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Mike Gerards

Showing results (11-20 of 29) with videos related to

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Mitochondrion|February 5, 2025
The unusual suspect: A novel role for intermediate filament proteins in mitochondrial morphologyIrene M G M Hemel, Carlijn Steen, Simon L I J Denil, et al.
Mitochondrion|January 25, 2019
A zebrafish model to study small-fiber neuropathy reveals a potential role for GDAP1Ivo Eijkenboom, Jo M Vanoevelen, Janneke G J Hoeijmakers, et al.
Molecular Systems Biology|June 23, 2014
Screen for mitochondrial DNA copy number maintenance genes reveals essential role for ATP synthaseAtsushi Fukuoh, Giuseppe Cannino, Mike Gerards, et al.
Mitochondrion|June 29, 2010
Nonsense mutations in CABC1/ADCK3 cause progressive cerebellar ataxia and atrophyMike Gerards, Bianca van den Bosch, Chantal Calis, et al.
Frontiers in Cell and Developmental Biology|June 30, 2020
<i>Tfam</i> Knockdown Results in Reduction of mtDNA Copy Number, OXPHOS Deficiency and Abnormalities in Zebrafish EmbryosAuke B C Otten, Rick Kamps, Patrick Lindsey, et al.
European Journal of Human Genetics : EJHG|July 23, 2015
Pathogenic CWF19L1 variants as a novel cause of autosomal recessive cerebellar ataxia and atrophyMinh Nguyen, Iris Boesten, Debby M E I Hellebrekers, et al.
Neuromuscular Disorders : NMD|August 22, 2021
Whole exome sequencing reveals a homozygous C1QBP deletion as the cause of progressive external ophthalmoplegia and multiple mtDNA deletionsLe Guo, Periyasamy Govindaraj, Mariëlle Kievit, et al.
Annals of Neurology|September 1, 2017
Thiamine deficiency in childhood with attention to genetic causes: Survival and outcome predictorsJuan Darío Ortigoza-Escobar, Majid Alfadhel, Marta Molero-Luis, et al.
Genetics|October 26, 2016
Replication Errors Made During Oogenesis Lead to Detectable De Novo mtDNA Mutations in Zebrafish Oocytes with a Low mtDNA Copy NumberAuke B C Otten, Alphons P M Stassen, Michiel Adriaens, et al.
Plos Genetics|October 5, 2019
Manipulating mtDNA in vivo reprograms metabolism via novel response mechanismsDiana Bahhir, Cagri Yalgin, Liina Ots, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Mitochondrion|February 5, 2025
The unusual suspect: A novel role for intermediate filament proteins in mitochondrial morphologyIrene M G M Hemel, Carlijn Steen, Simon L I J Denil, et al.
Mitochondrion|January 25, 2019
A zebrafish model to study small-fiber neuropathy reveals a potential role for GDAP1Ivo Eijkenboom, Jo M Vanoevelen, Janneke G J Hoeijmakers, et al.
Molecular Systems Biology|June 23, 2014
Screen for mitochondrial DNA copy number maintenance genes reveals essential role for ATP synthaseAtsushi Fukuoh, Giuseppe Cannino, Mike Gerards, et al.
Mitochondrion|June 29, 2010
Nonsense mutations in CABC1/ADCK3 cause progressive cerebellar ataxia and atrophyMike Gerards, Bianca van den Bosch, Chantal Calis, et al.
Frontiers in Cell and Developmental Biology|June 30, 2020
<i>Tfam</i> Knockdown Results in Reduction of mtDNA Copy Number, OXPHOS Deficiency and Abnormalities in Zebrafish EmbryosAuke B C Otten, Rick Kamps, Patrick Lindsey, et al.
European Journal of Human Genetics : EJHG|July 23, 2015
Pathogenic CWF19L1 variants as a novel cause of autosomal recessive cerebellar ataxia and atrophyMinh Nguyen, Iris Boesten, Debby M E I Hellebrekers, et al.
Neuromuscular Disorders : NMD|August 22, 2021
Whole exome sequencing reveals a homozygous C1QBP deletion as the cause of progressive external ophthalmoplegia and multiple mtDNA deletionsLe Guo, Periyasamy Govindaraj, Mariëlle Kievit, et al.
Annals of Neurology|September 1, 2017
Thiamine deficiency in childhood with attention to genetic causes: Survival and outcome predictorsJuan Darío Ortigoza-Escobar, Majid Alfadhel, Marta Molero-Luis, et al.
Genetics|October 26, 2016
Replication Errors Made During Oogenesis Lead to Detectable De Novo mtDNA Mutations in Zebrafish Oocytes with a Low mtDNA Copy NumberAuke B C Otten, Alphons P M Stassen, Michiel Adriaens, et al.
Plos Genetics|October 5, 2019
Manipulating mtDNA in vivo reprograms metabolism via novel response mechanismsDiana Bahhir, Cagri Yalgin, Liina Ots, et al.
Pageof 3