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17p13.2

A chromosome band present on 17p
National Institutes of Health

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5 relations
Chromosome 17 Short ArmChromosomesGP1BA wt AllelePELP1 wt Allele

Papers overview

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2016
2016
Comprehensive assessment of the expression of the SWI/SNF complex defines two distinct prognostic subtypes of ovarian clear cell carcinoma
Somatic mutations in the ARID1A tumor-suppressor gene have been frequently identified in ovarian clear cell carcinoma (CCC) cases… 
2016
2016
Olmsted Syndrome in a Family
Olmsted syndrome (OS) is a rare disorder characterized by the combination of periorificial, keratotic plaques, and bilateral… 
2014
2014
Rare De Novo Copy Number Variants in Patients with Congenital Pulmonary Atresia
Background Ongoing studies using genomic microarrays and next-generation sequencing have demonstrated that the genetic… 
2013
2013
Linkage Analysis in Familial Non-Lynch Syndrome Colorectal Cancer Families from Sweden
Family history is a major risk factor for colorectal cancer and many families segregate the disease as a seemingly monogenic… 
2010
2010
Evidence for three loci modifying age‐at‐onset of Alzheimer's disease in early‐onset PSEN2 families
Families with early‐onset Alzheimer's disease (AD) sharing a single PSEN2 mutation exhibit a wide range of age‐at‐onset… 
2010
2010
High-resolution oligonucleotide array comparative genomic hybridization study and methylation status of the RPS14 gene in de novo myelodysplastic syndromes.
2007
2007
Prognostic value of DNA alterations on chromosome 17p13.2 for intrahepatic cholangiocarcinoma.
AIM To characterize and evaluate DNA alterations among intrahepatic cholangiocarcinoma (ICC) patients. METHODS DNA from tumor… 
2004
2004
Chromosome 17p13.2 transfer reverts transformation phenotypes and fas‐mediated apoptosis in breast epithelial cells
Transformation of the human breast epithelial cells (HBEC) MCF‐10F with the carcinogen benz(a)pyrene (BP) into BP1‐E cells… 
2001
2001
Detailed deletion mapping in sporadic breast cancer at chromosomal region 17p13 distal to the TP53 gene: association with clinicopathological parameters
Chromosome 17p is among the most frequently deleted regions in a variety of human malignancies including breast cancer. This… 
2001
2001
A physical and expression map of the D17S1810–D17S1353 region spanning the central areolar choroidal dystrophy locus
Central areolar choroidal dystrophy (CACD) causes bilateral irreversible central visual loss in the 5th to 7th decades. The… 
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