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Anne Martin

Showing results (211-220 of 249) with videos related to

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Neuron|September 29, 2017
Heterophilic Type II Cadherins Are Required for High-Magnitude Synaptic Potentiation in the HippocampusRaunak Basu, Xin Duan, Matthew R Taylor, et al.
The Lancet. HIV|November 20, 2019
Doravirine versus ritonavir-boosted darunavir in antiretroviral-naive adults with HIV-1 (DRIVE-FORWARD): 96-week results of a randomised, double-blind, non-inferiority, phase 3 trialJean-Michel Molina, Kathleen Squires, Paul E Sax, et al.
Plos One|January 10, 2020
Assessment of peritoneal microbial features and tumor marker levels as potential diagnostic tools for ovarian cancerRuizhong Miao, Taylor C Badger, Kathleen Groesch, et al.
Medicine and Science in Sports and Exercise|October 18, 2017
Validation of a Novel Device to Measure and Provide Feedback on Sedentary BehaviorJason M R Gill, Nabeha S A Hawari, Douglas J Maxwell, et al.
Nature Genetics|March 2, 2011
Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndromeLouise S Bicknell, Sarah Walker, Anna Klingseisen, et al.
BMC Medical Informatics and Decision Making|December 19, 2019
Promoting healthy teenage behaviour across three European countries through the use of a novel smartphone technology platform, PEGASO fit for future: study protocol of a quasi-experimental, controlled, multi-Centre trialElisa Puigdomenech, Anne Martin, Alexandra Lang, et al.
American Journal of Ophthalmology|May 12, 2019
Clinical and Molecular Characterization of Familial Exudative Vitreoretinopathy Associated With MicrocephalySarah Hull, Gavin Arno, Pia Ostergaard, et al.
Experimental Neurology|June 13, 2017
Fumarate decreases edema volume and improves functional outcome after experimental strokeBettina Hjelm Clausen, Louise Lundberg, Minna Yli-Karjanmaa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2020
Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathyDavid A Parry, Carol-Anne Martin, Philip Greene, et al.
Plos One|April 27, 2022
Novel assays to investigate the mechanisms of latent infection with HIV-2Michael D Lu, Sushama Telwatte, Nitasha Kumar, et al.
Pageof 25

Showing results (211-220 of 249) with videos related to

Sort By:
Pageof 25
Neuron|September 29, 2017
Heterophilic Type II Cadherins Are Required for High-Magnitude Synaptic Potentiation in the HippocampusRaunak Basu, Xin Duan, Matthew R Taylor, et al.
The Lancet. HIV|November 20, 2019
Doravirine versus ritonavir-boosted darunavir in antiretroviral-naive adults with HIV-1 (DRIVE-FORWARD): 96-week results of a randomised, double-blind, non-inferiority, phase 3 trialJean-Michel Molina, Kathleen Squires, Paul E Sax, et al.
Plos One|January 10, 2020
Assessment of peritoneal microbial features and tumor marker levels as potential diagnostic tools for ovarian cancerRuizhong Miao, Taylor C Badger, Kathleen Groesch, et al.
Medicine and Science in Sports and Exercise|October 18, 2017
Validation of a Novel Device to Measure and Provide Feedback on Sedentary BehaviorJason M R Gill, Nabeha S A Hawari, Douglas J Maxwell, et al.
Nature Genetics|March 2, 2011
Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndromeLouise S Bicknell, Sarah Walker, Anna Klingseisen, et al.
BMC Medical Informatics and Decision Making|December 19, 2019
Promoting healthy teenage behaviour across three European countries through the use of a novel smartphone technology platform, PEGASO fit for future: study protocol of a quasi-experimental, controlled, multi-Centre trialElisa Puigdomenech, Anne Martin, Alexandra Lang, et al.
American Journal of Ophthalmology|May 12, 2019
Clinical and Molecular Characterization of Familial Exudative Vitreoretinopathy Associated With MicrocephalySarah Hull, Gavin Arno, Pia Ostergaard, et al.
Experimental Neurology|June 13, 2017
Fumarate decreases edema volume and improves functional outcome after experimental strokeBettina Hjelm Clausen, Louise Lundberg, Minna Yli-Karjanmaa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 9, 2020
Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathyDavid A Parry, Carol-Anne Martin, Philip Greene, et al.
Plos One|April 27, 2022
Novel assays to investigate the mechanisms of latent infection with HIV-2Michael D Lu, Sushama Telwatte, Nitasha Kumar, et al.
Pageof 25