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American Journal of Human Genetics
|
March 13, 2012
Haploinsufficiency of ARID1B, a member of the SWI/SNF-a chromatin-remodeling complex, is a frequent cause of intellectual disability
Juliane Hoyer, Arif B Ekici, Sabine Endele, et al.
Scientific Reports
|
October 1, 2020
DJ-1 (Park7) affects the gut microbiome, metabolites and the development of innate lymphoid cells (ILCs)
Yogesh Singh, Christoph Trautwein, Achal Dhariwal, et al.
Neurobiology of Disease
|
July 20, 2011
Olfactory neuron-specific expression of A30P α-synuclein exacerbates dopamine deficiency and hyperactivity in a novel conditional model of early Parkinson's disease stages
Silke Nuber, Elisabeth Petrasch-Parwez, Oscar Arias-Carrión, et al.
Human Mutation
|
September 15, 2004
Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7)
Robert Hering, Karsten M Strauss, Xiao Tao, et al.
Aging
|
March 25, 2020
Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease
Fulya Akçimen, Sandra Martins, Calwing Liao, et al.
Breast Cancer Research and Treatment
|
May 30, 2015
HBOC multi-gene panel testing: comparison of two sequencing centers
Christopher Schroeder, Ulrike Faust, Marc Sturm, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 29, 2018
Understanding the role of genetic variability in LRRK2 in Indian population
Asha Kishore, Ashwin Ashok Kumar Sreelatha, Marc Sturm, et al.
Brain : a Journal of Neurology
|
February 16, 2013
A progressive dopaminergic phenotype associated with neurotoxic conversion of α-synuclein in BAC-transgenic rats
Silke Nuber, Florian Harmuth, Zacharias Kohl, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
March 7, 2008
Neurodegeneration and motor dysfunction in a conditional model of Parkinson's disease
Silke Nuber, Elisabeth Petrasch-Parwez, Beate Winner, et al.
Neurology
|
September 17, 2017
Analysis of blood-based gene expression in idiopathic Parkinson disease
Ron Shamir, Christine Klein, David Amar, et al.
Page
of 32
Search research articles
Search
Showing results (231-240 of 313) with videos related to
Sort By:
Page
of 32
American Journal of Human Genetics
|
March 13, 2012
Haploinsufficiency of ARID1B, a member of the SWI/SNF-a chromatin-remodeling complex, is a frequent cause of intellectual disability
Juliane Hoyer, Arif B Ekici, Sabine Endele, et al.
Scientific Reports
|
October 1, 2020
DJ-1 (Park7) affects the gut microbiome, metabolites and the development of innate lymphoid cells (ILCs)
Yogesh Singh, Christoph Trautwein, Achal Dhariwal, et al.
Neurobiology of Disease
|
July 20, 2011
Olfactory neuron-specific expression of A30P α-synuclein exacerbates dopamine deficiency and hyperactivity in a novel conditional model of early Parkinson's disease stages
Silke Nuber, Elisabeth Petrasch-Parwez, Oscar Arias-Carrión, et al.
Human Mutation
|
September 15, 2004
Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7)
Robert Hering, Karsten M Strauss, Xiao Tao, et al.
Aging
|
March 25, 2020
Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease
Fulya Akçimen, Sandra Martins, Calwing Liao, et al.
Breast Cancer Research and Treatment
|
May 30, 2015
HBOC multi-gene panel testing: comparison of two sequencing centers
Christopher Schroeder, Ulrike Faust, Marc Sturm, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 29, 2018
Understanding the role of genetic variability in LRRK2 in Indian population
Asha Kishore, Ashwin Ashok Kumar Sreelatha, Marc Sturm, et al.
Brain : a Journal of Neurology
|
February 16, 2013
A progressive dopaminergic phenotype associated with neurotoxic conversion of α-synuclein in BAC-transgenic rats
Silke Nuber, Florian Harmuth, Zacharias Kohl, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
March 7, 2008
Neurodegeneration and motor dysfunction in a conditional model of Parkinson's disease
Silke Nuber, Elisabeth Petrasch-Parwez, Beate Winner, et al.
Neurology
|
September 17, 2017
Analysis of blood-based gene expression in idiopathic Parkinson disease
Ron Shamir, Christine Klein, David Amar, et al.
Page
of 32