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Andrew B Singleton

Showing results (31-40 of 397) with videos related to

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Neurobiology of Disease|February 22, 2012
A large study reveals no association between APOE and Parkinson's diseaseMonica Federoff, Belen Jimenez-Rolando, Michael A Nalls, et al.
Journal of Neurology|July 25, 2013
Exome sequencing expands the mutational spectrum of SPG8 in a family with spasticity responsive to L-DOPA treatmentConceição Bettencourt, Huw R Morris, Andrew B Singleton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 9, 2017
No clear support for a role for vitamin D in Parkinson's disease: A Mendelian randomization studySusanna C Larsson, Andrew B Singleton, Mike A Nalls, et al.
Neurobiology of Disease|January 29, 2020
Genetics of Parkinson's disease: An introspection of its journey towards precision medicineSara Bandres-Ciga, Monica Diez-Fairen, Jonggeol Jeff Kim, et al.
Neuroscience Letters|July 6, 2002
Normal localization of deltaF323-Y328 mutant torsinA in transfected human cellsCasey O'Farrell, Dena G Hernandez, Crystal Evey, et al.
Annals of Human Genetics|June 4, 2009
Parkinson's disease and low frequency alleles found together throughout LRRK2Coro Paisán-Ruiz, Nicole Washecka, Priti Nath, et al.
Human Mutation|January 24, 2008
Comprehensive analysis of LRRK2 in publicly available Parkinson's disease cases and neurologically normal controlsCoro Paisán-Ruíz, Priti Nath, Nicole Washecka, et al.
American Journal of Human Genetics|October 6, 2010
Exome sequencing in Brown-Vialetto-van Laere syndromeJanel O Johnson, J Raphael Gibbs, Lionel Van Maldergem, et al.
BMC Genomics|November 14, 2012
Cell population-specific expression analysis of human cerebellumAlexandre Kuhn, Azad Kumar, Alexandra Beilina, et al.
Neurobiology of Aging|July 28, 2005
Assessment of PINK1 (PARK6) polymorphisms in Finnish PDJordi Clarimón, Johanna Eerola, Olli Hellström, et al.
Pageof 40

Showing results (31-40 of 397) with videos related to

Sort By:
Pageof 40
Neurobiology of Disease|February 22, 2012
A large study reveals no association between APOE and Parkinson's diseaseMonica Federoff, Belen Jimenez-Rolando, Michael A Nalls, et al.
Journal of Neurology|July 25, 2013
Exome sequencing expands the mutational spectrum of SPG8 in a family with spasticity responsive to L-DOPA treatmentConceição Bettencourt, Huw R Morris, Andrew B Singleton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 9, 2017
No clear support for a role for vitamin D in Parkinson's disease: A Mendelian randomization studySusanna C Larsson, Andrew B Singleton, Mike A Nalls, et al.
Neurobiology of Disease|January 29, 2020
Genetics of Parkinson's disease: An introspection of its journey towards precision medicineSara Bandres-Ciga, Monica Diez-Fairen, Jonggeol Jeff Kim, et al.
Neuroscience Letters|July 6, 2002
Normal localization of deltaF323-Y328 mutant torsinA in transfected human cellsCasey O'Farrell, Dena G Hernandez, Crystal Evey, et al.
Annals of Human Genetics|June 4, 2009
Parkinson's disease and low frequency alleles found together throughout LRRK2Coro Paisán-Ruiz, Nicole Washecka, Priti Nath, et al.
Human Mutation|January 24, 2008
Comprehensive analysis of LRRK2 in publicly available Parkinson's disease cases and neurologically normal controlsCoro Paisán-Ruíz, Priti Nath, Nicole Washecka, et al.
American Journal of Human Genetics|October 6, 2010
Exome sequencing in Brown-Vialetto-van Laere syndromeJanel O Johnson, J Raphael Gibbs, Lionel Van Maldergem, et al.
BMC Genomics|November 14, 2012
Cell population-specific expression analysis of human cerebellumAlexandre Kuhn, Azad Kumar, Alexandra Beilina, et al.
Neurobiology of Aging|July 28, 2005
Assessment of PINK1 (PARK6) polymorphisms in Finnish PDJordi Clarimón, Johanna Eerola, Olli Hellström, et al.
Pageof 40