Proteolytic processing of OPA1 links mitochondrial dysfunction to alterations in mitochondrial morphology (Q40227379)

18 September 2017

title

Proteolytic processing of OPA1 links mitochondrial dysfunction to alterations in mitochondrial morphology (English)

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18 September 2017

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Stéphane Duvezin-Caubet

object named as

Stéphane Duvezin-Caubet

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Johannes Wagener

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Nils-Göran Larsson

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18 September 2017

Ravi Jagasia

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18 September 2017

Sabine Hofmann

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18 September 2017

Aleksandra Trifunovic

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18 September 2017

Anna Hansson

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18 September 2017

Anne Chomyn

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18 September 2017

Matthias F Bauer

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18 September 2017

Giuseppe Attardi

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18 September 2017

Walter Neupert

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18 September 2017

Andreas S Reichert

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18 September 2017

language of work or name

English

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publication date

26 September 2006

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Journal of Biological Chemistry

18 September 2017

published in

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18 September 2017

volume

281

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18 September 2017

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18 September 2017

page(s)

37972-37979

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A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine

18 September 2017

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OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

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Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

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Roles of the mammalian mitochondrial fission and fusion mediators Fis1, Drp1, and Opa1 in apoptosis

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21 January 2018

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OPA1 requires mitofusin 1 to promote mitochondrial fusion

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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

Identifiers

DOI

10.1074/JBC.M606059200

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18 September 2017

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