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1p34
A chromosome band present on 1p
National Institutes of Health
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Related topics
Related topics
8 relations
Chromosome 1 Short Arm
Chromosomes
EDN2 wt Allele
HDAC1 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2006
Highly Cited
2006
Combined microarray analysis of small cell lung cancer reveals altered apoptotic balance and distinct expression signatures of MYC family gene amplification
Y. Kim
,
L. Girard
,
+5 authors
J. Pollack
Oncogene
2006
Corpus ID: 21377251
DNA amplifications and deletions frequently contribute to the development and progression of lung cancer. To identify such novel…
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Highly Cited
2004
Highly Cited
2004
Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis.
Qing Wang
,
Shaoqi Rao
,
+8 authors
E. Topol
American journal of human genetics
2004
Corpus ID: 45359048
The most frequent causes of death and disability in the Western world are atherosclerotic coronary artery disease (CAD) and acute…
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Highly Cited
2003
Highly Cited
2003
A novel giant gene CSMD3 encoding a protein with CUB and sushi multiple domains: a candidate gene for benign adult familial myoclonic epilepsy on human chromosome 8q23.3-q24.1.
A. Shimizu
,
S. Asakawa
,
+6 authors
N. Shimizu
Biochemical and biophysical research…
2003
Corpus ID: 40048533
Highly Cited
2001
Highly Cited
2001
Genome-wide analyses on loss of heterozygosity in hepatocellular carcinoma in Southern China.
S. P. Li
,
H. Y. Wang
,
+7 authors
Y. Zeng
Journal of hepatology
2001
Corpus ID: 45268500
Highly Cited
2001
Highly Cited
2001
Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34
H. Koillinen
,
F. Wong
,
+8 authors
J. Kere
European Journal of Human Genetics
2001
Corpus ID: 10217201
The Van der Woude syndrome (VWS) is a dominantly inherited developmental disorder characterized by pits and/or sinuses of the…
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Highly Cited
1997
Highly Cited
1997
Loss of heterozygosity on the short arm of chromosomes 1 and 3 in sporadic pheochromocytoma and extra-adrenal paraganglioma.
M. P. Vargas
,
Z. Zhuang
,
C. Wang
,
A. Vortmeyer
,
W. Linehan
,
M. Merino
Human pathology
1997
Corpus ID: 19476684
Review
1992
Review
1992
Interleukin-6 and its receptor: a paradigm for cytokines.
T. Kishimoto
,
S. Akira
,
T. Taga
Science
1992
Corpus ID: 28661112
Many cytokines and cytokine receptors involved in the regulation of hematopoiesis, immune responses, and inflammation have been…
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Highly Cited
1992
Highly Cited
1992
A novel endothelial cell surface receptor tyrosine kinase with extracellular epidermal growth factor homology domains
J. Partanen
,
E. Armstrong
,
+6 authors
K. Alitalo
Molecular and cellular biology
1992
Corpus ID: 45677983
Endothelial cell surfaces play key roles in several important physiological and pathological processes such as blood clotting…
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Highly Cited
1992
Highly Cited
1992
Cloning of human lysyl hydroxylase: complete cDNA-derived amino acid sequence and assignment of the gene (PLOD) to chromosome 1p36.3----p36.2.
T. Hautala
,
M. Byers
,
R. Eddy
,
T. Shows
,
K. Kivirikko
,
R. Myllylä
Genomics
1992
Corpus ID: 24822820
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
,
M. Ishikawa
,
+4 authors
H. 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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