檢索結果 - Jennifer Orthmann‐Murphy

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  1. 1
    Gap Junctions Couple Astrocytes and Oligodendrocytes

    Gap Junctions Couple Astrocytes and Oligodendrocytes 由 Jennifer Orthmann‐Murphy, Charles K. Abrams, Steven S. Scherer

    出版 2008
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  2. 2
    Beyond relapses: How BTK inhibitors are shaping the future of progressive MS treatment

    Beyond relapses: How BTK inhibitors are shaping the future of progressive MS treatment 由 Laura R Naydovich, Jennifer Orthmann‐Murphy, Clyde Markowitz

    出版 2025
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  3. 3
    Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus–Merzbacher-like disease

    Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus–Merzbacher-like disease 由 Jennifer Orthmann‐Murphy, Alan D. Enriquez, Charles K. Abrams, Steven S. Scherer

    出版 2007
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  4. 4
    Myelin remodeling through experience-dependent oligodendrogenesis in the adult somatosensory cortex

    Myelin remodeling through experience-dependent oligodendrogenesis in the adult somatosensory cortex 由 Ethan G. Hughes, Jennifer Orthmann‐Murphy, Abraham J. Langseth, Dwight E. Bergles

    出版 2018
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  5. 5
    Two Distinct Heterotypic Channels Mediate Gap Junction Coupling between Astrocyte and Oligodendrocyte Connexins

    Two Distinct Heterotypic Channels Mediate Gap Junction Coupling between Astrocyte and Oligodendrocyte Connexins 由 Jennifer Orthmann‐Murphy, Mona M. Freidin, Esther Fischer, Steven S. Scherer, Charles K. Abrams

    出版 2007
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  6. 6
    Remyelination alters the pattern of myelin in the cerebral cortex

    Remyelination alters the pattern of myelin in the cerebral cortex 由 Jennifer Orthmann‐Murphy, Cody L. Call, Gian C Molina-Castro, Yu Chen Hsieh, Matthew N. Rasband, Peter A. Calabresi, Dwight E. Bergles

    出版 2020
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  7. 7
    Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations

    Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations 由 Jennifer Orthmann‐Murphy, Ettore Salsano, Charles K. Abrams, Alberto Bizzi, Graziella Uziel, Mona M. Freidin, Eleonora Lamantea, Massimo Zeviani, Steven S. Scherer, Davide Pareyson

    出版 2008
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  8. 8
    Lineage tracing reveals dynamic changes in oligodendrocyte precursor cells following cuprizone‐induced demyelination

    Lineage tracing reveals dynamic changes in oligodendrocyte precursor cells following cuprizone‐induced demyelination 由 Emily G. Baxi, Joseph DeBruin, Jing Jin, Hayley J. Strasburger, Matthew D. Smith, Jennifer Orthmann‐Murphy, Jason T. Schott, Amanda N. Fairchild, Dwight E. Bergles, Peter A. Calabresi

    出版 2017
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  9. 9
    Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia: Review of Clinical Manifestations as Foundations for Therapeutic Development

    Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia: Review of Clinical Manifestations as Foundations for Therapeutic Development 由 Spyros Papapetropoulos, Angela Pontius, Elizabeth Finger, Virginija Danylaité Karrenbauer, David S. Lynch, Matthew Brennan, Samantha Zappia, Wolfgang Koehler, Ludger Schoels, Stefanie N. Hayer, Takuya Konno, Takeshi Ikeuchi, Troy C. Lund, Jennifer Orthmann‐Murphy, Florian Eichler, Zbigniew K. Wszołek

    出版 2022
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