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Title
Recognition of the F&H motif by the Lowe syndrome protein OCRL
Authors
Keywords
-
Journal
NATURE STRUCTURAL & MOLECULAR BIOLOGY
Volume 18, Issue 7, Pages 789-795
Publisher
Springer Nature
Online
2011-06-13
DOI
10.1038/nsmb.2071
References
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Related references
Note: Only part of the references are listed.- A structural basis for Lowe syndrome caused by mutations in the Rab-binding domain of OCRL1
- (2011) Xiaomin Hou et al. EMBO JOURNAL
- The PH domain proteins IPIP27A and B link OCRL1 to receptor recycling in the endocytic pathway
- (2011) Christopher J. Noakes et al. MOLECULAR BIOLOGY OF THE CELL
- 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
- Identification of Phosphorylation Sites within the Signaling Adaptor APPL1 by Mass Spectrometry
- (2010) Randi L. Gant-Branum et al. JOURNAL OF PROTEOME RESEARCH
- 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
- Dali server: conservation mapping in 3D
- (2010) Liisa Holm et al. NUCLEIC ACIDS RESEARCH
- Two closely related endocytic proteins that share a common OCRL-binding motif with APPL1
- (2010) Laura E. Swan et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- MolProbity: all-atom structure validation for macromolecular crystallography
- (2009) Vincent B. Chen et al. ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY
- A Phosphoinositide Switch Controls the Maturation and Signaling Properties of APPL Endosomes
- (2009) Roberto Zoncu et al. CELL
- A PH domain within OCRL bridges clathrin-mediated membrane trafficking to phosphoinositide metabolism
- (2009) Yuxin Mao et al. EMBO JOURNAL
- Magnetic Resonance Imaging, Magnetic Resonance Spectroscopy, and Facial Dysmorphism in a Case of Lowe Syndrome with Novel OCRL1 Gene Mutation
- (2009) Adnan Yuksel et al. JOURNAL OF CHILD NEUROLOGY
- Dent-2 Disease: A Mild Variant of Lowe Syndrome
- (2009) Arend Bökenkamp et al. JOURNAL OF PEDIATRICS
- Inherited cerebrorenal syndromes
- (2009) Scott J. Schurman et al. Nature Reviews Nephrology
- OCRL1 Mutations in Dent 2 Patients Suggest a Mechanism for Phenotypic Variability
- (2009) Antony E. Shrimpton et al. NEPHRON PHYSIOLOGY
- Locus heterogeneity of Dent’s disease: OCRL1 and TMEM27 genes in patients with no CLCN5 mutations
- (2009) Enrica Tosetto et al. PEDIATRIC NEPHROLOGY
- All known patient mutations in the ASH-RhoGAP domains of OCRL affect targeting and APPL1 binding
- (2008) Heather J. McCrea et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Renal Phenotype in Lowe Syndrome: A Selective Proximal Tubular Dysfunction
- (2008) D. Bockenhauer et al. Clinical Journal of the American Society of Nephrology
- Large Scale Screening for Novel Rab Effectors Reveals Unexpected Broad Rab Binding Specificity
- (2008) Mitsunori Fukuda et al. MOLECULAR & CELLULAR PROTEOMICS
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