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5q34
A chromosome band present on 5q
National Institutes of Health
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Related topics
Related topics
7 relations
Chromosomes
DUSP1 wt Allele
EBF1 wt Allele
NKX2-5 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2007
2007
Bivariate Whole Genome Linkage Analysis for Femoral Neck Geometric Parameters and Total Body Lean Mass
F. Deng
,
P. Xiao
,
+7 authors
H. Deng
Journal of Bone and Mineral Research
2007
Corpus ID: 24831162
A genome‐wide bivariate analysis was conducted for femoral neck GPs and TBLM in a large white sample. We found QTLs shared by GPs…
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2006
2006
Serum Lipids in the GENECARD Study of Coronary Artery Disease Identify Quantitative Trait Loci and Phenotypic Subsets on Chromosomes 3q and 5q
Svati H. Shah
,
W. Kraus
,
+11 authors
E. Hauser
Annals of Human Genetics
2006
Corpus ID: 24239757
Coronary artery disease (CAD) and dyslipidemia have strong genetic components. Heterogeneity complicates evaluating genetics of…
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2006
2006
Delineation by molecular cytogenetics of 5q deletion breakpoints in myelodyplastic syndromes and acute myeloid leukemia.
B. Royer-Pokora
,
D. Trost
,
Nicola Müller
,
B. Hildebrandt
,
U. Germing
,
M. Beier
Cancer Genetics and Cytogenetics
2006
Corpus ID: 20946528
2004
2004
Evidence for Linkage between Juvenile Myoclonic Epilepsy–Related Idiopathic Generalized Epilepsy and 6p11‐12 in Dutch Families
D. Pinto
,
G. de Haan
,
+9 authors
B. Koeleman
Epilepsia
2004
Corpus ID: 25681816
Summary: Purpose: Previous linkage studies provided evidence for juvenile myoclonic epilepsy (JME) susceptibility loci at 6p11…
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2002
2002
ILAE Genetics Commission Conference Report: Molecular Analysis of Complex Genetic Epilepsies
E. Anderson
,
S. Berkovic
,
+18 authors
K. Weiss
Epilepsia
2002
Corpus ID: 44983979
Epilepsy is a diagnosis encompassing >40 clinical syndromes consisting of biochemical, anatomic, and physiologic changes that…
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Highly Cited
1998
Highly Cited
1998
The winged helix transcription factor Fkh10 is required for normal development of the inner ear
M. Hulander
,
W. Wurst
,
P. Carlsson
,
S. Enerbäck
Nature Genetics
1998
Corpus ID: 22999678
Fkh10 is a member of the forkhead family of winged helix transcriptional regulators. Genes encoding forkhead proteins are…
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1996
1996
Deletion mapping identifies loss of heterozygosity at 5p15.1-15.2, 5q11 and 5q34-35 in human male germ cell tumors.
Vundavalli V. Murty
,
Victor E. Reuter
,
G. Bosl
,
R. Chaganti
Oncogene
1996
Corpus ID: 25117372
Cytogenetic and loss of heterozygosity (LOH) studies of chromosome 5 in male germ cell tumors (GCTs) previously reported…
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1995
1995
Assignment of cardiac homeobox gene CSX to human chromosome 5q34.
I. Shiojima
,
I. Komuro
,
+5 authors
Y. Yazaki
Genomics
1995
Corpus ID: 9711651
Homeobox-containing genes play critical roles in regulating tissue-specific gene expression essential for tissue differentiation…
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1994
1994
The CL100 gene, which encodes a dual specificity (Tyr/Thr) MAP kinase phosphatase, is highly conserved and maps to human chromosome 5q34
E. Emslie
,
T. Jones
,
D. Sheer
,
S. Keyse
Human Genetics
1994
Corpus ID: 12590731
Expression of the human CL100 gene is induced in skin fibroblasts in response to oxidative/heat stress and growth factors. The…
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1985
1985
Nonreciprocal chromosome translocation t(5;14) in cancers of the kidney: adenocarcinoma of the renal parenchyma and transitional cell carcinoma of the kidney pelvis.
F. Hecht
,
C. Berger
,
A. Sandberg
Cancer Genetics and Cytogenetics
1985
Corpus ID: 3425784
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