NDP gene

Known as: NDP, NORRIN, Norrie disease (pseudoglioma) 
 
National Institutes of Health

Papers overview

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2015
2015
BACKGROUND AND PURPOSE Norrin and its receptor Frizzled-4 have important roles in the blood-brain barrier development. This study… (More)
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2012
Highly Cited
2012
The basal ganglia, a brain structure related to motor control, is implicated in the modulation of epileptic discharges… (More)
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2011
2011
PURPOSE. Mice deficient in the secreted protein Norrin or its receptor Frizzled-4 (FZD4) exhibit incomplete vascularization of… (More)
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2011
2011
The Norrie disease gene (Ndp) codes for a secreted protein, Norrin, that activates canonical Wnt signaling by binding to its… (More)
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2006
2006
BACKGROUND To examine the contribution of mutations within the Norrie disease (NDP) gene to the clinically similar retinal… (More)
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2004
Highly Cited
2004
Incomplete retinal vascularization occurs in both Norrie disease and familial exudative vitreoretinopathy (FEVR). Norrin, the… (More)
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2003
2003
Norrie disease is a rare X-inked recessive condition characterized by congenital blindness and occasionally deafness and mental… (More)
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1999
Highly Cited
1999
Coats' disease is characterized by abnormal retinal vascular development (so-called 'retinal telangiectasis') which results in… (More)
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Highly Cited
1993
Highly Cited
1993
Familial exudative vitreoretinopathy (FEVR) is a hereditary disorder characterized by an abnormality of the peripheral retina… (More)
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1992
1992
Levels of nm23 gene product/nucleoside diphosphate kinase (NDP kinase) expression have been demonstrated to correlate inversely… (More)
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