LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice (Q28181137)

object named as

Peter P De Deyn

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author name string

Alexander-Christian Gamp

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Yoshitaka Tanaka

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Renate Lüllmann-Rauch

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Dorothee Wittke

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Rudi D'Hooge

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Tobias Moser

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Hannes Maier

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Dieter Hartmann

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Karina Reiss

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Anna-Lena Illert

The biogenesis of lysosomes

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language of work or name

English

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publication date

15 March 2003

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published in

Human Molecular Genetics

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volume

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issue

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page(s)

631-46

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cites work

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Glycoproteins of the lysosomal membrane

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A Drosophila Gene Encoding an Epithelial Membrane Protein with Homology to CD36/LIMP II

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A di-leucine-based motif in the cytoplasmic tail of LIMP-II and tyrosinase mediates selective binding of AP-3

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Lysosomal integral membrane protein II binds thrombospondin-1. Structure-function homology with the cell adhesion molecule CD36 defines a conserved recognition motif

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Inactivation of lmpA, encoding a LIMPII-related endosomal protein, suppresses the internalization and endosomal trafficking defects in profilin-null mutants

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Identification of a suppressor of the Dictyostelium profilin-minus phenotype as a CD36/LIMP-II homologue

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A role for the lysosomal membrane protein LGP85 in the biogenesis and maintenance of endosomal and lysosomal morphology

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Ablation of uroplakin III gene results in small urothelial plaques, urothelial leakage, and vesicoureteral reflux

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Isolation and characterization of a novel membrane glycoprotein of 85,000 molecular weight from rat liver lysosomes

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Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease).

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Disease model: LAMP-2 enlightens Danon disease

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Consolidated OpenCitations Corpus – April 2017

21 January 2018

Identifiers

0 references

1 reference

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Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

12620969

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Consolidated OpenCitations Corpus – April 2017