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J Dowling

Showing results (381-390 of 493) with videos related to

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Orphanet Journal of Rare Diseases|August 8, 2013
Genotype-phenotype correlations in recessive RYR1-related myopathiesKimberly Amburgey, Angela Bailey, Jean H Hwang, et al.
Disease Models & Mechanisms|January 18, 2024
Standardization of zebrafish drug testing parameters for muscle diseasesMuthukumar Karuppasamy, Katherine G English, Clarissa A Henry, et al.
Plos Genetics|June 10, 2011
Pathogenic mechanism of the FIG4 mutation responsible for Charcot-Marie-Tooth disease CMT4JGuy M Lenk, Cole J Ferguson, Clement Y Chow, et al.
NPJ Quantum Information|September 29, 2025
A 2-Gbps low-SWaP quantum random number generator with photonic integrated circuits for satellite applicationsOliver M Crampton, Toby J Dowling, Thomas Roger, et al.
Plos Neglected Tropical Diseases|June 6, 2012
The Sigma class glutathione transferase from the liver fluke Fasciola hepaticaE James LaCourse, Samirah Perally, Russell M Morphew, et al.
Biorxiv : the Preprint Server for Biology|July 21, 2022
Adjuvant Discovery via a High Throughput Screen using Human Primary Mononuclear CellsKatherine Chew, Branden Lee, Simon D van Haren, et al.
Neuromuscular Disorders : NMD|April 26, 2011
King-Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) geneJames J Dowling, Suzanne Lillis, Kimberley Amburgey, et al.
Science Translational Medicine|July 24, 2024
Adjuvantation of a SARS-CoV-2 mRNA vaccine with controlled tissue-specific expression of an mRNA encoding IL-12p70Byron Brook, Valerie Duval, Soumik Barman, et al.
Human Mutation|December 26, 2001
Clinical and molecular basis of classical lissencephaly: Mutations in the LIS1 gene (PAFAH1B1)Carlos Cardoso, Richard J Leventer, James J Dowling, et al.
Disease Models & Mechanisms|May 31, 2012
Myotubular myopathy and the neuromuscular junction: a novel therapeutic approach from mouse modelsJames J Dowling, Romain Joubert, Sean E Low, et al.
Pageof 50

Showing results (381-390 of 493) with videos related to

Sort By:
Pageof 50
Orphanet Journal of Rare Diseases|August 8, 2013
Genotype-phenotype correlations in recessive RYR1-related myopathiesKimberly Amburgey, Angela Bailey, Jean H Hwang, et al.
Disease Models & Mechanisms|January 18, 2024
Standardization of zebrafish drug testing parameters for muscle diseasesMuthukumar Karuppasamy, Katherine G English, Clarissa A Henry, et al.
Plos Genetics|June 10, 2011
Pathogenic mechanism of the FIG4 mutation responsible for Charcot-Marie-Tooth disease CMT4JGuy M Lenk, Cole J Ferguson, Clement Y Chow, et al.
NPJ Quantum Information|September 29, 2025
A 2-Gbps low-SWaP quantum random number generator with photonic integrated circuits for satellite applicationsOliver M Crampton, Toby J Dowling, Thomas Roger, et al.
Plos Neglected Tropical Diseases|June 6, 2012
The Sigma class glutathione transferase from the liver fluke Fasciola hepaticaE James LaCourse, Samirah Perally, Russell M Morphew, et al.
Biorxiv : the Preprint Server for Biology|July 21, 2022
Adjuvant Discovery via a High Throughput Screen using Human Primary Mononuclear CellsKatherine Chew, Branden Lee, Simon D van Haren, et al.
Neuromuscular Disorders : NMD|April 26, 2011
King-Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) geneJames J Dowling, Suzanne Lillis, Kimberley Amburgey, et al.
Science Translational Medicine|July 24, 2024
Adjuvantation of a SARS-CoV-2 mRNA vaccine with controlled tissue-specific expression of an mRNA encoding IL-12p70Byron Brook, Valerie Duval, Soumik Barman, et al.
Human Mutation|December 26, 2001
Clinical and molecular basis of classical lissencephaly: Mutations in the LIS1 gene (PAFAH1B1)Carlos Cardoso, Richard J Leventer, James J Dowling, et al.
Disease Models & Mechanisms|May 31, 2012
Myotubular myopathy and the neuromuscular junction: a novel therapeutic approach from mouse modelsJames J Dowling, Romain Joubert, Sean E Low, et al.
Pageof 50