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Christopher R McMaster

Showing results (71-80 of 79) with videos related to

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JAMA Ophthalmology|August 16, 2014
Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutationsJohane M Robitaille, Roxanne M Gillett, Marissa A LeBlanc, et al.
Nature Communications|September 27, 2024
Computer-aided drug design to generate a unique antibiotic familyChristopher J Barden, Fan Wu, J Pedro Fernandez-Murray, et al.
Frontiers in Pediatrics|December 31, 2020
Barriers and Considerations for Diagnosing Rare Diseases in Indigenous PopulationsCarla S D'Angelo, Azure Hermes, Christopher R McMaster, et al.
Nature Communications|March 24, 2022
Mechanism of action and therapeutic route for a muscular dystrophy caused by a genetic defect in lipid metabolismMahtab Tavasoli, Sarah Lahire, Stanislav Sokolenko, et al.
Plos Genetics|October 24, 2014
Germline mutations in MAP3K6 are associated with familial gastric cancerDaniel Gaston, Samantha Hansford, Carla Oliveira, et al.
Brain : a Journal of Neurology|January 6, 2017
A mutation of EPT1 (SELENOI) underlies a new disorder of Kennedy pathway phospholipid biosynthesisMustafa Y Ahmed, Aisha Al-Khayat, Fathiya Al-Murshedi, et al.
Brain : a Journal of Neurology|February 24, 2022
Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephalyChiara Klöckner, J Pedro Fernández-Murray, Mahtab Tavasoli, et al.
American Journal of Human Genetics|February 8, 2020
The Canadian Rare Diseases Models and Mechanisms (RDMM) Network: Connecting Understudied Genes to Model OrganismsKym M Boycott, Philippe M Campeau, Heather E Howley, et al.
Autophagy|September 12, 2012
Guidelines for the use and interpretation of assays for monitoring autophagyDaniel J Klionsky, Fabio C Abdalla, Hagai Abeliovich, et al.
Pageof 8

Showing results (71-80 of 79) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 79 results.
JAMA Ophthalmology|August 16, 2014
Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutationsJohane M Robitaille, Roxanne M Gillett, Marissa A LeBlanc, et al.
Nature Communications|September 27, 2024
Computer-aided drug design to generate a unique antibiotic familyChristopher J Barden, Fan Wu, J Pedro Fernandez-Murray, et al.
Frontiers in Pediatrics|December 31, 2020
Barriers and Considerations for Diagnosing Rare Diseases in Indigenous PopulationsCarla S D'Angelo, Azure Hermes, Christopher R McMaster, et al.
Nature Communications|March 24, 2022
Mechanism of action and therapeutic route for a muscular dystrophy caused by a genetic defect in lipid metabolismMahtab Tavasoli, Sarah Lahire, Stanislav Sokolenko, et al.
Plos Genetics|October 24, 2014
Germline mutations in MAP3K6 are associated with familial gastric cancerDaniel Gaston, Samantha Hansford, Carla Oliveira, et al.
Brain : a Journal of Neurology|January 6, 2017
A mutation of EPT1 (SELENOI) underlies a new disorder of Kennedy pathway phospholipid biosynthesisMustafa Y Ahmed, Aisha Al-Khayat, Fathiya Al-Murshedi, et al.
Brain : a Journal of Neurology|February 24, 2022
Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephalyChiara Klöckner, J Pedro Fernández-Murray, Mahtab Tavasoli, et al.
American Journal of Human Genetics|February 8, 2020
The Canadian Rare Diseases Models and Mechanisms (RDMM) Network: Connecting Understudied Genes to Model OrganismsKym M Boycott, Philippe M Campeau, Heather E Howley, et al.
Autophagy|September 12, 2012
Guidelines for the use and interpretation of assays for monitoring autophagyDaniel J Klionsky, Fabio C Abdalla, Hagai Abeliovich, et al.
Pageof 8