Search research articles
Contact Us
Filters
Showing results (101-110 of 146) with videos related to
Page
of 15
Sort By:
Cancer Research
|
November 3, 2017
Rapid Intraoperative Diagnosis of Pediatric Brain Tumors Using Stimulated Raman Histology
Todd 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 disease
Jason 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 analysis
Paul D Piehowski, Vladislav A Petyuk, Daniel J Orton, et al.
Acta Neuropathologica
|
April 20, 2020
MEF2 impairment underlies skeletal muscle atrophy in polyglutamine disease
Samir 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 line
Elizabeth 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 myotubes
Carmelo 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 brains
Victor 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 Atrophy
Paola 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 disease
Mark 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 cataracts
Katherine I Oravecz-Wilson, Mark J Kiel, Lina Li, et al.
Page
of 15
Search research articles
Search
Showing results (101-110 of 146) with videos related to
Sort By:
Page
of 15
Cancer Research
|
November 3, 2017
Rapid Intraoperative Diagnosis of Pediatric Brain Tumors Using Stimulated Raman Histology
Todd 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 disease
Jason 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 analysis
Paul D Piehowski, Vladislav A Petyuk, Daniel J Orton, et al.
Acta Neuropathologica
|
April 20, 2020
MEF2 impairment underlies skeletal muscle atrophy in polyglutamine disease
Samir 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 line
Elizabeth 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 myotubes
Carmelo 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 brains
Victor 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 Atrophy
Paola 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 disease
Mark 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 cataracts
Katherine I Oravecz-Wilson, Mark J Kiel, Lina Li, et al.
Page
of 15