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L Oliver

Showing results (761-770 of 874) with videos related to

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 12, 2003
A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouseAdrian M Isaacs, Peter L Oliver, Emma L Jones, et al.
European Journal of Human Genetics : EJHG|March 24, 2020
Familial adult myoclonic epilepsy type 1 SAMD12 TTTCA repeat expansion arose 17,000 years ago and is present in Sri Lankan and Indian familiesMark F Bennett, Karen L Oliver, Brigid M Regan, et al.
American Journal of Physiology. Heart and Circulatory Physiology|July 14, 2023
Neurovascular coupling and cerebrovascular hemodynamics are modified by exercise training status at different stages of maturation during youthJack S Talbot, Dean R Perkins, Tony G Dawkins, et al.
Neurobiology of Disease|October 15, 2013
Region-specific deficits in dopamine, but not norepinephrine, signaling in a novel A30P α-synuclein BAC transgenic mouseTonya N Taylor, Dawid Potgieter, Sabina Anwar, et al.
Neurology|July 15, 2016
Diagnosis and misdiagnosis of adult neuronal ceroid lipofuscinosis (Kufs disease)Samuel F Berkovic, John F Staropoli, Stirling Carpenter, et al.
Stem Cell Research|April 28, 2009
Establishment and characterization of baboon embryonic stem cell lines: an Old World Primate model for regeneration and transplantation researchCalvin R Simerly, Christopher S Navara, Carlos A Castro, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 9, 2004
Mice lacking pro-opiomelanocortin are sensitive to high-fat feeding but respond normally to the acute anorectic effects of peptide-YY(3-36)B G Challis, A P Coll, G S H Yeo, et al.
Nature Structural & Molecular Biology|October 13, 2014
Cross-talking noncoding RNAs contribute to cell-specific neurodegeneration in SCA7Jennifer Y Tan, Keith W Vance, Miguel A Varela, et al.
Ebiomedicine|May 31, 2022
Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discoveryKaren L Oliver, Colin A Ellis, Ingrid E Scheffer, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2024
Loss of TDP-43 induces synaptic dysfunction that is rescued by <i>UNC13A</i> splice-switching ASOsMatthew J Keuss, Peter Harley, Eugeni Ryadnov, et al.
Pageof 88

Showing results (761-770 of 874) with videos related to

Sort By:
Pageof 88
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 12, 2003
A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouseAdrian M Isaacs, Peter L Oliver, Emma L Jones, et al.
European Journal of Human Genetics : EJHG|March 24, 2020
Familial adult myoclonic epilepsy type 1 SAMD12 TTTCA repeat expansion arose 17,000 years ago and is present in Sri Lankan and Indian familiesMark F Bennett, Karen L Oliver, Brigid M Regan, et al.
American Journal of Physiology. Heart and Circulatory Physiology|July 14, 2023
Neurovascular coupling and cerebrovascular hemodynamics are modified by exercise training status at different stages of maturation during youthJack S Talbot, Dean R Perkins, Tony G Dawkins, et al.
Neurobiology of Disease|October 15, 2013
Region-specific deficits in dopamine, but not norepinephrine, signaling in a novel A30P α-synuclein BAC transgenic mouseTonya N Taylor, Dawid Potgieter, Sabina Anwar, et al.
Neurology|July 15, 2016
Diagnosis and misdiagnosis of adult neuronal ceroid lipofuscinosis (Kufs disease)Samuel F Berkovic, John F Staropoli, Stirling Carpenter, et al.
Stem Cell Research|April 28, 2009
Establishment and characterization of baboon embryonic stem cell lines: an Old World Primate model for regeneration and transplantation researchCalvin R Simerly, Christopher S Navara, Carlos A Castro, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 9, 2004
Mice lacking pro-opiomelanocortin are sensitive to high-fat feeding but respond normally to the acute anorectic effects of peptide-YY(3-36)B G Challis, A P Coll, G S H Yeo, et al.
Nature Structural & Molecular Biology|October 13, 2014
Cross-talking noncoding RNAs contribute to cell-specific neurodegeneration in SCA7Jennifer Y Tan, Keith W Vance, Miguel A Varela, et al.
Ebiomedicine|May 31, 2022
Common risk variants for epilepsy are enriched in families previously targeted for rare monogenic variant discoveryKaren L Oliver, Colin A Ellis, Ingrid E Scheffer, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2024
Loss of TDP-43 induces synaptic dysfunction that is rescued by <i>UNC13A</i> splice-switching ASOsMatthew J Keuss, Peter Harley, Eugeni Ryadnov, et al.
Pageof 88