Publications of Klaus-Armin Nave
All genres
Journal Article (354)
281.
Journal Article
190 (1), pp. 213 - 223 (2004)
Early abnormalities in sciatic nerve function and structure in a rat model of Charcot-Marie-Tooth type 1A disease. Experimental Neurology 282.
Journal Article
40 (3), pp. 171 - 175 (2004)
Sox10-rtTA mouse line for tetracycline-inducible expression of transgenes in neural crest cells and oligodendrocytes. Genesis 283.
Journal Article
24 (17), pp. 7636 - 7642 (2004)
Cell depletion due to diphtheria toxin fragment A after Cre-mediated recombination. Molecular and Cellular Biology 284.
Journal Article
166 (1), pp. 121 - 131 (2004)
Oligodendroglial modulation of fast axonal transport in a mouse model of hereditary spastic paraplegia. Journal of Cell Biology 285.
Journal Article
304 (5671), pp. 700 - 703 (2004)
Axonal Neuregulin-1 Regulates Myelin Sheath Thickness. Science 286.
Journal Article
9 (12), pp. 1533 - 1537 (2003)
Therapeutic administration of progesterone antagonist in a model of Charcot-Marie-Tooth disease (CMT-1A). Nature Medicine 287.
Journal Article
40 (3), pp. 501 - 514 (2003)
FAK deficiency in cells contributing to the basal lamina results in cortical abnormalities resembling congenital muscular dystrophies. Neuron 288.
Journal Article
23 (14), pp. 6005 - 6012 (2003)
Hippocampal cGMP-dependent protein kinase I supports an age- and protein synthesis-dependent component of long-term potentiation but is not essential for spatial reference and contextual memory. The Journal of Neuroscience 289.
Journal Article
72 (1), pp. 12 - 24 (2003)
Genetic background determines phenotypic severity of the Plp rumpshaker mutation. Journal of Neuroscience Research 290.
Journal Article
71 (6), pp. 826 - 834 (2003)
Normal metabolism but different physical properties of myelin from mice deficient in proteolipid protein. Journal of Neuroscience Research 291.
Journal Article
33 (3), pp. 366 - 374 (2003)
Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelination. Nature Genetics 292.
Journal Article
278 (6), pp. 3590 - 3598 (2003)
The proteoglycan NG2 is complexed with α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors by the PDZ glutamate receptor interaction protein (GRIP) in glial progenitor cells - Implications for glial-neuronal signaling. The Journal of Biological Chemistry 293.
Journal Article
71 (3), pp. 326 - 337 (2003)
Differential expression of L- and S-MAG upon cAMP stimulated differentiation in oligodendroglial cells. Journal of Neuroscience Research 294.
Journal Article
12 (15), pp. 1881 - 1895 (2003)
Inactivation of ether lipid biosynthesis causes male infertility, defects in eye development and optic nerve hypoplasia in mice. Human Molecular Genetics 295.
Journal Article
23 (1), pp. 277 - 286 (2003)
The C264Y missense mutation in the extracellular domain of L1 impairs protein trafficking in vitro and in vivo. The Journal of Neuroscience 296.
Journal Article
39 (3), pp. 256 - 267 (2002)
Phenotypic analysis of mice deficient in the major myelin protein MOBP, and evidence for a novel Mobp isoform. Glia 297.
Journal Article
158 (4), pp. 719 - 729 (2002)
Survival of, and competition between, oligodendrocytes expressing different alleles of the Plp gene. Journal of Cell Biology 298.
Journal Article
158 (4), pp. 709 - 718 (2002)
Notch1 control of oligodendrocyte differentiation in the spinal cord. Journal of Cell Biology 299.
Journal Article
20 (1), pp. 93 - 109 (2002)
Identification of the Regulatory Region of the Peripheral Myelin Protein 22 (PMP22) Gene That Directs Temporal and Spatial Expression in Development and Regeneration of Peripheral Nerves. Molecular and Cellular Neuroscience 300.
Journal Article
157 (2), pp. 327 - 336 (2002)
Overexpression of the myelin proteolipid protein leads to accumulation of cholesterol and proteolipid protein in endosomes/lysosomes: implications for Pelizaeus-Merzbacher disease. The Journal of Cell Biology: JCB