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Richard J Rodenburg

Showing results (91-100 of 137) with videos related to

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Scientific Reports|March 19, 2021
Long-term treated HIV infection is associated with platelet mitochondrial dysfunctionWouter A van der Heijden, Lisa van de Wijer, Martin Jaeger, et al.
Translational Psychiatry|June 4, 2020
Impaired mitochondrial complex I function as a candidate driver in the biological stress response and a concomitant stress-induced brain metabolic reprogramming in male miceTim L Emmerzaal, Graeme Preston, Bram Geenen, et al.
American Journal of Human Genetics|January 31, 2012
Lack of the mitochondrial protein acylglycerol kinase causes Sengers syndromeJohannes A Mayr, Tobias B Haack, Elisabeth Graf, et al.
Human Molecular Genetics|April 12, 2012
Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencingSharita Timal, Alexander Hoischen, Ludwig Lehle, et al.
Biochimica Et Biophysica Acta|December 24, 2014
Mitochondrial dysfunction in primary human fibroblasts triggers an adaptive cell survival program that requires AMPK-αFelix Distelmaier, Federica Valsecchi, Dania C Liemburg-Apers, et al.
European Journal of Human Genetics : EJHG|January 19, 2018
Compound heterozygous SPATA5 variants in four families and functional studies of SPATA5 deficiencySanna Puusepp, Reka Kovacs-Nagy, Bader Alhaddad, et al.
Biochimica Et Biophysica Acta. Bioenergetics|April 27, 2020
NDUFS4 deletion triggers loss of NDUFA12 in Ndufs4<sup>-/-</sup> mice and Leigh syndrome patients: A stabilizing role for NDUFAF2Merel J W Adjobo-Hermans, Ria de Haas, Peter H G M Willems, et al.
The Journal of Clinical Investigation|February 24, 2007
Overexpression of Akt converts radial growth melanoma to vertical growth melanomaBaskaran Govindarajan, James E Sligh, Bethaney J Vincent, et al.
Plos One|October 17, 2013
New findings in a global approach to dissect the whole phenotype of PLA2G6 gene mutationsMustafa A Salih, Emeline Mundwiller, Arif O Khan, et al.
Free Radical Biology & Medicine|June 19, 2022
The decylTPP mitochondria-targeting moiety lowers electron transport chain supercomplex levels in primary human skin fibroblastsElianne P Bulthuis, Claudia Einer, Felix Distelmaier, et al.
Pageof 14

Showing results (91-100 of 137) with videos related to

Sort By:
Pageof 14
Scientific Reports|March 19, 2021
Long-term treated HIV infection is associated with platelet mitochondrial dysfunctionWouter A van der Heijden, Lisa van de Wijer, Martin Jaeger, et al.
Translational Psychiatry|June 4, 2020
Impaired mitochondrial complex I function as a candidate driver in the biological stress response and a concomitant stress-induced brain metabolic reprogramming in male miceTim L Emmerzaal, Graeme Preston, Bram Geenen, et al.
American Journal of Human Genetics|January 31, 2012
Lack of the mitochondrial protein acylglycerol kinase causes Sengers syndromeJohannes A Mayr, Tobias B Haack, Elisabeth Graf, et al.
Human Molecular Genetics|April 12, 2012
Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencingSharita Timal, Alexander Hoischen, Ludwig Lehle, et al.
Biochimica Et Biophysica Acta|December 24, 2014
Mitochondrial dysfunction in primary human fibroblasts triggers an adaptive cell survival program that requires AMPK-αFelix Distelmaier, Federica Valsecchi, Dania C Liemburg-Apers, et al.
European Journal of Human Genetics : EJHG|January 19, 2018
Compound heterozygous SPATA5 variants in four families and functional studies of SPATA5 deficiencySanna Puusepp, Reka Kovacs-Nagy, Bader Alhaddad, et al.
Biochimica Et Biophysica Acta. Bioenergetics|April 27, 2020
NDUFS4 deletion triggers loss of NDUFA12 in Ndufs4<sup>-/-</sup> mice and Leigh syndrome patients: A stabilizing role for NDUFAF2Merel J W Adjobo-Hermans, Ria de Haas, Peter H G M Willems, et al.
The Journal of Clinical Investigation|February 24, 2007
Overexpression of Akt converts radial growth melanoma to vertical growth melanomaBaskaran Govindarajan, James E Sligh, Bethaney J Vincent, et al.
Plos One|October 17, 2013
New findings in a global approach to dissect the whole phenotype of PLA2G6 gene mutationsMustafa A Salih, Emeline Mundwiller, Arif O Khan, et al.
Free Radical Biology & Medicine|June 19, 2022
The decylTPP mitochondria-targeting moiety lowers electron transport chain supercomplex levels in primary human skin fibroblastsElianne P Bulthuis, Claudia Einer, Felix Distelmaier, et al.
Pageof 14