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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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2018
2018
Title 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… 
2014
2014
Genetic association- and linkage studies in colorectal cancer
Colorectal cancer (CRC) is the third most common cancer type in the Western world. Over one million patients are diagnosed… 
2014
2014
Copy number variation in Han Chinese individuals with autism spectrum disorder
Autism spectrum disorders (ASDs) are a group of neurodevelopmental conditions with a demonstrated genetic etiology. Rare (<1… 
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… 
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… 
Review
2004
Review
2004
Neuro-Oncology in a Nutshell
Yu et al. vaccinated 12 patients suffering from malignant glioma (10 glioblastoma multiforme; 9 recurrent, one at initial… 
2002
2002
[Loss of heterozygosity fine mapping of chromosome 17p13 in transitional cell carcinoma of human urinary bladder].
OBJECTIVE To determine the frequency and common deletion region of allelic losses on chromosome 17p13 in transitional cell… 
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