VMA21 deficiency prevents vacuolar ATPase assembly and causes autophagic vacuolar myopathy (Q28283153)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23315026%20AND%20SRC:MED&resulttype=core&format=json

22 February 2020

title

VMA21 deficiency prevents vacuolar ATPase assembly and causes autophagic vacuolar myopathy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23315026%20AND%20SRC:MED&resulttype=core&format=json

Autophagic vacuolar myopathy

22 February 2020

main subject

autophagy

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1 reference

4

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22 February 2020

Ichizo Nishino

11

1 reference

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22 February 2020

Nicolas Levy

21

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22 February 2020

16

Michel Fardeau

1 reference

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22 February 2020

author name string

Nivetha Ramachandran

1

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22 February 2020

Iulia Munteanu

2

1 reference

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22 February 2020

Peixiang Wang

3

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22 February 2020

Jennifer J Rilstone

5

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22 February 2020

Nyrie Israelian

6

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22 February 2020

Taline Naranian

7

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22 February 2020

Paul Paroutis

8

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22 February 2020

Ray Guo

9

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22 February 2020

Zhi-Ping Ren

10

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22 February 2020

Brigitte Chabrol

12

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22 February 2020

Jean-Francois Pellissier

13

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22 February 2020

Carlo Minetti

14

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22 February 2020

Bjarne Udd

15

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22 February 2020

Chetankumar S Tailor

17

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22 February 2020

Don J Mahuran

18

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22 February 2020

John T Kissel

19

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22 February 2020

Hannu Kalimo

20

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22 February 2020

Morris F Manolson

22

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22 February 2020

Cameron A Ackerley

23

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22 February 2020

Berge A Minassian

24

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22 February 2020

language of work or name

English

0 references

publication date

12 January 2013

1 reference

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22 February 2020

published in

Acta Neuropathologica

1 reference

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22 February 2020

volume

125

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22 February 2020

issue

3

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22 February 2020

page(s)

439-457

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Regulation of targets of mTOR (mammalian target of rapamycin) signalling by intracellular amino acid availability

22 February 2020

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Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosis

21 January 2018

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Archazolid and apicularen: novel specific V-ATPase inhibitors

21 January 2018

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X-linked myopathy with excessive autophagy: a new hereditary muscle disease

21 January 2018

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Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

21 January 2018

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Impaired glycosylation and cutis laxa caused by mutations in the vesicular H+-ATPase subunit ATP6V0A2.

21 January 2018

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Lysosomal myopathies: an excessive build-up in autophagosomes is too much to handle.

21 January 2018

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Role of Vma21p in assembly and transport of the yeast vacuolar ATPase

21 January 2018

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Downstream of Akt: FoxO3 and mTOR in the regulation of autophagy in skeletal muscle

21 January 2018

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Consequences of the selective blockage of chaperone-mediated autophagy

21 January 2018

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21 January 2018

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21 January 2018

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Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease).

21 January 2018

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Anti-cancer agent siramesine is a lysosomotropic detergent that induces cytoprotective autophagosome accumulation

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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mTORC1 senses lysosomal amino acids through an inside-out mechanism that requires the vacuolar H(+)-ATPase

21 January 2018

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10.1007/S00401-012-1073-6

21 January 2018

Identifiers

DOI

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23315026%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

22 February 2020

1008787819

0 references

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23315026%20AND%20SRC:MED&resulttype=core&format=json