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9p13

A chromosome band present on 9p
National Institutes of Health

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10 relations
B4GALT1 wt AlleleCCL19 wt AlleleCCL21 wt AlleleCCL27 wt Allele

Papers overview

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2005
2005
Low-grade B-Cell lymphomas with plasmacytic differentiation lack PAX5 gene rearrangements.
2005
2005
Alterations of 9p in squamous cell carcinoma and adenocarcinoma of the lung: association with smoking, TP53, and survival.
Highly Cited
2000
Highly Cited
2000
Allelic loss at the D9S171 locus on chromosome 9p13 is associated with progression of papillary renal cell carcinoma
Papillary renal cell carcinomas (RCCs) have characteristic clinical and morphological features that separate them from the more… 
1996
1996
Chromosomal mapping of a family of human glutamine synthetase genes: functional gene (GLUL) on 1q25, pseudogene (GLULP) on 9p13, and three related genes (GLULL1, GLULL2, GLULL3) on 5q33, 11p15, and…
Glutamine synthetase (GS) is a ubiquitous enzyme that catalyzes the ATP-dependent conversion of glutamate to glutamine using… 
1996
1996
Molecular cloning and characterization of the human interleukin-11 receptor alpha-chain gene, IL11RA, located on chromosome 9p13.
The human gene coding for the interleukin-11 receptor (IL11RA) was cloned and its structure analyzed. The gene is composed of 13… 
1995
1995
Genomic organization and chromosomal localization of the human and mouse genes encoding the α receptor component for ciliary neurotrophic factor
1991
1991
Rearrangement of 9p13 as the primary chromosomal aberration in adenoid cystic carcinoma of the respiratory tract
Two adenoid cystic carcinomas, one of the nasal cavity, the other a bronchial tumor, were cytogenetically analyzed. The former… 
1991
1991
Involvement of the short arm of the derivative chromosome 9 in Philadelphia-positive acute lymphoblastic leukemia.
Highly Cited
1988
Highly Cited
1988
Frequent nonrandom chromosome abnormalities in 27 patients with untreated large cell lymphoma and immunoblastic lymphoma.
Fresh tumor samples from 27 patients with large cell lymphoma, either previously untreated (26 patients) or minimally treated… 
1987
1987
Partial trisomy 3q syndrome inherited from familal t(3;9) (q26.1;p23) *
A five‐year‐old girl was referred to prometaphase chromosome analysis because of mental retardation, facial dysmorphic features… 
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