(Q28208193)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14534547%20AND%20SRC:MED&resulttype=core&format=json

19 December 2019

title

Loss of Omi mitochondrial protease activity causes the neuromuscular disorder of mnd2 mutant mice (English)

1 reference

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19 December 2019

1 reference

9

1 reference

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19 December 2019

author name string

Julie M Jones

1

1 reference

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19 December 2019

Pinaki Datta

2

1 reference

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19 December 2019

Srinivasa M Srinivasula

3

1 reference

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19 December 2019

Weizhen Ji

4

1 reference

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19 December 2019

Sanjeev Gupta

5

1 reference

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19 December 2019

ZhiJia Zhang

6

1 reference

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19 December 2019

Erika Davies

7

1 reference

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19 December 2019

György Hajnóczky

8

1 reference

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19 December 2019

Margaret L Van Keuren

10

1 reference

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19 December 2019

Teresa Fernandes-Alnemri

11

1 reference

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19 December 2019

Miriam H Meisler

12

1 reference

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19 December 2019

Emad S Alnemri

13

1 reference

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19 December 2019

language of work or name

English

0 references

publication date

8 October 2003

1 reference

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19 December 2019

1 reference

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19 December 2019

volume

425

1 reference

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19 December 2019

page(s)

721-727

1 reference

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19 December 2019

issue

6959

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14534547%20AND%20SRC:MED&resulttype=core&format=json

mnd2: a new mouse model of inherited motor neuron disease

19 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

High-resolution genetic, physical, and transcript map of the mnd2 region of mouse chromosome 6

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

Progressive loss of striatal neurons causes motor dysfunction in MND2 mutant mice and is not prevented by Bcl-2.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

Aup1, a novel gene on mouse chromosome 6 and human chromosome 2p13.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

Localization of the rhotekin gene RTKN on the physical maps of mouse chromosome 6 and human chromosome 2p13 and exclusion as a candidate for mnd2 and LGMD2B

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

Mouse p150Glued (dynactin 1) cDNA sequence and evaluation as a candidate for the neuromuscular disease mutation mnd2.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

DQX1, an RNA-dependent ATPase homolog with a novel DEAQ box: expression pattern and genomic sequence comparison of the human and mouse genes

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

Structural insights into the pro-apoptotic function of mitochondrial serine protease HtrA2/Omi

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

Identification of Omi/HtrA2 as a mitochondrial apoptotic serine protease that disrupts inhibitor of apoptosis protein-caspase interaction

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

A serine protease, HtrA2, is released from the mitochondria and interacts with XIAP, inducing cell death

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

HtrA2 promotes cell death through its serine protease activity and its ability to antagonize inhibitor of apoptosis proteins

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

The serine protease Omi/HtrA2 regulates apoptosis by binding XIAP through a reaper-like motif

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

The serine protease Omi/HtrA2 is released from mitochondria during apoptosis. Omi interacts with caspase-inhibitor XIAP and induces enhanced caspase activity

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

The HtrA Family of Proteases

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

Love it or cleave it: tough choices in protein quality control

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

Inhibitor of apoptosis proteins are substrates for the mitochondrial serine protease Omi/HtrA2

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

Omi/HtrA2 catalytic cleavage of inhibitor of apoptosis (IAP) irreversibly inactivates IAPs and facilitates caspase activity in apoptosis

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

Increased susceptibility of striatal mitochondria to calcium-induced permeability transition

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

Apoptosis driven by IP(3)-linked mitochondrial calcium signals

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

Cytochrome c: can't live with it--can't live without it.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

Essential role of the mitochondrial apoptosis-inducing factor in programmed cell death

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

The harlequin mouse mutation downregulates apoptosis-inducing factor

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

OMP peptide signals initiate the envelope-stress response by activating DegS protease via relief of inhibition mediated by its PDZ domain

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

Intracellular adenosine triphosphate (ATP) concentration: a switch in the decision between apoptosis and necrosis

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

Molecular characterization of mitochondrial apoptosis-inducing factor

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

BAD and glucokinase reside in a mitochondrial complex that integrates glycolysis and apoptosis

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

ATP-dependent proteases controlling mitochondrial function in the yeast Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1038%2FNATURE02052

7 January 2021

Identifiers

DOI

10.1038/NATURE02052

2 references

Consolidated OpenCitations Corpus – April 2017

5585

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14534547%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

19 December 2019

1018343961

0 references

5585

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

5585

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14534547%20AND%20SRC:MED&resulttype=core&format=json