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David A Stroud

Showing results (91-100 of 109) with videos related to

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EMBO Molecular Medicine|September 12, 2018
<i>OXA1L</i> mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defectKyle Thompson, Nicole Mai, Monika Oláhová, et al.
Human Genetics|May 6, 2023
Deficiency of the mitochondrial ribosomal subunit, MRPL50, causes autosomal recessive syndromic premature ovarian insufficiencyShabnam Bakhshalizadeh, Daniella H Hock, Nicole A Siddall, et al.
The Journal of Clinical Endocrinology and Metabolism|September 8, 2022
Premature Ovarian Insufficiency in CLPB Deficiency: Transcriptomic, Proteomic and Phenotypic InsightsElena J Tucker, Megan J Baker, Daniella H Hock, et al.
American Journal of Human Genetics|April 7, 2018
Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh SyndromeNicole J Lake, Bryn D Webb, David A Stroud, et al.
Cell|November 20, 2025
Inhibition of heme biosynthesis triggers cuproptosis in acute myeloid leukemiaAlexander C Lewis, Emily Gruber, Rheana Franich, et al.
Bioscience|June 10, 2017
The Arctic in the Twenty-First Century: Changing Biogeochemical Linkages across a Paraglacial Landscape of GreenlandN John Anderson, Jasmine E Saros, Joanna E Bullard, et al.
Cell|May 12, 2023
Structure of the endosomal Commander complex linked to Ritscher-Schinzel syndromeMichael D Healy, Kerrie E McNally, Rebeka Butkovič, et al.
American Journal of Human Genetics|August 5, 2017
Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh SyndromeNicole J Lake, Bryn D Webb, David A Stroud, et al.
Nature Communications|February 23, 2023
TEFM variants impair mitochondrial transcription causing childhood-onset neurological diseaseLindsey Van Haute, Emily O'Connor, Héctor Díaz-Maldonado, et al.
Blood|April 7, 2021
Intact TP-53 function is essential for sustaining durable responses to BH3-mimetic drugs in leukemiasRachel Thijssen, Sarah T Diepstraten, Donia Moujalled, et al.
Pageof 11

Showing results (91-100 of 109) with videos related to

Sort By:
Pageof 11
EMBO Molecular Medicine|September 12, 2018
<i>OXA1L</i> mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defectKyle Thompson, Nicole Mai, Monika Oláhová, et al.
Human Genetics|May 6, 2023
Deficiency of the mitochondrial ribosomal subunit, MRPL50, causes autosomal recessive syndromic premature ovarian insufficiencyShabnam Bakhshalizadeh, Daniella H Hock, Nicole A Siddall, et al.
The Journal of Clinical Endocrinology and Metabolism|September 8, 2022
Premature Ovarian Insufficiency in CLPB Deficiency: Transcriptomic, Proteomic and Phenotypic InsightsElena J Tucker, Megan J Baker, Daniella H Hock, et al.
American Journal of Human Genetics|April 7, 2018
Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh SyndromeNicole J Lake, Bryn D Webb, David A Stroud, et al.
Cell|November 20, 2025
Inhibition of heme biosynthesis triggers cuproptosis in acute myeloid leukemiaAlexander C Lewis, Emily Gruber, Rheana Franich, et al.
Bioscience|June 10, 2017
The Arctic in the Twenty-First Century: Changing Biogeochemical Linkages across a Paraglacial Landscape of GreenlandN John Anderson, Jasmine E Saros, Joanna E Bullard, et al.
Cell|May 12, 2023
Structure of the endosomal Commander complex linked to Ritscher-Schinzel syndromeMichael D Healy, Kerrie E McNally, Rebeka Butkovič, et al.
American Journal of Human Genetics|August 5, 2017
Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh SyndromeNicole J Lake, Bryn D Webb, David A Stroud, et al.
Nature Communications|February 23, 2023
TEFM variants impair mitochondrial transcription causing childhood-onset neurological diseaseLindsey Van Haute, Emily O'Connor, Héctor Díaz-Maldonado, et al.
Blood|April 7, 2021
Intact TP-53 function is essential for sustaining durable responses to BH3-mimetic drugs in leukemiasRachel Thijssen, Sarah T Diepstraten, Donia Moujalled, et al.
Pageof 11