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MFN2 mutations in Charcot–Marie–Tooth disease alter mitochondria-associated ER membrane function but do not impair bioenergetics

Human molecular genetics, 2019-06, Vol.28 (11), p.1782-1800

2019

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The Arabian Cradle: Mitochondrial Relicts of the First Steps along the Southern Route out of Africa

American journal of human genetics, 2012-02, Vol.90 (2), p.347-355

2012

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Mitochondrial DNA Signals of Late Glacial Recolonization of Europe from Near Eastern Refugia

American journal of human genetics, 2012-05, Vol.90 (5), p.915-924

2012

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Pathogenic mtDNA variants, in particular single large-scale mtDNA deletions, are strongly associated with post-lingual onset sensorineural hearing loss in primary mitochondrial disease

Molecular genetics and metabolism, 2022-11, Vol.137 (3), p.230-238

2022

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Quantification and Characterization of UVB-Induced Mitochondrial Fragmentation in Normal Primary Human Keratinocytes

Scientific reports, 2016-10, Vol.6 (1), p.35065-35065, Article 35065

2016

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Expression of mitochondrial oxidative stress response genes in muscle is associated with mitochondrial respiration, physical performance, and muscle mass in the Study of Muscle, Mobility, and Aging

Aging cell, 2024-06, Vol.23 (6), p.e14114-n/a

2024

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Preserving mitochondria to treat hypertrophic cardiomyopathy: From rare mitochondrial DNA mutation to heart failure therapy?

The Journal of clinical investigation, 2023-07, Vol.133 (14)

Diwan, Abhinav

2023

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Mitochondrial miRNA (MitomiR): a new player in cardiovascular health

Canadian journal of physiology and pharmacology, 2015-10, Vol.93 (10), p.855-861

2015

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A Scoping Review Investigating the "Gene-Dosage Theory" of Mitochondrial DNA in the Healthy Skeletal Muscle

International journal of molecular sciences, 2023-05, Vol.24 (9), p.8154

2023

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Spatiotemporal Control of ULK1 Activation by NDP52 and TBK1 during Selective Autophagy

Molecular cell, 2019-04, Vol.74 (2), p.347-362.e6

2019

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voltage-dependent anion channel, a major component of the tRNA import machinery in plant mitochondria

Proceedings of the National Academy of Sciences - PNAS, 2006-11, Vol.103 (48), p.18362-18367

2006

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The Origin and Diversification of Mitochondria

Current biology, 2017-11, Vol.27 (21), p.R1177-R1192

2017

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Mechanisms of Mitochondrial Iron-Sulfur Protein Biogenesis

Annual review of biochemistry, 2020-06, Vol.89 (1), p.471-499

2020

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Mitochondrial ROS in myocardial ischemia reperfusion and remodeling

Biochimica et biophysica acta. Molecular basis of disease, 2020-07, Vol.1866 (7), p.165768-165768, Article 165768

2020

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Nevirapine induced mitochondrial dysfunction in HepG2 cells

Scientific reports, 2017-08, Vol.7 (1), p.9194-11, Article 9194

2017

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The alternative reality of plant mitochondrial DNA: One ring does not rule them all

PLoS genetics, 2019-08, Vol.15 (8), p.e1008373-e1008373

2019

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Plant organellar RNA editing: what 30 years of research has revealed

The Plant journal : for cell and molecular biology, 2020-03, Vol.101 (5), p.1040-1056

2020

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Mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delay

Journal of inherited metabolic disease, 2017-05, Vol.40 (3), p.385-394

2017

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Mitochondrial regulation of ferroptosis

The Journal of cell biology, 2021-09, Vol.220 (9), p.1

Gan, Boyi

2021

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Getting out what you put in: Copper in mitochondria and its impacts on human disease

Biochimica et biophysica acta. Molecular cell research, 2021-01, Vol.1868 (1), p.118867-118867, Article 118867

2021

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OrganellarGenomeDRAW (OGDRAW) version 1.3.1: expanded toolkit for the graphical visualization of organellar genomes

Nucleic acids research, 2019-07, Vol.47 (W1), p.W59-W64

2019

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Cellular adaptation to hypoxia through hypoxia inducible factors and beyond

Nature reviews. Molecular cell biology, 2020-05, Vol.21 (5), p.268-283

2020

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First description of a novel mitochondrial mutation in the MT-TI gene associated with multiple mitochondrial DNA deletion and depletion in family with severe dilated mitochondrial cardiomyopathy

Biochemical and biophysical research communications, 2018-03, Vol.497 (4), p.1049-1054

2018

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Mechanistic concepts of iron-sulfur protein biogenesis in Biology

Biochimica et biophysica acta. Molecular cell research, 2021-01, Vol.1868 (1), p.118863-118863, Article 118863

2021

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Dysregulated metabolism contributes to oncogenesis

Seminars in cancer biology, 2015-12, Vol.35, p.S129-S150

2015

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MFN2 mutations in Charcot–Marie–Tooth disease alter mitochondria-associated ER membrane function but do not impair bioenergetics

The Arabian Cradle: Mitochondrial Relicts of the First Steps along the Southern Route out of Africa

Mitochondrial DNA Signals of Late Glacial Recolonization of Europe from Near Eastern Refugia

Pathogenic mtDNA variants, in particular single large-scale mtDNA deletions, are strongly associated with post-lingual onset sensorineural hearing loss in primary mitochondrial disease

Quantification and Characterization of UVB-Induced Mitochondrial Fragmentation in Normal Primary Human Keratinocytes

Expression of mitochondrial oxidative stress response genes in muscle is associated with mitochondrial respiration, physical performance, and muscle mass in the Study of Muscle, Mobility, and Aging

Preserving mitochondria to treat hypertrophic cardiomyopathy: From rare mitochondrial DNA mutation to heart failure therapy?

Mitochondrial miRNA (MitomiR): a new player in cardiovascular health

A Scoping Review Investigating the "Gene-Dosage Theory" of Mitochondrial DNA in the Healthy Skeletal Muscle

Spatiotemporal Control of ULK1 Activation by NDP52 and TBK1 during Selective Autophagy

voltage-dependent anion channel, a major component of the tRNA import machinery in plant mitochondria

The Origin and Diversification of Mitochondria

Mechanisms of Mitochondrial Iron-Sulfur Protein Biogenesis

Mitochondrial ROS in myocardial ischemia reperfusion and remodeling

Nevirapine induced mitochondrial dysfunction in HepG2 cells

The alternative reality of plant mitochondrial DNA: One ring does not rule them all

Plant organellar RNA editing: what 30 years of research has revealed

Mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delay

Mitochondrial regulation of ferroptosis

Getting out what you put in: Copper in mitochondria and its impacts on human disease

OrganellarGenomeDRAW (OGDRAW) version 1.3.1: expanded toolkit for the graphical visualization of organellar genomes

Cellular adaptation to hypoxia through hypoxia inducible factors and beyond

First description of a novel mitochondrial mutation in the MT-TI gene associated with multiple mitochondrial DNA deletion and depletion in family with severe dilated mitochondrial cardiomyopathy

Mechanistic concepts of iron-sulfur protein biogenesis in Biology

Dysregulated metabolism contributes to oncogenesis

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