UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 39

Sortiert nach

Toxic gain of function from mutant FUS protein is crucial to trigger cell autonomous motor neuron loss

The EMBO journal, 2016-05, Vol.35 (10), p.1077-1097

2016

Volltextzugriff (PDF)

Peripheral monocytes are functionally altered and invade the CNS in ALS patients

Acta neuropathologica, 2016-09, Vol.132 (3), p.391-411

2016

Volltextzugriff (PDF)

Contrasting effects of selective MAGL and FAAH inhibition on dopamine depletion and GDNF expression in a chronic MPTP mouse model of Parkinson's disease

Neurochemistry international, 2017-11, Vol.110, p.14-24

2017

Volltextzugriff (PDF)

Alterations in the hypothalamic melanocortin pathway in amyotrophic lateral sclerosis

Brain (London, England : 1878), 2016-04, Vol.139 (Pt 4), p.1106-1122

2016

Volltextzugriff (PDF)

Effects of mitochondrial dysfunction on the immunological properties of microglia

Journal of neuroinflammation, 2010-08, Vol.7 (1), p.45-45, Article 45

2010

Volltextzugriff (PDF)

The Endocannabinoid Anandamide Protects Neurons during CNS Inflammation by Induction of MKP-1 in Microglial Cells

Neuron (Cambridge, Mass.), 2006-01, Vol.49 (1), p.67-79

2006

Volltextzugriff (PDF)

Nonpsychotropic Cannabinoid Receptors Regulate Microglial Cell Migration

The Journal of neuroscience, 2003-02, Vol.23 (4), p.1398-1405

2003

Volltextzugriff (PDF)

Evaluation of monoacylglycerol lipase as a therapeutic target in a transgenic mouse model of ALS

Neuropharmacology, 2017-09, Vol.124, p.157-169

2017

Volltextzugriff (PDF)

Fumaric acid esters stimulate astrocytic VEGF expression through HIF-1α and Nrf2

PloS one, 2013-10, Vol.8 (10), p.e76670

2013

Volltextzugriff (PDF)

ALS-causing mutations differentially affect PGC-1α expression and function in the brain vs. peripheral tissues

Neurobiology of disease, 2017-01, Vol.97 (Pt A), p.36-45

2017

Volltextzugriff (PDF)

Ribosomal transcription is regulated by PGC-1alpha and disturbed in Huntington's disease

Scientific reports, 2017-08, Vol.7 (1), p.8513-10, Article 8513

2017

Volltextzugriff (PDF)

P2X7 receptors control 2-arachidonoylglycerol production by microglial cells

Proceedings of the National Academy of Sciences - PNAS, 2004-03, Vol.101 (9), p.3214-3219

2004

Volltextzugriff (PDF)

High-resolution respirometry of fine-needle muscle biopsies in pre-manifest Huntington's disease expansion mutation carriers shows normal mitochondrial respiratory function

PloS one, 2017-04, Vol.12 (4), p.e0175248-e0175248

2017

Volltextzugriff (PDF)

Experimental Autoimmune Encephalomyelitis Disrupts Endocannabinoid-Mediated Neuroprotection

Proceedings of the National Academy of Sciences - PNAS, 2006-04, Vol.103 (16), p.6362-6367

2006

Volltextzugriff (PDF)

Comparison of Sirtuin 3 Levels in ALS and Huntington's Disease-Differential Effects in Human Tissue Samples vs. Transgenic Mouse Models

Frontiers in molecular neuroscience, 2017-05, Vol.10, p.156-156

2017

Volltextzugriff (PDF)

Astrocytes in Culture Produce Anandamide and Other Acylethanolamides

The Journal of biological chemistry, 2002-06, Vol.277 (23), p.20869-20876

2002

Volltextzugriff (PDF)

Age-dependent defects of alpha-synuclein oligomer uptake in microglia and monocytes

Acta neuropathologica, 2016-03, Vol.131 (3), p.379-391

2016

Volltextzugriff (PDF)

Comparative biochemical characterization of the monoacylglycerol lipase inhibitor KML29 in brain, spinal cord, liver, spleen, fat and muscle tissue

Neuropharmacology, 2015-04, Vol.91, p.148-156

2015

Volltextzugriff (PDF)

Mutual exacerbation of peroxisome proliferator-activated receptor γ coactivator 1α deregulation and α-synuclein oligomerization

Annals of neurology, 2015-01, Vol.77 (1), p.15-32

2015

Volltextzugriff (PDF)

