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Matthew W State

Showing results (31-40 of 123) with videos related to

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The Journal of Comparative Neurology|December 24, 2008
Developmentally regulated and evolutionarily conserved expression of SLITRK1 in brain circuits implicated in Tourette syndromeAlthea A Stillman, Zeljka Krsnik, Jinhao Sun, et al.
American Journal of Human Genetics|June 14, 2008
Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndromeThomas Fernandez, Thomas Morgan, Nicole Davis, et al.
Neuroscience Letters|March 29, 2011
High levels of histidine decarboxylase in the striatum of mice and ratsKuakarun Krusong, A Gulhan Ercan-Sencicek, Meiyu Xu, et al.
American Journal of Human Genetics|April 24, 2004
Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndromeThomas Fernandez, Thomas Morgan, Nicole Davis, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 16, 2007
Haplotype evolution of SLITRK1, a candidate gene for Gilles de la Tourette syndromeWilliam C Speed, Brian J O'Roak, Zsanett Tárnok, et al.
European Child & Adolescent Psychiatry|April 29, 2014
The Tourette International Collaborative Genetics (TIC Genetics) study, finding the genes causing Tourette syndrome: objectives and methodsAndrea Dietrich, Thomas V Fernandez, Robert A King, et al.
Development (Cambridge, England)|May 30, 2020
The neurodevelopmental disorder risk gene <i>DYRK1A</i> is required for ciliogenesis and control of brain size in <i>Xenopus</i> embryosHelen Rankin Willsey, Yuxiao Xu, Amanda Everitt, et al.
Development (Cambridge, England)|December 8, 2020
Correction: The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in <i>Xenopus</i> embryosHelen Rankin Willsey, Yuxiao Xu, Amanda Everitt, et al.
American Journal of Medical Genetics. Part A|April 2, 2010
A patient with Duchenne muscular dystrophy and autism demonstrates a hemizygous deletion affecting DystrophinOzdem Erturk, Kaya Bilguvar, Baris Korkmaz, et al.
The Journal of Clinical Investigation|February 3, 2006
A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103YLeigh D Plant, Peter N Bowers, Qianyong Liu, et al.
Pageof 13

Showing results (31-40 of 123) with videos related to

Sort By:
Pageof 13
The Journal of Comparative Neurology|December 24, 2008
Developmentally regulated and evolutionarily conserved expression of SLITRK1 in brain circuits implicated in Tourette syndromeAlthea A Stillman, Zeljka Krsnik, Jinhao Sun, et al.
American Journal of Human Genetics|June 14, 2008
Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndromeThomas Fernandez, Thomas Morgan, Nicole Davis, et al.
Neuroscience Letters|March 29, 2011
High levels of histidine decarboxylase in the striatum of mice and ratsKuakarun Krusong, A Gulhan Ercan-Sencicek, Meiyu Xu, et al.
American Journal of Human Genetics|April 24, 2004
Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndromeThomas Fernandez, Thomas Morgan, Nicole Davis, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 16, 2007
Haplotype evolution of SLITRK1, a candidate gene for Gilles de la Tourette syndromeWilliam C Speed, Brian J O'Roak, Zsanett Tárnok, et al.
European Child & Adolescent Psychiatry|April 29, 2014
The Tourette International Collaborative Genetics (TIC Genetics) study, finding the genes causing Tourette syndrome: objectives and methodsAndrea Dietrich, Thomas V Fernandez, Robert A King, et al.
Development (Cambridge, England)|May 30, 2020
The neurodevelopmental disorder risk gene <i>DYRK1A</i> is required for ciliogenesis and control of brain size in <i>Xenopus</i> embryosHelen Rankin Willsey, Yuxiao Xu, Amanda Everitt, et al.
Development (Cambridge, England)|December 8, 2020
Correction: The neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and control of brain size in <i>Xenopus</i> embryosHelen Rankin Willsey, Yuxiao Xu, Amanda Everitt, et al.
American Journal of Medical Genetics. Part A|April 2, 2010
A patient with Duchenne muscular dystrophy and autism demonstrates a hemizygous deletion affecting DystrophinOzdem Erturk, Kaya Bilguvar, Baris Korkmaz, et al.
The Journal of Clinical Investigation|February 3, 2006
A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103YLeigh D Plant, Peter N Bowers, Qianyong Liu, et al.
Pageof 13