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7p13

A chromosome band present on 7p
National Institutes of Health

Related topics

Related topics

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… Expand
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2009
2009
Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31.
OBJECTIVE The majority of research into functional psychosis has proceeded under the assumption that schizophrenia and bipolar… Expand
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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
Background Thioredoxins (Trx) are small redox proteins that function as general protein disulphide reductases and regulate… Expand
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… Expand
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Highly Cited
2000
Highly Cited
2000
Evidence for a Niemann-pick C (NPC) gene family: identification and characterization of NPC1L1.
Niemann-Pick type C1 (NPC1) disease is caused by defects in the NPC1 protein, which result in perturbation of subcellular… Expand
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… Expand
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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… Expand
Highly Cited
1997
Highly Cited
1997
Point mutations in human GLI3 cause Greig syndrome.
Greig cephalopolysyndactyly syndrome (GCPS, MIM 175700) is a rare autosomal dominant developmental disorder characterized by… Expand
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… Expand
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
Homologous clones that encode the beta chain of the T cell antigen receptor have been isolated recently from both murine and… Expand
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