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D Webb

Showing results (791-800 of 812) with videos related to

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Space Science Reviews|August 8, 2025
The Magnetic Search Coil (MSC) on the TRACERS MissionG B Hospodarsky, A J Carton, R T Dvorsky, et al.
Nature Genetics|April 30, 2008
Integrated genomic approaches implicate osteoglycin (Ogn) in the regulation of left ventricular massEnrico Petretto, Rizwan Sarwar, Ian Grieve, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 26, 2025
BiomarkersMolly Olzinski, Yann Cobigo, Rowan Saloner, et al.
Theranostics|June 7, 2021
Prodromal neuroinflammatory, cholinergic and metabolite dysfunction detected by PET and MRS in the TgF344-AD transgenic rat model of AD: a collaborative multi-modal studyAisling M Chaney, Francisco R Lopez-Picon, Sophie Serrière, et al.
Arthritis and Rheumatism|September 18, 2010
Genetically determined Amerindian ancestry correlates with increased frequency of risk alleles for systemic lupus erythematosusElena Sanchez, Ryan D Webb, Astrid Rasmussen, et al.
The Canadian Journal of Cardiology|April 23, 2022
Canadian Cardiovascular Society 2022 Guidelines for Cardiovascular Interventions in Adults With Congenital Heart DiseaseAriane Marelli, Luc Beauchesne, Jack Colman, et al.
American Journal of Human Genetics|April 7, 2018
Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh SyndromeNicole J Lake, Bryn D Webb, David A Stroud, et al.
American Journal of Human Genetics|August 5, 2017
Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh SyndromeNicole J Lake, Bryn D Webb, David A Stroud, et al.
Nature Communications|July 7, 2017
A defect in myoblast fusion underlies Carey-Fineman-Ziter syndromeSilvio Alessandro Di Gioia, Samantha Connors, Norisada Matsunami, et al.
Human Genetics|October 15, 2021
TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathyMary C Whitman, Brenda J Barry, Caroline D Robson, et al.
Pageof 82

Showing results (791-800 of 812) with videos related to

Sort By:
Pageof 82
Space Science Reviews|August 8, 2025
The Magnetic Search Coil (MSC) on the TRACERS MissionG B Hospodarsky, A J Carton, R T Dvorsky, et al.
Nature Genetics|April 30, 2008
Integrated genomic approaches implicate osteoglycin (Ogn) in the regulation of left ventricular massEnrico Petretto, Rizwan Sarwar, Ian Grieve, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 26, 2025
BiomarkersMolly Olzinski, Yann Cobigo, Rowan Saloner, et al.
Theranostics|June 7, 2021
Prodromal neuroinflammatory, cholinergic and metabolite dysfunction detected by PET and MRS in the TgF344-AD transgenic rat model of AD: a collaborative multi-modal studyAisling M Chaney, Francisco R Lopez-Picon, Sophie Serrière, et al.
Arthritis and Rheumatism|September 18, 2010
Genetically determined Amerindian ancestry correlates with increased frequency of risk alleles for systemic lupus erythematosusElena Sanchez, Ryan D Webb, Astrid Rasmussen, et al.
The Canadian Journal of Cardiology|April 23, 2022
Canadian Cardiovascular Society 2022 Guidelines for Cardiovascular Interventions in Adults With Congenital Heart DiseaseAriane Marelli, Luc Beauchesne, Jack Colman, et al.
American Journal of Human Genetics|April 7, 2018
Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh SyndromeNicole J Lake, Bryn D Webb, David A Stroud, et al.
American Journal of Human Genetics|August 5, 2017
Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh SyndromeNicole J Lake, Bryn D Webb, David A Stroud, et al.
Nature Communications|July 7, 2017
A defect in myoblast fusion underlies Carey-Fineman-Ziter syndromeSilvio Alessandro Di Gioia, Samantha Connors, Norisada Matsunami, et al.
Human Genetics|October 15, 2021
TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathyMary C Whitman, Brenda J Barry, Caroline D Robson, et al.
Pageof 82