Lysosomal amino acid transporter LYAAT-1 in the rat central nervous system: an in situ hybridization and immunohistochemical study (Q44450298)

3 December 2017

title

Lysosomal amino acid transporter LYAAT-1 in the rat central nervous system: an in situ hybridization and immunohistochemical study (English)

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3 December 2017

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6

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3 December 2017

Cendra Agulhon

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Philippe Ravassard

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Philippe Ravassard

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author name string

Philippe Rostaing

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3 December 2017

Corinne Sagné

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3 December 2017

Antoine Triller

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3 December 2017

language of work or name

English

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publication date

1 July 2003

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The Journal of Comparative Neurology

3 December 2017

published in

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3 December 2017

volume

462

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3 December 2017

issue

1

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3 December 2017

page(s)

71-89

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Hyperammonemia with reduced ornithine, citrulline, arginine and proline: a new inborn error caused by a mutation in the gene encoding delta(1)-pyrroline-5-carboxylate synthase

3 December 2017

cites work

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Functional characterization of two novel mammalian electrogenic proton-dependent amino acid cotransporters

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Enzymatically active lysosomal proteases are associated with amyloid deposits in Alzheimer brain

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Lysosomal proteinase antigens are prominently localized within senile plaques of Alzheimer's disease: evidence for a neuronal origin

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Lysosomal hydrolases of different classes are abnormally distributed in brains of patients with Alzheimer disease

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Localization of the brain-specific high-affinity l-proline transporter in cultured hippocampal neurons: molecular heterogeneity of synaptic terminals

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Transmembrane molecular pump activity of Niemann-Pick C1 protein

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Pyridoxal phosphate de-activation by pyrroline-5-carboxylic acid. Increased risk of vitamin B6 deficiency and seizures in hyperprolinemia type II

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Type II hyperprolinaemia in a pedigree of Irish travellers (nomads)

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Molecular cloning and expression of a high affinity L-proline transporter expressed in putative glutamatergic pathways of rat brain

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Sorting of mannose 6-phosphate receptors and lysosomal membrane proteins in endocytic vesicles

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The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

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Defective hydroxyproline metabolism in type II hyperprolinemia

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Trans-Golgi network sorting

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Transport of the lysosomal membrane glycoprotein lgp120 (lgp-A) to lysosomes does not require appearance on the plasma membrane

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A comparison of cathepsin B processing and distribution during neuronal death in rats following global ischemia or decapitation necrosis

21 January 2018

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Is hyperprolinemia type I actually a benign trait? Report of a case with severe neurologic involvement and vigabatrin intolerance.

21 January 2018

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Proline, glutamate and glutamine metabolism in mouse brain synaptosomes

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Lysosomal transport disorders

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

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

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The endosomal-lysosomal system of neurons: new roles

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The endosomal-lysosomal system of neurons in Alzheimer's disease pathogenesis: a review

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Segregation of MHC class II molecules from MHC class I molecules in the Golgi complex for transport to lysosomal compartments

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Defective sialic acid egress from isolated fibroblast lysosomes of patients with Salla disease

21 January 2018

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Identification and characterization of a lysosomal transporter for small neutral amino acids

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Familial hyperprolinemia and mental retardation: A second metabolic type

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High urinary excretion of N-(pyrrole-2-carboxyl) glycine in type II hyperprolinemia

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21 January 2018

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Immunocytochemical localization of cathepsin D in rat neural tissue

21 January 2018

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A new synaptosomal biosynthetic pathway of glutamate and GABA from ornithine and its negative feedback inhibition by GABA.

21 January 2018

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The lysosomal membrane glycoprotein lamp-1 is transported to lysosomes by two alternative pathways

21 January 2018

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Immuno-localization of H+/peptide cotransporter in rat digestive tract

21 January 2018

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Type I hyperprolinemia

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Mammalian Brain-specific L-Proline Transporter

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Cellular pathology of lysosomal storage disorders.

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Characterization of an oligopeptide transporter in renal lysosomes

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Properties of the endosomal-lysosomal system in the human central nervous system: disturbances mark most neurons in populations at risk to degenerate in Alzheimer's disease.

21 January 2018

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7 January 2021

The mammalian brain high-affinity L-proline transporter is enriched preferentially in synaptic vesicles in a subpopulation of excitatory nerve terminals in rat forebrain.

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7 January 2021

Aggregation of vasopressin mRNA in a subset of axonal swellings of the median eminence and posterior pituitary: light and electron microscopic evidence.

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7 January 2021

Glial cells transform glucose to alanine, which fuels the neurons in the honeybee retina.

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7 January 2021

Identifiers

DOI

10.1002/CNE.10712

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3 December 2017

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