Compensatory Role of Inositol 5-Phosphatase INPP5B to OCRL in Primary Cilia Formation in Oculocerebrorenal Syndrome of Lowe
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Title
Compensatory Role of Inositol 5-Phosphatase INPP5B to OCRL in Primary Cilia Formation in Oculocerebrorenal Syndrome of Lowe
Authors
Keywords
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Journal
PLoS One
Volume 8, Issue 6, Pages e66727
Publisher
Public Library of Science (PLoS)
Online
2013-06-22
DOI
10.1371/journal.pone.0066727
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Related references
Note: Only part of the references are listed.- Inositol polyphosphate 5-phosphatases; new players in the regulation of cilia and ciliopathies
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- OCRL localizes to the primary cilium: a new role for cilia in Lowe syndrome
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- ARL13B, PDE6D, and CEP164 form a functional network for INPP5E ciliary targeting
- (2012) M. C. Humbert et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- OCRL1 Modulates Cilia Length in Renal Epithelial Cells
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- (2010) C. A. Murga-Zamalloa et al. HUMAN MOLECULAR GENETICS
- From lowe syndrome to Dent disease: correlations between mutations of the OCRL1 gene and clinical and biochemical phenotypes
- (2010) Haifa Hichri et al. HUMAN MUTATION
- Amot Recognizes a Juxtanuclear Endocytic Recycling Compartment via a Novel Lipid Binding Domain
- (2010) Brigitte Heller et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Mouse Model for Lowe Syndrome/Dent Disease 2 Renal Tubulopathy
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- X-inactivation analysis of embryonic lethality in Ocrl wt/−;Inpp5b −/− mice
- (2010) David J. Bernard et al. MAMMALIAN GENOME
- Species-specific difference in expression and splice-site choice in Inpp5b, an inositol polyphosphate 5-phosphatase paralogous to the enzyme deficient in Lowe Syndrome
- (2010) Susan P. Bothwell et al. MAMMALIAN GENOME
- Functional genomic screen for modulators of ciliogenesis and cilium length
- (2010) Joon Kim et al. NATURE
- Lowe syndrome patient fibroblasts display Ocrl1-specific cell migration defects that cannot be rescued by the homologous Inpp5b phosphatase
- (2009) Brian G. Coon et al. HUMAN MOLECULAR GENETICS
- Human retinopathy-associated ciliary protein retinitis pigmentosa GTPase regulator mediates cilia-dependent vertebrate development
- (2009) Amiya K. Ghosh et al. HUMAN MOLECULAR GENETICS
- INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse
- (2009) Monique Jacoby et al. NATURE GENETICS
- Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies
- (2009) Stephanie L Bielas et al. NATURE GENETICS
- Inherited cerebrorenal syndromes
- (2009) Scott J. Schurman et al. Nature Reviews Nephrology
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