The Cellular and Physiological Functions of the Lowe Syndrome Protein OCRL1-Reference-Cited by-同舟云学术

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The Cellular and Physiological Functions of the Lowe Syndrome Protein OCRL1

Published:2014-03-07 Issue:5 Volume:15 Page:471-487
ISSN:1398-9219
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language:en
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Author:

Mehta Zenobia B.¹²,Pietka Grzegorz¹³,Lowe Martin¹

Affiliation:

1. Faculty of Life Sciences University of Manchester The Michael Smith Building, Oxford Road Manchester M13 9PT UK

2. Current address: Faculty of Medicine, Imperial College, London, UK

3. Current address: Cancer Institute, Faculty of Medical Sciences, UCL, London, UK

Publisher

Wiley

Subject

Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/tra.12160

Reference109 articles.

1. Phosphoinositides in cell regulation and membrane dynamics

2. Phosphoinositide Signaling: New Tools and Insights

3. Mammalian phosphoinositide kinases and phosphatases

4. Inositol-lipid binding motifs: signal integrators through protein-lipid and protein-protein interactions

5. Membrane recognition by phospholipid-binding domains

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1. Is hyperammonemia helpful in detecting syndromic tubulopathies with early extrarenal manifestations? A case report of Lowe’s syndrome;Egyptian Pediatric Association Gazette;2024-08-16

2. Two cases of Lowe syndrome caused by a novel mutation in OCRL gene in a family;2024-08-11

3. OCRL1 Deficiency Affects the Intracellular Traffic of ApoER2 and Impairs Reelin-Induced Responses;Biomolecules;2024-07-05

4. WHAMM functions in kidney reabsorption and polymerizes actin to promote autophagosomal membrane closure and cargo sequestration;Molecular Biology of the Cell;2024-06-01

5. Atypical phenotypes and novel OCRL variations in southern Chinese patients with Lowe syndrome;Pediatric Nephrology;2024-04-08

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