UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Oligodendrocyte gene expression is reduced by and influences effects of chronic social stress in mice

Genes, brain and behavior, 2019-01, Vol.18 (1), p.e12475-n/a

2019

Volltextzugriff (PDF)

Inactivation of ether lipid biosynthesis causes male infertility, defects in eye development and optic nerve hypoplasia in mice

Human molecular genetics, 2003-08, Vol.12 (15), p.1881-1895

2003

Volltextzugriff (PDF)

Axonal Swellings and Degeneration in Mice Lacking the Major Proteolipid of Myelin

Science (American Association for the Advancement of Science), 1998-06, Vol.280 (5369), p.1610-1613

1998

Volltextzugriff (PDF)

The transcription factor Sox10 is a key regulator of peripheral glial development

Genes & development, 2001-01, Vol.15 (1), p.66-78

2001

Volltextzugriff (PDF)

The septin cytoskeleton in myelinating glia

Molecular and cellular neuroscience, 2009-02, Vol.40 (2), p.156-166

2009

Volltextzugriff (PDF)

Shaping of the autoreactive T-cell repertoire by a splice variant of self protein expressed in thymic epithelial cells

Nature medicine, 2000-01, Vol.6 (1), p.56-61

2000

Volltextzugriff (PDF)

Mice with Conditional Inactivation of Fibroblast Growth Factor Receptor-2 Signaling in Oligodendrocytes Have Normal Myelin But Display Dramatic Hyperactivity when Combined with Cnp1 Inactivation

The Journal of neuroscience, 2006-11, Vol.26 (47), p.12339-12350

2006

Volltextzugriff (PDF)

Elevated phosphatidylinositol 3,4,5-trisphosphate in glia triggers cell-autonomous membrane wrapping and myelination

The Journal of neuroscience, 2010-06, Vol.30 (26), p.8953-8964

2010

Volltextzugriff (PDF)

Patients lacking the major CNS myelin protein, proteolipid protein 1, develop length-dependent axonal degeneration in the absence of demyelination and inflammation

Brain (London, England : 1878), 2002-03, Vol.125 (Pt 3), p.551-561

2002

Volltextzugriff (PDF)

Neuronal Basic Helix-Loop-Helix Proteins (NEX and BETA2/Neuro D) Regulate Terminal Granule Cell Differentiation in the Hippocampus

The Journal of neuroscience, 2000-05, Vol.20 (10), p.3714-3724

2000

Volltextzugriff (PDF)

Revisiting adult neurogenesis and the role of erythropoietin for neuronal and oligodendroglial differentiation in the hippocampus

Molecular psychiatry, 2016-12, Vol.21 (12), p.1752-1767

2016

Volltextzugriff (PDF)

Late-onset neurodegeneration in mice with increased dosage of the proteolipid protein gene

Journal of comparative neurology (1911), 1998-05, Vol.394 (4), p.506-519

1998

Volltextzugriff (PDF)

Assembly of CNS Myelin in the Absence of Proteolipid Protein

Neuron (Cambridge, Mass.), 1997-01, Vol.18 (1), p.59-70

1997

Volltextzugriff (PDF)

Clonal expansions of pathogenic CD8+ effector cells in the CNS of myelin mutant mice

Molecular and cellular neuroscience, 2007-11, Vol.36 (3), p.416-424

2007

Volltextzugriff (PDF)

Genetic background determines phenotypic severity of the Plp rumpshaker mutation

Journal of neuroscience research, 2003-04, Vol.72 (1), p.12-24

2003

Volltextzugriff (PDF)

Axonal Neuregulin-1 Regulates Myelin Sheath Thickness

Science (American Association for the Advancement of Science), 2004-04, Vol.304 (5671), p.700-703

2004

Volltextzugriff (PDF)

Neurological mouse mutants and the genes of myelin

Journal of neuroscience research, 1994-08, Vol.38 (6), p.607-612

Nave, K.-A.

