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10q22

A chromosome band present on 10q
National Institutes of Health

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4 relations
10qChromosomesPRF1 wt AlleleVDAC2 wt Allele

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2012
Highly Cited
2012
Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci.
Highly Cited
2009
Highly Cited
2009
Common variants at five new loci associated with early-onset inflammatory bowel disease
The inflammatory bowel diseases (IBD) Crohn's disease and ulcerative colitis are common causes of morbidity in children and young… 
Highly Cited
2005
Highly Cited
2005
Maternal segregation of the Dutch preeclampsia locus at 10q22 with a new member of the winged helix gene family
Preeclampsia is a pregnancy-associated disease with maternal symptoms but placental origin. Epigenetic inheritance is involved in… 
Highly Cited
2005
Highly Cited
2005
Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder
The large conductance calcium-sensitive potassium (BK) channel is widely expressed in many organs and tissues, but its in vivo… 
Highly Cited
2001
Highly Cited
2001
Discovery of new DNA amplification loci in prostate cancer by comparative genomic hybridization *
DNA sequence amplifications are involved in the progression of many tumor types, and have also been found in advanced prostate… 
Review
2000
Review
2000
A Novel Human Opsin in the Inner Retina
Here we report the identification of a novel human opsin, melanopsin, that is expressed in cells of the mammalian inner retina… 
Highly Cited
2000
Highly Cited
2000
Will the real Cowden syndrome please stand up: revised diagnostic criteria.
  • C. Eng
  • Journal of medical genetics
  • 2000
  • Corpus ID: 27076421
Cowden syndrome (CS, MIM 158350) is an autosomal dominant disorder with age related penetrance characterised by multiple… 
Review
2000
Review
2000
PTEN, a unique tumor suppressor gene.
  • P. Dahia
  • Endocrine-related cancer
  • 2000
  • Corpus ID: 27405328
For many years, it has been thought that the chromosome region 10q22-24 includes one or more genes that appear to play a role in… 
Highly Cited
1999
Highly Cited
1999
Immunohistochemical evidence of loss of PTEN expression in primary ductal adenocarcinomas of the breast.
Highly Cited
1997
Highly Cited
1997
Germline mutations in the PTEN/MMAC1 gene in patients with Cowden disease.
Cowden disease, also known as multiple hamartoma syndrome, is an autosomal dominant cancer syndrome with a high risk of breast… 
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