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Chromosomes, Human, Pair 9

Known as: 9 chromosome, Chromosome 9 
The designation for each member of the ninth largest human autosomal chromosome pair. Chromosome 9 spans about 145 million base pairs of nucleic… 
National Institutes of Health

Related topics

Related topics

27 relations

Narrower (9)

9p partial monosomy syndrome9q22.3 MicrodeletionCHROMOSOME 9p DELETION SYNDROMEChromosome 9, partial trisomy 9p
ChromatinChromosome 9 Short ArmDS Stage I Plasma Cell MyelomaDS Stage II Plasma Cell Myeloma

Broader (1)

Chromosomes, Human, 6-12 and X

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2001
Highly Cited
2001
The high molecular mass rhoptry protein, RhopH1, is encoded by members of the clag multigene family in Plasmodium falciparum and Plasmodium yoelii.
Highly Cited
1997
Highly Cited
1997
Recurrent DNA copy number changes in 1q, 4q, 6q, 9p, 13q, 14q and 22q detected by comparative genomic hybridization in malignant mesothelioma.
Comparative genomic hybridization (CGH) analyses were performed on 27 human pleural mesothelioma tumour specimens, consisting of… 
Highly Cited
1997
Highly Cited
1997
Human Lysophosphatidic Acid Acyltransferase
Lysophosphatidic acid (1-acyl-sn-glycero-3-phosphate (LPA)) is a phospholipid with diverse biological activities. The mediator… 
Highly Cited
1994
Highly Cited
1994
Homozygous deletion on chromosome 9p and loss of heterozygosity on 9q, 6p, and 6q in primary human small cell lung cancer.
Highly Cited
1993
Highly Cited
1993
Preliminary mapping of the deleted region of chromosome 9 in bladder cancer.
Inactivation of a suppressor gene by deletion of chromosome 9 is a candidate initiating event in bladder carcinogenesis. We have… 
Highly Cited
1993
Highly Cited
1993
Confirmation of chromosome 9p linkage in familial melanoma.
Malignant melanoma occurs as a familial cancer in 5%-10% of cases where it segregates in a manner consistent with autosomal… 
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.
Highly Cited
1989
Highly Cited
1989
Nucleotide sequence of both reciprocal translocation junction regions in a patient with Ph positive acute lymphoblastic leukaemia, with a breakpoint within the first intron of the BCR gene.
Breakpoints on chromosome 22 in the translocation t(9;22) found in Philadelphia positive acute lymphoblastic leukaemia patients… 
Highly Cited
1989
Highly Cited
1989
Detection by enzymatic amplification of bcr-abl mRNA in peripheral blood and bone marrow cells of patients with chronic myelogenous leukemia.
The Philadelphia chromosome of chronic myelogenous leukemia (CML) patients is caused by a translocation of the c-abl gene from… 
Highly Cited
1987
Highly Cited
1987
The cellular retinol binding protein II gene. Sequence analysis of the rat gene, chromosomal localization in mice and humans, and documentation of its close linkage to the cellular retinol binding…
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