17p13.2

A chromosome band present on 17p
National Institutes of Health

Topic mentions per year

Topic mentions per year

2000-2016
02420002016

Papers overview

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2014
2014
Cystinosis is caused by mutations in the CTNS gene (17p13.2), which encodes for a lysosomal cystine/proton symporter termed… (More)
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2014
2014
Autism spectrum disorders (ASDs) are a group of neurodevelopmental conditions with a demonstrated genetic etiology. Rare (<1… (More)
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2010
2010
Families with early-onset Alzheimer's disease (AD) sharing a single PSEN2 mutation exhibit a wide range of age-at-onset… (More)
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2007
2007
AIM To characterize and evaluate DNA alterations among intrahepatic cholangiocarcinoma (ICC) patients. METHODS DNA from tumor… (More)
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2004
2004
Aneurysmal bone cyst is a benign, cystic lesion of bone composed of blood-filled spaces separated by fibrous septa. Relatively… (More)
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Highly Cited
2004
Highly Cited
2004
Hedgehog signaling is suggested to be a major oncogenic pathway in medulloblastoma, which arises from aberrant development of… (More)
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Highly Cited
2003
Highly Cited
2003
X-linked inhibitor of apoptosis (XIAP) is the most potent member of the IAP family that exerts antiapoptotic effects by… (More)
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2001
2001
Type A receptors of gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter, contain alpha, beta, delta, gamma, and rho… (More)
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2001
2001
Chromosome 17p is among the most frequently deleted regions in a variety of human malignancies including breast cancer. This… (More)
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Highly Cited
2000
Highly Cited
2000
X-linked inhibitor of apoptosis protein (XIAP) is a potent modulator of programmed cell death. XIAP specifically binds and… (More)
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