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S Scherer

Showing results (381-390 of 519) with videos related to

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Neurology|December 1, 2017
Neurofascin antibodies in autoimmune, genetic, and idiopathic neuropathiesElisabeth Burnor, Li Yang, Hao Zhou, et al.
Journal of the Peripheral Nervous System : JPNS|June 4, 2023
Recruiting for an International Rare Disease Clinical Trial Readiness Study during the COVID-19 pandemic: Challenges and solutionsKaty Eichinger, Steffen Behrens-Spraggins, Janet E Sowden, et al.
Neurology|April 24, 2015
A novel AARS mutation in a family with dominant myeloneuropathyWilliam W Motley, Laurie B Griffin, Inès Mademan, et al.
Biomaterials|April 25, 2015
Novel micropatterns mechanically control fibrotic reactions at the surface of silicone implantsHicham Majd, Saja S Scherer, Stellar Boo, et al.
Science (New York, N.Y.)|March 19, 1993
Released form of CNTF receptor alpha component as a soluble mediator of CNTF responsesS Davis, T H Aldrich, N Y Ip, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|September 25, 2007
Reduction of gangliosides, phospholipids and cholesterol content in cerebral cortex of rats caused by chronic hypermethioninemiaFrancieli M Stefanello, Fernando Kreutz, Emilene B S Scherer, et al.
Journal of Lipid Research|May 1, 1999
Comprehensive evaluation of isoprenoid biosynthesis regulation in Saccharomyces cerevisiae utilizing the Genome Reporter MatrixD Dimster-Denk, J Rine, J Phillips, et al.
Journal of Palliative Medicine|February 28, 2019
The Cambia Sojourns Scholars Leadership Program: Projects and Reflections on Leadership in Palliative CareConstance Dahlin, Justin Sanders, Brook Calton, et al.
Nature Neuroscience|June 15, 2007
A central role for Necl4 (SynCAM4) in Schwann cell-axon interaction and myelinationIvo Spiegel, Konstantin Adamsky, Yael Eshed, et al.
Genomics|November 1, 1996
Chromosomal localization in mouse and human of the vasoactive intestinal peptide receptor type 2 gene: a possible contributor to the holoprosencephaly 3 phenotypeM Mackay, J Fantes, S Scherer, et al.
Pageof 52

Showing results (381-390 of 519) with videos related to

Sort By:
Pageof 52
Neurology|December 1, 2017
Neurofascin antibodies in autoimmune, genetic, and idiopathic neuropathiesElisabeth Burnor, Li Yang, Hao Zhou, et al.
Journal of the Peripheral Nervous System : JPNS|June 4, 2023
Recruiting for an International Rare Disease Clinical Trial Readiness Study during the COVID-19 pandemic: Challenges and solutionsKaty Eichinger, Steffen Behrens-Spraggins, Janet E Sowden, et al.
Neurology|April 24, 2015
A novel AARS mutation in a family with dominant myeloneuropathyWilliam W Motley, Laurie B Griffin, Inès Mademan, et al.
Biomaterials|April 25, 2015
Novel micropatterns mechanically control fibrotic reactions at the surface of silicone implantsHicham Majd, Saja S Scherer, Stellar Boo, et al.
Science (New York, N.Y.)|March 19, 1993
Released form of CNTF receptor alpha component as a soluble mediator of CNTF responsesS Davis, T H Aldrich, N Y Ip, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|September 25, 2007
Reduction of gangliosides, phospholipids and cholesterol content in cerebral cortex of rats caused by chronic hypermethioninemiaFrancieli M Stefanello, Fernando Kreutz, Emilene B S Scherer, et al.
Journal of Lipid Research|May 1, 1999
Comprehensive evaluation of isoprenoid biosynthesis regulation in Saccharomyces cerevisiae utilizing the Genome Reporter MatrixD Dimster-Denk, J Rine, J Phillips, et al.
Journal of Palliative Medicine|February 28, 2019
The Cambia Sojourns Scholars Leadership Program: Projects and Reflections on Leadership in Palliative CareConstance Dahlin, Justin Sanders, Brook Calton, et al.
Nature Neuroscience|June 15, 2007
A central role for Necl4 (SynCAM4) in Schwann cell-axon interaction and myelinationIvo Spiegel, Konstantin Adamsky, Yael Eshed, et al.
Genomics|November 1, 1996
Chromosomal localization in mouse and human of the vasoactive intestinal peptide receptor type 2 gene: a possible contributor to the holoprosencephaly 3 phenotypeM Mackay, J Fantes, S Scherer, et al.
Pageof 52