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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 study
Arundhati 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 retina
Panagiotis 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 humans
Peter 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 organisms
Joshua 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 humans
Giulia 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 therapy
Mei Hong Tan, Donna S Mackay, Jill Cowing, et al.
Nature Communications
|
November 12, 2022
Site-selective photocatalytic functionalization of peptides and proteins at selenocysteine
Luke 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 research
Peter J H Jones, Maryam Shamloo, Dylan S MacKay, et al.
Nature Genetics
|
July 31, 2012
NMNAT1 mutations cause Leber congenital amaurosis
Marni 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 correlations
Donna S Mackay, Arundhati Dev Borman, Ruifang Sui, et al.
Page
of 32
Search research articles
Search
Showing results (301-310 of 312) with videos related to
Sort By:
Page
of 32
Investigative Ophthalmology & Visual Science
|
May 10, 2012
Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic study
Arundhati 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 retina
Panagiotis 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 humans
Peter 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 organisms
Joshua 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 humans
Giulia 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 therapy
Mei Hong Tan, Donna S Mackay, Jill Cowing, et al.
Nature Communications
|
November 12, 2022
Site-selective photocatalytic functionalization of peptides and proteins at selenocysteine
Luke 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 research
Peter J H Jones, Maryam Shamloo, Dylan S MacKay, et al.
Nature Genetics
|
July 31, 2012
NMNAT1 mutations cause Leber congenital amaurosis
Marni 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 correlations
Donna S Mackay, Arundhati Dev Borman, Ruifang Sui, et al.
Page
of 32