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Stephan Frank

Showing results (31-40 of 144) with videos related to

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Virchows Archiv : an International Journal of Pathology|June 27, 2020
NUT midline carcinomas and their differentials by a single molecular profiling method: a new promising diagnostic strategy illustrated by a case reportSimon Haefliger, Alexandar Tzankov, Stephan Frank, et al.
Cells|November 27, 2021
Silencing of the ER and Integrative Stress Responses in the Liver of Mice with Error-Prone TranslationJames Moore, Ivan Osinnii, Amandine Grimm, et al.
RNA (New York, N.Y.)|December 2, 2020
Mitochondrial misreading in skeletal muscle accelerates metabolic aging and confers lipid accumulation and increased inflammationDimitri Scherbakov, Stefan Duscha, Reda Juskeviciene, et al.
Cells|October 22, 2020
Clock-Controlled Mitochondrial Dynamics Correlates with Cyclic Pregnenolone SynthesisMelissa Witzig, Amandine Grimm, Karen Schmitt, et al.
Pharmaceutics|November 17, 2020
Evaluation of Actinium-225 Labeled Minigastrin Analogue [<sup>225</sup>Ac]Ac-DOTA-PP-F11N for Targeted Alpha Particle TherapyYun Qin, Stefan Imobersteg, Alain Blanc, et al.
Journal of Neurosurgery. Case Lessons|March 10, 2025
Rare glioblastoma subtype masquerading as a poorly differentiated carcinoma: illustrative caseKim Harnisch, Alberto Consuegra, Ali Fuat Okuducu, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 24, 2013
Impaired complex IV activity in response to loss of LRPPRC function can be compensated by mitochondrial hyperfusionStéphane G Rolland, Elisa Motori, Nadin Memar, et al.
Plos One|January 4, 2013
Inactivation of MARCH5 prevents mitochondrial fragmentation and interferes with cell death in a neuronal cell modelLei Fang, Charles Hemion, David Goldblum, et al.
Neuromuscular Disorders : NMD|April 2, 2014
Congenital muscular dystrophy with dropped head phenotype and cognitive impairment due to a novel mutation in the LMNA geneUlrike Bonati, Nina Bechtel, Karl Heinimann, et al.
The British Journal of Ophthalmology|July 19, 2014
Novel mitochondrial tRNA(Ile) m.4282A>G gene mutation leads to chronic progressive external ophthalmoplegia plus phenotypeChristopher B Jackson, Christoph Neuwirth, Dagmar Hahn, et al.
Pageof 15

Showing results (31-40 of 144) with videos related to

Sort By:
Pageof 15
Virchows Archiv : an International Journal of Pathology|June 27, 2020
NUT midline carcinomas and their differentials by a single molecular profiling method: a new promising diagnostic strategy illustrated by a case reportSimon Haefliger, Alexandar Tzankov, Stephan Frank, et al.
Cells|November 27, 2021
Silencing of the ER and Integrative Stress Responses in the Liver of Mice with Error-Prone TranslationJames Moore, Ivan Osinnii, Amandine Grimm, et al.
RNA (New York, N.Y.)|December 2, 2020
Mitochondrial misreading in skeletal muscle accelerates metabolic aging and confers lipid accumulation and increased inflammationDimitri Scherbakov, Stefan Duscha, Reda Juskeviciene, et al.
Cells|October 22, 2020
Clock-Controlled Mitochondrial Dynamics Correlates with Cyclic Pregnenolone SynthesisMelissa Witzig, Amandine Grimm, Karen Schmitt, et al.
Pharmaceutics|November 17, 2020
Evaluation of Actinium-225 Labeled Minigastrin Analogue [<sup>225</sup>Ac]Ac-DOTA-PP-F11N for Targeted Alpha Particle TherapyYun Qin, Stefan Imobersteg, Alain Blanc, et al.
Journal of Neurosurgery. Case Lessons|March 10, 2025
Rare glioblastoma subtype masquerading as a poorly differentiated carcinoma: illustrative caseKim Harnisch, Alberto Consuegra, Ali Fuat Okuducu, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 24, 2013
Impaired complex IV activity in response to loss of LRPPRC function can be compensated by mitochondrial hyperfusionStéphane G Rolland, Elisa Motori, Nadin Memar, et al.
Plos One|January 4, 2013
Inactivation of MARCH5 prevents mitochondrial fragmentation and interferes with cell death in a neuronal cell modelLei Fang, Charles Hemion, David Goldblum, et al.
Neuromuscular Disorders : NMD|April 2, 2014
Congenital muscular dystrophy with dropped head phenotype and cognitive impairment due to a novel mutation in the LMNA geneUlrike Bonati, Nina Bechtel, Karl Heinimann, et al.
The British Journal of Ophthalmology|July 19, 2014
Novel mitochondrial tRNA(Ile) m.4282A>G gene mutation leads to chronic progressive external ophthalmoplegia plus phenotypeChristopher B Jackson, Christoph Neuwirth, Dagmar Hahn, et al.
Pageof 15