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K Koenig

Showing results (91-100 of 113) with videos related to

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Neurology|January 4, 2020
Safety and efficacy of omaveloxolone in patients with mitochondrial myopathy: MOTOR trialKaren L Madsen, Astrid E Buch, Bruce H Cohen, et al.
Molecular Genetics and Metabolism|June 18, 2016
Solid organ transplantation in primary mitochondrial disease: Proceed with cautionSumit Parikh, Amel Karaa, Amy Goldstein, et al.
Journal of Clinical Medicine|November 23, 2019
Clinical Spectrum and Functional Consequences Associated with Bi-Allelic Pathogenic <i>PNPT1</i> VariantsRocio Rius, Nicole J Van Bergen, Alison G Compton, et al.
Genome Announcements|January 11, 2014
Genome Sequence of Escherichia coli O157:H7 Strain 2886-75, Associated with the First Reported Case of Human Infection in the United StatesFatemeh Sanjar, Tracy H Hazen, Sadiq M Shah, et al.
Environmental Science & Technology|November 19, 2025
Bihourly Monitoring Reveals the Significance of Photochemical Removal of PAHs in the Urban AtmosphereZhen Cheng, Xinghua Qiu, Xiaodi Shi, et al.
American Journal of Medical Genetics. Part A|April 13, 2021
Heterozygous variants in SPTBN1 cause intellectual disability and autismJill A Rosenfeld, Rui Xiao, Mir Reza Bekheirnia, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Atomistic TCR-ligand interactions instruct memory T-cell differentiationAoi Akitsu, Kemin Tan, Robert J Mallis, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 2015
Active and widespread halogen chemistry in the tropical and subtropical free troposphereSiyuan Wang, Johan A Schmidt, Sunil Baidar, et al.
Brain : a Journal of Neurology|February 11, 2022
DNAJC30 defect: a frequent cause of recessive Leber hereditary optic neuropathy and Leigh syndromeSarah L Stenton, Marketa Tesarova, Natalia L Sheremet, et al.
Human Mutation|January 31, 2020
BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorderTiana M Scott, Hui Guo, Evan E Eichler, et al.
Pageof 12

Showing results (91-100 of 113) with videos related to

Sort By:
Pageof 12
Neurology|January 4, 2020
Safety and efficacy of omaveloxolone in patients with mitochondrial myopathy: MOTOR trialKaren L Madsen, Astrid E Buch, Bruce H Cohen, et al.
Molecular Genetics and Metabolism|June 18, 2016
Solid organ transplantation in primary mitochondrial disease: Proceed with cautionSumit Parikh, Amel Karaa, Amy Goldstein, et al.
Journal of Clinical Medicine|November 23, 2019
Clinical Spectrum and Functional Consequences Associated with Bi-Allelic Pathogenic <i>PNPT1</i> VariantsRocio Rius, Nicole J Van Bergen, Alison G Compton, et al.
Genome Announcements|January 11, 2014
Genome Sequence of Escherichia coli O157:H7 Strain 2886-75, Associated with the First Reported Case of Human Infection in the United StatesFatemeh Sanjar, Tracy H Hazen, Sadiq M Shah, et al.
Environmental Science & Technology|November 19, 2025
Bihourly Monitoring Reveals the Significance of Photochemical Removal of PAHs in the Urban AtmosphereZhen Cheng, Xinghua Qiu, Xiaodi Shi, et al.
American Journal of Medical Genetics. Part A|April 13, 2021
Heterozygous variants in SPTBN1 cause intellectual disability and autismJill A Rosenfeld, Rui Xiao, Mir Reza Bekheirnia, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
Atomistic TCR-ligand interactions instruct memory T-cell differentiationAoi Akitsu, Kemin Tan, Robert J Mallis, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 2015
Active and widespread halogen chemistry in the tropical and subtropical free troposphereSiyuan Wang, Johan A Schmidt, Sunil Baidar, et al.
Brain : a Journal of Neurology|February 11, 2022
DNAJC30 defect: a frequent cause of recessive Leber hereditary optic neuropathy and Leigh syndromeSarah L Stenton, Marketa Tesarova, Natalia L Sheremet, et al.
Human Mutation|January 31, 2020
BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorderTiana M Scott, Hui Guo, Evan E Eichler, et al.
Pageof 12