Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation (Q28117328)

4 January 2017

title

Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation (English)

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mitochondrial protein catabolic process

4 January 2017

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GOA release 2020-03-11

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YME1-like 1 (S. cerevisiae)

GOA release 2020-03-11

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GOA release 2020-03-11

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1 reference

1 reference

10

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Thomas MacVicar

4

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Luciana Musante

5

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Björn Fischer-Zirnsak

6

object named as

Björn Fischer-Zirnsak

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Angela Kaindl

object named as

Angela M. Kaindl

14

1 reference

4 January 2017

Lambert P van den Heuvel

9

object named as

Lambert van den Heuvel

1 reference

4 January 2017

Bianca Hartmann

1

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4 January 2017

Timothy Wai

2

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4 January 2017

Hao Hu

3

1 reference

4 January 2017

Björn Fischer-Zirnsak

6

1 reference

4 January 2017

Werner Stenzel

7

1 reference

4 January 2017

Ralph Gräf

8

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4 January 2017

Thomas F. Wienker

11

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4 January 2017

Christoph Hübner

12

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4 January 2017

Thomas Langer

13

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4 January 2017

language of work or name

English

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publication date

6 August 2016

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4 January 2017

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4 January 2017

volume

5

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describes a project that uses

4 January 2017

ImageJ

1 reference

Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4991934/fullTextXML

inferred from PubMed Central ID database lookup

cites work

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The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission

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29 September 2017

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29 September 2017

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2 June 2018

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Impaired Folding of the Mitochondrial Small TIM Chaperones Induces Clearance by the i-AAA Protease

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Mutation detection in four candidate genes (OXA1L, MRS2L, YME1L and MIPEP) for combined deficiencies in the oxidative phosphorylation system

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