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The Lancet. Neurology
|
June 24, 2017
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study
Davina J Hensman Moss, Antonio F Pardiñas, Douglas Langbehn, et al.
Human Molecular Genetics
|
May 13, 2016
RNA-Seq of Huntington's disease patient myeloid cells reveals innate transcriptional dysregulation associated with proinflammatory pathway activation
James R C Miller, Kitty K Lo, Ralph Andre, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 26, 2007
Expression profiling of Huntington's disease models suggests that brain-derived neurotrophic factor depletion plays a major role in striatal degeneration
Andrew D Strand, Zachary C Baquet, Aaron K Aragaki, et al.
Health Technology Assessment (Winchester, England)
|
September 23, 2015
Does home oxygen therapy (HOT) in addition to standard care reduce disease severity and improve symptoms in people with chronic heart failure? A randomised trial of home oxygen therapy for patients with chronic heart failure
Andrew L Clark, Miriam Johnson, Caroline Fairhurst, et al.
Journal of Huntington'S Disease
|
February 13, 2021
Huntington's Disease Pathogenesis: Two Sequential Components
Eun Pyo Hong, Marcy E MacDonald, Vanessa C Wheeler, et al.
Neurology
|
March 26, 2021
Timing and Impact of Psychiatric, Cognitive, and Motor Abnormalities in Huntington Disease
Branduff McAllister, James F Gusella, G Bernhard Landwehrmeyer, et al.
Journal of Huntington'S Disease
|
October 8, 2015
The Genetic Modifiers of Motor OnsetAge (GeM MOA) Website: Genome-wide Association Analysis for Genetic Modifiers of Huntington's Disease
Kevin Correia, Denise Harold, Kyung-Hee Kim, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
|
June 29, 2018
Cross-species evidence from human and rat brain transcriptome for growth factor signaling pathway dysregulation in major depression
Lucia Carboni, Luca Marchetti, Mario Lauria, et al.
Human Molecular Genetics
|
June 9, 2012
Early transcriptional changes linked to naturally occurring Huntington's disease mutations in neural derivatives of human embryonic stem cells
Maxime Feyeux, Fany Bourgois-Rocha, Amanda Redfern, et al.
Human Molecular Genetics
|
January 10, 2008
Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1
Nicholas J Bray, Peter A Holmans, Marianne B van den Bree, et al.
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of 14
Search research articles
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Showing results (81-90 of 138) with videos related to
Sort By:
Page
of 14
The Lancet. Neurology
|
June 24, 2017
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study
Davina J Hensman Moss, Antonio F Pardiñas, Douglas Langbehn, et al.
Human Molecular Genetics
|
May 13, 2016
RNA-Seq of Huntington's disease patient myeloid cells reveals innate transcriptional dysregulation associated with proinflammatory pathway activation
James R C Miller, Kitty K Lo, Ralph Andre, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
October 26, 2007
Expression profiling of Huntington's disease models suggests that brain-derived neurotrophic factor depletion plays a major role in striatal degeneration
Andrew D Strand, Zachary C Baquet, Aaron K Aragaki, et al.
Health Technology Assessment (Winchester, England)
|
September 23, 2015
Does home oxygen therapy (HOT) in addition to standard care reduce disease severity and improve symptoms in people with chronic heart failure? A randomised trial of home oxygen therapy for patients with chronic heart failure
Andrew L Clark, Miriam Johnson, Caroline Fairhurst, et al.
Journal of Huntington'S Disease
|
February 13, 2021
Huntington's Disease Pathogenesis: Two Sequential Components
Eun Pyo Hong, Marcy E MacDonald, Vanessa C Wheeler, et al.
Neurology
|
March 26, 2021
Timing and Impact of Psychiatric, Cognitive, and Motor Abnormalities in Huntington Disease
Branduff McAllister, James F Gusella, G Bernhard Landwehrmeyer, et al.
Journal of Huntington'S Disease
|
October 8, 2015
The Genetic Modifiers of Motor OnsetAge (GeM MOA) Website: Genome-wide Association Analysis for Genetic Modifiers of Huntington's Disease
Kevin Correia, Denise Harold, Kyung-Hee Kim, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
|
June 29, 2018
Cross-species evidence from human and rat brain transcriptome for growth factor signaling pathway dysregulation in major depression
Lucia Carboni, Luca Marchetti, Mario Lauria, et al.
Human Molecular Genetics
|
June 9, 2012
Early transcriptional changes linked to naturally occurring Huntington's disease mutations in neural derivatives of human embryonic stem cells
Maxime Feyeux, Fany Bourgois-Rocha, Amanda Redfern, et al.
Human Molecular Genetics
|
January 10, 2008
Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1
Nicholas J Bray, Peter A Holmans, Marianne B van den Bree, et al.
Page
of 14