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Article

Inositol 5-phosphatases: insights from the Lowe syndrome protein OCRL

29 Feb 2012

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 22381590
DOI: 10.1016/j.tibs.2012.01.002

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Inositol 5-phosphatases: insights from the Lowe syndrome protein OCRLPMID 22381590Read ↗

The cellular and physiological functions of the Lowe syndrome protein OCRL1.Semantic proximity Read ↗

The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphataseSemantic proximity Read ↗

Structure and function of the Lowe syndrome protein OCRL1.Semantic proximity Read ↗

The oculocerebrorenal syndrome of Lowe: an update.Semantic proximity Read ↗

The PH domain proteins IPIP27A and B link OCRL1 to receptor recycling in the endocytic pathway.Semantic proximity Read ↗

The 5-phosphatase OCRL in Lowe syndrome and Dent disease 2.Semantic proximity Read ↗

Genotype & Phenotype in Lowe Syndrome: Specific <i>OCRL1</i> patient mutations differentially impact cellular phenotypesSemantic proximity Read ↗

Genotype & phenotype in Lowe Syndrome: specific OCRL1 patient mutations differentially impact cellular phenotypes.Semantic proximity Read ↗

Prenatal diagnosis of lowe syndrome: identification of a novel pathogenic variation in the OCRL1gene.Semantic proximity Read ↗

A novel OCRL1 mutation in a patient with the mild phenotype of Lowe syndrome.Semantic proximity Read ↗

Phosphoinositide phosphatases and disease.Semantic proximity Read ↗

"Lowe syndrome: A particularly severe phenotype without clinical kidney involvement".Semantic proximity Read ↗

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