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Age-related decline in oligodendrogenesis retards white matter repair in mice. [electronic resource] by
- Miyamoto, Nobukazu
- Pham, Loc-Duyen D
- Hayakawa, Kazuhide
- Matsuzaki, Toshinori
- Seo, Ji Hae
- Magnain, Caroline
- Ayata, Cenk
- Kim, Kyu-Won
- Boas, David
- Lo, Eng H
- Arai, Ken
Producer: 20131118
In:
Stroke vol. 44
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16562.
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Endogenous GABA controls oligodendrocyte lineage cell number, myelination, and CNS internode length. [electronic resource] by
- Hamilton, Nicola B
- Clarke, Laura E
- Arancibia-Carcamo, I Lorena
- Kougioumtzidou, Eleni
- Matthey, Moritz
- Káradóttir, Ragnhildur
- Whiteley, Louise
- Bergersen, Linda H
- Richardson, William D
- Attwell, David
Producer: 20180112
In:
Glia vol. 65
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16564.
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16565.
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16566.
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Vitamin D receptor-retinoid X receptor heterodimer signaling regulates oligodendrocyte progenitor cell differentiation. [electronic resource] by
- de la Fuente, Alerie Guzman
- Errea, Oihana
- van Wijngaarden, Peter
- Gonzalez, Ginez A
- Kerninon, Christophe
- Jarjour, Andrew A
- Lewis, Hilary J
- Jones, Clare A
- Nait-Oumesmar, Brahim
- Zhao, Chao
- Huang, Jeffrey K
- ffrench-Constant, Charles
- Franklin, Robin J M
Producer: 20160405
In:
The Journal of cell biology vol. 211
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16567.
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GD1a Overcomes Inhibition of Myelination by Fibronectin via Activation of Protein Kinase A: Implications for Multiple Sclerosis. [electronic resource] by
- Qin, Jing
- Sikkema, Arend H
- van der Bij, Kristine
- de Jonge, Jenny C
- Klappe, Karin
- Nies, Vera
- Jonker, Johan W
- Kok, Jan Willem
- Hoekstra, Dick
- Baron, Wia
Producer: 20171023
In:
The Journal of neuroscience : the official journal of the Society for Neuroscience vol. 37
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16569.
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Loss of mTORC2 signaling in oligodendrocyte precursor cells delays myelination. [electronic resource] by
- Grier, Mark D
- West, Kathryn L
- Kelm, Nathaniel D
- Fu, Cary
- Does, Mark D
- Parker, Brittany
- McBrier, Eleanor
- Lagrange, Andre H
- Ess, Kevin C
- Carson, Robert P
Producer: 20171205
In:
PloS one vol. 12
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16570.
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Combined fetal inflammation and postnatal hypoxia causes myelin deficits and autism-like behavior in a rat model of diffuse white matter injury. [electronic resource] by
- van Tilborg, Erik
- Achterberg, E J Marijke
- van Kammen, Caren M
- van der Toorn, Annette
- Groenendaal, Floris
- Dijkhuizen, Rick M
- Heijnen, Cobi J
- Vanderschuren, Louk J M J
- Benders, Manon N J L
- Nijboer, Cora H A
Producer: 20180702
In:
Glia vol. 66
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16573.
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Homozygous mutation in MFSD2A, encoding a lysolipid transporter for docosahexanoic acid, is associated with microcephaly and hypomyelination. [electronic resource] by
- Harel, Tamar
- Quek, Debra Q Y
- Wong, Bernice H
- Cazenave-Gassiot, Amaury
- Wenk, Markus R
- Fan, Hao
- Berger, Itai
- Shmueli, Dorit
- Shaag, Avraham
- Silver, David L
- Elpeleg, Orly
- Edvardson, Shimon
Producer: 20190925
In:
Neurogenetics vol. 19
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16574.
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16575.
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16576.
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16577.
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16578.
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16579.
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16580.
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