298 related articles for article (PubMed ID: 12805295)
21. Pathologic and phenotypic alterations in a mouse expressing a connexin47 missense mutation that causes Pelizaeus-Merzbacher-like disease in humans.
Tress O; Maglione M; Zlomuzica A; May D; Dicke N; Degen J; Dere E; Kettenmann H; Hartmann D; Willecke K
PLoS Genet; 2011 Jul; 7(7):e1002146. PubMed ID: 21750683
[TBL] [Abstract][Full Text] [Related]
22. Deletion of oligodendrocyte Cx32 and astrocyte Cx43 causes white matter vacuolation, astrocyte loss and early mortality.
Magnotti LM; Goodenough DA; Paul DL
Glia; 2011 Jul; 59(7):1064-74. PubMed ID: 21538560
[TBL] [Abstract][Full Text] [Related]
23. Investigating oligodendrocyte connexins: Heteromeric interactions between Cx32 and mutant or wild-type forms of Cx47 do not contribute to or modulate gap junction function.
Abrams CK; Flores-Obando RE; Dungan GD; Cherepanova E; Freidin MM
Glia; 2021 Aug; 69(8):1882-1896. PubMed ID: 33835612
[TBL] [Abstract][Full Text] [Related]
24. Abnormal myelinogenesis both in the white and gray matter of the attractin-deficient mv rat.
Izawa T; Yamate J; Franklin RJ; Kuwamura M
Brain Res; 2010 Feb; 1312():145-55. PubMed ID: 19931230
[TBL] [Abstract][Full Text] [Related]
25. Dysmyelination and reduced myelin basic protein gene expression by oligodendrocytes of SHP-1-deficient mice.
Massa PT; Wu C; Fecenko-Tacka K
J Neurosci Res; 2004 Jul; 77(1):15-25. PubMed ID: 15197735
[TBL] [Abstract][Full Text] [Related]
26. Severe Convulsions and Dysmyelination in Both Jimpy and Cx32/47
Chaban YHG; Chen Y; Hertz E; Hertz L
Neurochem Res; 2017 Jun; 42(6):1747-1766. PubMed ID: 28214987
[TBL] [Abstract][Full Text] [Related]
27. Oligodendroglial connexin 47 regulates neuroinflammation upon autoimmune demyelination in a novel mouse model of multiple sclerosis.
Zhao Y; Yamasaki R; Yamaguchi H; Nagata S; Une H; Cui Y; Masaki K; Nakamuta Y; Iinuma K; Watanabe M; Matsushita T; Isobe N; Kira JI
Proc Natl Acad Sci U S A; 2020 Jan; 117(4):2160-2169. PubMed ID: 31932428
[TBL] [Abstract][Full Text] [Related]
28. Myelination defects and neuronal hyperexcitability in the neocortex of connexin 32-deficient mice.
Sutor B; Schmolke C; Teubner B; Schirmer C; Willecke K
Cereb Cortex; 2000 Jul; 10(7):684-97. PubMed ID: 10906315
[TBL] [Abstract][Full Text] [Related]
29. Genetic and physiological evidence that oligodendrocyte gap junctions contribute to spatial buffering of potassium released during neuronal activity.
Menichella DM; Majdan M; Awatramani R; Goodenough DA; Sirkowski E; Scherer SS; Paul DL
J Neurosci; 2006 Oct; 26(43):10984-91. PubMed ID: 17065440
[TBL] [Abstract][Full Text] [Related]
30. Gap junction disorders of myelinating cells.
Kleopa KA; Orthmann-Murphy J; Sargiannidou I
Rev Neurosci; 2010; 21(5):397-419. PubMed ID: 21280457
[TBL] [Abstract][Full Text] [Related]
31. Alterations in the oligodendrocyte lineage, myelin, and white matter in adult mice lacking the chemokine receptor CXCR2.
Padovani-Claudio DA; Liu L; Ransohoff RM; Miller RH
Glia; 2006 Oct; 54(5):471-83. PubMed ID: 16886211
[TBL] [Abstract][Full Text] [Related]
32. Activated immune response in an inherited leukodystrophy disease caused by the loss of oligodendrocyte gap junctions.
Wasseff SK; Scherer SS
Neurobiol Dis; 2015 Oct; 82():86-98. PubMed ID: 26051537
[TBL] [Abstract][Full Text] [Related]
33. Kir4.1 potassium channel subunit is crucial for oligodendrocyte development and in vivo myelination.
Neusch C; Rozengurt N; Jacobs RE; Lester HA; Kofuji P
J Neurosci; 2001 Aug; 21(15):5429-38. PubMed ID: 11466414
[TBL] [Abstract][Full Text] [Related]
34. Cx32 and Cx47 mediate oligodendrocyte:astrocyte and oligodendrocyte:oligodendrocyte gap junction coupling.
Wasseff SK; Scherer SS
Neurobiol Dis; 2011 Jun; 42(3):506-13. PubMed ID: 21396451
[TBL] [Abstract][Full Text] [Related]
35. Connexin32 in oligodendrocytes and association with myelinated fibers in mouse and rat brain.
Li J; Hertzberg EL; Nagy JI
J Comp Neurol; 1997 Mar; 379(4):571-91. PubMed ID: 9067844
[TBL] [Abstract][Full Text] [Related]
36. Loss-of-function GJA12/Connexin47 mutations cause Pelizaeus-Merzbacher-like disease.
Orthmann-Murphy JL; Enriquez AD; Abrams CK; Scherer SS
Mol Cell Neurosci; 2007 Apr; 34(4):629-41. PubMed ID: 17344063
[TBL] [Abstract][Full Text] [Related]
37. Directional coupling of oligodendrocyte connexin-47 and astrocyte connexin-43 gap junctions.
Fasciani I; Pluta P; González-Nieto D; Martínez-Montero P; Molano J; Paíno CL; Millet O; Barrio LC
Glia; 2018 Nov; 66(11):2340-2352. PubMed ID: 30144323
[TBL] [Abstract][Full Text] [Related]
38. In vivo evidence that TRAF4 is required for central nervous system myelin homeostasis.
Blaise S; Kneib M; Rousseau A; Gambino F; Chenard MP; Messadeq N; Muckenstrum M; Alpy F; Tomasetto C; Humeau Y; Rio MC
PLoS One; 2012; 7(2):e30917. PubMed ID: 22363515
[TBL] [Abstract][Full Text] [Related]
39. The transmembrane semaphorin Sema4D/CD100, an inhibitor of axonal growth, is expressed on oligodendrocytes and upregulated after CNS lesion.
Moreau-Fauvarque C; Kumanogoh A; Camand E; Jaillard C; Barbin G; Boquet I; Love C; Jones EY; Kikutani H; Lubetzki C; Dusart I; Chédotal A
J Neurosci; 2003 Oct; 23(27):9229-39. PubMed ID: 14534257
[TBL] [Abstract][Full Text] [Related]
40. Abnormal myelinogenesis in the central nervous system of the VF mutant rat with recoverable tremor.
Tanaka M; Soma K; Izawa T; Yamate J; Franklin RJ; Kuramoto T; Serikawa T; Kuwamura M
Brain Res; 2012 Dec; 1488():104-12. PubMed ID: 23036276
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]