Resultados de procura - Michele D. Binder
- Mostrando 1 - 6 Resultados de 6
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Gas6 Deficiency Increases Oligodendrocyte Loss and Microglial Activation in Response to Cuprizone-Induced Demyelination por Michele D. Binder, Holly S. Cate, Anne L. Prieto, Dennis Kemper, Helmut Butzkueven, Melissa Gresle, Tania Cipriani, Vilija Jokubaitis, Peter Carmeliet, Trevor J. Kilpatrick
Publicado 2008Artigo -
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MRI identification of the rostral‐caudal pattern of pathology within the corpus callosum in the cuprizone mouse model por Qizhu Wu, Qing Yang, Holly S. Cate, Dennis Kemper, Michele D. Binder, Hongxin Wang, Ke Fang, Melissa J. Quick, Mark Marriott, Trevor J. Kilpatrick, Gary F. Egan
Publicado 2007Artigo -
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Suppressor of cytokine signaling 3 limits protection of leukemia inhibitory factor receptor signaling against central demyelination por Ben Emery, Holly S. Cate, Mark Marriott, Tobias D. Merson, Michele D. Binder, Cameron Snell, Pik Ying Soo, Simon S. Murray, Ben A. Croker, Jian‐Guo Zhang, Warren S. Alexander, Helen Cooper, Helmut Butzkueven, Trevor J. Kilpatrick
Publicado 2006Artigo -
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Common and Low Frequency Variants in MERTK Are Independently Associated with Multiple Sclerosis Susceptibility with Discordant Association Dependent upon HLA-DRB1*15:01 Status por Michele D. Binder, Andrew Fox, Daniel Merlo, Laura Johnson, Lauren Giuffrida, Sarah E. Calvert, Rainer Akkermann, Z. M. Gerry, Ashwyn A Perera, Melissa Gresle, Louise Laverick, Grace Foo, Marzena J. Fabis‐Pedrini, Timothy Spelman, Margaret A. Jordan, Alan G. Baxter, Simon J. Foote, Helmut Butzkueven, Trevor J. Kilpatrick, Judith Field
Publicado 2016Artigo
Ferramentas de procura:
Materias Relacionadas
Biology
Immunology
Central nervous system
Medicine
Multiple sclerosis
Myelin
Receptor tyrosine kinase
Cell biology
Internal medicine
MERTK
Neuroscience
Oligodendrocyte
Receptor
Signal transduction
Corpus callosum
GAS6
Gene
Genetics
Pathology
Anatomy
Biochemistry
Cancer research
Cytokine
Diffusion MRI
Disease
Effective diffusion coefficient
Endocrinology
Genetic association
Genetic predisposition
Genotype