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1p34.3
A chromosome band present on 1p
National Institutes of Health
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Related topics
Related topics
12 relations
CDCA8 wt Allele
CLSPN wt Allele
Chromosome 1 Short Arm
Chromosomes
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2010
Review
2010
ZC3H12A (MCPIP1): molecular characteristics and clinical implications.
Ricardo A Cifuentes
,
Paola Cruz-Tapias
,
A. Rojas-Villarraga
,
J. Anaya
Clinica chimica acta; international journal of…
2010
Corpus ID: 38013969
2008
2008
Functional copy number changes in Sézary syndrome: toward an integrated molecular cytogenetic map III.
X. Mao
,
S. McElwaine
Cancer Genetics and Cytogenetics
2008
Corpus ID: 32197015
2008
2008
Comparative analysis of an unusual gene arrangement in the human chromosome 1.
I. Makałowska
Gene
2008
Corpus ID: 31879804
2006
2006
Microarray‐based CGH of sporadic and syndrome‐related pheochromocytomas using a 0.1–0.2 Mb bacterial artificial chromosome array spanning chromosome arm 1p
M. Aarts
,
H. Dannenberg
,
+7 authors
R. D. de Krijger
Genes, Chromosomes and Cancer
2006
Corpus ID: 37995683
Pheochromocytomas (PCC) are relatively rare neuroendocrine tumors, mainly of the adrenal medulla. They arise sporadically or…
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2004
2004
Gene structure and evolution of testicular haploid germ cell-specific genes, Oxct2a and Oxct2b.
M. Onishi
,
T. Yasunaga
,
Hiromitsu Tanaka
,
Y. Nishimune
,
M. Nozaki
Genomics
2004
Corpus ID: 41285040
Review
2002
Review
2002
Genome wide detection of oncogene amplifications in nasopharyngeal carcinoma by array based comparative genomic hybridization.
A. Hui
,
K. Lo
,
P. Teo
,
K. To
,
D. Huang
International Journal of Oncology
2002
Corpus ID: 14758564
We have applied the method of genomic microarray to investigate amplification of oncogenes throughout the genome of…
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Highly Cited
2001
Highly Cited
2001
An early lesion in hepatic carcinogenesis: Loss of heterozygosity in human cirrhotic livers and dysplastic nodules at the 1p36‐p34 region
Min Sun
,
J. Eshleman
,
+5 authors
O. Sudilovsky
Hepatology
2001
Corpus ID: 20480097
Loss of heterozygosity (LOH) of chromosome 1 has been suggested, by karyotyping, to be an initial episode in human…
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Highly Cited
2000
Highly Cited
2000
Characterization of the human and mouse HEY1, HEY2, and HEYL genes: cloning, mapping, and mutation screening of a new bHLH gene family.
Christian Steidl
,
C. Leimeister
,
+6 authors
Manfred Gessler
Genomics
2000
Corpus ID: 33433866
Many basic helix-loop-helix (bHLH) transcription factors are known as key regulators of embryonic development or differentiation…
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2000
2000
Allelotype and loss of heterozygosity around the L-myc gene locus in primary lung cancers.
C. Mendoza
,
H. Sato
,
+6 authors
M. Yamakido
Lung Cancer
2000
Corpus ID: 31518373
1996
1996
Reassignment of MYCL1 to human chromosome 1p34.3 by fluorescence in situ hybridization.
F. Speleman
,
G. V. Camp
,
N. V. Roy
Cytogenetics and Cell Genetics
1996
Corpus ID: 21145700
MYCL1 has been previously mapped to 1p32. This position was in contradiction with our mapping data of 1p deletions in…
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