A greatly extended PPARGC1A genomic locus encodes several new brain-specific isoforms and influences Huntington disease age of onset

Human molecular genetics, 2012-08, Vol.21 (15), p.3461-3473

2012

Volltextzugriff (PDF)

PGC-1 is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis

Human molecular genetics, 2013-09, Vol.22 (17), p.3477-3484

2013

Volltextzugriff (PDF)

PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis

Human molecular genetics, 2013-09, Vol.22 (17), p.3477-3484

2013

Volltextzugriff (PDF)

Endocannabinoids accumulate in spinal cord of SOD1G93A transgenic mice

Journal of neurochemistry, 2004-06, Vol.89 (6), p.1555-1557

2004

Volltextzugriff (PDF)

B30 Integrated mitochondrial function in human fine-needle muscle biopsies of huntington’s disease mutation carriers and in tissues of HdhQ111 mice

Journal of neurology, neurosurgery and psychiatry, 2016-09, Vol.87 (Suppl 1), p.A19-A20

2016

Volltextzugriff (PDF)

1 – 25 von 39

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(37)
Mit Volltextzugriff
(38)

Publikationsform

Artikel
(38)
Buchkapitel
(1)

Sprache

Englisch
(39)
Japanisch
(13)

Erscheinungsjahr

n.n

Thema

Animals
(25)
Science & Technology
(25)
Life Sciences & Biomedicine
(21)
Mice
(20)
Neurosciences
(15)
Neurosciences & Neurology
(15)
Humans
(14)
Male
(12)
Mice, Transgenic
(12)
Female
(11)
Cells, Cultured
(10)
Disease Models, Animal
(10)
Neurons
(10)
Amyotrophic Lateral Sclerosis
(9)
Microglia
(8)
Mutation
(8)
Amyotrophic Lateral Sclerosis - Metabolism
(7)
Biochemistry & Molecular Biology
(7)
Mice, Inbred C57bl
(7)
Neurology
(7)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Toxic gain of function from mutant FUS protein is crucial to trigger cell autonomous motor neuron loss

Peripheral monocytes are functionally altered and invade the CNS in ALS patients

Contrasting effects of selective MAGL and FAAH inhibition on dopamine depletion and GDNF expression in a chronic MPTP mouse model of Parkinson's disease

Alterations in the hypothalamic melanocortin pathway in amyotrophic lateral sclerosis

Effects of mitochondrial dysfunction on the immunological properties of microglia

The Endocannabinoid Anandamide Protects Neurons during CNS Inflammation by Induction of MKP-1 in Microglial Cells

Nonpsychotropic Cannabinoid Receptors Regulate Microglial Cell Migration

Evaluation of monoacylglycerol lipase as a therapeutic target in a transgenic mouse model of ALS

Fumaric acid esters stimulate astrocytic VEGF expression through HIF-1α and Nrf2

ALS-causing mutations differentially affect PGC-1α expression and function in the brain vs. peripheral tissues

Ribosomal transcription is regulated by PGC-1alpha and disturbed in Huntington's disease

P2X7 receptors control 2-arachidonoylglycerol production by microglial cells

High-resolution respirometry of fine-needle muscle biopsies in pre-manifest Huntington's disease expansion mutation carriers shows normal mitochondrial respiratory function

Experimental Autoimmune Encephalomyelitis Disrupts Endocannabinoid-Mediated Neuroprotection

Comparison of Sirtuin 3 Levels in ALS and Huntington's Disease-Differential Effects in Human Tissue Samples vs. Transgenic Mouse Models

Astrocytes in Culture Produce Anandamide and Other Acylethanolamides

Age-dependent defects of alpha-synuclein oligomer uptake in microglia and monocytes

Comparative biochemical characterization of the monoacylglycerol lipase inhibitor KML29 in brain, spinal cord, liver, spleen, fat and muscle tissue

Mutual exacerbation of peroxisome proliferator-activated receptor γ coactivator 1α deregulation and α-synuclein oligomerization

A greatly extended PPARGC1A genomic locus encodes several new brain-specific isoforms and influences Huntington disease age of onset

PGC-1 is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis

PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis

Endocannabinoids accumulate in spinal cord of SOD1G93A transgenic mice

Serotonin 2B receptor slows disease progression and prevents degeneration of spinal cord mononuclear phagocytes in amyotrophic lateral sclerosis

B30 Integrated mitochondrial function in human fine-needle muscle biopsies of huntington’s disease mutation carriers and in tissues of HdhQ111 mice

Suchergebnisse filtern