Search research articles
Contact Us
Filters
Showing results (741-750 of 949) with videos related to
Page
of 95
Sort By:
Neurogenetics
|
July 21, 2009
Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot-Marie-Tooth type 2A disease
Virginie Guillet, Naïg Gueguen, Christophe Verny, et al.
Neurogenetics
|
May 10, 2020
Oligogenicity, C9orf72 expansion, and variant severity in ALS
Jay P Ross, Claire S Leblond, Sandra B Laurent, et al.
Neurogenetics
|
May 24, 2015
Variable expression of microglial DAP12 and TREM2 genes in Nasu-Hakola disease
Atsushi Sasaki, Akiyoshi Kakita, Kunihiro Yoshida, et al.
Neurogenetics
|
April 28, 2015
The fused in sarcoma protein forms cytoplasmic aggregates in motor neurons derived from integration-free induced pluripotent stem cells generated from a patient with familial amyotrophic lateral sclerosis carrying the FUS-P525L mutation
Xinxiu Liu, Jiayu Chen, Wenchao Liu, et al.
Neurogenetics
|
September 6, 2025
Huntington's chorea: emerging fields in therapeutics (Review)
Aisha Tahir, Sania Jamal, Usman Ali Shams, et al.
Neurogenetics
|
February 7, 2001
Dystrobrevin- and dystrophin-like mutants display similar phenotypes in the nematode Caenorhabditis elegans
K Gieseler, C Bessou, L Ségalat
Neurogenetics
|
February 7, 2001
Two novel point mutations of mitochondrial tRNA genes in histologically confirmed Parkinson disease
E M Grasbon-Frodl, S Kösel, M Sprinzl, et al.
Neurogenetics
|
March 29, 2000
Clinical and molecular genetics of primary dystonias
U Müller, D Steinberger, A H Németh
Neurogenetics
|
March 29, 2000
Genetic fine mapping of the Miyoshi myopathy locus and exclusion of eight candidate genes
K Bejaoui, J Liu, D McKenna-Yasek, et al.
Neurogenetics
|
March 29, 2000
Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease
S Kösel, E M Grasbon-Frodl, U Mautsch, et al.
Page
of 95
Search research articles
Search
Showing results (741-750 of 949) with videos related to
Sort By:
Page
of 95
Neurogenetics
|
July 21, 2009
Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot-Marie-Tooth type 2A disease
Virginie Guillet, Naïg Gueguen, Christophe Verny, et al.
Neurogenetics
|
May 10, 2020
Oligogenicity, C9orf72 expansion, and variant severity in ALS
Jay P Ross, Claire S Leblond, Sandra B Laurent, et al.
Neurogenetics
|
May 24, 2015
Variable expression of microglial DAP12 and TREM2 genes in Nasu-Hakola disease
Atsushi Sasaki, Akiyoshi Kakita, Kunihiro Yoshida, et al.
Neurogenetics
|
April 28, 2015
The fused in sarcoma protein forms cytoplasmic aggregates in motor neurons derived from integration-free induced pluripotent stem cells generated from a patient with familial amyotrophic lateral sclerosis carrying the FUS-P525L mutation
Xinxiu Liu, Jiayu Chen, Wenchao Liu, et al.
Neurogenetics
|
September 6, 2025
Huntington's chorea: emerging fields in therapeutics (Review)
Aisha Tahir, Sania Jamal, Usman Ali Shams, et al.
Neurogenetics
|
February 7, 2001
Dystrobrevin- and dystrophin-like mutants display similar phenotypes in the nematode Caenorhabditis elegans
K Gieseler, C Bessou, L Ségalat
Neurogenetics
|
February 7, 2001
Two novel point mutations of mitochondrial tRNA genes in histologically confirmed Parkinson disease
E M Grasbon-Frodl, S Kösel, M Sprinzl, et al.
Neurogenetics
|
March 29, 2000
Clinical and molecular genetics of primary dystonias
U Müller, D Steinberger, A H Németh
Neurogenetics
|
March 29, 2000
Genetic fine mapping of the Miyoshi myopathy locus and exclusion of eight candidate genes
K Bejaoui, J Liu, D McKenna-Yasek, et al.
Neurogenetics
|
March 29, 2000
Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease
S Kösel, E M Grasbon-Frodl, U Mautsch, et al.
Page
of 95