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Neurogenetics

Showing results (781-790 of 949) with videos related to

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Neurogenetics|November 3, 2021
Myoclonic status epilepticus and cerebellar hypoplasia associated with a novel variant in the GRIA3 geneBerardo Rinaldi, Yu-Han Ge, Elena Freri, et al.
Neurogenetics|May 13, 2014
PARK20 caused by SYNJ1 homozygous Arg258Gln mutation in a new Italian familySimone Olgiati, Anna De Rosa, Marialuisa Quadri, et al.
Neurogenetics|March 24, 2019
Celia's encephalopathy and c.974dupG in BSCL2 gene: a hidden change in a known variantSofía Sánchez-Iglesias, Melissa Crocker, Mar O'Callaghan, et al.
Neurogenetics|July 4, 2012
RNA-based analysis of two SMARCB1 mutations associated with familial schwannomatosis with meningiomasGerman Melean, Ana Velasco, Elisabete Hernández-Imaz, et al.
Neurogenetics|September 15, 2012
Mammalian sleep geneticsJessica M Kelly, Matt T Bianchi
Neurogenetics|September 19, 2012
TMEM70: a mutational hot spot in nuclear ATP synthase deficiency with a pivotal role in complex V biogenesisAlessandra Torraco, Daniela Verrigni, Teresa Rizza, et al.
Neurogenetics|March 23, 2004
Evidence of linkage and association on chromosome 20 for late-onset Alzheimer diseaseKatrina A B Goddard, Jane M Olson, Haydeh Payami, et al.
Neurogenetics|March 19, 2005
Novel mutations and repeated findings of mutations in familial Alzheimer diseaseUlrich Finckh, Christian Kuschel, Maria Anagnostouli, et al.
Neurogenetics|April 14, 2005
Diagnosis of Pelizaeus-Merzbacher disease: detection of proteolipid protein gene copy number by real-time PCRStefano Regis, Serena Grossi, Susanna Lualdi, et al.
Neurogenetics|March 3, 2005
Functional polymorphisms in the human beta4 subunit of nicotinic acetylcholine receptorsYong Liang, Ramiro Salas, Lisa Marubio, et al.
Pageof 95

Showing results (781-790 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|November 3, 2021
Myoclonic status epilepticus and cerebellar hypoplasia associated with a novel variant in the GRIA3 geneBerardo Rinaldi, Yu-Han Ge, Elena Freri, et al.
Neurogenetics|May 13, 2014
PARK20 caused by SYNJ1 homozygous Arg258Gln mutation in a new Italian familySimone Olgiati, Anna De Rosa, Marialuisa Quadri, et al.
Neurogenetics|March 24, 2019
Celia's encephalopathy and c.974dupG in BSCL2 gene: a hidden change in a known variantSofía Sánchez-Iglesias, Melissa Crocker, Mar O'Callaghan, et al.
Neurogenetics|July 4, 2012
RNA-based analysis of two SMARCB1 mutations associated with familial schwannomatosis with meningiomasGerman Melean, Ana Velasco, Elisabete Hernández-Imaz, et al.
Neurogenetics|September 15, 2012
Mammalian sleep geneticsJessica M Kelly, Matt T Bianchi
Neurogenetics|September 19, 2012
TMEM70: a mutational hot spot in nuclear ATP synthase deficiency with a pivotal role in complex V biogenesisAlessandra Torraco, Daniela Verrigni, Teresa Rizza, et al.
Neurogenetics|March 23, 2004
Evidence of linkage and association on chromosome 20 for late-onset Alzheimer diseaseKatrina A B Goddard, Jane M Olson, Haydeh Payami, et al.
Neurogenetics|March 19, 2005
Novel mutations and repeated findings of mutations in familial Alzheimer diseaseUlrich Finckh, Christian Kuschel, Maria Anagnostouli, et al.
Neurogenetics|April 14, 2005
Diagnosis of Pelizaeus-Merzbacher disease: detection of proteolipid protein gene copy number by real-time PCRStefano Regis, Serena Grossi, Susanna Lualdi, et al.
Neurogenetics|March 3, 2005
Functional polymorphisms in the human beta4 subunit of nicotinic acetylcholine receptorsYong Liang, Ramiro Salas, Lisa Marubio, et al.
Pageof 95