1994

Volltextzugriff (PDF)

Myelin proteolipid proteins promote the interaction of oligodendrocytes and axons

Journal of neuroscience research, 2001-01, Vol.63 (2), p.151-164

2001

Volltextzugriff (PDF)

Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelination

Nature genetics, 2003-03, Vol.33 (3), p.366-374

2003

Volltextzugriff (PDF)

Membrane traffic in myelinating oligodendrocytes

Microscopy research and technique, 2001-03, Vol.52 (6), p.656-671

2001

Volltextzugriff (PDF)

Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice

Journal of neuroscience research, 1997-12, Vol.50 (5), p.829-843

1997

Volltextzugriff (PDF)

FAK Deficiency in Cells Contributing to the Basal Lamina Results in Cortical Abnormalities Resembling Congenital Muscular Dystrophies

Neuron (Cambridge, Mass.), 2003-10, Vol.40 (3), p.501-514

2003

Volltextzugriff (PDF)

Uncoupling of hypomyelination and glial cell death by a mutation in the proteolipid protein gene

Nature (London), 1992-08, Vol.358 (6389), p.758-761

1992

Volltextzugriff (PDF)

Phenotypic analysis of mice deficient in the major myelin protein MOBP, and evidence for a novel Mobp isoform

Glia, 2002-09, Vol.39 (3), p.256-267

2002

Volltextzugriff (PDF)

Mice deficient for the myelin-associated glycoprotein show subtle abnormalities in myelin

Neuron (Cambridge, Mass.), 1994-07, Vol.13 (1), p.229-246

1994

Volltextzugriff (PDF)

1 – 25 von 94

Suche als RSS-Feed

Aktive Filter

ThemaMice

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(93)
Mit Volltextzugriff
(89)

Publikationsform

Artikel
(94)

Sprache

Englisch
(94)

Erscheinungsjahr

n.n

Thema

Animals
(94)
Science & Technology
(89)
Life Sciences & Biomedicine
(82)
Neurosciences
(57)
Neurosciences & Neurology
(56)
Mice, Transgenic
(37)
Mice, Inbred C57bl
(22)
Mice, Knockout
(22)
Myelin Proteolipid Protein - Genetics
(22)
Oligodendroglia - Metabolism
(22)
Myelin
(21)
Myelin Sheath - Metabolism
(21)
Humans
(20)
Male
(20)
Female
(17)
Biological And Medical Sciences
(16)
Myelin Proteins - Genetics
(16)
Cell Biology
(15)
Mutation
(15)

14 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Oligodendrocyte gene expression is reduced by and influences effects of chronic social stress in mice

Inactivation of ether lipid biosynthesis causes male infertility, defects in eye development and optic nerve hypoplasia in mice

Axonal Swellings and Degeneration in Mice Lacking the Major Proteolipid of Myelin

The transcription factor Sox10 is a key regulator of peripheral glial development

The septin cytoskeleton in myelinating glia

Shaping of the autoreactive T-cell repertoire by a splice variant of self protein expressed in thymic epithelial cells

Mice with Conditional Inactivation of Fibroblast Growth Factor Receptor-2 Signaling in Oligodendrocytes Have Normal Myelin But Display Dramatic Hyperactivity when Combined with Cnp1 Inactivation

Elevated phosphatidylinositol 3,4,5-trisphosphate in glia triggers cell-autonomous membrane wrapping and myelination

Patients lacking the major CNS myelin protein, proteolipid protein 1, develop length-dependent axonal degeneration in the absence of demyelination and inflammation

Neuronal Basic Helix-Loop-Helix Proteins (NEX and BETA2/Neuro D) Regulate Terminal Granule Cell Differentiation in the Hippocampus

Revisiting adult neurogenesis and the role of erythropoietin for neuronal and oligodendroglial differentiation in the hippocampus

Late-onset neurodegeneration in mice with increased dosage of the proteolipid protein gene

Assembly of CNS Myelin in the Absence of Proteolipid Protein

Clonal expansions of pathogenic CD8+ effector cells in the CNS of myelin mutant mice

Genetic background determines phenotypic severity of the Plp rumpshaker mutation

Axonal Neuregulin-1 Regulates Myelin Sheath Thickness

Neurological mouse mutants and the genes of myelin

Myelin proteolipid proteins promote the interaction of oligodendrocytes and axons

Disruption of Cnp1 uncouples oligodendroglial functions in axonal support and myelination

Membrane traffic in myelinating oligodendrocytes

Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice

FAK Deficiency in Cells Contributing to the Basal Lamina Results in Cortical Abnormalities Resembling Congenital Muscular Dystrophies

Uncoupling of hypomyelination and glial cell death by a mutation in the proteolipid protein gene

Phenotypic analysis of mice deficient in the major myelin protein MOBP, and evidence for a novel Mobp isoform

Mice deficient for the myelin-associated glycoprotein show subtle abnormalities in myelin

Aktive Filter

Suchergebnisse filtern