10q24

A chromosome band present on 10q
National Institutes of Health

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19 relations
10qABCC2 wt AlleleCYP2C18 wt AlleleCYP2C9 wt Allele
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Papers overview

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Highly Cited
2013
Highly Cited
2013
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
BACKGROUND Findings from family and twin studies suggest that genetic contributions to psychiatric disorders do not in all cases… (More)
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Highly Cited
2013
Highly Cited
2013
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis
We performed a genome-wide association study of non-Hispanic, white individuals with fibrotic idiopathic interstitial pneumonias… (More)
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Highly Cited
2009
Highly Cited
2009
Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy.
CONTEXT Clopidogrel therapy improves cardiovascular outcomes in patients with acute coronary syndromes and following percutaneous… (More)
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Highly Cited
2005
Highly Cited
2005
Infantile onset spinocerebellar ataxia is caused by recessive mutations in mitochondrial proteins Twinkle and Twinky.
Infantile onset spinocerebellar ataxia (IOSCA) (MIM 271245) is a severe autosomal recessively inherited neurodegenerative… (More)
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Highly Cited
2005
Highly Cited
2005
Somatic mutations in the PTCH, SMOH, SUFUH and TP53 genes in sporadic basal cell carcinomas.
BACKGROUND Basal cell carcinoma (BCC) of the skin is the most common human cancer. The genetic alterations underlying BCC… (More)
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Highly Cited
2004
Highly Cited
2004
Combined histopathological and molecular cytogenetic stratification of medulloblastoma patients.
This study examined the utility of stratifying children with medulloblastomas by a combination of refined histopathological… (More)
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Review
2003
Review
2003
PTEN signaling pathways in melanoma
Phosphatase and tensin homolog deleted in from chromosome ten (PTEN), initially also known as mutated in multiple advanced… (More)
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Highly Cited
2002
Highly Cited
2002
Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy.
Autosomal dominant lateral temporal epilepsy (EPT; OMIM 600512) is a form of epilepsy characterized by partial seizures, usually… (More)
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Highly Cited
1998
Highly Cited
1998
A novel gene, LGI1, from 10q24 is rearranged and downregulated in malignant brain tumors
Loss of heterozygosity for 10q23–26 is seen in over 80% of glioblastoma multiforme tumors. We have used a positional cloning… (More)
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Highly Cited
1996
Highly Cited
1996
A human canalicular multispecific organic anion transporter (cMOAT) gene is overexpressed in cisplatin-resistant human cancer cell lines with decreased drug accumulation.
By targeting the ATP binding conserved domain in three ATP binding cassette superfamily proteins (P-glycoprotein, multidrug… (More)
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