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20q13.2-q13.3
A chromosome band present on 20q
National Institutes of Health
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6 relations
20q
AURKA wt Allele
Chromosomes
GNAS wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2009
2009
Polymorphisms in the neural nicotinic acetylcholine receptor α4 subunit (CHRNA4) are associated with ADHD in a genetic isolate
Deeann Wallis
,
Deeann Wallis
,
+12 authors
M. Muenke
Attention deficit and hyperactivity disorders
2009
Corpus ID: 23770324
The neural nicotinic acetylcholine receptor α4 subunit (CHRNA4), at 20q13.2–q13.3, is an important candidate gene for conferring…
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Review
2008
Review
2008
AURKA overexpression accompanies dysregulation of DNA-damage response genes in invasive urothelial cell carcinoma
A. Veerakumarasivam
,
L. Goldstein
,
+7 authors
J. Kelly
Cell Cycle
2008
Corpus ID: 2397168
Invasive urothelial cell carcinoma (UCC) is characterized by increased chromosomal instability (CIN) and follows an aggressive…
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Highly Cited
2000
Highly Cited
2000
The hD52 (TPD52) gene is a candidate target gene for events resulting in increased 8q21 copy number in human breast carcinoma
R. Balleine
,
M. Fejzo
,
Pavani Sathasivam
,
P. Basset
,
C. Clarke
,
J. A. Byrne
Genes, Chromosomes and Cancer
2000
Corpus ID: 8775668
Chromosome band 8q21 is frequently overrepresented in human cancer, but to date no 8q21 target gene has been proposed. The hD52…
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1999
1999
Functional analysis and chromosomal mapping of Gata5, a gene encoding a zinc finger DNA-binding protein
G. Nemer
,
S. Qureshi
,
D. Malo
,
M. Nemer
Mammalian Genome
1999
Corpus ID: 23837090
Abstract. The GATA family of zinc finger proteins are transcriptional regulators with critical functions in lineage…
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Highly Cited
1998
Highly Cited
1998
Cloning of a third member of the D52 gene family indicates alternative coding sequence usage in D52-like transcripts.
C. Nourse
,
M. Mattei
,
P. Gunning
,
J. A. Byrne
Biochimica et Biophysica Acta
1998
Corpus ID: 6265720
Highly Cited
1997
Highly Cited
1997
Tissue‐specific expression of the human laminin α5‐chain, and mapping of the gene to human chromosome 20q13.2‐13.3 and to distal mouse chromosome 2 near the locus for the ragged (Ra) mutation
M. Durkin
,
F. Loechel
,
M. Mattei
,
B. Gilpin
,
R. Albrechtsen
,
U. Wewer
FEBS Letters
1997
Corpus ID: 45286880
Highly Cited
1994
Highly Cited
1994
Refinement of the localization of the gene for neuronal nicotinic acetylcholine receptor alpha 4 subunit (CHRNA4) to human chromosome 20q13.2-q13.3.
O. Steinlein
,
R. Smigrodzki
,
+4 authors
F. Vogel
Genomics
1994
Corpus ID: 39049756
Using a human fetal brain genomic library and a P1 clone library from Genome Systems Inc, a cosmid and P1-clone walk has been…
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Highly Cited
1993
Highly Cited
1993
Localization of the genes encoding the melanocortin-2 (adrenocorticotropic hormone) and melanocortin-3 receptors to chromosomes 18p11.2 and 20q13.2-q13.3 by fluorescence in situ hybridization.
I. Gantz
,
T. Tashiro
,
+6 authors
T. Yamada
Genomics
1993
Corpus ID: 34460739
Adrenocorticotropic hormone (ACTH) and [alpha]-, [beta]-, and [gamma]-melanocyte-stimulating hormone (MSH) are products of…
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Highly Cited
1991
Highly Cited
1991
Chromosomal assignments of the human endothelin family genes: the endothelin-1 gene (EDN1) to 6p23-p24, the endothelin-2 gene (EDN2) to 1p34, and the endothelin-3 gene (EDN3) to 20q13.2-q13.3.
T. Arinami
,
Mikiyo Ishikawa
,
+4 authors
Hideo Hamaguchi
American Journal of Human Genetics
1991
Corpus ID: 37550466
Chromosomal assignments of the genes for the human endothelin family, the endothelin-1 gene (EDN1), the endothelin-2 gene (EDN2…
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1991
1991
The gene for the novel vasoactive peptide endothelin 3 (EDN3) is localized to human chromosome 20q13.2-qter.
V. Rao
,
C. Löffler
,
I. Hansmann
Genomics
1991
Corpus ID: 46224642
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