CCT3 gene

Known as: CHAPERONIN CONTAINING TCP1, SUBUNIT 3, CCT-GAMMA, CCTG 
 
National Institutes of Health

Papers overview

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Review
2017
Review
2017
Postoperative chemoradiation and perioperative chemotherapy using epirubicin/cisplatin/5-fluorouracil (ECF) represent two… (More)
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Highly Cited
2012
Highly Cited
2012
BACKGROUND PAPA syndrome is a recently identified hereditary autoinflammatory syndrome clinically characterized by pyogenic… (More)
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Highly Cited
2009
Highly Cited
2009
Myotonic dystrophy (DM) is a genetic disorder caused by the expression (as RNA) of expanded CTG or CCTG repeats. The alternative… (More)
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Review
2005
Review
2005
Myotonic dystrophy (dystrophia myotonica, DM) is the most common form of muscular dystrophy in adults. The presence of two… (More)
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Highly Cited
2004
Highly Cited
2004
Myotonic dystrophy (DM) is caused by either an untranslated CTG expansion in the 3' untranslated region of the DMPK gene on… (More)
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Highly Cited
2004
Highly Cited
2004
Myotonic dystrophy (DM) type 1 is caused by an expansion of a CTG repeat in the DMPK gene and type 2 by a CCTG repeat in the ZNF9… (More)
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Highly Cited
2003
Highly Cited
2003
BACKGROUND Myotonic dystrophy types 1 (DM1) and 2 (DM2/proximal myotonic myopathy PROMM) are dominantly inherited disorders with… (More)
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Highly Cited
2003
Highly Cited
2003
Myotonic dystrophy (DM), the most common form of muscular dystrophy in adults, is a clinically and genetically heterogeneous… (More)
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Highly Cited
2002
Highly Cited
2002
Myotonic dystrophy is a complex neuromuscular disorder associated with DNA expansion mutations in two different genes. In DM1 a… (More)
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Highly Cited
2001
Highly Cited
2001
Myotonic dystrophy (DM), the most common form of muscular dystrophy in adults, can be caused by a mutation on either chromosome… (More)
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