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CLUH granules coordinate translation of mitochondrial proteins with mTORC1 signaling and mitophagy

The EMBO journal, 2020-05, Vol.39 (9), p.e102731-n/a

2020

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Mitochondrial membrane proteins and VPS35 orchestrate selective removal of mtDNA

Nature communications, 2022-11, Vol.13 (1), p.6704-6704, Article 6704

2022

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Combined fibre atrophy and decreased muscle regeneration capacity driven by mitochondrial DNA alterations underlie the development of sarcopenia

Journal of cachexia, sarcopenia and muscle, 2022-08, Vol.13 (4), p.2132-2145

2022

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Endosomal-dependent mitophagy coordinates mitochondrial nucleoid and mtDNA elimination

Autophagy, 2023-09, Vol.19 (9), p.2609-2610

2023

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Selective Neuron Vulnerability in Common and Rare Diseases—Mitochondria in the Focus

Frontiers in molecular biosciences, 2021-06, Vol.8, p.676187-676187

2021

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Junctophilin-1 is a modifier gene of GDAP1-related Charcot-Marie-Tooth disease

Human molecular genetics, 2015-01, Vol.24 (1), p.213-229

2015

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Silencing of the Charcot–Marie–Tooth disease-associated gene GDAP1 induces abnormal mitochondrial distribution and affects Ca2+ homeostasis by reducing store-operated Ca2+ entry

Neurobiology of disease, 2013-07, Vol.55, p.140-151

2013

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CMT-linked loss-of-function mutations in GDAP1 impair store-operated Ca2+ entry-stimulated respiration

Scientific reports, 2017-02, Vol.7 (1), p.42993-42993, Article 42993

2017

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Extraocular Muscle Reveals Selective Vulnerability of Type IIB Fibers to Respiratory Chain Defects Induced by Mitochondrial DNA Alterations

Investigative ophthalmology & visual science, 2020-10, Vol.61 (12), p.14

2020

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Charcot-Marie-Tooth-related Gene GDAP1 Complements Cell Cycle Delay at G2/M Phase in Saccharomyces cerevisiae fis1 Gene-defective Cells

The Journal of biological chemistry, 2011-10, Vol.286 (42), p.36777-36786

2011

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Mitochondrial dysfunction induced by frataxin deficiency is associated with cellular senescence and abnormal calcium metabolism

Frontiers in cellular neuroscience, 2014-05, Vol.8, p.124-124

2014

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The role of mitochondrial network dynamics in the pathogenesis of Charcot-Marie-Tooth disease

Advances in experimental medicine and biology, 2009-01, Vol.652, p.129

2009

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Reshaping membranes to build mitochondrial DNA

PLoS genetics, 2019-06, Vol.15 (6), p.e1008140

2019

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CLUH regulates mitochondrial biogenesis by binding mRNAs of nuclear-encoded mitochondrial proteins

The Journal of cell biology, 2014-10, Vol.207 (2), p.213-223

2014

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CLUH regulates mitochondrial metabolism by controlling translation and decay of target mRNAs

The Journal of cell biology, 2017-03, Vol.216 (3), p.675-693

2017

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Inner membrane turns inside out to exit mitochondrial organelles

Nature (London), 2024-08, Vol.632 (8027), p.987-988

2024

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Lack of GDAP1 induces neuronal calcium and mitochondrial defects in a knockout mouse model of charcot-marie-tooth neuropathy

PLoS genetics, 2015-04, Vol.11 (4), p.e1005115-e1005115

2015

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Localization of Mitochondrial Nucleoids by Transmission Electron Microscopy Using the Transgenic Expression of the Mitochondrial Helicase Twinkle and APEX2

Methods in molecular biology (Clifton, N.J.), 2023, Vol.2615, p.173

2023

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Author Response: K320E-Twinkle skm Mice Are Genetically Heterogeneous for Secondary mtDNA Deletions Impairing Comparison With Controls

Investigative ophthalmology & visual science, 2021-01, Vol.62 (1), p.13

2021

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CMT-linked loss-of-function mutations in GDAP1 impair store-operated Ca 2+ entry-stimulated respiration

