検索結果 - D. A. Yool
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1
The proteolipid protein gene and myelin disorders in man and animal models 著者: D. A. Yool
出版事項 2000Revisão -
2
Oligodendroglial modulation of fast axonal transport in a mouse model of hereditary spastic paraplegia 著者: Julia M. Edgar, Marκ McLaughlin, D. A. Yool, Su-Chun Zhang, Jill H. Fowler, Paul Montague, Jennifer A. Barrie, Mailis C. McCulloch, Ian D. Duncan, James Garbern, Klaus Armin Nave, Ian R. Griffiths
出版事項 2004Artigo -
3
Patients lacking the major CNS myelin protein, proteolipid protein 1, develop length-dependent axonal degeneration in the absence of demyelination and inflammation 著者: James Garbern, D. A. Yool, Gregory J. Moore, Ian B Wilds, Michael W. Faulk, Matthias Klugmann, K.-A. Nave, Erik A. Sistermans, Marjo S. van der Knaap, Thomas D. Bird, Michael E. Shy, John Kamholz, Ian R. Griffiths
出版事項 2002Artigo -
4
Effect of clinical signs, endocrinopathies, timing of surgery, hyperlipidemia, and hyperbilirubinemia on outcome in dogs with gallbladder mucocele 著者: Jared A. Jaffey, Michelle Pavlick, Cynthia R. L. Webster, G. E. Moore, Kristen A. McDaniel, Shauna L. Blois, Évelin Maria Brand, Colin F. Reich, Laura O. Motschenbacher, Eric T. Hostnik, Dong-Shuai Su, Jonathan A. Lidbury, O. Raab, Susan Venn Carr, Kasey Mabry, W. Alexander Fox‐Alvarez, S. Townsend, Shannon M. Palermo, Y. Nakazono, Koichi Ohno, E. VanEerde, Hille Fieten, Alma H. Hulsman, K. Cooley-Lock, Mark Dunning, Caroline Kisielewicz, Andrea Zoia, Marco Caldín, Andreza Conti‐Patara, Lcyda Ross, Caroline Mansfield, O. Lynn, Melissa A. Claus, Penny Watson, Adam Swallow, D. A. Yool, Kris Gommeren, Michael Knops, V. Ceplecha, H. de Rooster, Remo Lobetti, Olivier Dossin, Florence Jolivet, Lysimachos G. Papazoglou, M Pappalardo, Ferenc Manczur, Zoltán Dudás-Györki, Emma J. O’Neill, Clara Galán Martínez, Arnon Gal, Robert L. Owen, Elizabeth Gunn, K. Brown, Lena Harder, Christine Griebsch, Kristin P. Anfinsen, Tone K. Grøn, Veronica Marchetti, Romy M. Heilmann, P. Pazzi, Amy E. DeClue
出版事項 2019Artigo
関連主題
Biology
Central nervous system
Myelin
Neuroscience
Gene
Genetics
Medicine
Myelin basic protein
Phenotype
Proteolipid protein 1
Axon
Axonal degeneration
Axoplasmic transport
Cell biology
Degeneration (medical)
Gallbladder
Gastroenterology
Hereditary spastic paraplegia
Immunology
Internal medicine
Jaundice
Loss function
Magnetic resonance imaging
Missense mutation
Multiple sclerosis
Mutation
Myelin proteolipid protein
Odds ratio
Oligodendrocyte
Pathology