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Alexandre Janer

Showing results (1-10 of 18) with videos related to

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Life Science Alliance|March 28, 2023
The role of the mitochondrial outer membrane protein SLC25A46 in mitochondrial fission and fusionJana Schuettpelz, Alexandre Janer, Hana Antonicka, et al.
Nucleic Acids Research|October 12, 2023
BOLA3 and NFU1 link mitoribosome iron-sulfur cluster assembly to multiple mitochondrial dysfunctions syndromeHui Zhong, Alexandre Janer, Oleh Khalimonchuk, et al.
Human Molecular Genetics|November 10, 2017
Loss of CHCHD10-CHCHD2 complexes required for respiration underlies the pathogenicity of a CHCHD10 mutation in ALSIsabella R Straub, Alexandre Janer, Woranontee Weraarpachai, et al.
Cell Metabolism|September 3, 2020
A High-Density Human Mitochondrial Proximity Interaction NetworkHana Antonicka, Zhen-Yuan Lin, Alexandre Janer, et al.
The Journal of Cell Biology|July 5, 2006
PML clastosomes prevent nuclear accumulation of mutant ataxin-7 and other polyglutamine proteinsAlexandre Janer, Elodie Martin, Marie-Paule Muriel, et al.
Molecular Genetics and Metabolism|December 29, 2012
Subcellular location of MMACHC and MMADHC, two human proteins central to intracellular vitamin B(12) metabolismWayne Mah, Justin C Deme, David Watkins, et al.
Human Molecular Genetics|October 22, 2009
SUMOylation attenuates the aggregation propensity and cellular toxicity of the polyglutamine expanded ataxin-7Alexandre Janer, Andreas Werner, Junko Takahashi-Fujigasaki, et al.
American Journal of Human Genetics|October 2, 2012
An RMND1 Mutation causes encephalopathy associated with multiple oxidative phosphorylation complex deficiencies and a mitochondrial translation defectAlexandre Janer, Hana Antonicka, Emilie Lalonde, et al.
American Journal of Human Genetics|September 28, 2011
Mutations in iron-sulfur cluster scaffold genes NFU1 and BOLA3 cause a fatal deficiency of multiple respiratory chain and 2-oxoacid dehydrogenase enzymesJessie M Cameron, Alexandre Janer, Valeriy Levandovskiy, et al.
Developmental Neurobiology|February 17, 2023
Loss of mitochondrial Chchd10 or Chchd2 in zebrafish leads to an ALS-like phenotype and Complex I deficiency independent of the mitochondrial integrated stress responseVirginie Petel Légaré, Christian J Rampal, Tyler J N Gurberg, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Life Science Alliance|March 28, 2023
The role of the mitochondrial outer membrane protein SLC25A46 in mitochondrial fission and fusionJana Schuettpelz, Alexandre Janer, Hana Antonicka, et al.
Nucleic Acids Research|October 12, 2023
BOLA3 and NFU1 link mitoribosome iron-sulfur cluster assembly to multiple mitochondrial dysfunctions syndromeHui Zhong, Alexandre Janer, Oleh Khalimonchuk, et al.
Human Molecular Genetics|November 10, 2017
Loss of CHCHD10-CHCHD2 complexes required for respiration underlies the pathogenicity of a CHCHD10 mutation in ALSIsabella R Straub, Alexandre Janer, Woranontee Weraarpachai, et al.
Cell Metabolism|September 3, 2020
A High-Density Human Mitochondrial Proximity Interaction NetworkHana Antonicka, Zhen-Yuan Lin, Alexandre Janer, et al.
The Journal of Cell Biology|July 5, 2006
PML clastosomes prevent nuclear accumulation of mutant ataxin-7 and other polyglutamine proteinsAlexandre Janer, Elodie Martin, Marie-Paule Muriel, et al.
Molecular Genetics and Metabolism|December 29, 2012
Subcellular location of MMACHC and MMADHC, two human proteins central to intracellular vitamin B(12) metabolismWayne Mah, Justin C Deme, David Watkins, et al.
Human Molecular Genetics|October 22, 2009
SUMOylation attenuates the aggregation propensity and cellular toxicity of the polyglutamine expanded ataxin-7Alexandre Janer, Andreas Werner, Junko Takahashi-Fujigasaki, et al.
American Journal of Human Genetics|October 2, 2012
An RMND1 Mutation causes encephalopathy associated with multiple oxidative phosphorylation complex deficiencies and a mitochondrial translation defectAlexandre Janer, Hana Antonicka, Emilie Lalonde, et al.
American Journal of Human Genetics|September 28, 2011
Mutations in iron-sulfur cluster scaffold genes NFU1 and BOLA3 cause a fatal deficiency of multiple respiratory chain and 2-oxoacid dehydrogenase enzymesJessie M Cameron, Alexandre Janer, Valeriy Levandovskiy, et al.
Developmental Neurobiology|February 17, 2023
Loss of mitochondrial Chchd10 or Chchd2 in zebrafish leads to an ALS-like phenotype and Complex I deficiency independent of the mitochondrial integrated stress responseVirginie Petel Légaré, Christian J Rampal, Tyler J N Gurberg, et al.
Pageof 2