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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 report
Simon 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 Translation
James 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 inflammation
Dimitri Scherbakov, Stefan Duscha, Reda Juskeviciene, et al.
Cells
|
October 22, 2020
Clock-Controlled Mitochondrial Dynamics Correlates with Cyclic Pregnenolone Synthesis
Melissa 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 Therapy
Yun 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 case
Kim 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 hyperfusion
Stéphane 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 model
Lei 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 gene
Ulrike 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 phenotype
Christopher B Jackson, Christoph Neuwirth, Dagmar Hahn, et al.
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of 15
Search research articles
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Showing results (31-40 of 144) with videos related to
Sort By:
Page
of 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 report
Simon 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 Translation
James 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 inflammation
Dimitri Scherbakov, Stefan Duscha, Reda Juskeviciene, et al.
Cells
|
October 22, 2020
Clock-Controlled Mitochondrial Dynamics Correlates with Cyclic Pregnenolone Synthesis
Melissa 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 Therapy
Yun 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 case
Kim 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 hyperfusion
Stéphane 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 model
Lei 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 gene
Ulrike 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 phenotype
Christopher B Jackson, Christoph Neuwirth, Dagmar Hahn, et al.
Page
of 15