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19q13.31
A chromosome band present on 19q
National Institutes of Health
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Related topics
Related topics
3 relations
19q
Chromosomes
POU2F2 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Knockdown of ZNF233 suppresses hepatocellular carcinoma cell proliferation and tumorigenesis.
Wenjuan Xie
,
Xiaojing Qiao
,
+4 authors
Yanhua Wu
Gene
2018
Corpus ID: 52156073
2017
2017
Identification of breast cancer associated variants that modulate transcription factor binding
Yunxian Liu
,
Ninad M Walavalkar
,
M. Dozmorov
,
S. Rich
,
M. Civelek
,
M. Guertin
PLoS genetics
2017
Corpus ID: 14018260
Genome-wide association studies (GWAS) have discovered thousands loci associated with disease risk and quantitative traits, yet…
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Highly Cited
2012
Highly Cited
2012
Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients
Linlu Zhao
,
E. Triche
,
+4 authors
A. Dewan
BMC Pregnancy and Childbirth
2012
Corpus ID: 3486487
BackgroundSpecific genetic contributions for preeclampsia (PE) are currently unknown. This genome-wide association study (GWAS…
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Review
2011
Review
2011
The genetics of the human APOE polymorphism.
D. Seripa
,
G. D’Onofrio
,
F. Panza
,
L. Cascavilla
,
C. Masullo
,
A. Pilotto
Rejuvenation research
2011
Corpus ID: 11506105
Abstract The genetic origin of the three common variants of the human apolipoprotein E (apoE) protein, known as E2, E3 and E4…
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2010
2010
Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family.
H. Reutter
,
F. Rüschendorf
,
+9 authors
M. Ludwig
Birth defects research. Part A, Clinical and…
2010
Corpus ID: 20398592
BACKGROUND The bladder exstrophy-epispadias complex (BEEC) is a spectrum of anomalies involving the abdominal wall, pelvis…
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Highly Cited
2009
Highly Cited
2009
Chromosomal imbalances and partial uniparental disomies in primary central nervous system lymphoma
H. Schwindt
,
I. Vater
,
+9 authors
R. Siebert
Leukemia
2009
Corpus ID: 2013202
To determine the pattern of genetic alterations in primary central nervous system lymphomas (PCNSL), 19 PCNSL were studied by…
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Highly Cited
2006
Highly Cited
2006
Integration specificity of phage phiC31 integrase in the human genome.
T. Chalberg
,
Joylette L. Portlock
,
+5 authors
M. Calos
Journal of molecular biology
2006
Corpus ID: 7344796
Highly Cited
2006
Highly Cited
2006
Molecular analysis of chromosomal rearrangements in mammalian cells after phiC31-mediated integration.
A. Ehrhardt
,
J. Engler
,
Hui Xu
,
A. Cherry
,
M. Kay
Human gene therapy
2006
Corpus ID: 15126392
Reports on insertional mutagenesis due to integration of gene therapy vectors into the host genome have raised concerns about the…
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2006
2006
The gene overexpressed in polycythemia rubra vera, PRV‐1, and the gene encoding a neutrophil alloantigen, NB1, are alleles of a single gene, CD177, in chromosome band 19q13.31
L. Caruccio
,
M. Bettinotti
,
A. Director-Myska
,
D. Arthur
,
D. Stroncek
Transfusion
2006
Corpus ID: 12855915
BACKGROUND: PRV‐1 mRNA is overexpressed by neutrophils from polycythemia vera patients and is homologous to NB1 a gene…
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2005
2005
Meta-analysis of four new genome scans for lipid parameters and analysis of positional candidates in positive linkage regions
B. Heijmans
,
M. Beekman
,
+8 authors
P. Slagboom
European Journal of Human Genetics
2005
Corpus ID: 9414939
Lipid levels in plasma strongly influence the risk for coronary heart disease. To localise and subsequently identify genes…
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