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Retinitis Pigmentosa 10

Known as: RP10 
 
National Institutes of Health

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Retinitis Pigmentosa

Papers overview

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2017
2017
Pluvial flooding in European cities - A continental approach to urban flood modelling
Pluvial flooding is caused by localized intense rainfall and the flood models used to assess it are normally applied on a city… Expand
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2017
2017
VARIABILIDADE ESPACIAL DA RESISTÊNCIA DO SOLO À PENETRAÇÃO E DA PRODUTIVIDADE DO MILHO
O presente trabalho teve como objetivo estudar a variabilidade espacial da resistencia do solo a penetracao (RP), teor de agua no… Expand
2011
2011
Molecular recruitment as a basis for negative dominant inheritance? propagation of misfolding in oligomers of IMPDH1, the mutated enzyme in the RP10 form of retinitis pigmentosa.
Retinitis pigmentosa, causing progressive blindness, is genetically heterogeneous. RP10, due to a defect in inosine monophosphate… Expand
Highly Cited
2008
Highly Cited
2008
Therapeutic benefit derived from RNAi-mediated ablation of IMPDH1 transcripts in a murine model of autosomal dominant retinitis pigmentosa (RP10).
Mutations within the inosine 5'-monophosphate dehydrogenase 1 (IMPDH1) gene cause the RP10 form of autosomal dominant retinitis… Expand
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Highly Cited
2006
Highly Cited
2006
Genome‐wide identification of pseudogenes capable of disease‐causing gene conversion
Pseudogenes are remnants of gene duplication (nonprocessed pseudogenes) and retrotransposition (processed pseudogenes) events… Expand
Highly Cited
2004
Highly Cited
2004
On the molecular pathology of neurodegeneration in IMPDH1-based retinitis pigmentosa.
Retinitis pigmentosa (RP), the hereditary degenerative disease of the photoreceptor neurons of the retina, probably represents… Expand
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2004
2004
Evidence for a major gene (RP10) for autosomal dominant retinitis pigmentosa on chromosome 7q: linkage mapping in a second, unrelated family
Retinitis pigmentosa is a genetically heterogeneous form of retinal degeneration, which has X-linked, autosomal recessive and… Expand
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Highly Cited
2002
Highly Cited
2002
Mutations in the inosine monophosphate dehydrogenase 1 gene (IMPDH1) cause the RP10 form of autosomal dominant retinitis pigmentosa.
Autosomal dominant retinitis pigmentosa (adRP) is a heterogeneous set of progressive retinopathies caused by several distinct… Expand
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1996
1996
Reversible injury: creatinine kinase recovery restores bioenergetics and function.
In postischemia hearts, cytoplasmic creatinine kinase (CK) inactivation resulting from toxic oxygen metabolite injury may lead to… Expand
1995
1995
Structure and regulation of a Candida albicans RP10 gene which encodes an immunogenic protein homologous to Saccharomyces cerevisiae ribosomal protein 10.
The Candida albicans clone cDNA10 was isolated on the basis that it encodes a protein which is immunogenic during infections in… Expand
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