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Frank Baas

Showing results (61-70 of 231) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|May 15, 2009
Screening for dystonia genes DYT1, 11 and 16 in patients with writer's crampKatja Ritz, Justus L Groen, Jose J M Kruisdijk, et al.
Journal of Neuroscience Research|January 27, 2005
Expression profiling of sciatic nerve in a Charcot-Marie-Tooth disease type 1a mouse modelAnneloor L M A ten Asbroek, Camiel Verhamme, Marjon van Groenigen, et al.
Behavioral and Brain Functions : BBF|April 21, 2007
Association between the DTNBP1 gene and intelligence: a case-control study in young patients with schizophrenia and related disorders and unaffected siblingsJanneke R Zinkstok, Odette de Wilde, Therese A M J van Amelsvoort, et al.
American Journal of Hypertension|November 22, 2008
Are RGS2 gene polymorphisms associated with high blood pressure in an ethnicity- and gender-specific manner?Ines N Hahntow, Gideon Mairuhu, Irene G M van Valkengoed, et al.
Journal of Psychopharmacology (Oxford, England)|March 31, 2011
Dopamine metabolism in adults with 22q11 deletion syndrome, with and without schizophrenia--relationship with COMT Val¹⁰⁸/¹⁵⁸Met polymorphism, gender and symptomatologyErik Boot, Jan Booij, Nico Abeling, et al.
Annals of Neurology|March 24, 2005
Early onset neuropathy in a compound form of Charcot-Marie-Tooth diseaseFarid Meggouh, Marianne de Visser, Willem F M Arts, et al.
Chembiochem : a European Journal of Chemical Biology|April 30, 2005
On the in vitro and in vivo properties of four locked nucleic acid nucleotides incorporated into an anti-H-Ras antisense oligonucleotideKees Fluiter, Miriam Frieden, Jeroen Vreijling, et al.
Human Molecular Genetics|January 29, 2011
Impairment of the tRNA-splicing endonuclease subunit 54 (tsen54) gene causes neurological abnormalities and larval death in zebrafish models of pontocerebellar hypoplasiaPaul R Kasher, Yasmin Namavar, Paula van Tijn, et al.
Orphanet Journal of Rare Diseases|March 21, 2014
PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure PalsiesBarbara W van Paassen, Anneke J van der Kooi, Karin Y van Spaendonck-Zwarts, et al.
Addiction Biology|September 6, 2016
Neural response to alcohol taste cues in youth: effects of the OPRM1 geneOzlem Korucuoglu, Thomas E Gladwin, Frank Baas, et al.
Pageof 24

Showing results (61-70 of 231) with videos related to

Sort By:
Pageof 24
Movement Disorders : Official Journal of the Movement Disorder Society|May 15, 2009
Screening for dystonia genes DYT1, 11 and 16 in patients with writer's crampKatja Ritz, Justus L Groen, Jose J M Kruisdijk, et al.
Journal of Neuroscience Research|January 27, 2005
Expression profiling of sciatic nerve in a Charcot-Marie-Tooth disease type 1a mouse modelAnneloor L M A ten Asbroek, Camiel Verhamme, Marjon van Groenigen, et al.
Behavioral and Brain Functions : BBF|April 21, 2007
Association between the DTNBP1 gene and intelligence: a case-control study in young patients with schizophrenia and related disorders and unaffected siblingsJanneke R Zinkstok, Odette de Wilde, Therese A M J van Amelsvoort, et al.
American Journal of Hypertension|November 22, 2008
Are RGS2 gene polymorphisms associated with high blood pressure in an ethnicity- and gender-specific manner?Ines N Hahntow, Gideon Mairuhu, Irene G M van Valkengoed, et al.
Journal of Psychopharmacology (Oxford, England)|March 31, 2011
Dopamine metabolism in adults with 22q11 deletion syndrome, with and without schizophrenia--relationship with COMT Val¹⁰⁸/¹⁵⁸Met polymorphism, gender and symptomatologyErik Boot, Jan Booij, Nico Abeling, et al.
Annals of Neurology|March 24, 2005
Early onset neuropathy in a compound form of Charcot-Marie-Tooth diseaseFarid Meggouh, Marianne de Visser, Willem F M Arts, et al.
Chembiochem : a European Journal of Chemical Biology|April 30, 2005
On the in vitro and in vivo properties of four locked nucleic acid nucleotides incorporated into an anti-H-Ras antisense oligonucleotideKees Fluiter, Miriam Frieden, Jeroen Vreijling, et al.
Human Molecular Genetics|January 29, 2011
Impairment of the tRNA-splicing endonuclease subunit 54 (tsen54) gene causes neurological abnormalities and larval death in zebrafish models of pontocerebellar hypoplasiaPaul R Kasher, Yasmin Namavar, Paula van Tijn, et al.
Orphanet Journal of Rare Diseases|March 21, 2014
PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure PalsiesBarbara W van Paassen, Anneke J van der Kooi, Karin Y van Spaendonck-Zwarts, et al.
Addiction Biology|September 6, 2016
Neural response to alcohol taste cues in youth: effects of the OPRM1 geneOzlem Korucuoglu, Thomas E Gladwin, Frank Baas, et al.
Pageof 24