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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
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
2007
Highly Cited
2007
Significant evidence of one or more susceptibility loci for endometriosis with near-Mendelian inheritance on chromosome 7p13-15.
BACKGROUND Endometriosis is a common disease with a heritable component. The collaborative International Endogene Study consists… 
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
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
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
Point mutations in human GLI3 cause Greig syndrome.
Greig cephalopolysyndactyly syndrome (GCPS, MIM 175700) is a rare autosomal dominant developmental disorder characterized by… 
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… 
1987
1987
Fragile sites limited to lymphocytes: molecular recombination and malignancy.
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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