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Jeroen P Vreijling

Showing results (1-10 of 9) with videos related to

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Human Molecular Genetics|December 10, 2003
Expression of complement components in the peripheral nervous systemRosalein R de Jonge, Ivo N van Schaik, Jeroen P Vreijling, et al.
Genomics|July 3, 2003
Transcriptional profile of the human peripheral nervous system by serial analysis of gene expressionRosalein R de Jonge, Jeroen P Vreijling, Asker Meintjes, et al.
Diabetologia|February 10, 2019
Diurnal rhythms in the white adipose tissue transcriptome are disturbed in obese individuals with type 2 diabetes compared with lean control individualsDirk Jan Stenvers, Aldo Jongejan, Sadaf Atiqi, et al.
Annals of Surgery|January 11, 2021
Whole-exome Sequencing Identifies SLC52A1 and ZNF106 Variants as Novel Genetic Risk Factors for (Early) Multiple-organ Failure in Acute PancreatitisFons F van den Berg, Yama Issa, Jeroen P Vreijling, et al.
Journal of Lipid Research|March 13, 2026
Longitudinal analysis of lipid changes in the sciatic nerve caused by overexpression of PMP22 in murine models of CMT1ATom P Hellings, Naima Lamzira-Arichi, Jeroen P Vreijling, et al.
Human Molecular Genetics|October 4, 2018
Cis D4Z4 repeat duplications associated with facioscapulohumeral muscular dystrophy type 2Richard J L F Lemmers, Patrick J van der Vliet, Jeroen P Vreijling, et al.
Journal of the American Heart Association|February 14, 2025
Neurovascular Decoupling Is Associated With Lobar Intracerebral Hemorrhages and White Matter HyperintensitiesSuzanne E van Dijk, Nadieh Drenth, Anne Hafkemeijer, et al.
Acta Neuropathologica Communications|May 5, 2018
Systemic inhibition of the membrane attack complex impedes neuroinflammation in chronic relapsing experimental autoimmune encephalomyelitisIliana Michailidou, Aldo Jongejan, Jeroen P Vreijling, et al.
Neurology|August 29, 2025
Small Vessel Disease Phenotype Associated With Monoallelic <i>NOTCH3</i> Loss-of-Function VariantsJosephine S van Asbeck, Gido Gravesteijn, Minne N Cerfontaine, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Human Molecular Genetics|December 10, 2003
Expression of complement components in the peripheral nervous systemRosalein R de Jonge, Ivo N van Schaik, Jeroen P Vreijling, et al.
Genomics|July 3, 2003
Transcriptional profile of the human peripheral nervous system by serial analysis of gene expressionRosalein R de Jonge, Jeroen P Vreijling, Asker Meintjes, et al.
Diabetologia|February 10, 2019
Diurnal rhythms in the white adipose tissue transcriptome are disturbed in obese individuals with type 2 diabetes compared with lean control individualsDirk Jan Stenvers, Aldo Jongejan, Sadaf Atiqi, et al.
Annals of Surgery|January 11, 2021
Whole-exome Sequencing Identifies SLC52A1 and ZNF106 Variants as Novel Genetic Risk Factors for (Early) Multiple-organ Failure in Acute PancreatitisFons F van den Berg, Yama Issa, Jeroen P Vreijling, et al.
Journal of Lipid Research|March 13, 2026
Longitudinal analysis of lipid changes in the sciatic nerve caused by overexpression of PMP22 in murine models of CMT1ATom P Hellings, Naima Lamzira-Arichi, Jeroen P Vreijling, et al.
Human Molecular Genetics|October 4, 2018
Cis D4Z4 repeat duplications associated with facioscapulohumeral muscular dystrophy type 2Richard J L F Lemmers, Patrick J van der Vliet, Jeroen P Vreijling, et al.
Journal of the American Heart Association|February 14, 2025
Neurovascular Decoupling Is Associated With Lobar Intracerebral Hemorrhages and White Matter HyperintensitiesSuzanne E van Dijk, Nadieh Drenth, Anne Hafkemeijer, et al.
Acta Neuropathologica Communications|May 5, 2018
Systemic inhibition of the membrane attack complex impedes neuroinflammation in chronic relapsing experimental autoimmune encephalomyelitisIliana Michailidou, Aldo Jongejan, Jeroen P Vreijling, et al.
Neurology|August 29, 2025
Small Vessel Disease Phenotype Associated With Monoallelic <i>NOTCH3</i> Loss-of-Function VariantsJosephine S van Asbeck, Gido Gravesteijn, Minne N Cerfontaine, et al.
Pageof 1