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Dirk Goossens

Showing results (31-40 of 41) with videos related to

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Neurobiology of Aging|December 11, 2007
Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALSIlse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, et al.
Molecular Neuropsychiatry|May 31, 2016
Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental IllnessMandy Johnstone, Alan Maclean, Lien Heyrman, et al.
Nature Genetics|November 11, 2008
Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosisYurii S Aulchenko, Ilse A Hoppenbrouwers, Sreeram V Ramagopalan, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 11, 2012
Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage-dependent calcium channels in psychiatric disordersMaarten J Van Den Bossche, Mojca Strazisar, Stephan De Bruyne, et al.
Human Mutation|July 26, 2006
Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patientsArvid Suls, Kristl G Claeys, Dirk Goossens, et al.
Neurogenetics|September 19, 2014
Unraveling the genetic landscape of autosomal recessive Charcot-Marie-Tooth neuropathies using a homozygosity mapping approachMagdalena Zimoń, Esra Battaloğlu, Yesim Parman, et al.
Nature Genetics|December 15, 2010
Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel diseaseYukihide Momozawa, Myriam Mni, Kayo Nakamura, et al.
Nature Genetics|September 28, 2005
Mutations in SEPT9 cause hereditary neuralgic amyotrophyGregor Kuhlenbäumer, Mark C Hannibal, Eva Nelis, et al.
Brain : a Journal of Neurology|June 26, 2008
Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1Arvid Suls, Peter Dedeken, Karolien Goffin, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 14, 2018
<i>TP53</i> Outperforms Other Androgen Receptor Biomarkers to Predict Abiraterone or Enzalutamide Outcome in Metastatic Castration-Resistant Prostate CancerBram De Laere, Steffi Oeyen, Markus Mayrhofer, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Neurobiology of Aging|December 11, 2007
Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALSIlse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, et al.
Molecular Neuropsychiatry|May 31, 2016
Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental IllnessMandy Johnstone, Alan Maclean, Lien Heyrman, et al.
Nature Genetics|November 11, 2008
Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosisYurii S Aulchenko, Ilse A Hoppenbrouwers, Sreeram V Ramagopalan, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 11, 2012
Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage-dependent calcium channels in psychiatric disordersMaarten J Van Den Bossche, Mojca Strazisar, Stephan De Bruyne, et al.
Human Mutation|July 26, 2006
Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patientsArvid Suls, Kristl G Claeys, Dirk Goossens, et al.
Neurogenetics|September 19, 2014
Unraveling the genetic landscape of autosomal recessive Charcot-Marie-Tooth neuropathies using a homozygosity mapping approachMagdalena Zimoń, Esra Battaloğlu, Yesim Parman, et al.
Nature Genetics|December 15, 2010
Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel diseaseYukihide Momozawa, Myriam Mni, Kayo Nakamura, et al.
Nature Genetics|September 28, 2005
Mutations in SEPT9 cause hereditary neuralgic amyotrophyGregor Kuhlenbäumer, Mark C Hannibal, Eva Nelis, et al.
Brain : a Journal of Neurology|June 26, 2008
Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1Arvid Suls, Peter Dedeken, Karolien Goffin, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 14, 2018
<i>TP53</i> Outperforms Other Androgen Receptor Biomarkers to Predict Abiraterone or Enzalutamide Outcome in Metastatic Castration-Resistant Prostate CancerBram De Laere, Steffi Oeyen, Markus Mayrhofer, et al.
Pageof 5