NLRP2 gene

Known as: NLR family, pyrin domain containing 2, PYPAF2, nucleotide-binding oligomerization domain, leucine rich repeat and pyrin domain containing 2 
This gene plays a role in the modulation of apoptotic signaling.
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
Central nervous system (CNS) trauma involves extensive cellular damage that is due, in part, to an innate inflammatory response… (More)
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Highly Cited
2009
Highly Cited
2009
Beckwith-Wiedemann syndrome (BWS) is a fetal overgrowth and human imprinting disorder resulting from the deregulation of a number… (More)
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Highly Cited
2007
Highly Cited
2007
MRE11-RAD50-NBS1 (MRN) is a conserved nuclease complex that exhibits properties of a DNA damage sensor and is critical in… (More)
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Highly Cited
2005
Highly Cited
2005
ATM has a central role in controlling the cellular responses to DNA damage. It and other phosphoinositide 3-kinase-related… (More)
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Review
2004
Review
2004
Nijmegen breakage syndrome is a recessive genetic disorder, characterized by elevated sensitivity to ionizing radiation… (More)
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Highly Cited
2002
Highly Cited
2002
DNA double-strand breaks represent the most potentially serious damage to a genome; hence, many repair proteins are recruited to… (More)
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Highly Cited
2002
Highly Cited
2002
Nijmegen breakage syndrome (NBS) is an autosomal recessive hereditary disease that shares some common defects with ataxia… (More)
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Highly Cited
2000
Highly Cited
2000
Ataxia-telangiectasia (A-T) and Nijmegen breakage syndrome (NBS) are recessive genetic disorders with susceptibility to cancer… (More)
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Highly Cited
1998
Highly Cited
1998
Nijmegen breakage syndrome (NBS), also known as ataxia-telangiectasia (AT) variant, is an autosomal recessive disorder… (More)
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Highly Cited
1998
Highly Cited
1998
A genetic screen for factors required for endocytosis in the budding yeast Saccharomyces cerevisiae previously identified PAN1… (More)
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