Publikationen von K.-A. Nave
Alle Typen
Zeitschriftenartikel (360)
321.
Zeitschriftenartikel
883 (1), S. 234 - 246 (1999)
Distinct Phenotypes Associated with Increasing Dosage of the PLP Gene: Implications for CMT1A Due toPMP22Gene Duplication. Annals of the New York Academy of Sciences 322.
Zeitschriftenartikel
883 (1), S. 254 - 261 (1999)
The “CMT Rat”: Peripheral Neuropathy and Dysmyelination Caused by Transgenic Overexpression ofPMP22. Annals of the New York Academy of Sciences 323.
Zeitschriftenartikel
883 (1), S. 247 - 253 (1999)
Transgenic Mouse Models of CMT1A and HNPP. Annals of the New York Academy of Sciences 324.
Zeitschriftenartikel
14 (1), S. 41 - 51 (1999)
Myelination in the Absence of Galactolipids and Proteolipid Proteins. Molecular and Cellular Neuroscience 325.
Zeitschriftenartikel
97, S. 595 - 606 (1999)
Transgenic Lewis rats overexpressing the proteolipid protein gene: myelin degeneration and its effect on T cell-mediated experimental autoimmune encephalomyelitis. Acta Neuropathologica 326.
Zeitschriftenartikel
9, S. 903 - 904 (1998)
Evidence against altered forms of MAG in the dysmyelinated mouse mutant claw paw. Mammalian Genome 327.
Zeitschriftenartikel
8 (4), S. 771 - 793 (1998)
Mouse Models of Myelin Diseases. Brain Pathology 328.
Zeitschriftenartikel
52 (6), S. 633 - 640 (1998)
Molecular cloning and transfection studies of M6b-2, a novel splice variant of a member of the PLP-DM20/M6 gene family. Journal of Neuroscience Research 329.
Zeitschriftenartikel
280 (5369), S. 1610 - 1613 (1998)
Axonal Swellings and Degeneration in Mice Lacking the Major Proteolipid of Myelin. Science 330.
Zeitschriftenartikel
41 (5), S. 344 - 358 (1998)
Current concepts of PLP and its role in the nervous system. Microscopy Research and Technique 331.
Zeitschriftenartikel
394 (4), S. 506 - 519 (1998)
Late-onset neurodegeneration in mice with increased dosage of the proteolipid protein gene. The Journal of Comparative Neurology 332.
Zeitschriftenartikel
18 (4), S. 1408 - 1418 (1998)
Neuronal Basic Helix-Loop-Helix Proteins (NEX, neuroD, NDRF): Spatiotemporal Expression and Targeted Disruption of the NEX Gene in Transgenic Mice. The Journal of Neuroscience 333.
Zeitschriftenartikel
50 (5), S. 829 - 843 (1997)
Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice. Journal of Neuroscience Research 334.
Zeitschriftenartikel
50 (5), S. 684 - 701 (1997)
Helix-loop-helix proteins in Schwann cells: A study of regulation and subcellular localization of Ids, REB, and E12/47 during embryonic and postnatal development. Journal of Neuroscience Research 335.
Zeitschriftenartikel
50 (1), S. 13 - 22 (1997)
Modification of Schwann cell phenotype withPlp transgenes: Evidence that the PLP and DM20 isoproteins are targeted to different cellular domains. Journal of Neuroscience Research 336.
Zeitschriftenartikel
20 (4), S. 322 - 332 (1997)
Phenotypic severity of murinePlp mutants reflects in vivo and in vitro variatioans in transport of PLP isoproteins. Glia 337.
Zeitschriftenartikel
18 (1), S. 59 - 70 (1997)
Assembly of CNS Myelin in the Absence of Proteolipid Protein. Neuron 338.
Zeitschriftenartikel
9 (5-6), S. 460 - 475 (1997)
SHARPs: MammalianEnhancer-of-Split- and Hairy-Related Proteins Coupled to Neuronal Stimulation. Molecular and Cellular Neuroscience 339.
Zeitschriftenartikel
16 (24), S. 7920 - 7929 (1996)
Monoclonal Antibody O10 Defines a Conformationally Sensitive Cell-Surface Epitope of Proteolipid Protein (PLP): Evidence that PLP Misfolding Underlies Dysmyelination in Mutant Mice. The Journal of Neuroscience 340.
Zeitschriftenartikel
16 (5), S. 1049 - 1060 (1996)
A Transgenic Rat Model of Charcot-Marie-Tooth Disease. Neuron