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9p22

A chromosome band present on 9p
National Institutes of Health

Related topics

Related topics

4 relations
Chromosome 9 Short ArmChromosomesIFNA2 wt AlleleMLLT3 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2006
Review
2006
Constitutional complex chromosomal rearrangements in azoospermic men--case report and literature review.
2004
2004
Characterization of gains, losses, and regional amplification in testicular germ cell tumor cell lines by comparative genomic hybridization.
2001
2001
Frequently deleted loci on chromosome 9 may harbor several tumor suppressor genes in human renal cell carcinoma.
Highly Cited
1995
Highly Cited
1995
Evidence for u.v. induction of CDKN2 mutations in melanoma cell lines.
The CDKN2 gene, encoding the cyclin dependent kinase inhibitor p16, is a tumour suppressor gene involved in melanoma and maps to… 
1995
1995
Loss of heterozygosity at 9p and 17q in human laryngeal tumors.
Highly Cited
1995
Highly Cited
1995
Frequent microsatellite alterations on chromosome 3p in esophageal squamous cell carcinoma.
By the microsatellite assay, two types of genetic alterations, loss of heterozygosity (LOH) and replication error (RER), were… 
Highly Cited
1995
Highly Cited
1995
Microsatellite instability and loss of heterozygosity in melanoma.
Alterations in the repeat length of microsatellites have been identified recently in tumors arising in patients with hereditary… 
Review
1993
Review
1993
MLLT3 gene on 9p22 involved in t(9;11) leukemia encodes a serine/proline rich protein homologous to MLLT1 on 19p13.
Recently, the MLL gene at 11q23 was found to be involved in a subset of leukemias with an 11q23 abnormality. In the present study… 
Highly Cited
1993
Highly Cited
1993
Molecular deletion of 9p sequences in non‐small cell lung cancer and malignant mesothelioma
Previously we have reported non‐random cytogenetic abnormalities involving the short arm of chromosome 9 (9p) in the majority of… 
Highly Cited
1992
Highly Cited
1992
Mapping of the shortest region of overlap of deletions of the short arm of chromosome 9 associated with human neoplasia.
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