UB Paderborn / Katalog / Suche / in CDI

Microsomal prostaglandin E synthase-1 is a critical factor in dopaminergic neurodegeneration in Parkinson's disease

Neurobiology of disease, 2019-04, Vol.124, p.81-92

2019

Link zum Volltext

Verfügbarkeit prüfen

Proteomics-based identification of differentially expressed genes in human gliomas: down-regulation of SIRT2 gene

Biochemical and biophysical research communications, 2003-09, Vol.309 (3), p.558-566

2003

Link zum Volltext

Verfügbarkeit prüfen

Pyramidal tract abnormalities in the human fetus and infant with trisomy 18 syndrome

Neuropathology, 2014-06, Vol.34 (3), p.219-226

2014

Link zum Volltext

Verfügbarkeit prüfen

Neuropathology of Idiopathic Normal Pressure Hydrocephalus: A Study of Three Autopsy Cases and a Literature Review

Brain and nerve = Shinkei kenkyū no shinpo, 2024-02, Vol.76 (2), p.135

2024

Link zum Volltext

Verfügbarkeit prüfen

Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1

Science (American Association for the Advancement of Science), 1998-09, Vol.281 (5384), p.1851-1854

1998

Link zum Volltext

Verfügbarkeit prüfen

White Matter Changes in Elderly People: MR-pathologic Correlations

Magnetic Resonance in Medical Sciences, 2006, Vol.5(2), pp.99-104

2006

Link zum Volltext

Verfügbarkeit prüfen

Expression of ubiquitin-binding protein p62 in ubiquitin-immunoreactive intraneuronal inclusions in amyotrophic lateral sclerosis with dementia: analysis of five autopsy cases with broad clinicopathological spectrum

Acta neuropathologica, 2004-04, Vol.107 (4), p.359-364

2004

Link zum Volltext

Verfügbarkeit prüfen

Redox system expression in the motor neurons in amyotrophic lateral sclerosis (ALS): immunohistochemical studies on sporadic ALS, superoxide dismutase 1 (SOD1)-mutated familial ALS, and SOD1-mutated ALS animal models

Acta neuropathologica, 2005-08, Vol.110 (2), p.101-112

2005

Link zum Volltext

Verfügbarkeit prüfen

Immunohistochemical expression of fibroblast growth factor-2 in developing human cerebrum and epilepsy-associated malformations of cortical development

Neuropathology, 2011-12, Vol.31 (6), p.589-598

2011

Link zum Volltext

Verfügbarkeit prüfen

Immunohistochemical expression of fibroblast growth factor (FGF)-2 in epilepsy-associated malformations of cortical development (MCDs)

Neuropathology, 2008-08, Vol.28 (4), p.372-381

2008

Link zum Volltext

Verfügbarkeit prüfen

Pro-apoptotic protein glyceraldehyde-3-phosphate dehydrogenase promotes the formation of Lewy body-like inclusions

The European journal of neuroscience, 2005-01, Vol.21 (2), p.317-326

2005

Link zum Volltext

Verfügbarkeit prüfen

Role of proteasomes in the formation of neurofilamentous inclusions in spinal motor neurons of aluminum-treated rabbits

Neuropathology, 2007-12, Vol.27 (6), p.522-530

2007

Link zum Volltext

Verfügbarkeit prüfen

Histological evidence of redox system breakdown caused by superoxide dismutase 1 (SOD1) aggregation is common to SOD1-mutated motor neurons in humans and animal models

Acta neuropathologica, 2004-02, Vol.107 (2), p.149-158

2004

Link zum Volltext

Verfügbarkeit prüfen

Advanced glycation endproduct-modified superoxide dismutase-1 (SOD1)-positive inclusions are common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutations and transgenic mice expressing human SOD1 with a G85R mutation

Acta neuropathologica, 2000-11, Vol.100 (5), p.490-505

2000

Link zum Volltext

Verfügbarkeit prüfen

Copper chaperone for superoxide dismutase co-aggregates with superoxide dismutase 1 (SOD1) in neuronal Lewy body-like hyaline inclusions : an immunohistochemical study on familial amyotrophic lateral sclerosis with SOD1 gene mutation

Acta neuropathologica, 2001-09, Vol.102 (3), p.233-238

2001

Link zum Volltext

Verfügbarkeit prüfen

Midkine, a new neurotrophic factor, is present in glial cytoplasmic inclusions of multiple system atrophy brains

Acta neuropathologica, 2000-11, Vol.100 (5), p.481-489

2000

Link zum Volltext

Verfügbarkeit prüfen

Fragmentation of Golgi apparatus of nigral neurons with alpha-synuclein-positive inclusions in patients with Parkinson's disease

Acta neuropathologica, 2006-09, Vol.112 (3), p.261-265

2006

Link zum Volltext

Verfügbarkeit prüfen

Intravascular Large B-cell Lymphoma Following a Relapsing Stroke with Temporary Fever: A Brain Biopsy Case

Internal Medicine, 2006, Vol.45(10), pp.693-695

2006

Link zum Volltext

Verfügbarkeit prüfen

Development of Purkinje cells in humans: an immunohistochemical study using a monoclonal antibody against the inositol 1,4,5-triphosphate type 1 receptor (IP3R1)

