Mice deficient in lysosomal acid phosphatase develop lysosomal storage in the kidney and central nervous system
about
RAB26 and RAB3D are direct transcriptional targets of MIST1 that regulate exocrine granule maturationIncreased expression of lysosomal acid phosphatase in CLN3-defective cells and mouse brain tissueNormal lysosomal morphology and function in LAMP-1-deficient miceMice lacking tartrate-resistant acid phosphatase (Acp 5) have disordered macrophage inflammatory responses and reduced clearance of the pathogen, Staphylococcus aureusLysosome dysfunction triggers Atg7-dependent neural apoptosis.DeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis.Quantitative trait loci, genes, and polymorphisms that regulate bone mineral density in mouseIntegrating comparative expression profiling data and association of SNPs with Salmonella shedding for improved food safety and porcine disease resistance.Morphological, biochemical and molecular biology approaches for the diagnosis of lysosomal storage diseases.Purkinje cell compartmentation in the cerebellum of the lysosomal Acid phosphatase 2 mutant mouse (nax - naked-ataxia mutant mouse).Proximal 11p deletion syndrome (P11pDS): additional evaluation of the clinical and molecular aspects.Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphismsEfficacy of phosphodiesterase-4 inhibitors in juvenile Batten disease (CLN3).Acid phosphatase 2 (ACP2) is required for membrane fusion during influenza virus entry.Lysosomal acid phosphatase 2 is an unfavorable prognostic factor but is associated with better survival in stage II colorectal cancer patients receiving chemotherapy.Mannose 6 dephosphorylation of lysosomal proteins mediated by acid phosphatases Acp2 and Acp5.Picrotoxin-induced convulsions and lysosomal function in the rat brainCerebellar Expression of the Neurotrophin Receptor p75 in Naked-Ataxia Mutant Mouse.Biosynthesis of phosphatidylcholine from a phosphocholine precursor pool derived from the late endosomal/lysosomal degradation of sphingomyelin.Spatial and temporal expression of lysosomal acid phosphatase 2 (ACP2) reveals dynamic patterning of the mouse cerebellar cortex.Potocki-Shaffer deletion encompassing ALX4 in a patient with frontonasal dysplasia phenotype.
P2860
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P2860
Mice deficient in lysosomal acid phosphatase develop lysosomal storage in the kidney and central nervous system
description
1997 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1997 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
article publié dans la revue scientifique Journal of Biological Chemistry
@fr
artículu científicu espublizáu en 1997
@ast
im Juli 1997 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1997/07/25)
@sk
vědecký článek publikovaný v roce 1997
@cs
wetenschappelijk artikel (gepubliceerd op 1997/07/25)
@nl
наукова стаття, опублікована в липні 1997
@uk
name
Mice deficient in lysosomal ac ...... ney and central nervous system
@ast
Mice deficient in lysosomal ac ...... ney and central nervous system
@en
Mice deficient in lysosomal ac ...... ney and central nervous system
@nl
type
label
Mice deficient in lysosomal ac ...... ney and central nervous system
@ast
Mice deficient in lysosomal ac ...... ney and central nervous system
@en
Mice deficient in lysosomal ac ...... ney and central nervous system
@nl
prefLabel
Mice deficient in lysosomal ac ...... ney and central nervous system
@ast
Mice deficient in lysosomal ac ...... ney and central nervous system
@en
Mice deficient in lysosomal ac ...... ney and central nervous system
@nl
P2093
P2860
P356
P1476
Mice deficient in lysosomal ac ...... ney and central nervous system
@en
P2093
D. Hartmann
K. von Figura
R. Lüllmann-Rauch
P2860
P304
18628–18635
P356
10.1074/JBC.272.30.18628
P407
P577
1997-07-25T00:00:00Z