(Q24290722)

Journal of Biological Chemistry

GOA release 2020-03-11

S Cherqui

1

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Vasiliki Kalatzis

object named as

V Kalatzis

series ordinal

2

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author name string

G Trugnan

series ordinal

3

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C Antignac

series ordinal

4

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language of work or name

English

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publication date

20 April 2001

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published in

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volume

276

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page(s)

13314-21

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issue

16

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cites work

Intracellular trafficking of lysosomal membrane proteins.

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Mutations of CTNS causing intermediate cystinosis

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Autophagy and other vacuolar protein degradation mechanisms

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Kinase activity controls the sorting of the epidermal growth factor receptor within the multivesicular body

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The role of clathrin, adaptors and dynamin in endocytosis

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Peptide sequences that target cytosolic proteins for lysosomal proteolysis

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Use of the green fluorescent protein and its mutants in quantitative fluorescence microscopy

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The AP-3 complex: a coat of many colours

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Lysosomal transport disorders

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A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis

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Characteristics of cystine counter-transport in normal and cystinotic lysosome-rich leucocyte granular fractions

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Improved renal function in children with cystinosis treated with cysteamine

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Expression cloning of a Na(+)-independent neutral amino acid transporter from rat kidney

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Endocytosis and lysosomal targeting of epidermal growth factor receptors are mediated by distinct sequences independent of the tyrosine kinase domain

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Lysosomal targeting of epidermal growth factor receptors via a kinase-dependent pathway is mediated by the receptor carboxyl-terminal residues 1022-1123.

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Lysosomal targeting of P-selectin is mediated by a novel sequence within its cytoplasmic tail

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A cytoplasmic sequence in human tyrosinase defines a second class of di-leucine-based sorting signals for late endosomal and lysosomal delivery

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The steroidogenic acute regulatory protein homolog MLN64, a late endosomal cholesterol-binding protein.

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A cysteine-specific lysosomal transport system provides a major route for the delivery of thiol to human fibroblast lysosomes: possible role in supporting lysosomal proteolysis

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Accumulation of membrane glycoproteins in lysosomes requires a tyrosine residue at a particular position in the cytoplasmic tail

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An endogenous MDCK lysosomal membrane glycoprotein is targeted basolaterally before delivery to lysosomes

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Cytoplasmic determinants involved in direct lysosomal sorting, endocytosis, and basolateral targeting of rat lgp120 (lamp-I) in MDCK cells.

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Molecular bases for the recognition of tyrosine-based sorting signals

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The genomic region encompassing the nephropathic cystinosis gene (CTNS): complete sequencing of a 200-kb segment and discovery of a novel gene within the common cystinosis-causing deletion

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Coat proteins and vesicle budding

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Cystine transport is defective in isolated leukocyte lysosomes from patients with cystinosis

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Acidification of the endocytic and exocytic pathways

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Lysosomal storage diseases

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Cystinosis. Intracellular cystine depletion by aminothiols in vitro and in vivo

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7 January 2021

Identifiers

DOI

10.1074/JBC.M010562200

1 reference

Consolidated OpenCitations Corpus – April 2017

1839284

1839284

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference