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Showing results (151-160 of 176) with videos related to

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The Journal of Pathology|November 1, 2017
Myoepithelial cell-specific expression of stefin A as a suppressor of early breast cancer invasionHendrika M Duivenvoorden, Jai Rautela, Laura E Edgington-Mitchell, et al.
The EMBO Journal|July 21, 2022
AIFM1 is a component of the mitochondrial disulfide relay that drives complex I assembly through efficient import of NDUFS5Silja Lucia Salscheider, Sarah Gerlich, Alfredo Cabrera-Orefice, et al.
Science Advances|December 1, 2021
De novo macrocyclic peptides for inhibiting, stabilizing, and probing the function of the retromer endosomal trafficking complexKai-En Chen, Qian Guo, Timothy A Hill, et al.
International Journal of Molecular Sciences|January 21, 2022
Biallelic Variants in <i>PYROXD2</i> Cause a Severe Infantile Metabolic Disorder Affecting Mitochondrial FunctionNicole J Van Bergen, Daniella H Hock, Lucy Spencer, et al.
American Journal of Human Genetics|March 31, 2026
Bi-allelic variants in NDUFA5 cause a mitochondriopathy with complex I deficiencyNatalie B Tan, Matthias Gautschi, Michael Raum, et al.
Journal of Inherited Metabolic Disease|January 28, 2026
A Nonketotic Hyperglycinemia Mouse Shows Wide-Ranging Biochemical Consequences of Elevated Glycine, Reduced Folate One-Carbon Charging, and Serine DeficiencyMichael A Swanson, Hua Jiang, Lakshmi Divya Kolora, et al.
Nature Communications|March 13, 2020
Mitochondrial peptide BRAWNIN is essential for vertebrate respiratory complex III assemblyShan Zhang, Boris Reljić, Chao Liang, et al.
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.
Pageof 18

Showing results (151-160 of 176) with videos related to

Sort By:
Pageof 18
The Journal of Pathology|November 1, 2017
Myoepithelial cell-specific expression of stefin A as a suppressor of early breast cancer invasionHendrika M Duivenvoorden, Jai Rautela, Laura E Edgington-Mitchell, et al.
The EMBO Journal|July 21, 2022
AIFM1 is a component of the mitochondrial disulfide relay that drives complex I assembly through efficient import of NDUFS5Silja Lucia Salscheider, Sarah Gerlich, Alfredo Cabrera-Orefice, et al.
Science Advances|December 1, 2021
De novo macrocyclic peptides for inhibiting, stabilizing, and probing the function of the retromer endosomal trafficking complexKai-En Chen, Qian Guo, Timothy A Hill, et al.
International Journal of Molecular Sciences|January 21, 2022
Biallelic Variants in <i>PYROXD2</i> Cause a Severe Infantile Metabolic Disorder Affecting Mitochondrial FunctionNicole J Van Bergen, Daniella H Hock, Lucy Spencer, et al.
American Journal of Human Genetics|March 31, 2026
Bi-allelic variants in NDUFA5 cause a mitochondriopathy with complex I deficiencyNatalie B Tan, Matthias Gautschi, Michael Raum, et al.
Journal of Inherited Metabolic Disease|January 28, 2026
A Nonketotic Hyperglycinemia Mouse Shows Wide-Ranging Biochemical Consequences of Elevated Glycine, Reduced Folate One-Carbon Charging, and Serine DeficiencyMichael A Swanson, Hua Jiang, Lakshmi Divya Kolora, et al.
Nature Communications|March 13, 2020
Mitochondrial peptide BRAWNIN is essential for vertebrate respiratory complex III assemblyShan Zhang, Boris Reljić, Chao Liang, et al.
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.
Pageof 18