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Neurogenetics

Showing results (361-370 of 1,080) with videos related to

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Neurogenetics|September 13, 2008
Identification of a heterozygous genomic deletion in the spatacsin gene in SPG11 patients using high-resolution comparative genomic hybridizationPeter Bauer, Beate Winner, Rebecca Schüle, et al.
Neurogenetics|July 8, 2020
Metachromatic leukodystrophy genotypes in The Netherlands reveal novel pathogenic ARSA variants in non-Caucasian patientsShanice Beerepoot, Silvy J M van Dooren, Gajja S Salomons, et al.
Neurogenetics|May 25, 2023
COLQ-related congenital myasthenic syndrome: An integrative viewTina Eshaghian, Bahareh Rabbani, Reza Shervin Badv, et al.
Neurogenetics|December 18, 2002
A novel presenilin 1 mutation (L174 M) in a large Cuban family with early onset Alzheimer diseaseA M Bertoli Avella, B Marcheco Teruel, J J Llibre Rodriguez, et al.
Neurogenetics|May 28, 2002
A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small familyBora E Baysal, Joan E Willett-Brozick, Judith A Badner, et al.
Neurogenetics|August 29, 2001
Mapping of the second Friedreich's ataxia (FRDA2) locus to chromosome 9p23-p11: evidence for further locus heterogeneityK Christodoulou, F Deymeer, P Serdaroğlu, et al.
Neurogenetics|April 11, 2003
Genetic animal models of anxietyDeborah A Finn, Mark T Rutledge-Gorman, John C Crabbe
Neurogenetics|June 27, 2003
Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson's diseaseAlexander Zimprich, Friedrich Asmus, Petra Leitner, et al.
Neurogenetics|December 17, 2002
Identification of genetic loci affecting mouse-adapted bovine spongiform encephalopathy incubation time in miceSarah E Lloyd, James B Uphill, Paul V Targonski, et al.
Neurogenetics|December 17, 2002
A novel NF-L mutation Pro22Ser is associated with CMT2 in a large Slovenian familyDonna-Maria Georgiou, Janez Zidar, Marko Korosec, et al.
Pageof 108

Showing results (361-370 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|September 13, 2008
Identification of a heterozygous genomic deletion in the spatacsin gene in SPG11 patients using high-resolution comparative genomic hybridizationPeter Bauer, Beate Winner, Rebecca Schüle, et al.
Neurogenetics|July 8, 2020
Metachromatic leukodystrophy genotypes in The Netherlands reveal novel pathogenic ARSA variants in non-Caucasian patientsShanice Beerepoot, Silvy J M van Dooren, Gajja S Salomons, et al.
Neurogenetics|May 25, 2023
COLQ-related congenital myasthenic syndrome: An integrative viewTina Eshaghian, Bahareh Rabbani, Reza Shervin Badv, et al.
Neurogenetics|December 18, 2002
A novel presenilin 1 mutation (L174 M) in a large Cuban family with early onset Alzheimer diseaseA M Bertoli Avella, B Marcheco Teruel, J J Llibre Rodriguez, et al.
Neurogenetics|May 28, 2002
A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small familyBora E Baysal, Joan E Willett-Brozick, Judith A Badner, et al.
Neurogenetics|August 29, 2001
Mapping of the second Friedreich's ataxia (FRDA2) locus to chromosome 9p23-p11: evidence for further locus heterogeneityK Christodoulou, F Deymeer, P Serdaroğlu, et al.
Neurogenetics|April 11, 2003
Genetic animal models of anxietyDeborah A Finn, Mark T Rutledge-Gorman, John C Crabbe
Neurogenetics|June 27, 2003
Point mutations in exon 1 of the NR4A2 gene are not a major cause of familial Parkinson's diseaseAlexander Zimprich, Friedrich Asmus, Petra Leitner, et al.
Neurogenetics|December 17, 2002
Identification of genetic loci affecting mouse-adapted bovine spongiform encephalopathy incubation time in miceSarah E Lloyd, James B Uphill, Paul V Targonski, et al.
Neurogenetics|December 17, 2002
A novel NF-L mutation Pro22Ser is associated with CMT2 in a large Slovenian familyDonna-Maria Georgiou, Janez Zidar, Marko Korosec, et al.
Pageof 108