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Neurogenetics

Showing results (151-160 of 1,080) with videos related to

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Neurogenetics|June 29, 2007
A de novo SPAST mutation leading to somatic mosaicism is associated with a later age at onset in HSPChristel Depienne, Estelle Fedirko, Jean-Marc Faucheux, et al.
Neurogenetics|August 5, 2009
Sequence variation in SORL1 and dementia risk in SwedesChandra A Reynolds, Mun-Gwan Hong, Ulrika K Eriksson, et al.
Neurogenetics|October 2, 2009
A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardationGinevra Zanni, Hilde van Esch, Anissa Bensalem, et al.
Neurogenetics|October 2, 2009
A Copine family member, Cpne8, is a candidate quantitative trait gene for prion disease incubation time in mouseSarah E Lloyd, Emma G Maytham, Julia Grizenkova, et al.
Neurogenetics|August 29, 2009
Congenital bovine spinal dysmyelination is caused by a missense mutation in the SPAST geneBo Thomsen, Peter H Nissen, Jørgen S Agerholm, et al.
Neurogenetics|October 7, 2009
Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variantNadia Bahi-Buisson, Juliette Nectoux, Benoit Girard, et al.
Neurogenetics|August 9, 2011
Late-onset Alzheimer's disease is associated with mitochondrial DNA 7028C/haplogroup H and D310 poly-C tract heteroplasmyEliecer Coto, Juan Gómez, Belén Alonso, et al.
Neurogenetics|August 11, 2011
A novel deletion-insertion mutation identified in exon 3 of FXN in two siblings with a severe Friedreich ataxia phenotypeMarguerite V Evans-Galea, Louise A Corben, Justin Hasell, et al.
Neurogenetics|February 1, 2012
Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47) Peter Bauer, Esther Leshinsky-Silver, Lubov Blumkin, et al.
Neurogenetics|January 13, 2012
Genome-scale methylation analysis of Parkinson's disease patients' brains reveals DNA hypomethylation and increased mRNA expression of cytochrome P450 2E1Oliver Kaut, Ina Schmitt, Ullrich Wüllner
Pageof 108

Showing results (151-160 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|June 29, 2007
A de novo SPAST mutation leading to somatic mosaicism is associated with a later age at onset in HSPChristel Depienne, Estelle Fedirko, Jean-Marc Faucheux, et al.
Neurogenetics|August 5, 2009
Sequence variation in SORL1 and dementia risk in SwedesChandra A Reynolds, Mun-Gwan Hong, Ulrika K Eriksson, et al.
Neurogenetics|October 2, 2009
A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardationGinevra Zanni, Hilde van Esch, Anissa Bensalem, et al.
Neurogenetics|October 2, 2009
A Copine family member, Cpne8, is a candidate quantitative trait gene for prion disease incubation time in mouseSarah E Lloyd, Emma G Maytham, Julia Grizenkova, et al.
Neurogenetics|August 29, 2009
Congenital bovine spinal dysmyelination is caused by a missense mutation in the SPAST geneBo Thomsen, Peter H Nissen, Jørgen S Agerholm, et al.
Neurogenetics|October 7, 2009
Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variantNadia Bahi-Buisson, Juliette Nectoux, Benoit Girard, et al.
Neurogenetics|August 9, 2011
Late-onset Alzheimer's disease is associated with mitochondrial DNA 7028C/haplogroup H and D310 poly-C tract heteroplasmyEliecer Coto, Juan Gómez, Belén Alonso, et al.
Neurogenetics|August 11, 2011
A novel deletion-insertion mutation identified in exon 3 of FXN in two siblings with a severe Friedreich ataxia phenotypeMarguerite V Evans-Galea, Louise A Corben, Justin Hasell, et al.
Neurogenetics|February 1, 2012
Mutation in the AP4B1 gene cause hereditary spastic paraplegia type 47 (SPG47) Peter Bauer, Esther Leshinsky-Silver, Lubov Blumkin, et al.
Neurogenetics|January 13, 2012
Genome-scale methylation analysis of Parkinson's disease patients' brains reveals DNA hypomethylation and increased mRNA expression of cytochrome P450 2E1Oliver Kaut, Ina Schmitt, Ullrich Wüllner
Pageof 108