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… (More)
National Institutes of Health

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Narrower (9)

9p partial monosomy syndrome9q22.3 MicrodeletionCHROMOSOME 9p DELETION SYNDROMEChromosome 9, partial trisomy 9p
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ChromatinChromosome 9 Short ArmDS Stage I Plasma Cell MyelomaDS Stage II Plasma Cell Myeloma
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Broader (1)

Chromosomes, Human, 6-12 and X

Papers overview

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Highly Cited
2011
Highly Cited
2011
Incomplete DNA methylation underlies a transcriptional memory of somatic cells in human iPS cells
Human induced pluripotent stem (iPS) cells are remarkably similar to embryonic stem (ES) cells, but recent reports indicate that… (More)
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Highly Cited
2007
Highly Cited
2007
A common allele on chromosome 9 associated with coronary heart disease.
Coronary heart disease (CHD) is a major cause of death in Western countries. We used genome-wide association scanning to identify… (More)
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Highly Cited
2005
Highly Cited
2005
A gain-of-function mutation of JAK2 in myeloproliferative disorders.
BACKGROUND Polycythemia vera, essential thrombocythemia, and idiopathic myelofibrosis are clonal myeloproliferative disorders… (More)
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Highly Cited
2003
Highly Cited
2003
DNA sequence and analysis of human chromosome 9
Chromosome 9 is highly structurally polymorphic. It contains the largest autosomal block of heterochromatin, which is… (More)
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Highly Cited
1994
Highly Cited
1994
A cell cycle regulator potentially involved in genesis of many tumor types.
A putative tumor suppressor locus on the short arm of human chromosome 9 has been localized to a region of less than 40 kilobases… (More)
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Highly Cited
1994
Highly Cited
1994
pl5INK4B is a potentia| effector of TGF-β-induced cell cycle arrest
TRANSFORMING growth factor-beta (TGF-β) inhibits cell proliferation by inducing a Gl-phase cell cycle arrest1. Normal progression… (More)
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Highly Cited
1991
Highly Cited
1991
TAN-1, the human homolog of the Drosophila notch gene, is broken by chromosomal translocations in T lymphoblastic neoplasms.
Previously we described joining of DNA in the beta T cell receptor gene to DNA of an uncharacterized locus in a t(7;9)(q34;q34.3… (More)
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Highly Cited
1991
Highly Cited
1991
Human platelet/erythroleukemia cell prostaglandin G/H synthase: cDNA cloning, expression, and gene chromosomal assignment.
Platelets metabolize arachidonic acid to thromboxane A2, a potent platelet aggregator and vasoconstrictor compound. The first… (More)
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Highly Cited
1986
Highly Cited
1986
The chronic myelogenous leukemia-specific P210 protein is the product of the bcr/abl hybrid gene.
Chronic myelogenous leukemia (CML) is a human disease associated with a consistent chromosomal translocation that results in… (More)
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Highly Cited
1982
Highly Cited
1982
A cellular oncogene is translocated to the Philadelphia chromosome in chronic myelocytic leukaemia
The transforming genes of oncogenic retroviruses are homologous to a group of evolutionary conserved cellular onc genes1. The… (More)
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