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S MacKay

Showing results (291-300 of 312) with videos related to

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Blood|March 8, 2024
Mutations causing premature termination codons discriminate and generate cellular and clinical variability in HHTMaria E Bernabéu-Herrero, Dilipkumar Patel, Adrianna Bielowka, et al.
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology|August 21, 2025
NOURISH-US: a mixed-methods, randomized crossover study of a program designed to reduce the financial burden of food allergyMichael A Golding, Sarah Baldwin, Brandon Kim, et al.
JAMA Ophthalmology|July 9, 2016
Expanding the Phenotype of TRNT1-Related Immunodeficiency to Include Childhood Cataract and Inner Retinal DysfunctionSarah Hull, Aeesha N J Malik, Gavin Arno, et al.
The Veterinary Record|March 26, 2005
Multiple antimicrobial resistant Salmonella enterica serovar Paratyphi B variant Java in cattle: a case reportS J Evans, R H Davies, S H Binns, et al.
Molecular Vision|November 9, 2011
RDH12 retinopathy: novel mutations and phenotypic descriptionDonna S Mackay, Arundhati Dev Borman, Phillip Moradi, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|July 19, 2017
Nonnutritive sweeteners and cardiometabolic health: a systematic review and meta-analysis of randomized controlled trials and prospective cohort studiesMeghan B Azad, Ahmed M Abou-Setta, Bhupendrasinh F Chauhan, et al.
Molecular Vision|March 20, 2010
Novel mutations in MERTK associated with childhood onset rod-cone dystrophyDonna S Mackay, Robert H Henderson, Panagiotis I Sergouniotis, et al.
Angewandte Chemie (International Ed. in English)|October 11, 2023
Electrochemical Modification of Polypeptides at SelenocysteineAngus S Mackay, Joshua W C Maxwell, Max J Bedding, et al.
Human Mutation|December 31, 2013
A homozygous mutation in the TUB gene associated with retinal dystrophy and obesityArundhati Dev Borman, Laura R Pearce, Donna S Mackay, et al.
American Journal of Ophthalmology|March 19, 2013
A longitudinal study of stargardt disease: clinical and electrophysiologic assessment, progression, and genotype correlationsKaoru Fujinami, Noemi Lois, Alice E Davidson, et al.
Pageof 32

Showing results (291-300 of 312) with videos related to

Sort By:
Pageof 32
Blood|March 8, 2024
Mutations causing premature termination codons discriminate and generate cellular and clinical variability in HHTMaria E Bernabéu-Herrero, Dilipkumar Patel, Adrianna Bielowka, et al.
Allergy, Asthma, and Clinical Immunology : Official Journal of the Canadian Society of Allergy and Clinical Immunology|August 21, 2025
NOURISH-US: a mixed-methods, randomized crossover study of a program designed to reduce the financial burden of food allergyMichael A Golding, Sarah Baldwin, Brandon Kim, et al.
JAMA Ophthalmology|July 9, 2016
Expanding the Phenotype of TRNT1-Related Immunodeficiency to Include Childhood Cataract and Inner Retinal DysfunctionSarah Hull, Aeesha N J Malik, Gavin Arno, et al.
The Veterinary Record|March 26, 2005
Multiple antimicrobial resistant Salmonella enterica serovar Paratyphi B variant Java in cattle: a case reportS J Evans, R H Davies, S H Binns, et al.
Molecular Vision|November 9, 2011
RDH12 retinopathy: novel mutations and phenotypic descriptionDonna S Mackay, Arundhati Dev Borman, Phillip Moradi, et al.
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|July 19, 2017
Nonnutritive sweeteners and cardiometabolic health: a systematic review and meta-analysis of randomized controlled trials and prospective cohort studiesMeghan B Azad, Ahmed M Abou-Setta, Bhupendrasinh F Chauhan, et al.
Molecular Vision|March 20, 2010
Novel mutations in MERTK associated with childhood onset rod-cone dystrophyDonna S Mackay, Robert H Henderson, Panagiotis I Sergouniotis, et al.
Angewandte Chemie (International Ed. in English)|October 11, 2023
Electrochemical Modification of Polypeptides at SelenocysteineAngus S Mackay, Joshua W C Maxwell, Max J Bedding, et al.
Human Mutation|December 31, 2013
A homozygous mutation in the TUB gene associated with retinal dystrophy and obesityArundhati Dev Borman, Laura R Pearce, Donna S Mackay, et al.
American Journal of Ophthalmology|March 19, 2013
A longitudinal study of stargardt disease: clinical and electrophysiologic assessment, progression, and genotype correlationsKaoru Fujinami, Noemi Lois, Alice E Davidson, et al.
Pageof 32