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Stephan Kemp

Showing results (51-60 of 107) with videos related to

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The Biochemical Journal|April 12, 2011
Conservation of targeting but divergence in function and quality control of peroxisomal ABC transporters: an analysis using cross-kingdom expressionXuebin Zhang, Carine De Marcos Lousa, Nellie Schutte-Lensink, et al.
Annals of Clinical and Translational Neurology|October 13, 2020
Plasma NfL and GFAP as biomarkers of spinal cord degeneration in adrenoleukodystrophyWouter J C van Ballegoij, Stephanie I W van de Stadt, Irene C Huffnagel, et al.
Plos One|August 23, 2012
Bezafibrate for X-linked adrenoleukodystrophyMarc Engelen, Luc Tran, Rob Ofman, et al.
Orphanet Journal of Rare Diseases|February 9, 2019
Disease progression in women with X-linked adrenoleukodystrophy is slowIrene C Huffnagel, Marcel G W Dijkgraaf, Georges E Janssens, et al.
Annals of Clinical and Translational Neurology|September 30, 2020
Targeting foam cell formation in inflammatory brain diseases by the histone modifier MS-275Bettina Zierfuss, Isabelle Weinhofer, Agnieszka Buda, et al.
Molecular Genetics and Metabolism|April 13, 2016
Pathogenicity of novel ABCD1 variants: The need for biochemical testing in the era of advanced geneticsMartin J A Schackmann, Rob Ofman, Björn M van Geel, et al.
Human Molecular Genetics|April 30, 2003
A very long-chain acyl-CoA synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophyAnn K Heinzer, Paul A Watkins, Jyh-Feng Lu, et al.
Frontiers in Pediatrics|October 25, 2021
Expanding Neonatal Bloodspot Screening: A Multi-Stakeholder PerspectiveTessa van Dijk, Adriana Kater, Marleen Jansen, et al.
Human Molecular Genetics|March 18, 2008
Early oxidative damage underlying neurodegeneration in X-adrenoleukodystrophyStéphane Fourcade, Jone López-Erauskin, Jorge Galino, et al.
Journal of Inherited Metabolic Disease|December 20, 2024
Altered lipid profile and reduced neuronal support in human induced pluripotent stem cell-derived astrocytes from adrenoleukodystrophy patientsRoberto Montoro Ferrer, Yorrick R J Jaspers, Inge M E Dijkstra, et al.
Pageof 11

Showing results (51-60 of 107) with videos related to

Sort By:
Pageof 11
The Biochemical Journal|April 12, 2011
Conservation of targeting but divergence in function and quality control of peroxisomal ABC transporters: an analysis using cross-kingdom expressionXuebin Zhang, Carine De Marcos Lousa, Nellie Schutte-Lensink, et al.
Annals of Clinical and Translational Neurology|October 13, 2020
Plasma NfL and GFAP as biomarkers of spinal cord degeneration in adrenoleukodystrophyWouter J C van Ballegoij, Stephanie I W van de Stadt, Irene C Huffnagel, et al.
Plos One|August 23, 2012
Bezafibrate for X-linked adrenoleukodystrophyMarc Engelen, Luc Tran, Rob Ofman, et al.
Orphanet Journal of Rare Diseases|February 9, 2019
Disease progression in women with X-linked adrenoleukodystrophy is slowIrene C Huffnagel, Marcel G W Dijkgraaf, Georges E Janssens, et al.
Annals of Clinical and Translational Neurology|September 30, 2020
Targeting foam cell formation in inflammatory brain diseases by the histone modifier MS-275Bettina Zierfuss, Isabelle Weinhofer, Agnieszka Buda, et al.
Molecular Genetics and Metabolism|April 13, 2016
Pathogenicity of novel ABCD1 variants: The need for biochemical testing in the era of advanced geneticsMartin J A Schackmann, Rob Ofman, Björn M van Geel, et al.
Human Molecular Genetics|April 30, 2003
A very long-chain acyl-CoA synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophyAnn K Heinzer, Paul A Watkins, Jyh-Feng Lu, et al.
Frontiers in Pediatrics|October 25, 2021
Expanding Neonatal Bloodspot Screening: A Multi-Stakeholder PerspectiveTessa van Dijk, Adriana Kater, Marleen Jansen, et al.
Human Molecular Genetics|March 18, 2008
Early oxidative damage underlying neurodegeneration in X-adrenoleukodystrophyStéphane Fourcade, Jone López-Erauskin, Jorge Galino, et al.
Journal of Inherited Metabolic Disease|December 20, 2024
Altered lipid profile and reduced neuronal support in human induced pluripotent stem cell-derived astrocytes from adrenoleukodystrophy patientsRoberto Montoro Ferrer, Yorrick R J Jaspers, Inge M E Dijkstra, et al.
Pageof 11