Publications of K.-A. Nave
All genres
Journal Article (358)
321.
Journal Article
883 (1), pp. 247 - 253 (1999)
Transgenic Mouse Models of CMT1A and HNPP. Annals of the New York Academy of Sciences 322.
Journal Article
14 (1), pp. 41 - 51 (1999)
Myelination in the Absence of Galactolipids and Proteolipid Proteins. Molecular and Cellular Neuroscience 323.
Journal Article
97, pp. 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 324.
Journal Article
9, pp. 903 - 904 (1998)
Evidence against altered forms of MAG in the dysmyelinated mouse mutant claw paw. Mammalian Genome 325.
Journal Article
8 (4), pp. 771 - 793 (1998)
Mouse Models of Myelin Diseases. Brain Pathology 326.
Journal Article
52 (6), pp. 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 327.
Journal Article
280 (5369), pp. 1610 - 1613 (1998)
Axonal Swellings and Degeneration in Mice Lacking the Major Proteolipid of Myelin. Science 328.
Journal Article
41 (5), pp. 344 - 358 (1998)
Current concepts of PLP and its role in the nervous system. Microscopy Research and Technique 329.
Journal Article
394 (4), pp. 506 - 519 (1998)
Late-onset neurodegeneration in mice with increased dosage of the proteolipid protein gene. The Journal of Comparative Neurology 330.
Journal Article
18 (4), pp. 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 331.
Journal Article
50 (5), pp. 829 - 843 (1997)
Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice. Journal of Neuroscience Research 332.
Journal Article
50 (5), pp. 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 333.
Journal Article
50 (1), pp. 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 334.
Journal Article
20 (4), pp. 322 - 332 (1997)
Phenotypic severity of murinePlp mutants reflects in vivo and in vitro variatioans in transport of PLP isoproteins. Glia 335.
Journal Article
18 (1), pp. 59 - 70 (1997)
Assembly of CNS Myelin in the Absence of Proteolipid Protein. Neuron 336.
Journal Article
9 (5-6), pp. 460 - 475 (1997)
SHARPs: MammalianEnhancer-of-Split- and Hairy-Related Proteins Coupled to Neuronal Stimulation. Molecular and Cellular Neuroscience 337.
Journal Article
16 (24), pp. 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 338.
Journal Article
16 (5), pp. 1049 - 1060 (1996)
A Transgenic Rat Model of Charcot-Marie-Tooth Disease. Neuron 339.
Journal Article
5 (3), pp. 275 - 281 (1995)
Transgenic and Natural Mouse Models of Proteolipid Protein (PLP)-Related Dysmyelination and Demyelination. Brain Pathology 340.
Journal Article
5 (3), pp. 231 - 232 (1995)
Myelin Genetics: New Insight Into Old Diseases. Brain Pathology