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7p13

A chromosome band present on 7p
National Institutes of Health

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4 relations
Chromosome 7 Short ArmChromosomesGLI3 wt AlleleNPC1L1 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
Pancreatic cancer is the fourth leading cause of cancer death in the developed world. Both inherited high-penetrance mutations in… 
Highly Cited
2014
Highly Cited
2014
Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations.
2010
2010
Identification of gene copy number variations in patients with mental retardation using array-CGH: Novel syndromes in a large French series.
Highly Cited
2009
Highly Cited
2009
Genome-wide association study of exercise behavior in Dutch and American adults.
INTRODUCTION The objective of this study was to identify genetic variants that are associated with adult leisure time exercise… 
Highly Cited
2001
Highly Cited
2001
Deletions of PURA, at 5q31, and PURB, at 7p13, in myelodysplastic syndrome and progression to acute myelogenous leukemia
Deletions or monosomy of chromosomes 5 and 7 are frequently observed in myelodysplastic syndromes (MDS) and acute myelogenous… 
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
Background Thioredoxins (Trx) are small redox proteins that function as general protein disulphide reductases and regulate… 
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.
Cerebral cavernous malformation (CCM) is a Mendelian model of stroke, characterized by focal abnormalities in small intracranial… 
Highly Cited
1997
Highly Cited
1997
GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome
Pallister-Hall syndrome (PHS, M146510) was first described in 1980 in six newborns. It is a pleiotropic disorder of human… 
Highly Cited
1990
Highly Cited
1990
GLI3 encodes a 190-kilodalton protein with multiple regions of GLI similarity
The GLI oncogene, discovered by virtue of its amplification in human tumors, encodes a sequence-specific DNA-binding protein… 
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
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