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10q22

A chromosome band present on 10q
National Institutes of Health

Topic mentions per year

Topic mentions per year

1982-2018
05101519822018

Related topics

Related topics

3 relations
10qChromosomesVDAC2 wt Allele

Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
10q22
Chromosomes
10q
VDAC2 wt Allele

Papers overview

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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… (More)
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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… (More)
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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… (More)
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Highly Cited
2000
Highly Cited
2000
Will the real Cowden syndrome please stand up: revised diagnostic criteria.
Cowden syndrome (CS, MIM 158350) is an autosomal dominant disorder with age related penetrance characterised by multiple… (More)
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2000
2000
Human sphingosine-1-phosphate lyase: cDNA cloning, functional expression studies and mapping to chromosome 10q22(1).
Sphingosine-1-phosphate lyase catalyzes the last step in sphingolipid breakdown, the cleavage of phosphorylated sphingoid bases… (More)
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Highly Cited
1999
Highly Cited
1999
Immunohistochemical evidence of loss of PTEN expression in primary ductal adenocarcinomas of the breast.
Germline mutations in PTEN, encoding a dual-specificity phosphatase on 10q23.3, cause Cowden syndrome (CS), which is… (More)
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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… (More)
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1997
1997
Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome.
Juvenile polyposis syndrome (JPS; MIM 174900) is an autosomal dominant condition with incomplete penetrance characterized by… (More)
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1994
1994
Loss of heterozygosity for 10q22-10qter in malignant melanoma progression.
Karyotypic and molecular data indicate that genetic events involving the chromosome region 10q22-10qter may be related to… (More)
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1993
1993
Involvement of 10q22 in leiomyoma.
Cytogenetic investigation of uterine leiomyomas revealed a rearranged 10q22 present in nine tumors as a clonal change in most of… (More)
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