NPHP4 gene

Known as: SLSN4, KIAA0673, nephronophthisis 4 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2002-2014
02420022014

Papers overview

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2014
2014
The protein nephrocystin-4 (NPHP4) is widespread in ciliated organisms, and defects in NPHP4 cause nephronophthisis and blindness… (More)
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2011
2011
Nephronophthisis (NPHP) is an autosomal recessive kidney disease that is often associated with vision and/or brain defects. To… (More)
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2008
2008
Cone-rod dystrophy is a retinal degenerative disorder occurring naturally in man and dog. Here we identify a novel gene for early… (More)
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Highly Cited
2007
Highly Cited
2007
Cerebello-oculo-renal syndrome (CORS), also called Joubert syndrome type B, and Meckel (MKS) syndrome belong to the group of… (More)
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Highly Cited
2007
Highly Cited
2007
Protein-protein interaction analyses have uncovered a ciliary and basal body protein network that, when disrupted, can result in… (More)
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2005
2005
Nephronophthisis (NPH) is a cystic kidney disorder that causes end-stage renal failure in children. Five nephrocystin… (More)
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Highly Cited
2005
Highly Cited
2005
RPGR-interacting protein 1 (RPGRIP1) is a key component of cone and rod photoreceptor cells, where it interacts with RPGR… (More)
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2004
2004
Nephronophthisis (NPH) is an autosomal recessive kidney disease characterized by tubular basement membrane disruption… (More)
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Highly Cited
2003
Highly Cited
2003
Nephronophthisis (NPHP), a group of autosomal recessive cystic kidney disorders, is the most common genetic cause of progressive… (More)
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Highly Cited
2002
Highly Cited
2002
Nephronophthisis (NPHP) comprises a group of autosomal recessive cystic kidney diseases, which constitute the most frequent… (More)
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