Scientific reports, 2017-02, Vol.7, p.42993

2017

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Author Response: K320E-Twinkleskm Mice Are Genetically Heterogeneous for Secondary mtDNA Deletions Impairing Comparison With Controls

Investigative ophthalmology & visual science, 2021-01, Vol.62 (1), p.13-13

2021

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Mitochondrial organelles turn inside out

Nature (London), 2024-08, Vol.632 (8027), p.987-988

2024

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Silencing of the Charcot–Marie–Tooth disease-associated gene GDAP1 induces abnormal mitochondrial distribution and affects Ca 2 + homeostasis by reducing store-operated Ca 2 + entry

Neurobiology of disease, 2013, Vol.55, p.140-151

2013

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mtDNA In and Out: On the Tightrope of Cellular Health

The Dynamic Nature of Mitochondria, 2024, Vol.1, p.111-127

1, 2024

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Silencing of the CharcotaMarieaTooth disease-associated gene GDAP1 induces abnormal mitochondrial distribution and affects Ca2 + homeostasis by reducing store-operated Ca2 + entry

Neurobiology of disease, 2013-07, Vol.55, p.140-151

2013

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CLUH granules coordinate translation of mitochondrial proteins with mTORC1 signaling and mitophagy

Mitochondrial membrane proteins and VPS35 orchestrate selective removal of mtDNA

Combined fibre atrophy and decreased muscle regeneration capacity driven by mitochondrial DNA alterations underlie the development of sarcopenia

Endosomal-dependent mitophagy coordinates mitochondrial nucleoid and mtDNA elimination

Selective Neuron Vulnerability in Common and Rare Diseases—Mitochondria in the Focus

Junctophilin-1 is a modifier gene of GDAP1-related Charcot-Marie-Tooth disease

Silencing of the Charcot–Marie–Tooth disease-associated gene GDAP1 induces abnormal mitochondrial distribution and affects Ca2+ homeostasis by reducing store-operated Ca2+ entry

CMT-linked loss-of-function mutations in GDAP1 impair store-operated Ca2+ entry-stimulated respiration

Extraocular Muscle Reveals Selective Vulnerability of Type IIB Fibers to Respiratory Chain Defects Induced by Mitochondrial DNA Alterations

Charcot-Marie-Tooth-related Gene GDAP1 Complements Cell Cycle Delay at G2/M Phase in Saccharomyces cerevisiae fis1 Gene-defective Cells

Mitochondrial dysfunction induced by frataxin deficiency is associated with cellular senescence and abnormal calcium metabolism

The role of mitochondrial network dynamics in the pathogenesis of Charcot-Marie-Tooth disease

Reshaping membranes to build mitochondrial DNA

CLUH regulates mitochondrial biogenesis by binding mRNAs of nuclear-encoded mitochondrial proteins

CLUH regulates mitochondrial metabolism by controlling translation and decay of target mRNAs

Inner membrane turns inside out to exit mitochondrial organelles

Lack of GDAP1 induces neuronal calcium and mitochondrial defects in a knockout mouse model of charcot-marie-tooth neuropathy

Localization of Mitochondrial Nucleoids by Transmission Electron Microscopy Using the Transgenic Expression of the Mitochondrial Helicase Twinkle and APEX2

Author Response: K320E-Twinkle skm Mice Are Genetically Heterogeneous for Secondary mtDNA Deletions Impairing Comparison With Controls

CMT-linked loss-of-function mutations in GDAP1 impair store-operated Ca 2+ entry-stimulated respiration

Author Response: K320E-Twinkleskm Mice Are Genetically Heterogeneous for Secondary mtDNA Deletions Impairing Comparison With Controls

Mitochondrial organelles turn inside out

Silencing of the Charcot–Marie–Tooth disease-associated gene GDAP1 induces abnormal mitochondrial distribution and affects Ca 2 + homeostasis by reducing store-operated Ca 2 + entry

mtDNA In and Out: On the Tightrope of Cellular Health

Silencing of the CharcotaMarieaTooth disease-associated gene GDAP1 induces abnormal mitochondrial distribution and affects Ca2 + homeostasis by reducing store-operated Ca2 + entry

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