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S MacKay

Showing results (301-310 of 312) with videos related to

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Investigative Ophthalmology & Visual Science|May 10, 2012
Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic studyArundhati Dev Borman, Louise A Ocaka, Donna S Mackay, et al.
American Journal of Human Genetics|December 6, 2011
Biallelic mutations in PLA2G5, encoding group V phospholipase A2, cause benign fleck retinaPanagiotis I Sergouniotis, Alice E Davidson, Donna S Mackay, et al.
Atherosclerosis|December 22, 2014
High-oleic canola oil consumption enriches LDL particle cholesteryl oleate content and reduces LDL proteoglycan binding in humansPeter J H Jones, Dylan S MacKay, Vijitha K Senanayake, et al.
Chemical Science|September 17, 2025
Engineering ultrapotent trivalent anticoagulants through hybridisation of salivary peptides from multiple haematophagous organismsJoshua W C Maxwell, Jorge Ripoll-Rozada, Angus S Mackay, et al.
Nature Communications|May 6, 2025
Perinatal SSRI exposure impacts innate fear circuit activation and behavior in mice and humansGiulia Zanni, Milenna T van Dijk, Martha Caffrey Cagliostro, et al.
Plos One|March 14, 2012
Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapyMei Hong Tan, Donna S Mackay, Jill Cowing, et al.
Nature Communications|November 12, 2022
Site-selective photocatalytic functionalization of peptides and proteins at selenocysteineLuke J Dowman, Sameer S Kulkarni, Juan V Alegre-Requena, et al.
Nutrition Reviews|August 14, 2018
Progress and perspectives in plant sterol and plant stanol researchPeter J H Jones, Maryam Shamloo, Dylan S MacKay, et al.
Nature Genetics|July 31, 2012
NMNAT1 mutations cause Leber congenital amaurosisMarni J Falk, Qi Zhang, Eiko Nakamaru-Ogiso, et al.
Human Mutation|August 16, 2013
Screening of a large cohort of leber congenital amaurosis and retinitis pigmentosa patients identifies novel LCA5 mutations and new genotype-phenotype correlationsDonna S Mackay, Arundhati Dev Borman, Ruifang Sui, et al.
Pageof 32

Showing results (301-310 of 312) with videos related to

Sort By:
Pageof 32
Investigative Ophthalmology & Visual Science|May 10, 2012
Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic studyArundhati Dev Borman, Louise A Ocaka, Donna S Mackay, et al.
American Journal of Human Genetics|December 6, 2011
Biallelic mutations in PLA2G5, encoding group V phospholipase A2, cause benign fleck retinaPanagiotis I Sergouniotis, Alice E Davidson, Donna S Mackay, et al.
Atherosclerosis|December 22, 2014
High-oleic canola oil consumption enriches LDL particle cholesteryl oleate content and reduces LDL proteoglycan binding in humansPeter J H Jones, Dylan S MacKay, Vijitha K Senanayake, et al.
Chemical Science|September 17, 2025
Engineering ultrapotent trivalent anticoagulants through hybridisation of salivary peptides from multiple haematophagous organismsJoshua W C Maxwell, Jorge Ripoll-Rozada, Angus S Mackay, et al.
Nature Communications|May 6, 2025
Perinatal SSRI exposure impacts innate fear circuit activation and behavior in mice and humansGiulia Zanni, Milenna T van Dijk, Martha Caffrey Cagliostro, et al.
Plos One|March 14, 2012
Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapyMei Hong Tan, Donna S Mackay, Jill Cowing, et al.
Nature Communications|November 12, 2022
Site-selective photocatalytic functionalization of peptides and proteins at selenocysteineLuke J Dowman, Sameer S Kulkarni, Juan V Alegre-Requena, et al.
Nutrition Reviews|August 14, 2018
Progress and perspectives in plant sterol and plant stanol researchPeter J H Jones, Maryam Shamloo, Dylan S MacKay, et al.
Nature Genetics|July 31, 2012
NMNAT1 mutations cause Leber congenital amaurosisMarni J Falk, Qi Zhang, Eiko Nakamaru-Ogiso, et al.
Human Mutation|August 16, 2013
Screening of a large cohort of leber congenital amaurosis and retinitis pigmentosa patients identifies novel LCA5 mutations and new genotype-phenotype correlationsDonna S Mackay, Arundhati Dev Borman, Ruifang Sui, et al.
Pageof 32