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The Journal of Biological Chemistry
|
October 28, 2011
Methicillin-resistant Staphylococcus aureus (MRSA) pyruvate kinase as a target for bis-indole alkaloids with antibacterial activities
Roya Zoraghi, Liam Worrall, Raymond H See, et al.
Human Genetics
|
June 25, 2013
A novel rearrangement of occludin causes brain calcification and renal dysfunction
Marissa A LeBlanc, Lynette S Penney, Daniel Gaston, et al.
The Journal of Biological Chemistry
|
February 13, 2022
A mouse model of inherited choline kinase β-deficiency presents with specific cardiac abnormalities and a predisposition to arrhythmia
Mahtab Tavasoli, Tiam Feridooni, Hirad Feridooni, et al.
Investigative Ophthalmology & Visual Science
|
February 7, 2025
Gene Variant Spectrum in Probands With Familial Exudative Vitreoretinopathy Using an Expanded Panel
Sarah van der Ende, Karen Bedard, Karin Wallace, et al.
JAMA Ophthalmology
|
August 16, 2014
Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutations
Johane M Robitaille, Roxanne M Gillett, Marissa A LeBlanc, et al.
Nature Communications
|
September 27, 2024
Computer-aided drug design to generate a unique antibiotic family
Christopher J Barden, Fan Wu, J Pedro Fernandez-Murray, et al.
Nature Genetics
|
March 2, 2011
Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome
Duane L Guernsey, Makoto Matsuoka, Haiyan Jiang, et al.
ACS Chemical Biology
|
November 10, 2011
Cheminformatics-driven discovery of selective, nanomolar inhibitors for staphylococcal pyruvate kinase
Peter Axerio-Cilies, Raymond H See, Roya Zoraghi, et al.
Frontiers in Pediatrics
|
December 31, 2020
Barriers and Considerations for Diagnosing Rare Diseases in Indigenous Populations
Carla 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 metabolism
Mahtab Tavasoli, Sarah Lahire, Stanislav Sokolenko, et al.
Page
of 28
Search research articles
Search
Showing results (261-270 of 278) with videos related to
Sort By:
Page
of 28
The Journal of Biological Chemistry
|
October 28, 2011
Methicillin-resistant Staphylococcus aureus (MRSA) pyruvate kinase as a target for bis-indole alkaloids with antibacterial activities
Roya Zoraghi, Liam Worrall, Raymond H See, et al.
Human Genetics
|
June 25, 2013
A novel rearrangement of occludin causes brain calcification and renal dysfunction
Marissa A LeBlanc, Lynette S Penney, Daniel Gaston, et al.
The Journal of Biological Chemistry
|
February 13, 2022
A mouse model of inherited choline kinase β-deficiency presents with specific cardiac abnormalities and a predisposition to arrhythmia
Mahtab Tavasoli, Tiam Feridooni, Hirad Feridooni, et al.
Investigative Ophthalmology & Visual Science
|
February 7, 2025
Gene Variant Spectrum in Probands With Familial Exudative Vitreoretinopathy Using an Expanded Panel
Sarah van der Ende, Karen Bedard, Karin Wallace, et al.
JAMA Ophthalmology
|
August 16, 2014
Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutations
Johane M Robitaille, Roxanne M Gillett, Marissa A LeBlanc, et al.
Nature Communications
|
September 27, 2024
Computer-aided drug design to generate a unique antibiotic family
Christopher J Barden, Fan Wu, J Pedro Fernandez-Murray, et al.
Nature Genetics
|
March 2, 2011
Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome
Duane L Guernsey, Makoto Matsuoka, Haiyan Jiang, et al.
ACS Chemical Biology
|
November 10, 2011
Cheminformatics-driven discovery of selective, nanomolar inhibitors for staphylococcal pyruvate kinase
Peter Axerio-Cilies, Raymond H See, Roya Zoraghi, et al.
Frontiers in Pediatrics
|
December 31, 2020
Barriers and Considerations for Diagnosing Rare Diseases in Indigenous Populations
Carla 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 metabolism
Mahtab Tavasoli, Sarah Lahire, Stanislav Sokolenko, et al.
Page
of 28