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Timothy Wai

Showing results (21-30 of 56) with videos related to

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Molecular Genetics and Metabolism|September 16, 2020
Mitochondrial dysfunction caused by novel ATAD3A mutationsNathalie Dorison, Pauline Gaignard, Aurélien Bayot, et al.
Human Molecular Genetics|December 10, 2002
Identification of the gene responsible for the cblB complementation group of vitamin B12-dependent methylmalonic aciduriaC Melissa Dobson, Timothy Wai, Daniel Leclerc, et al.
Nature|May 6, 2021
Distinct fission signatures predict mitochondrial degradation or biogenesisTatjana Kleele, Timo Rey, Julius Winter, et al.
Plos Genetics|October 27, 2010
Gimap3 regulates tissue-specific mitochondrial DNA segregationRiikka Jokinen, Paula Marttinen, Helen Katarin Sandell, et al.
Molecular Genetics and Metabolism|June 13, 2006
A hemizygous SCO2 mutation in an early onset rapidly progressive, fatal cardiomyopathyScot C Leary, Andre Mattman, Timothy Wai, et al.
Human Mutation|November 4, 2004
Mutations in the MMAA gene in patients with the cblA disorder of vitamin B12 metabolismJordan P Lerner-Ellis, C Melissa Dobson, Timothy Wai, et al.
EMBO Reports|October 15, 2016
The membrane scaffold SLP2 anchors a proteolytic hub in mitochondria containing PARL and the i-AAA protease YME1LTimothy Wai, Shotaro Saita, Hendrik Nolte, et al.
EMBO Molecular Medicine|November 4, 2018
Loss of the mitochondrial <i>i</i>-AAA protease YME1L leads to ocular dysfunction and spinal axonopathyHans-Georg Sprenger, Gulzar Wani, Annika Hesseling, et al.
Brain : a Journal of Neurology|November 23, 2022
MPC2 variants disrupt mitochondrial pyruvate metabolism and cause an early-onset mitochondriopathyClaire Pujol, Elise Lebigot, Pauline Gaignard, et al.
Brain : a Journal of Neurology|June 3, 2022
CHCHD10 and SLP2 control the stability of the PHB complex: a key factor for motor neuron viabilityEmmanuelle C Genin, Sylvie Bannwarth, Baptiste Ropert, et al.
Pageof 6

Showing results (21-30 of 56) with videos related to

Sort By:
Pageof 6
Molecular Genetics and Metabolism|September 16, 2020
Mitochondrial dysfunction caused by novel ATAD3A mutationsNathalie Dorison, Pauline Gaignard, Aurélien Bayot, et al.
Human Molecular Genetics|December 10, 2002
Identification of the gene responsible for the cblB complementation group of vitamin B12-dependent methylmalonic aciduriaC Melissa Dobson, Timothy Wai, Daniel Leclerc, et al.
Nature|May 6, 2021
Distinct fission signatures predict mitochondrial degradation or biogenesisTatjana Kleele, Timo Rey, Julius Winter, et al.
Plos Genetics|October 27, 2010
Gimap3 regulates tissue-specific mitochondrial DNA segregationRiikka Jokinen, Paula Marttinen, Helen Katarin Sandell, et al.
Molecular Genetics and Metabolism|June 13, 2006
A hemizygous SCO2 mutation in an early onset rapidly progressive, fatal cardiomyopathyScot C Leary, Andre Mattman, Timothy Wai, et al.
Human Mutation|November 4, 2004
Mutations in the MMAA gene in patients with the cblA disorder of vitamin B12 metabolismJordan P Lerner-Ellis, C Melissa Dobson, Timothy Wai, et al.
EMBO Reports|October 15, 2016
The membrane scaffold SLP2 anchors a proteolytic hub in mitochondria containing PARL and the i-AAA protease YME1LTimothy Wai, Shotaro Saita, Hendrik Nolte, et al.
EMBO Molecular Medicine|November 4, 2018
Loss of the mitochondrial <i>i</i>-AAA protease YME1L leads to ocular dysfunction and spinal axonopathyHans-Georg Sprenger, Gulzar Wani, Annika Hesseling, et al.
Brain : a Journal of Neurology|November 23, 2022
MPC2 variants disrupt mitochondrial pyruvate metabolism and cause an early-onset mitochondriopathyClaire Pujol, Elise Lebigot, Pauline Gaignard, et al.
Brain : a Journal of Neurology|June 3, 2022
CHCHD10 and SLP2 control the stability of the PHB complex: a key factor for motor neuron viabilityEmmanuelle C Genin, Sylvie Bannwarth, Baptiste Ropert, et al.
Pageof 6