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7p13
A chromosome band present on 7p
National Institutes of Health
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Related topics
Related topics
4 relations
Chromosome 7 Short Arm
Chromosomes
GLI3 wt Allele
NPC1L1 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2015
Highly Cited
2015
Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer
Erica J. Childs
,
E. Mocci
,
+59 authors
A. Klein
Nature Genetics
2015
Corpus ID: 17039820
Pancreatic cancer is the fourth leading cause of cancer death in the developed world. Both inherited high-penetrance mutations in…
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Highly Cited
2014
Highly Cited
2014
Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations.
S. Ganesh
,
D. Chasman
,
+51 authors
A. Chakravarti
American Journal of Human Genetics
2014
Corpus ID: 22851291
2010
2010
Identification of gene copy number variations in patients with mental retardation using array-CGH: Novel syndromes in a large French series.
S. Jaillard
,
S. Drunat
,
+21 authors
C. Dubourg
European Journal of Medical Genetics
2010
Corpus ID: 26127821
Highly Cited
2009
Highly Cited
2009
Genome-wide association study of exercise behavior in Dutch and American adults.
M. de Moor
,
Yong-jun Liu
,
+14 authors
H. Deng
Medicine & Science in Sports & Exercise
2009
Corpus ID: 604975
INTRODUCTION The objective of this study was to identify genetic variants that are associated with adult leisure time exercise…
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Highly Cited
2001
Highly Cited
2001
Deletions of PURA, at 5q31, and PURB, at 7p13, in myelodysplastic syndrome and progression to acute myelogenous leukemia
K. Lezon-Geyda
,
V. Najfeld
,
E. Johnson
Leukemia
2001
Corpus ID: 7186291
Deletions or monosomy of chromosomes 5 and 7 are frequently observed in myelodysplastic syndromes (MDS) and acute myelogenous…
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Highly Cited
2001
Highly Cited
2001
Sptrx‐2, a fusion protein composed of one thioredoxin and three tandemly repeated NDP‐kinase domains is expressed in human testis germ cells
C. Sadek
,
A. Damdimopoulos
,
M. Pelto-huikko
,
J. Gustafsson
,
G. Spyrou
,
A. Miranda-Vizuete
Genes to Cells
2001
Corpus ID: 20869820
Background Thioredoxins (Trx) are small redox proteins that function as general protein disulphide reductases and regulate…
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Highly Cited
1998
Highly Cited
1998
Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27.
H. Craig
,
M. Günel
,
+15 authors
R. Lifton
Human Molecular Genetics
1998
Corpus ID: 19471693
Cerebral cavernous malformation (CCM) is a Mendelian model of stroke, characterized by focal abnormalities in small intracranial…
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Highly Cited
1997
Highly Cited
1997
GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome
Seongman Kang
,
J. Graham
,
A. Olney
,
L. Biesecker
Nature Genetics
1997
Corpus ID: 31776794
Pallister-Hall syndrome (PHS, M146510) was first described in 1980 in six newborns. It is a pleiotropic disorder of human…
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Highly Cited
1990
Highly Cited
1990
GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity
J. Ruppert
,
B. Vogelstein
,
K. Arheden
,
K. Kinzler
Molecular and Cellular Biology
1990
Corpus ID: 10562788
The GLI oncogene, discovered by virtue of its amplification in human tumors, encodes a sequence-specific DNA-binding protein…
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Highly Cited
1984
Highly Cited
1984
The T cell receptor β chain genes are located on chromosome 6 in mice and chromosome 7 in humans
N. Caccia
,
M. Kronenberg
,
+9 authors
T. Mak
Cell
1984
Corpus ID: 26615965
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