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Edwin Yip

Showing results (1-10 of 6) with videos related to

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Journal of Immunology (Baltimore, Md. : 1950)|January 29, 2014
Type 2 innate lymphoid cells drive CD4+ Th2 cell responsesAnanda S Mirchandani, Anne-Gaelle Besnard, Edwin Yip, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 24, 2006
Novel SPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegiaSatoshi Kaneko, Toshitaka Kawarai, Edwin Yip, et al.
Neurobiology of Aging|July 23, 2008
LRRK2 and Parkin mutations in a family with parkinsonism-Lack of genotype-phenotype correlationConnie Marras, Christine Klein, Anthony E Lang, et al.
Nature Communications|August 8, 2014
Nitric oxide enhances Th9 cell differentiation and airway inflammationWanda Niedbala, Anne-Gaelle Besnard, Daniele Carvalho Nascimento, et al.
Orphanet Journal of Rare Diseases|March 1, 2023
Mitochondrial diseases in Hong Kong: prevalence, clinical characteristics and genetic landscapeTsz-Sum Wong, Kiran M Belaramani, Chun-Kong Chan, et al.
Neurology|January 30, 2025
Characterization of Factors Associated With Death in Deceased Patients With Mitochondrial Disorders: A Multicenter Cross-Sectional SurveyAlina Ivaniuk, Irina A Anselm, Aaron Bowen, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Journal of Immunology (Baltimore, Md. : 1950)|January 29, 2014
Type 2 innate lymphoid cells drive CD4+ Th2 cell responsesAnanda S Mirchandani, Anne-Gaelle Besnard, Edwin Yip, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 24, 2006
Novel SPG6 mutation p.A100T in a Japanese family with autosomal dominant form of hereditary spastic paraplegiaSatoshi Kaneko, Toshitaka Kawarai, Edwin Yip, et al.
Neurobiology of Aging|July 23, 2008
LRRK2 and Parkin mutations in a family with parkinsonism-Lack of genotype-phenotype correlationConnie Marras, Christine Klein, Anthony E Lang, et al.
Nature Communications|August 8, 2014
Nitric oxide enhances Th9 cell differentiation and airway inflammationWanda Niedbala, Anne-Gaelle Besnard, Daniele Carvalho Nascimento, et al.
Orphanet Journal of Rare Diseases|March 1, 2023
Mitochondrial diseases in Hong Kong: prevalence, clinical characteristics and genetic landscapeTsz-Sum Wong, Kiran M Belaramani, Chun-Kong Chan, et al.
Neurology|January 30, 2025
Characterization of Factors Associated With Death in Deceased Patients With Mitochondrial Disorders: A Multicenter Cross-Sectional SurveyAlina Ivaniuk, Irina A Anselm, Aaron Bowen, et al.
Pageof 1