Acta neuropathologica, 1999-09, Vol.98 (3), p.226-232

1999

Link zum Volltext

Verfügbarkeit prüfen

6-Formylpterin protects retinal neurons from transient ischemia-reperfusion injury in rats: A morphological and immunohistochemical study

Neuropathology, 2003-09, Vol.23 (3), p.161-168

2003

Link zum Volltext

Verfügbarkeit prüfen

A Japanese girl with leukoencephalopathy with vanishing white matter

Brain & development (Tokyo. 1979), 2001-03, Vol.23 (1), p.58-61

2001

Link zum Volltext

Verfügbarkeit prüfen

Putaminal lesion in multiple system atrophy: postmortem MR-pathological correlations

Neuroradiology, 2008-07, Vol.50 (7), p.559-567

2008

Link zum Volltext

Verfügbarkeit prüfen

Clinically silent choroid plexus cyst : evaluation by diffusion-weighted MRI

Neuroradiology, 2005-04, Vol.47 (4), p.251-255

2005

Link zum Volltext

Verfügbarkeit prüfen

Mixed germ cell tumors with abundant sarcomatous component in the temporal lobe after radiochemotherapy of neurohypophyseal germinoma: a case report

Brain tumor pathology, 2006-10, Vol.23 (2), p.83-89

2006

Link zum Volltext

Verfügbarkeit prüfen

Application of Energy-dispersive X-ray Microanalysis on the Diagnosis of Atypical Calcific Band Keratopathy

Okajimas Folia Anatomica Japonica, 2005, Vol.82(1), pp.19-24

2005

Link zum Volltext

Verfügbarkeit prüfen

Menü

Weitere Dienste

Einstellungen

Microsomal prostaglandin E synthase-1 is a critical factor in dopaminergic neurodegeneration in Parkinson's disease

Proteomics-based identification of differentially expressed genes in human gliomas: down-regulation of SIRT2 gene

Pyramidal tract abnormalities in the human fetus and infant with trisomy 18 syndrome

Neuropathology of Idiopathic Normal Pressure Hydrocephalus: A Study of Three Autopsy Cases and a Literature Review

Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1

White Matter Changes in Elderly People: MR-pathologic Correlations

Expression of ubiquitin-binding protein p62 in ubiquitin-immunoreactive intraneuronal inclusions in amyotrophic lateral sclerosis with dementia: analysis of five autopsy cases with broad clinicopathological spectrum

Redox system expression in the motor neurons in amyotrophic lateral sclerosis (ALS): immunohistochemical studies on sporadic ALS, superoxide dismutase 1 (SOD1)-mutated familial ALS, and SOD1-mutated ALS animal models

Immunohistochemical expression of fibroblast growth factor-2 in developing human cerebrum and epilepsy-associated malformations of cortical development

Immunohistochemical expression of fibroblast growth factor (FGF)-2 in epilepsy-associated malformations of cortical development (MCDs)

Pro-apoptotic protein glyceraldehyde-3-phosphate dehydrogenase promotes the formation of Lewy body-like inclusions

Role of proteasomes in the formation of neurofilamentous inclusions in spinal motor neurons of aluminum-treated rabbits

Histological evidence of redox system breakdown caused by superoxide dismutase 1 (SOD1) aggregation is common to SOD1-mutated motor neurons in humans and animal models

Advanced glycation endproduct-modified superoxide dismutase-1 (SOD1)-positive inclusions are common to familial amyotrophic lateral sclerosis patients with SOD1 gene mutations and transgenic mice expressing human SOD1 with a G85R mutation

Copper chaperone for superoxide dismutase co-aggregates with superoxide dismutase 1 (SOD1) in neuronal Lewy body-like hyaline inclusions : an immunohistochemical study on familial amyotrophic lateral sclerosis with SOD1 gene mutation

Midkine, a new neurotrophic factor, is present in glial cytoplasmic inclusions of multiple system atrophy brains

Fragmentation of Golgi apparatus of nigral neurons with alpha-synuclein-positive inclusions in patients with Parkinson's disease

Intravascular Large B-cell Lymphoma Following a Relapsing Stroke with Temporary Fever: A Brain Biopsy Case

Development of Purkinje cells in humans: an immunohistochemical study using a monoclonal antibody against the inositol 1,4,5-triphosphate type 1 receptor (IP3R1)

6-Formylpterin protects retinal neurons from transient ischemia-reperfusion injury in rats: A morphological and immunohistochemical study

A Japanese girl with leukoencephalopathy with vanishing white matter

Putaminal lesion in multiple system atrophy: postmortem MR-pathological correlations

Clinically silent choroid plexus cyst : evaluation by diffusion-weighted MRI

Mixed germ cell tumors with abundant sarcomatous component in the temporal lobe after radiochemotherapy of neurohypophyseal germinoma: a case report

Application of Energy-dispersive X-ray Microanalysis on the Diagnosis of Atypical Calcific Band Keratopathy

Suchergebnisse filtern