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Thomas Robertson

Showing results (91-100 of 115) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|February 19, 2024
Loss-of-function variants in <i>JPH1</i> cause congenital myopathy with prominent facial involvementMridul Johari, Ana Topf, Chiara Folland, et al.
Journal of General Internal Medicine|June 3, 2022
Elements Influencing Recruitment and Retention of Millennial Hospitalists Born in or after 1982: a Survey-Based StudyAmteshwar Singh, Tiffani Panek, Sean Tackett, et al.
The Chinese Journal of Physiology|July 13, 2006
Redistribution of blood flow and lung volume between lungs in lateral decubitus postures during unilateral atelectasis and PEEPHung Chang, Stephen J Lai-Fook, Karen B Domino, et al.
Acta Neuropathologica Communications|November 21, 2013
G-protein coupled receptor expression patterns delineate medulloblastoma subgroupsKelsey L Whittier, Erin A Boese, Katherine N Gibson-Corley, et al.
Scientific Reports|January 20, 2018
The ten-year evolutionary trajectory of a highly recurrent paediatric high grade neuroepithelial tumour with MN1:BEND2 fusionAnna Burford, Alan Mackay, Sergey Popov, et al.
Acta Neuropathologica|February 14, 2023
SMARCA4-associated schwannomatosisFiona Chan-Pak-Choon, Carla Roca, Anne-Sophie Chong, et al.
Journal of Medical Genetics|August 29, 2024
Loss-of-function variants in <i>JPH1</i> cause congenital myopathy with prominent facial and ocular involvementMridul Johari, Ana Topf, Chiara Folland, et al.
Genome Medicine|May 1, 2023
Spatial transcriptomic analysis of Sonic hedgehog medulloblastoma identifies that the loss of heterogeneity and promotion of differentiation underlies the response to CDK4/6 inhibitionTuan Vo, Brad Balderson, Kahli Jones, et al.
Molecular Genetics and Metabolism|June 28, 2024
Molecular genetic analysis of candidate genes for glutaric aciduria type II in a cohort of patients from Queensland, AustraliaKalliope Demetriou, Janelle Nisbet, David Coman, et al.
Journal of Medical Genetics|February 22, 2023
Germline pathogenic <i>SMARCA4</i> variants in neuroblastomaLeora Witkowski, Kim E Nichols, Marjolijn Jongmans, et al.
Pageof 12

Showing results (91-100 of 115) with videos related to

Sort By:
Pageof 12
Medrxiv : the Preprint Server for Health Sciences|February 19, 2024
Loss-of-function variants in <i>JPH1</i> cause congenital myopathy with prominent facial involvementMridul Johari, Ana Topf, Chiara Folland, et al.
Journal of General Internal Medicine|June 3, 2022
Elements Influencing Recruitment and Retention of Millennial Hospitalists Born in or after 1982: a Survey-Based StudyAmteshwar Singh, Tiffani Panek, Sean Tackett, et al.
The Chinese Journal of Physiology|July 13, 2006
Redistribution of blood flow and lung volume between lungs in lateral decubitus postures during unilateral atelectasis and PEEPHung Chang, Stephen J Lai-Fook, Karen B Domino, et al.
Acta Neuropathologica Communications|November 21, 2013
G-protein coupled receptor expression patterns delineate medulloblastoma subgroupsKelsey L Whittier, Erin A Boese, Katherine N Gibson-Corley, et al.
Scientific Reports|January 20, 2018
The ten-year evolutionary trajectory of a highly recurrent paediatric high grade neuroepithelial tumour with MN1:BEND2 fusionAnna Burford, Alan Mackay, Sergey Popov, et al.
Acta Neuropathologica|February 14, 2023
SMARCA4-associated schwannomatosisFiona Chan-Pak-Choon, Carla Roca, Anne-Sophie Chong, et al.
Journal of Medical Genetics|August 29, 2024
Loss-of-function variants in <i>JPH1</i> cause congenital myopathy with prominent facial and ocular involvementMridul Johari, Ana Topf, Chiara Folland, et al.
Genome Medicine|May 1, 2023
Spatial transcriptomic analysis of Sonic hedgehog medulloblastoma identifies that the loss of heterogeneity and promotion of differentiation underlies the response to CDK4/6 inhibitionTuan Vo, Brad Balderson, Kahli Jones, et al.
Molecular Genetics and Metabolism|June 28, 2024
Molecular genetic analysis of candidate genes for glutaric aciduria type II in a cohort of patients from Queensland, AustraliaKalliope Demetriou, Janelle Nisbet, David Coman, et al.
Journal of Medical Genetics|February 22, 2023
Germline pathogenic <i>SMARCA4</i> variants in neuroblastomaLeora Witkowski, Kim E Nichols, Marjolijn Jongmans, et al.
Pageof 12