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

12

object named as

Kurt von Figura

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Renate Lüllmann-Rauch

object named as

Renate Lüllmann-Rauch

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author name string

Alexander-Christian Gamp

1

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Yoshitaka Tanaka

2

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Renate Lüllmann-Rauch

3

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Dorothee Wittke

4

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Rudi D'Hooge

5

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Peter P De Deyn

6

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Tobias Moser

7

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Hannes Maier

8

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Dieter Hartmann

9

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Karina Reiss

10

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Anna-Lena Illert

The biogenesis of lysosomes

11

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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

12

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page(s)

631-46

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issue

6

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cites work

1 reference

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Biogenesis of lysosomal membranes

21 January 2018

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Glycoproteins of the lysosomal membrane

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Croquemort, a novel Drosophila hemocyte/macrophage receptor that recognizes apoptotic cells.

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A Drosophila gene encoding an epithelial membrane protein with homology to CD36/LIMP II.

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The C. elegans genome sequencing project: a beginning

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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

21 January 2018

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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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KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential

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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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Normal lysosomal morphology and function in LAMP-1-deficient mice

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Accumulation of autophagic vacuoles and cardiomyopathy in LAMP-2-deficient mice

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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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Lumenal plasma membrane of the urinary bladder. I. Three-dimensional reconstruction from freeze-etch images

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ADAMTS-1: a metalloproteinase-disintegrin essential for normal growth, fertility, and organ morphology and function

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ADAMTS: a novel family of proteases with an ADAM protease domain and thrombospondin 1 repeats

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Cycling of the integral membrane glycoprotein, LEP100, between plasma membrane and lysosomes: kinetic and morphological analysis

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Purification and characterization of human lysosomal membrane glycoproteins

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The pathway and targeting signal for delivery of the integral membrane glycoprotein LEP100 to lysosomes

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Cochlear distribution of Na,K-ATPase and corticosteroid receptors in two mouse strains with congenital hearing disorders

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KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

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Expression and localization of the Na-K-2Cl cotransporter in the rat cochlea.

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Inner ear defects induced by null mutation of the isk gene

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Mouse models of myelin diseases.

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Trembler mouse carries a point mutation in a myelin gene

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The effect of changes in endolymphatic ion concentrations on the tectorial membrane

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The two mannose 6-phosphate receptors transport distinct complements of lysosomal proteins.

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Metachromatic leukodystrophy: arylsulfatase-A deficiency in skin fibroblast cultures

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Incorporation of cytoplasmic vesicles into apical membrane of mammalian urinary bladder epithelium

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Consolidated OpenCitations Corpus – April 2017

21 January 2018

Identifiers

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1 reference

4218071

4218071

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference