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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…
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National Institutes of Health
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Related topics
Related topics
32 relations
BRK1 gene
C3CER1 gene
Central Nervous System Hemangioblastoma
Cerebellar hemangioblastoma
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Narrower (6)
Chromosome 3, monosomy 3p
Chromosome 3, monosomy 3p14 p11
Chromosome 3, trisomy 3p
Chromosome 3, trisomy 3q
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Broader (1)
Chromosomes, Human, 1-3
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2003
Highly Cited
2003
A large rearrangement involving genes and low-copy DNA interrupts the microcollinearity between rice and barley at the Rph7 locus.
S. Brunner
,
B. Keller
,
C. Feuillet
Genetics
2003
Corpus ID: 26987738
Grass genomes differ greatly in chromosome number, ploidy level, and size. Despite these differences, very good conservation of…
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Highly Cited
2002
Highly Cited
2002
Chromosome-wide SNPs reveal an ancient origin for Plasmodium falciparum
Jianbing Mu
,
J. Duan
,
+5 authors
X. Su
Nature
2002
Corpus ID: 4409397
The Malaria's Eve hypothesis, proposing a severe recent population bottleneck (about 3,000–5,000 years ago) of the human malaria…
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Highly Cited
2002
Highly Cited
2002
Generation of Multiple Isoforms of Eukaryotic Translation Initiation Factor 4GI by Use of Alternate Translation Initiation Codons
Marshall P Byrd
,
M. Zamora
,
R. Lloyd
Molecular and Cellular Biology
2002
Corpus ID: 7426403
ABSTRACT Eukaryotic translation initiation factor 4GI (eIF4GI) is an essential protein that is the target for translational…
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Review
2001
Review
2001
A genome-wide survey of reproductive barriers in an intraspecific hybrid.
Y. Harushima
,
M. Nakagahra
,
Masahiro Yano
,
Takuji Sasaki
,
Nori Kurata
Genetics
2001
Corpus ID: 29974128
Genetic study of the reproductive barriers between related species plays an essential role in understanding the process of…
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Highly Cited
1999
Highly Cited
1999
A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23–24.2
Mounira Hmani
,
A. Ghorbel
,
+6 authors
H. Ayadi
European Journal of Human Genetics
1999
Corpus ID: 25794766
Usher type II syndrome is defined by the association of retinitis pigmentosa, appearing in the late second to early third decade…
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Highly Cited
1994
Highly Cited
1994
Organization of the gene for human platelet/endothelial cell adhesion molecule-1 shows alternatively spliced isoforms and a functionally complex cytoplasmic domain.
N. Kirschbaum
,
R. J. Gumina
,
P. Newman
Blood
1994
Corpus ID: 1132652
Platelet endothelial cell adhesion molecule-1 (PECAM-1) is a cell-cell adhesion molecule that is expressed on circulating…
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Highly Cited
1993
Highly Cited
1993
Linkage on chromosome 3 of autoimmune diabetes and defective Fc receptor for IgG in NOD mice.
J. Prins
,
John A Todd
,
+7 authors
A. Sirotina
Science
1993
Corpus ID: 21280690
A congenic, non-obese diabetic (NOD) mouse strain that contains a segment of chromosome 3 from the diabetes-resistant mouse…
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Highly Cited
1989
Highly Cited
1989
Definition of mouse chromosome 1 and 3 gene linkage groups that are conserved on human chromosome 1: evidence that a conserved linkage group spans the centromere of human chromosome 1.
W. S. Moseley
,
M. F. Seldin
Genomics
1989
Corpus ID: 34591544
Highly Cited
1978
Highly Cited
1978
The association of chromosome 3 duplication and the Cornelia de Lange syndrome.
Golder N Wilson
,
V. Hieber
,
R. Schmickel
Jornal de Pediatria
1978
Corpus ID: 40232583
Highly Cited
1975
Highly Cited
1975
Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).
P. Allderdice
,
N. Browne
,
D. P. Murphy
American Journal of Human Genetics
1975
Corpus ID: 43475901
Close phenotypic similarity between two cases carrying a rec(3) dup q,inv(3) (p25q21), 12 additional infants from the same inv (3…
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