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Neurogenetics

Showing results (281-290 of 1,080) with videos related to

Pageof 108
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Neurogenetics|July 28, 2007
CCM3 interacts with CCM2 indicating common pathogenesis for cerebral cavernous malformationsKatrin Voss, Sonja Stahl, Elisa Schleider, et al.
Neurogenetics|July 5, 2007
Association of progesterone receptor with migraine-associated vertigoHane Lee, Lauren Sininger, Joanna C Jen, et al.
Neurogenetics|September 15, 2006
Microcephaly and simplified gyral pattern of the brain associated with early onset insulin-dependent diabetes mellitusM C Y de Wit, I F M de Coo, C Julier, et al.
Neurogenetics|January 17, 2007
Leucine-rich repeat kinase 1: a paralog of LRRK2 and a candidate gene for Parkinson's diseaseJulie P Taylor, Mary M Hulihan, Jennifer M Kachergus, et al.
Neurogenetics|December 1, 2006
Mutations of the LMNA gene can mimic autosomal dominant proximal spinal muscular atrophySabine Rudnik-Schöneborn, Elke Botzenhart, Thomas Eggermann, et al.
Neurogenetics|August 26, 2006
Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromesE Stogmann, P Lichtner, C Baumgartner, et al.
Neurogenetics|September 14, 2006
Frameshift mutation in GJA12 leading to nystagmus, spastic ataxia and CNS dys-/demyelinationNicole I Wolf, Maria Cundall, Paul Rutland, et al.
Neurogenetics|April 29, 2020
Loss of mitochondrial ClpP, Lonp1, and Tfam triggers transcriptional induction of Rnf213, a susceptibility factor for moyamoya diseaseJana Key, Antonia Maletzko, Aneesha Kohli, et al.
Neurogenetics|August 15, 2021
Increased unfolded protein responses caused by MED17 mutationsTakeshi Terabayashi, Satoru Hashimoto
Neurogenetics|August 2, 2021
Fetal brain arrest broadens the spectrum of WDR81-related developmental brain malformationsMohamed S Abdel-Hamid, Sahar Sabry, Sherif F Abdel-Ghafar, et al.
Pageof 108

Showing results (281-290 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|July 28, 2007
CCM3 interacts with CCM2 indicating common pathogenesis for cerebral cavernous malformationsKatrin Voss, Sonja Stahl, Elisa Schleider, et al.
Neurogenetics|July 5, 2007
Association of progesterone receptor with migraine-associated vertigoHane Lee, Lauren Sininger, Joanna C Jen, et al.
Neurogenetics|September 15, 2006
Microcephaly and simplified gyral pattern of the brain associated with early onset insulin-dependent diabetes mellitusM C Y de Wit, I F M de Coo, C Julier, et al.
Neurogenetics|January 17, 2007
Leucine-rich repeat kinase 1: a paralog of LRRK2 and a candidate gene for Parkinson's diseaseJulie P Taylor, Mary M Hulihan, Jennifer M Kachergus, et al.
Neurogenetics|December 1, 2006
Mutations of the LMNA gene can mimic autosomal dominant proximal spinal muscular atrophySabine Rudnik-Schöneborn, Elke Botzenhart, Thomas Eggermann, et al.
Neurogenetics|August 26, 2006
Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromesE Stogmann, P Lichtner, C Baumgartner, et al.
Neurogenetics|September 14, 2006
Frameshift mutation in GJA12 leading to nystagmus, spastic ataxia and CNS dys-/demyelinationNicole I Wolf, Maria Cundall, Paul Rutland, et al.
Neurogenetics|April 29, 2020
Loss of mitochondrial ClpP, Lonp1, and Tfam triggers transcriptional induction of Rnf213, a susceptibility factor for moyamoya diseaseJana Key, Antonia Maletzko, Aneesha Kohli, et al.
Neurogenetics|August 15, 2021
Increased unfolded protein responses caused by MED17 mutationsTakeshi Terabayashi, Satoru Hashimoto
Neurogenetics|August 2, 2021
Fetal brain arrest broadens the spectrum of WDR81-related developmental brain malformationsMohamed S Abdel-Hamid, Sahar Sabry, Sherif F Abdel-Ghafar, et al.
Pageof 108