples by… 
2002
2002
Sibling pair linkage and association studies between peak bone mineral density and the gene locus for the osteoclast-specific subunit (OC116) of the vacuolar proton pump on chromosome 11p12-13.
A major determinant of the risk of osteoporosis is peak bone mineral density (BMD), which has been shown to have substantial… 
2001
2001
EEG1, a putative transporter expressed during epithelial organogenesis: comparison with embryonic transporter expression during nephrogenesis.
A screen for genes differentially regulated in a model of kidney development identified the novel gene embryonic epithelia gene 1… 
2001
2001
A Novel WT1 Gene Mutation Associated with Wilms' Tumor and Congenital Male Genitourinary Malformation
WT1 is located on the short arm of human chromosome 11 and consists of 10 coding exons. Mutations of this gene have been reported… 
1997
1997
Tandem duplication of 11p12-p13 in a child with borderline development delay and eye abnormalities: dose effect of the PAX6 gene product?
We report on a girl with a duplication of chromosome band 11p12-->13, which includes the Wilms tumor gene (WT1) and the aniridia… 
Review
1991
Review
1991
Interstitial deletions without phenotypic effect: Prenatal diagnosis of a new family and brief review
A 39‐year‐old woman (G4P1SAB2) was referred for amniocentesis for advanced maternal age. An interstitial deletion of the G‐dark… 
Highly Cited
1985
Highly Cited
1985
Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome.
We describe five individuals who have constitutional deletions of the short arm of one chromosome 11, including all or part of… 
1985
1985
Localization of the oncogene c-Ha-ras1 outside the aniridia-Wilms' tumor-associated deletion of chromosome 11(del 11p13) using somatic cell hybrids.
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