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Showing results (491-500 of 571) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
Statistical Challenges when Analyzing SARS-CoV-2 RNA Measurements Below the Assay Limit of Quantification in COVID-19 Clinical TrialsCarlee B Moser, Kara W Chew, Mark J Giganti, et al.
Molecular Genetics and Metabolism|November 26, 2013
Newborn screening for X-linked adrenoleukodystrophy: further evidence high throughput screening is feasibleChristiane Theda, Katy Gibbons, Todd E Defor, et al.
Cell Metabolism|December 3, 2014
Hif-2α promotes degradation of mammalian peroxisomes by selective autophagyKatharina M Walter, Miriam J Schönenberger, Martin Trötzmüller, et al.
Communications Biology|September 9, 2022
Peroxisomal very long-chain fatty acid transport is targeted by herpesviruses and the antiviral host responseIsabelle Weinhofer, Agnieszka Buda, Markus Kunze, et al.
Molecular Genetics and Metabolism|February 8, 2014
The Pex1-G844D mouse: a model for mild human Zellweger spectrum disorderShandi Hiebler, Tomohiro Masuda, Joseph G Hacia, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|May 12, 2019
Biomarker Identification, Safety, and Efficacy of High-Dose Antioxidants for Adrenomyeloneuropathy: a Phase II Pilot StudyCarlos Casasnovas, Montserrat Ruiz, Agatha Schlüter, et al.
Human Molecular Genetics|August 30, 2014
A novel bile acid biosynthesis defect due to a deficiency of peroxisomal ABCD3Sacha Ferdinandusse, Gerardo Jimenez-Sanchez, Janet Koster, et al.
American Journal of Human Genetics|May 7, 2002
Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disordersDeyanira Corzo, William Gibson, Kisha Johnson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 9, 2018
A metabolomic map of Zellweger spectrum disorders reveals novel disease biomarkersMichael F Wangler, Leroy Hubert, Taraka R Donti, et al.
Journal of Molecular Biology|May 23, 2020
Structural and Mechanistic Studies of the Rare Myristoylation Signal of the Feline Immunodeficiency VirusJanae B Brown, Holly R Summers, Lola A Brown, et al.
Pageof 58

Showing results (491-500 of 571) with videos related to

Sort By:
Pageof 58
Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
Statistical Challenges when Analyzing SARS-CoV-2 RNA Measurements Below the Assay Limit of Quantification in COVID-19 Clinical TrialsCarlee B Moser, Kara W Chew, Mark J Giganti, et al.
Molecular Genetics and Metabolism|November 26, 2013
Newborn screening for X-linked adrenoleukodystrophy: further evidence high throughput screening is feasibleChristiane Theda, Katy Gibbons, Todd E Defor, et al.
Cell Metabolism|December 3, 2014
Hif-2α promotes degradation of mammalian peroxisomes by selective autophagyKatharina M Walter, Miriam J Schönenberger, Martin Trötzmüller, et al.
Communications Biology|September 9, 2022
Peroxisomal very long-chain fatty acid transport is targeted by herpesviruses and the antiviral host responseIsabelle Weinhofer, Agnieszka Buda, Markus Kunze, et al.
Molecular Genetics and Metabolism|February 8, 2014
The Pex1-G844D mouse: a model for mild human Zellweger spectrum disorderShandi Hiebler, Tomohiro Masuda, Joseph G Hacia, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|May 12, 2019
Biomarker Identification, Safety, and Efficacy of High-Dose Antioxidants for Adrenomyeloneuropathy: a Phase II Pilot StudyCarlos Casasnovas, Montserrat Ruiz, Agatha Schlüter, et al.
Human Molecular Genetics|August 30, 2014
A novel bile acid biosynthesis defect due to a deficiency of peroxisomal ABCD3Sacha Ferdinandusse, Gerardo Jimenez-Sanchez, Janet Koster, et al.
American Journal of Human Genetics|May 7, 2002
Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disordersDeyanira Corzo, William Gibson, Kisha Johnson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 9, 2018
A metabolomic map of Zellweger spectrum disorders reveals novel disease biomarkersMichael F Wangler, Leroy Hubert, Taraka R Donti, et al.
Journal of Molecular Biology|May 23, 2020
Structural and Mechanistic Studies of the Rare Myristoylation Signal of the Feline Immunodeficiency VirusJanae B Brown, Holly R Summers, Lola A Brown, et al.
Pageof 58