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Chromosomes, Human, Pair 3

Known as: 3 chromosome, 3 chromosomes, Chromosome 3 
The designation for each member of the third largest human autosomal chromosome pair. Chromosome 3 spans almost 200 million base pairs and represents… Expand
National Institutes of Health

Related topics

Related topics

32 relations
BRK1 geneC3CER1 geneCentral Nervous System HemangioblastomaCerebellar hemangioblastoma
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Narrower (6)

Chromosome 3, monosomy 3pChromosome 3, monosomy 3p14 p11Chromosome 3, trisomy 3pChromosome 3, trisomy 3q
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Broader (1)

Chromosomes, Human, 1-3

Papers overview

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Highly Cited
2009
Highly Cited
2009
HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin
Drug-induced liver injury (DILI) is an important cause of serious liver disease. The antimicrobial agent flucloxacillin is a… Expand
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Highly Cited
2006
Highly Cited
2006
GS3, a major QTL for grain length and weight and minor QTL for grain width and thickness in rice, encodes a putative transmembrane protein
The GS3 locus located in the pericentromeric region of rice chromosome 3 has been frequently identified as a major QTL for both… Expand
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Highly Cited
2005
Highly Cited
2005
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia
We have previously reported a large Danish pedigree with autosomal dominant frontotemporal dementia (FTD) linked to chromosome 3… Expand
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Highly Cited
2004
Highly Cited
2004
Gene Expression Profiling in Uveal Melanoma Reveals Two Molecular Classes and Predicts Metastatic Death
Melanomas are notoriously difficult to classify because of a lack of discrete clinical and pathological stages. Here, we show… Expand
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Highly Cited
1996
Highly Cited
1996
Prognostic implications of monosomy 3 in uveal melanoma
BACKGROUND A high proportion of patients with uveal melanoma die of metastatic disease. In a subgroup of uveal melanomas there is… Expand
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Highly Cited
1995
Highly Cited
1995
The Drosophila tumor suppressor gene warts encodes a homolog of human myotonic dystrophy kinase and is required for the control of cell shape and proliferation.
Homozygous loss of the warts (wts) gene of Drosophila, caused by mitotic recombination in somatic cells, leads to the formation… Expand
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Highly Cited
1994
Highly Cited
1994
Mutation in the DNA mismatch repair gene homologue hMLH 1 is associated with hereditary non-polyposis colon cancer
THE human DNA mismatch repair gene homologue, hMSH2, on chromosome 2p is involved in hereditary non-polyposis colon cancer (HNPCC… Expand
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Highly Cited
1990
Highly Cited
1990
The murine mutation osteopetrosis is in the coding region of the macrophage colony stimulating factor gene
MICE homozygous for the recessive mutation osteopetrosis (op) on chromosome 3 have a restricted capacity for bone remodelling… Expand
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Highly Cited
1990
Highly Cited
1990
Total absence of colony-stimulating factor 1 in the macrophage-deficient osteopetrotic (op/op) mouse.
Osteopetrotic (op/op) mutant mice suffer from congenital osteopetrosis due to a severe deficiency of osteoclasts. Furthermore… Expand
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Highly Cited
1990
Highly Cited
1990
A point mutation of the rhodopsin gene in one form of retinitis pigmentosa
THE gene for autosomal dominant retinitis pigmentosa in a large pedigree of Irish origin has recently been found to be linked to… Expand
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