Two closely related endocytic proteins that share a common OCRL-binding motif with APPL1 (Q24624573)

22 June 2017

title

Two closely related endocytic proteins that share a common OCRL-binding motif with APPL1 (English)

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22 June 2017

3

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Pietro De Camilli

5

object named as

Pietro De Camilli

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22 June 2017

Laura E Swan

1

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author name string

Livia Tomasini

2

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22 June 2017

Joël Lunardi

4

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22 June 2017

Michelle Pirruccello

3

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22 June 2017

language of work or name

English

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publication date

2 February 2010

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Proceedings of the National Academy of Sciences of the United States of America

22 June 2017

published in

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22 June 2017

volume

107

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22 June 2017

issue

8

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22 June 2017

page(s)

3511-3516

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describes a project that uses

22 June 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2840420/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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Opacities of the lens indicating carrier status in the oculo-cerebro-renal (Lowe) syndrome

27 September 2017

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Fanconi or not Fanconi? Lowe syndrome revisited

30 May 2018

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Evidence for a discrete behavioral phenotype in the oculocerebrorenal syndrome of Lowe.

21 January 2018

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Renal manifestations of Dent disease and Lowe syndrome.

21 January 2018

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Large scale screening for novel rab effectors reveals unexpected broad Rab binding specificity

21 January 2018

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OCRL mutation analysis in Italian patients with Lowe syndrome

21 January 2018

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The effect of missense mutations in the RhoGAP-homology domain on ocrl1 function.

21 January 2018

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Magnetic resonance imaging, magnetic resonance spectroscopy, and facial dysmorphism in a case of Lowe syndrome with novel OCRL1 gene mutation.

21 January 2018

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https://api.crossref.org/works/10.1073%2FPNAS.0914658107

OCRL1 mutation analysis in French Lowe syndrome patients: implications for molecular diagnosis strategy and genetic counseling.

21 January 2018

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Novel OCRL1 mutations in patients with the phenotype of Dent disease.

21 January 2018

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28 November 2018

Identifiers

DOI

10.1073/PNAS.0914658107

1 reference

22 June 2017

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1 reference