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A Cumming

Showing results (141-150 of 192) with videos related to

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Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|September 26, 2025
Human Cases of Carbapenemase-Producing Escherichia coli Linked to Spread Between Animals and the Environment in a Veterinary Facility -Massachusetts, USA, 2023Ian M DeStefano, Claire L Fellman, Paula M Snippes Vagnone, et al.
European Journal of Human Genetics : EJHG|July 4, 2018
De novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1Sarah A Cumming, Mark J Hamilton, Yvonne Robb, et al.
Bioorganic & Medicinal Chemistry Letters|September 1, 2010
A novel series of positive modulators of the AMPA receptor: discovery and structure based hit-to-lead studiesCraig Jamieson, Stephanie Basten, Robert A Campbell, et al.
Ebiomedicine|October 15, 2019
A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomesMarc Ciosi, Alastair Maxwell, Sarah A Cumming, et al.
Genes|November 11, 2020
Preliminary Findings on CTG Expansion Determination in Different Tissues from Patients with Myotonic Dystrophy Type 1Alfonsina Ballester-Lopez, Emma Koehorst, Ian Linares-Pardo, et al.
Genes|July 11, 2020
The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1Alfonsina Ballester-Lopez, Ian Linares-Pardo, Emma Koehorst, et al.
The Review of Scientific Instruments|February 2, 2011
Invited article: CO2 laser production of fused silica fibers for use in interferometric gravitational wave detector mirror suspensionsA Heptonstall, M A Barton, A Bell, et al.
Science Translational Medicine|February 12, 2025
Antisense oligonucleotide-mediated MSH3 suppression reduces somatic CAG repeat expansion in Huntington's disease iPSC-derived striatal neuronsEmma L Bunting, Jasmine Donaldson, Sarah A Cumming, et al.
Bioorganic & Medicinal Chemistry|April 19, 2022
Identification and optimisation of a pyrimidopyridone series of IRAK4 inhibitorsIain A Cumming, Sébastien L Degorce, Anna Aagaard, et al.
Human Mutation|October 15, 2019
A DM1 family with interruptions associated with atypical symptoms and late onset but not with a milder phenotypeAlfonsina Ballester-Lopez, Emma Koehorst, Miriam Almendrote, et al.
Pageof 20

Showing results (141-150 of 192) with videos related to

Sort By:
Pageof 20
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|September 26, 2025
Human Cases of Carbapenemase-Producing Escherichia coli Linked to Spread Between Animals and the Environment in a Veterinary Facility -Massachusetts, USA, 2023Ian M DeStefano, Claire L Fellman, Paula M Snippes Vagnone, et al.
European Journal of Human Genetics : EJHG|July 4, 2018
De novo repeat interruptions are associated with reduced somatic instability and mild or absent clinical features in myotonic dystrophy type 1Sarah A Cumming, Mark J Hamilton, Yvonne Robb, et al.
Bioorganic & Medicinal Chemistry Letters|September 1, 2010
A novel series of positive modulators of the AMPA receptor: discovery and structure based hit-to-lead studiesCraig Jamieson, Stephanie Basten, Robert A Campbell, et al.
Ebiomedicine|October 15, 2019
A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomesMarc Ciosi, Alastair Maxwell, Sarah A Cumming, et al.
Genes|November 11, 2020
Preliminary Findings on CTG Expansion Determination in Different Tissues from Patients with Myotonic Dystrophy Type 1Alfonsina Ballester-Lopez, Emma Koehorst, Ian Linares-Pardo, et al.
Genes|July 11, 2020
The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1Alfonsina Ballester-Lopez, Ian Linares-Pardo, Emma Koehorst, et al.
The Review of Scientific Instruments|February 2, 2011
Invited article: CO2 laser production of fused silica fibers for use in interferometric gravitational wave detector mirror suspensionsA Heptonstall, M A Barton, A Bell, et al.
Science Translational Medicine|February 12, 2025
Antisense oligonucleotide-mediated MSH3 suppression reduces somatic CAG repeat expansion in Huntington's disease iPSC-derived striatal neuronsEmma L Bunting, Jasmine Donaldson, Sarah A Cumming, et al.
Bioorganic & Medicinal Chemistry|April 19, 2022
Identification and optimisation of a pyrimidopyridone series of IRAK4 inhibitorsIain A Cumming, Sébastien L Degorce, Anna Aagaard, et al.
Human Mutation|October 15, 2019
A DM1 family with interruptions associated with atypical symptoms and late onset but not with a milder phenotypeAlfonsina Ballester-Lopez, Emma Koehorst, Miriam Almendrote, et al.
Pageof 20