Zeitschriftenartikel (674)
601.
Zeitschriftenartikel
40 (3), S. 501 - 514 (2003)
FAK deficiency in cells contributing to the basal lamina results in cortical abnormalities resembling congenital muscular dystrophies. Neuron 602.
Zeitschriftenartikel
23 (14), S. 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 603.
Zeitschriftenartikel
23 (12), S. 5004 - 5011 (2003)
Bone marrow-derived cells expressing green fluorescent protein under the control of the glial fibrillary acidic protein promoter do not differentiate into astrocytes In Vitro and In Vivo. The Journal of Neuroscience 604.
Zeitschriftenartikel
72 (1), S. 12 - 24 (2003)
Genetic background determines phenotypic severity of the Plp rumpshaker mutation. Journal of Neuroscience Research 605.
Zeitschriftenartikel
71 (6), S. 826 - 834 (2003)
Normal metabolism but different physical properties of myelin from mice deficient in proteolipid protein. Journal of Neuroscience Research 606.
Zeitschriftenartikel
37 (5), S. 751 - 764 (2003)
Neuronal or glial progeny: Regional differences in radial glia fate. Neuron 607.
Zeitschriftenartikel
33 (3), S. 366 - 374 (2003)
Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelination. Nature Genetics 608.
Zeitschriftenartikel
23 (5), S. 1750 - 1758 (2003)
Segregated expression of AMPA-type glutamate receptors and glutamate transporters defines distinct astrocyte populations in the mouse hippocampus. The Journal of Neuroscience 609.
Zeitschriftenartikel
278 (6), S. 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 610.
Zeitschriftenartikel
71 (3), S. 326 - 337 (2003)
Differential expression of L- and S-MAG upon cAMP stimulated differentiation in oligodendroglial cells. Journal of Neuroscience Research 611.
Zeitschriftenartikel
12 (15), S. 1881 - 1895 (2003)
Inactivation of ether lipid biosynthesis causes male infertility, defects in eye development and optic nerve hypoplasia in mice. Human Molecular Genetics 612.
Zeitschriftenartikel
23 (1), S. 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 613.
Zeitschriftenartikel
39 (3), S. 256 - 267 (2002)
Phenotypic analysis of mice deficient in the major myelin protein MOBP, and evidence for a novel Mobp isoform. Glia 614.
Zeitschriftenartikel
158 (4), S. 719 - 729 (2002)
Survival of, and competition between, oligodendrocytes expressing different alleles of the Plp gene. Journal of Cell Biology 615.
Zeitschriftenartikel
158 (4), S. 709 - 718 (2002)
Notch1 control of oligodendrocyte differentiation in the spinal cord. Journal of Cell Biology 616.
Zeitschriftenartikel
20 (1), S. 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 617.
Zeitschriftenartikel
157 (2), S. 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 618.
Zeitschriftenartikel
125 (3), S. 551 - 561 (2002)
Patients lacking the major CNS myelin protein, proteolipid protein 1, develop length-dependent axonal degeneration in the absence of demyelination and inflammation. Brain 619.
Zeitschriftenartikel
67 (4), S. 443 - 449 (2002)
Proliferation of Schwann cells and regulation of cyclin D1 expression in an animal model of Charcot-Marie-Tooth disease type 1A. Journal of Neuroscience Research 620.
Zeitschriftenartikel
16 (2), S. 1 - 16 (2002)
Astrocyte Ca2+ waves trigger responses in microglial cells in brain slices. The FASEB Journal 621.
Zeitschriftenartikel
40 (1), S. 61 - 71 (2002)
Molecular cloning of an extracellular aspartic proteinase from Rhizopus microsporus and evidence for its expression during infection. Medical Mycology 622.
Zeitschriftenartikel
28 (1), S. 75 - 78 (2002)
Observations on the structure of myelin lacking the major proteolipid protein. Neuropathology and Applied Neurobiology 623.
