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3p21.1
A chromosome band present on 3p
National Institutes of Health
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Related topics
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7 relations
ALAS1 wt Allele
Chromosome 3 Short Arm
Chromosomes
IL17RB wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2010
2010
Replication of association of 3p21.1 with susceptibility to bipolar disorder but not major depression
G. Breen
,
C. Lewis
,
+8 authors
P. McGuffin
Nature Genetics
2010
Corpus ID: 205341319
Replication of association of 3p21.1 with susceptibility to bipolar disorder but not major depression
Highly Cited
2010
Highly Cited
2010
Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p.
M. Gunay‐Aygun
,
Yifat Zivony-Elboum
,
+34 authors
T. Falik-Zaccai
Blood
2010
Corpus ID: 10116621
Gray platelet syndrome (GPS) is an inherited bleeding disorder characterized by macrothrombocytopenia and absence of platelet…
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Highly Cited
2009
Highly Cited
2009
Meta-analysis of genome-wide association data detects a risk locus for major mood disorders on chromosome 3p21.1
F. McMahon
,
N. Akula
,
+17 authors
M. Rietschel
Nature Genetics
2009
Corpus ID: 18799998
The major mood disorders, which include bipolar disorder and major depressive disorder (MDD), are considered heritable traits…
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2009
2009
Role of air pollution Particulate Matter (PM(2.5)) in the occurrence of loss of heterozygosity in multiple critical regions of 3p chromosome in human epithelial lung cells (L132).
F. Saint-Georges
,
G. Garçon
,
+5 authors
P. Shirali
Toxicology Letters
2009
Corpus ID: 31453681
Highly Cited
2003
Highly Cited
2003
Cloning and characterization of human CADPS and CADPS2, new members of the Ca2+-dependent activator for secretion protein family.
Felipe A. Cisternas
,
J. Vincent
,
S. Scherer
,
P. Ray
Genomics
2003
Corpus ID: 21091674
Highly Cited
2000
Highly Cited
2000
Linkage of a gene for familial hypobetalipoproteinemia to chromosome 3p21.1-22.
B. Yuan
,
R. Neuman
,
+6 authors
G. Schonfeld
American Journal of Human Genetics
2000
Corpus ID: 21925186
Familial hypobetalipoproteinemia (FHBL) is an apparently autosomal dominant disorder of lipid metabolism characterized by less…
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2000
2000
In vivo metabolism of ApoB, ApoA-I, and VLDL triglycerides in a form of hypobetalipoproteinemia not linked to the ApoB gene.
N. Elias
,
B. Patterson
,
G. Schonfeld
Arteriosclerosis, Thrombosis and Vascular Biology
2000
Corpus ID: 1449216
Familial hypobetalipoproteinemia (FHBL) is an autosomal codominant disorder that may result from different mutations in the…
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Highly Cited
2000
Highly Cited
2000
Loss of expression of the DRR 1 gene at chromosomal segment 3p21.1 in renal cell carcinoma
Liang Wang
,
J. Darling
,
+9 authors
David I. Smith
Genes, Chromosomes and Cancer
2000
Corpus ID: 24765920
Consistent deletion of DNA sequences in chromosomal band 3p21 observed in a variety of human tumors suggests the presence of one…
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Highly Cited
1996
Highly Cited
1996
A gene from human chromosomal band 3p21.1 encodes a highly conserved arginine-rich protein and is mutated in renal cell carcinomas.
V. Shridhar
,
S. Rivard
,
+6 authors
D. Smith
Oncogene
1996
Corpus ID: 42191461
We have identified a gene, called ARP for Arginine-rich protein, in human chromosomal band 3p21. It is approximately 600 Kb…
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1989
1989
Regional and physical mapping studies characterizing the Greig polysyndactyly 3;7 chromosome translocation, t(3;7)(p21.1;p13).
H. Drabkin
,
M. Sage
,
+7 authors
F. Ruddle
Genomics
1989
Corpus ID: 22010027
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