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Frank Baas

Showing results (91-100 of 231) with videos related to

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Stroke|March 1, 2008
Genomewide linkage in a large Dutch family with intracranial aneurysms: replication of 2 loci for intracranial aneurysms to chromosome 1p36.11-p36.13 and Xp22.2-p22.32Ynte M Ruigrok, Cisca Wijmenga, Gabriel J E Rinkel, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|October 12, 2022
Tackling Neuroinflammation After Traumatic Brain Injury: Complement Inhibition as a Therapy for Secondary InjuryInge A M van Erp, Iliana Michailidou, Thomas A van Essen, 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.
Experimental Gerontology|March 28, 2006
The unfolded protein response affects neuronal cell cycle protein expression: implications for Alzheimer's disease pathogenesisJeroen J M Hoozemans, Jens Stieler, Elise S van Haastert, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|April 27, 2010
Which patient will feel down, which will be happy? The need to study the genetic disposition of emotional statesMirjam A G Sprangers, Meike Bartels, Ruut Veenhoven, et al.
Acta Neuropathologica|November 20, 2013
Plasminogen activator inhibitor-1 influences cerebrovascular complications and death in pneumococcal meningitisMatthijs C Brouwer, Joost C M Meijers, Frank Baas, et al.
Stem Cell Research|June 3, 2020
Generation and genetic repair of 2 iPSC clones from a patient bearing a heterozygous c.1120del18 mutation in the ACVRL1 gene leading to Hereditary Hemorrhagic Telangiectasia (HHT) type 2Marga J Bouma, Valeria Orlova, Francijna E van den Hil, et al.
JIMD Reports|September 30, 2016
RARS2 Mutations: Is Pontocerebellar Hypoplasia Type 6 a Mitochondrial Encephalopathy?Tessa van Dijk, Fred van Ruissen, Bregje Jaeger, et al.
The Journal of Pediatrics|November 1, 2002
Cardiolipin deficiency in X-linked cardioskeletal myopathy and neutropenia (Barth syndrome, MIM 302060): a study in cultured skin fibroblastsFredoen Valianpour, Ronald J A Wanders, Henk Overmars, et al.
Journal of Neuropathology and Experimental Neurology|April 14, 2011
Myelin and axon pathology in a long-term study of PMP22-overexpressing miceCamiel Verhamme, Rosalind H M King, Anneloor L M A ten Asbroek, et al.
Pageof 24

Showing results (91-100 of 231) with videos related to

Sort By:
Pageof 24
Stroke|March 1, 2008
Genomewide linkage in a large Dutch family with intracranial aneurysms: replication of 2 loci for intracranial aneurysms to chromosome 1p36.11-p36.13 and Xp22.2-p22.32Ynte M Ruigrok, Cisca Wijmenga, Gabriel J E Rinkel, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|October 12, 2022
Tackling Neuroinflammation After Traumatic Brain Injury: Complement Inhibition as a Therapy for Secondary InjuryInge A M van Erp, Iliana Michailidou, Thomas A van Essen, 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.
Experimental Gerontology|March 28, 2006
The unfolded protein response affects neuronal cell cycle protein expression: implications for Alzheimer's disease pathogenesisJeroen J M Hoozemans, Jens Stieler, Elise S van Haastert, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|April 27, 2010
Which patient will feel down, which will be happy? The need to study the genetic disposition of emotional statesMirjam A G Sprangers, Meike Bartels, Ruut Veenhoven, et al.
Acta Neuropathologica|November 20, 2013
Plasminogen activator inhibitor-1 influences cerebrovascular complications and death in pneumococcal meningitisMatthijs C Brouwer, Joost C M Meijers, Frank Baas, et al.
Stem Cell Research|June 3, 2020
Generation and genetic repair of 2 iPSC clones from a patient bearing a heterozygous c.1120del18 mutation in the ACVRL1 gene leading to Hereditary Hemorrhagic Telangiectasia (HHT) type 2Marga J Bouma, Valeria Orlova, Francijna E van den Hil, et al.
JIMD Reports|September 30, 2016
RARS2 Mutations: Is Pontocerebellar Hypoplasia Type 6 a Mitochondrial Encephalopathy?Tessa van Dijk, Fred van Ruissen, Bregje Jaeger, et al.
The Journal of Pediatrics|November 1, 2002
Cardiolipin deficiency in X-linked cardioskeletal myopathy and neutropenia (Barth syndrome, MIM 302060): a study in cultured skin fibroblastsFredoen Valianpour, Ronald J A Wanders, Henk Overmars, et al.
Journal of Neuropathology and Experimental Neurology|April 14, 2011
Myelin and axon pathology in a long-term study of PMP22-overexpressing miceCamiel Verhamme, Rosalind H M King, Anneloor L M A ten Asbroek, et al.
Pageof 24