Zeitschriftenartikel
45 (S1), S. 53 - 56 (2002)
Blood coagulation with domestic deep-seated mycoses. Mycoses 624.
Zeitschriftenartikel
18 (6), S. 593 - 605 (2001)
Multiple Splice Isoforms of Proteolipid M6B in Neurons and Oligodendrocytes. Molecular and Cellular Neuroscience 625.
Zeitschriftenartikel
30 (9-10), S. 841 - 855 (2001)
Differential expression of apoptotic markers in jimpy and in Plp overexpressors: evidence for different apoptotic pathways. Journal of Neurocytology 626.
Zeitschriftenartikel
50 (1), S. 47 - 55 (2001)
PMP22 transgenic dorsal root ganglia cultures show myelin abnormalities similar to those of human CMT1A. Annals of Neurology 627.
Zeitschriftenartikel
26, S. 639 - 645 (2001)
Mutant PLP/DM20 Cannot Be Processed to Secrete PLP-Related Oligodendrocyte Differentiation/Survival Factor. Neurochemical Research 628.
Zeitschriftenartikel
52 (6), S. 656 - 671 (2001)
Membrane traffic in myelinating oligodendrocytes. Microscopy Research and Technique 629.
Zeitschriftenartikel
21 (3), S. 920 - 933 (2001)
The AN2 Protein Is a Novel Marker for the Schwann Cell Lineage Expressed by Immature and Nonmyelinating Schwann Cells. The Journal of Neuroscience 630.
Zeitschriftenartikel
63 (2), S. 151 - 164 (2001)
Myelin proteolipid proteins promote the interaction of oligodendrocytes and axons. Journal of Neuroscience Research 631.
Zeitschriftenartikel
15, S. 66 - 78 (2001)
The transcription factor Sox10 is a key regulator of peripheral glial development. Genes and Development 632.
Zeitschriftenartikel
20 (11), S. 4120 - 4128 (2000)
Uncoupling of Myelin Assembly and Schwann Cell Differentiation by Transgenic Overexpression of Peripheral Myelin Protein 22. The Journal of Neuroscience 633.
Zeitschriftenartikel
20 (10), S. 3714 - 3724 (2000)
Neuronal Basic Helix-Loop-Helix Proteins (NEX and BETA2/Neuro D) Regulate Terminal Granule Cell Differentiation in the Hippocampus. The Journal of Neuroscience 634.
Zeitschriftenartikel
6, S. 56 - 61 (2000)
Shaping of the autoreactive T-cell repertoire by a splice variant of self protein expressed in thymic epithelial cells. Nature Medicine 635.
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 636.
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 637.
Zeitschriftenartikel
883 (1), S. 247 - 253 (1999)
Transgenic Mouse Models of CMT1A and HNPP. Annals of the New York Academy of Sciences 638.
Zeitschriftenartikel
14 (1), S. 41 - 51 (1999)
Myelination in the Absence of Galactolipids and Proteolipid Proteins. Molecular and Cellular Neuroscience 639.
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 640.
Zeitschriftenartikel
9, S. 903 - 904 (1998)
Evidence against altered forms of MAG in the dysmyelinated mouse mutant claw paw. Mammalian Genome 641.
Zeitschriftenartikel
8 (4), S. 771 - 793 (1998)
Mouse Models of Myelin Diseases. Brain Pathology 642.
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 643.
Zeitschriftenartikel
280 (5369), S. 1610 - 1613 (1998)
Axonal Swellings and Degeneration in Mice Lacking the Major Proteolipid of Myelin. Science 644.
Zeitschriftenartikel
41 (5), S. 344 - 358 (1998)
Current concepts of PLP and its role in the nervous system. Microscopy Research and Technique 645.
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 646.
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 647.
Zeitschriftenartikel
50 (5), S. 829 - 843 (1997)
Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice. Journal of Neuroscience Research 648.
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 649.
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 650.
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