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Andrew P Lieberman

Showing results (101-110 of 146) with videos related to

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Cancer Research|November 3, 2017
Rapid Intraoperative Diagnosis of Pediatric Brain Tumors Using Stimulated Raman HistologyTodd C Hollon, Spencer Lewis, Balaji Pandian, et al.
The Journal of Clinical Investigation|January 22, 2015
Disrupting SUMOylation enhances transcriptional function and ameliorates polyglutamine androgen receptor-mediated diseaseJason P Chua, Satya L Reddy, Zhigang Yu, et al.
Journal of Proteome Research|March 19, 2013
Sources of technical variability in quantitative LC-MS proteomics: human brain tissue sample analysisPaul D Piehowski, Vladislav A Petyuk, Daniel J Orton, et al.
Acta Neuropathologica|April 20, 2020
MEF2 impairment underlies skeletal muscle atrophy in polyglutamine diseaseSamir R Nath, Matthew L Lieberman, Zhigang Yu, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 11, 2007
Genetic variation in C57BL/6 ES cell lines and genetic instability in the Bruce4 C57BL/6 ES cell lineElizabeth D Hughes, Yun Yan Qu, Suzanne J Genik, et al.
Scientific Reports|January 25, 2017
Beta-agonist stimulation ameliorates the phenotype of spinal and bulbar muscular atrophy mice and patient-derived myotubesCarmelo Milioto, Adriana Malena, Eleonora Maino, et al.
Journal of Proteome Research|May 8, 2012
Label-free quantitative LC-MS proteomics of Alzheimer's disease and normally aged human brainsVictor P Andreev, Vladislav A Petyuk, Heather M Brewer, et al.
Scientific Reports|October 23, 2015
Aberrant Autophagic Response in The Muscle of A Knock-in Mouse Model of Spinal and Bulbar Muscular AtrophyPaola Rusmini, Maria Josefa Polanco, Riccardo Cristofani, et al.
JCI Insight|October 27, 2022
Species-specific differences in NPC1 protein trafficking govern therapeutic response in Niemann-Pick type C diseaseMark L Schultz, Kylie J Schache, Ruth D Azaria, et al.
Human Molecular Genetics|March 5, 2004
Huntingtin Interacting Protein 1 mutations lead to abnormal hematopoiesis, spinal defects and cataractsKatherine I Oravecz-Wilson, Mark J Kiel, Lina Li, et al.
Pageof 15

Showing results (101-110 of 146) with videos related to

Sort By:
Pageof 15
Cancer Research|November 3, 2017
Rapid Intraoperative Diagnosis of Pediatric Brain Tumors Using Stimulated Raman HistologyTodd C Hollon, Spencer Lewis, Balaji Pandian, et al.
The Journal of Clinical Investigation|January 22, 2015
Disrupting SUMOylation enhances transcriptional function and ameliorates polyglutamine androgen receptor-mediated diseaseJason P Chua, Satya L Reddy, Zhigang Yu, et al.
Journal of Proteome Research|March 19, 2013
Sources of technical variability in quantitative LC-MS proteomics: human brain tissue sample analysisPaul D Piehowski, Vladislav A Petyuk, Daniel J Orton, et al.
Acta Neuropathologica|April 20, 2020
MEF2 impairment underlies skeletal muscle atrophy in polyglutamine diseaseSamir R Nath, Matthew L Lieberman, Zhigang Yu, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 11, 2007
Genetic variation in C57BL/6 ES cell lines and genetic instability in the Bruce4 C57BL/6 ES cell lineElizabeth D Hughes, Yun Yan Qu, Suzanne J Genik, et al.
Scientific Reports|January 25, 2017
Beta-agonist stimulation ameliorates the phenotype of spinal and bulbar muscular atrophy mice and patient-derived myotubesCarmelo Milioto, Adriana Malena, Eleonora Maino, et al.
Journal of Proteome Research|May 8, 2012
Label-free quantitative LC-MS proteomics of Alzheimer's disease and normally aged human brainsVictor P Andreev, Vladislav A Petyuk, Heather M Brewer, et al.
Scientific Reports|October 23, 2015
Aberrant Autophagic Response in The Muscle of A Knock-in Mouse Model of Spinal and Bulbar Muscular AtrophyPaola Rusmini, Maria Josefa Polanco, Riccardo Cristofani, et al.
JCI Insight|October 27, 2022
Species-specific differences in NPC1 protein trafficking govern therapeutic response in Niemann-Pick type C diseaseMark L Schultz, Kylie J Schache, Ruth D Azaria, et al.
Human Molecular Genetics|March 5, 2004
Huntingtin Interacting Protein 1 mutations lead to abnormal hematopoiesis, spinal defects and cataractsKatherine I Oravecz-Wilson, Mark J Kiel, Lina Li, et al.
Pageof 15