Reduced cathepsins B and D cause impaired autophagic degradation that can be almost completely restored by overexpression of these two proteases in Sap C-deficient fibroblasts (Q28116738)

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English	Reduced cathepsins B and D cause impaired autophagic degradation that can be almost completely restored by overexpression of these two proteases in Sap C-deficient fibroblasts	scientific journal article

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scholarly article

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4 January 2017

Reduced cathepsins B and D cause impaired autophagic degradation that can be almost completely restored by overexpression of these two proteases in Sap C-deficient fibroblasts (English)

1 reference

4 January 2017

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GOA release 2020-03-11

regulation of autophagy

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GOA release 2020-03-11

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based on heuristic

inferred from title

Francesco Cecconi

6

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Sabrina Di Bartolomeo

object named as

Sabrina Di Bartolomeo

3

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Valentina Cianfanelli

object named as

Valentina Cianfanelli

5

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author name string

Massimo Tatti

1

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4 January 2017

Marialetizia Motta

2

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4 January 2017

Susanna Scarpa

4

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4 January 2017

Rosa Salvioli

7

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4 January 2017

publication date

1 December 2012

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4 January 2017

Human Molecular Genetics

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4 January 2017

21

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4 January 2017

5159–5173

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4 January 2017

23

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4 January 2017

Further studies on the reconstitution of glucosylceramidase activity by Sap C and anionic phospholipids

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Molecular imaging of membrane interfaces reveals mode of beta-glucosidase activation by saposin C.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Mutation in the sphingolipid activator protein 2 in a patient with a variant of Gaucher disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Mutational analysis in a patient with a variant form of Gaucher disease caused by SAP-2 deficiency

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Neuronopathic juvenile glucosylceramidosis due to sap-C deficiency: clinical course, neuropathology and brain lipid composition in this Gaucher disease variant.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

A mutation within the saposin D domain in a Gaucher disease patient with normal glucocerebrosidase activity.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Non-neuronopathic Gaucher disease due to saposin C deficiency.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Saposin C mutations in Gaucher disease patients resulting in lysosomal lipid accumulation, saposin C deficiency, but normal prosaposin processing and sorting

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Participation of autophagy in storage of lysosomes in neurons from mouse models of neuronal ceroid-lipofuscinoses (Batten disease).

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Autophagy in Niemann-Pick C disease is dependent upon Beclin-1 and responsive to lipid trafficking defects

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Enhanced autophagy and mitochondrial aberrations in murine G(M1)-gangliosidosis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

mTOR regulation of autophagy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Apoptotic pathways: involvement of lysosomal proteases

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Assays to assess autophagy induction and fusion of autophagic vacuoles with a degradative compartment, using monodansylcadaverine (MDC) and DQ-BSA.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Termination of autophagy and reformation of lysosomes regulated by mTOR

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Lysosomal positioning coordinates cellular nutrient responses.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

A block of autophagy in lysosomal storage disorders

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Dysfunction of endocytic and autophagic pathways in a lysosomal storage disease.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Potential artefacts in proteome analysis of plasma of Gaucher patients due to protease abnormalities.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Altered expression and distribution of cathepsins in neuronopathic forms of Gaucher disease and in other sphingolipidoses.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Microglial activation precedes acute neurodegeneration in Sandhoff disease and is suppressed by bone marrow transplantation

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Molecular pathophysiology in Tay-Sachs and Sandhoff diseases as revealed by gene expression profiling.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

A mutation in the ovine cathepsin D gene causes a congenital lysosomal storage disease with profound neurodegeneration

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Cathepsin D deficiency underlies congenital human neuronal ceroid-lipofuscinosis

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Neuronal loss and brain atrophy in mice lacking cathepsins B and L

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Impaired autophagy in sporadic inclusion-body myositis and in endoplasmic reticulum stress-provoked cultured human muscle fibers

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Cathepsin B-mediated autophagy flux facilitates the anthrax toxin receptor 2-mediated delivery of anthrax lethal factor into the cytoplasm

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

The dynamic interaction of AMBRA1 with the dynein motor complex regulates mammalian autophagy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

LC3 conjugation system in mammalian autophagy

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Characterization of new fluorogenic substrates for the rapid and sensitive assay of cathepsin E and cathepsin D

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

Cathepsin B, Cathepsin H, and cathepsin L

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS367

21 January 2018

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