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Showing results (691-700 of 726) with videos related to

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Nature Ecology & Evolution|February 11, 2018
Author Correction: Genome expansion and lineage-specific genetic innovations in the forest pathogenic fungi ArmillariaGyörgy Sipos, Arun N Prasanna, Mathias C Walter, et al.
JAMA Oncology|January 28, 2021
Individualizing Surveillance Mammography for Older Patients After Treatment for Early-Stage Breast Cancer: Multidisciplinary Expert Panel and International Society of Geriatric Oncology Consensus StatementRachel A Freedman, Christina A Minami, Eric P Winer, et al.
Neurology. Clinical Practice|December 18, 2023
Life-Saving Treatments for Spinal Muscular Atrophy: Global Access and AvailabilityVictor D Armengol, Basil T Darras, Ahmad A Abulaban, et al.
Brain : a Journal of Neurology|September 2, 2009
Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathyRita Horvath, John P Kemp, Helen A L Tuppen, et al.
Neuromuscular Disorders : NMD|August 3, 2014
Selected items from the Charcot-Marie-Tooth (CMT) Neuropathy Score and secondary clinical outcome measures serve as sensitive clinical markers of disease severity in CMT1A patientsManoj Mannil, Alessandra Solari, Andreas Leha, et al.
Nature Cell Biology|June 10, 2021
ELOF1 is a transcription-coupled DNA repair factor that directs RNA polymerase II ubiquitylationYana van der Weegen, Klaas de Lint, Diana van den Heuvel, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|September 22, 2021
NCCN Guidelines® Insights: Older Adult Oncology, Version 1.2021Efrat Dotan, Louise C Walter, Ilene S Browner, et al.
Brain : a Journal of Neurology|February 17, 2024
Biallelic variants in SNUPN cause a limb girdle muscular dystrophy with myofibrillar-like featuresPablo Iruzubieta, Alberto Damborenea, Mihaela Ioghen, et al.
Muscle & Nerve|February 18, 2022
Cardiac and pulmonary findings in dysferlinopathy: A 3-year, longitudinal studyUrsula Moore, Roberto Fernandez-Torron, Marni Jacobs, et al.
Disease Models & Mechanisms|November 19, 2021
A scalable, clinically severe pig model for Duchenne muscular dystrophyMichael Stirm, Lina Marie Fonteyne, Bachuki Shashikadze, et al.
Pageof 73

Showing results (691-700 of 726) with videos related to

Sort By:
Pageof 73
Nature Ecology & Evolution|February 11, 2018
Author Correction: Genome expansion and lineage-specific genetic innovations in the forest pathogenic fungi ArmillariaGyörgy Sipos, Arun N Prasanna, Mathias C Walter, et al.
JAMA Oncology|January 28, 2021
Individualizing Surveillance Mammography for Older Patients After Treatment for Early-Stage Breast Cancer: Multidisciplinary Expert Panel and International Society of Geriatric Oncology Consensus StatementRachel A Freedman, Christina A Minami, Eric P Winer, et al.
Neurology. Clinical Practice|December 18, 2023
Life-Saving Treatments for Spinal Muscular Atrophy: Global Access and AvailabilityVictor D Armengol, Basil T Darras, Ahmad A Abulaban, et al.
Brain : a Journal of Neurology|September 2, 2009
Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathyRita Horvath, John P Kemp, Helen A L Tuppen, et al.
Neuromuscular Disorders : NMD|August 3, 2014
Selected items from the Charcot-Marie-Tooth (CMT) Neuropathy Score and secondary clinical outcome measures serve as sensitive clinical markers of disease severity in CMT1A patientsManoj Mannil, Alessandra Solari, Andreas Leha, et al.
Nature Cell Biology|June 10, 2021
ELOF1 is a transcription-coupled DNA repair factor that directs RNA polymerase II ubiquitylationYana van der Weegen, Klaas de Lint, Diana van den Heuvel, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|September 22, 2021
NCCN Guidelines® Insights: Older Adult Oncology, Version 1.2021Efrat Dotan, Louise C Walter, Ilene S Browner, et al.
Brain : a Journal of Neurology|February 17, 2024
Biallelic variants in SNUPN cause a limb girdle muscular dystrophy with myofibrillar-like featuresPablo Iruzubieta, Alberto Damborenea, Mihaela Ioghen, et al.
Muscle & Nerve|February 18, 2022
Cardiac and pulmonary findings in dysferlinopathy: A 3-year, longitudinal studyUrsula Moore, Roberto Fernandez-Torron, Marni Jacobs, et al.
Disease Models & Mechanisms|November 19, 2021
A scalable, clinically severe pig model for Duchenne muscular dystrophyMichael Stirm, Lina Marie Fonteyne, Bachuki Shashikadze, et al.
Pageof 73