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Fuencisla Matesanz

Showing results (51-60 of 58) with videos related to

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Human Molecular Genetics|July 9, 2015
A functional variant that affects exon-skipping and protein expression of SP140 as genetic mechanism predisposing to multiple sclerosisFuencisla Matesanz, Victor Potenciano, Maria Fedetz, et al.
Brain : a Journal of Neurology|April 14, 2020
NLRP3 inflammasome as prognostic factor and therapeutic target in primary progressive multiple sclerosis patientsSunny Malhotra, Carme Costa, Herena Eixarch, et al.
Plos Genetics|June 7, 2019
Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of diseaseCarles Vilariño-Güell, Alexander Zimprich, Filippo Martinelli-Boneschi, et al.
Journal of Medical Genetics|January 15, 2013
Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis riskChristina M Lill, Brit-Maren M Schjeide, Christiane Graetz, et al.
Journal of Medical Genetics|September 14, 2012
Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjectsChristina M Lill, Tian Liu, Brit-Maren M Schjeide, et al.
G3 (Bethesda, Md.)|May 20, 2016
Analysis of Plasminogen Genetic Variants in Multiple Sclerosis PatientsA Dessa Sadovnick, Anthony L Traboulsee, Cecily Q Bernales, et al.
Brain : a Journal of Neurology|June 7, 2013
MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis, Christina M Lill, Brit-Maren M Schjeide, et al.
Journal of Medical Genetics|October 18, 2015
Genome-wide significant association with seven novel multiple sclerosis risk lociChristina M Lill, Felix Luessi, Antonio Alcina, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
Human Molecular Genetics|July 9, 2015
A functional variant that affects exon-skipping and protein expression of SP140 as genetic mechanism predisposing to multiple sclerosisFuencisla Matesanz, Victor Potenciano, Maria Fedetz, et al.
Brain : a Journal of Neurology|April 14, 2020
NLRP3 inflammasome as prognostic factor and therapeutic target in primary progressive multiple sclerosis patientsSunny Malhotra, Carme Costa, Herena Eixarch, et al.
Plos Genetics|June 7, 2019
Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of diseaseCarles Vilariño-Güell, Alexander Zimprich, Filippo Martinelli-Boneschi, et al.
Journal of Medical Genetics|January 15, 2013
Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis riskChristina M Lill, Brit-Maren M Schjeide, Christiane Graetz, et al.
Journal of Medical Genetics|September 14, 2012
Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjectsChristina M Lill, Tian Liu, Brit-Maren M Schjeide, et al.
G3 (Bethesda, Md.)|May 20, 2016
Analysis of Plasminogen Genetic Variants in Multiple Sclerosis PatientsA Dessa Sadovnick, Anthony L Traboulsee, Cecily Q Bernales, et al.
Brain : a Journal of Neurology|June 7, 2013
MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis, Christina M Lill, Brit-Maren M Schjeide, et al.
Journal of Medical Genetics|October 18, 2015
Genome-wide significant association with seven novel multiple sclerosis risk lociChristina M Lill, Felix Luessi, Antonio Alcina, et al.
Pageof 6