Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Steven J Steinberg

Showing results (1-10 of 25) with videos related to

Pageof 3
Sort By:
The Journal of Pastoral Care & Counseling : JPCC|November 12, 2005
The pastoral visit as Pas de deuxSteven J Steinberg
The Journal of Pastoral Care & Counseling : JPCC|November 12, 2005
Clinical Pastoral Education for Jews an enriching experienceSteven J Steinberg
Pediatric Neurology|August 1, 2014
Late-onset Zellweger spectrum disorder caused by PEX6 mutations mimicking X-linked adrenoleukodystrophyChristel Tran, Stacy Hewson, Steven J Steinberg, et al.
Human Mutation|December 24, 2008
Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disordersWing Yan Yik, Steven J Steinberg, Ann B Moser, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 12, 2019
Laboratory diagnosis of disorders of peroxisomal biogenesis and function: a technical standard of the American College of Medical Genetics and Genomics (ACMG)Irene De Biase, Silvia Tortorelli, Lisa Kratz, et al.
Biochimica Et Biophysica Acta|October 24, 2006
Peroxisome biogenesis disordersSteven J Steinberg, Gabriele Dodt, Gerald V Raymond, et al.
Journal of Pediatric Surgery|February 24, 2009
A novel SOX9 mutation, 972delC, causes 46,XY sex-reversed campomelic dysplasia with nephrocalcinosis, urolithiasis, and dysgerminomaNicholas G Cost, Aaron T Ludwig, Duncan T Wilcox, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 24, 2006
Bap31 enhances the endoplasmic reticulum export and quality control of human class I MHC moleculesJohn J Ladasky, Sarah Boyle, Malini Seth, et al.
Journal of Cellular Biochemistry|April 6, 2011
Nonsense suppressor therapies rescue peroxisome lipid metabolism and assembly in cells from patients with specific PEX gene mutationsPatricia K Dranchak, Erminia Di Pietro, Ann Snowden, et al.
The Journal of Biological Chemistry|September 17, 2003
The acyl-CoA synthetase "bubblegum" (lipidosin): further characterization and role in neuronal fatty acid beta-oxidationZhengtong Pei, Nadia A Oey, Maartje M Zuidervaart, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
The Journal of Pastoral Care & Counseling : JPCC|November 12, 2005
The pastoral visit as Pas de deuxSteven J Steinberg
The Journal of Pastoral Care & Counseling : JPCC|November 12, 2005
Clinical Pastoral Education for Jews an enriching experienceSteven J Steinberg
Pediatric Neurology|August 1, 2014
Late-onset Zellweger spectrum disorder caused by PEX6 mutations mimicking X-linked adrenoleukodystrophyChristel Tran, Stacy Hewson, Steven J Steinberg, et al.
Human Mutation|December 24, 2008
Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disordersWing Yan Yik, Steven J Steinberg, Ann B Moser, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 12, 2019
Laboratory diagnosis of disorders of peroxisomal biogenesis and function: a technical standard of the American College of Medical Genetics and Genomics (ACMG)Irene De Biase, Silvia Tortorelli, Lisa Kratz, et al.
Biochimica Et Biophysica Acta|October 24, 2006
Peroxisome biogenesis disordersSteven J Steinberg, Gabriele Dodt, Gerald V Raymond, et al.
Journal of Pediatric Surgery|February 24, 2009
A novel SOX9 mutation, 972delC, causes 46,XY sex-reversed campomelic dysplasia with nephrocalcinosis, urolithiasis, and dysgerminomaNicholas G Cost, Aaron T Ludwig, Duncan T Wilcox, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 24, 2006
Bap31 enhances the endoplasmic reticulum export and quality control of human class I MHC moleculesJohn J Ladasky, Sarah Boyle, Malini Seth, et al.
Journal of Cellular Biochemistry|April 6, 2011
Nonsense suppressor therapies rescue peroxisome lipid metabolism and assembly in cells from patients with specific PEX gene mutationsPatricia K Dranchak, Erminia Di Pietro, Ann Snowden, et al.
The Journal of Biological Chemistry|September 17, 2003
The acyl-CoA synthetase "bubblegum" (lipidosin): further characterization and role in neuronal fatty acid beta-oxidationZhengtong Pei, Nadia A Oey, Maartje M Zuidervaart, et al.
Pageof 3