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...

Cytoplasmic and nuclear polyglutamine aggregates in SCA6 Purkinje cells

Neurology, 2001-06, Vol.56 (12), p.1753-1756

2001

Volltextzugriff (PDF)

Brain hydrogen sulfide is severely decreased in Alzheimer's disease

Biochemical and biophysical research communications, 2002-05, Vol.293 (5), p.1485-1488

2002

Volltextzugriff (PDF)

Corticobasal degeneration: etiopathological significance of the cytoskeletal alterations

Acta neuropathologica, 1994-06, Vol.87 (6), p.545-553

1994

Volltextzugriff (PDF)

Hereditary spastic paraplegia with frontal lobe dysfunction: a clinicopathologic study

Neurology, 2004-12, Vol.63 (11), p.2149-2152

2004

Volltextzugriff (PDF)

A patient with dementia with Lewy bodies and codon 232 mutation of PRNP

Neurology, 2002-11, Vol.59 (10), p.1619-1621

2002

Volltextzugriff (PDF)

Sporadic Creutzfeldt-Jakob disease with MM1-type prion protein and plaques

Neurology, 2003-02, Vol.60 (3), p.514-517

2003

Volltextzugriff (PDF)

Prefrontal Abnormality of Schizophrenia Revealed by DNA Microarray: Impact on Glial and Neurotrophic Gene Expression

Annals of the New York Academy of Sciences, 2004-10, Vol.1025 (1), p.84-91

2004

Volltextzugriff (PDF)

White matter hyperintensities on MRI in a patient with corticobasal degeneration

Acta neurologica Scandinavica, 1999-03, Vol.99 (3), p.199-201

1999

Volltextzugriff (PDF)

Hereditary dentatorubral-pallidoluysian atrophy: clinical and pathologic variants in a family

Neurology, 1988-07, Vol.38 (7), p.1065-1065

1988

Volltextzugriff (PDF)

Wobble modification deficiency in mutant tRNAs in patients with mitochondrial diseases

FEBS letters, 2005-05, Vol.579 (13), p.2948-2952

2005

Volltextzugriff (PDF)

Selective reduction of a PDZ protein, SAP‐97, in the prefrontal cortex of patients with chronic schizophrenia

Journal of neurochemistry, 2002-11, Vol.83 (4), p.797-806

2002

Volltextzugriff (PDF)

Development and characterization of a TAPIR-like mouse monoclonal antibody to amyloid-beta

Journal of Alzheimer's disease, 2008-06, Vol.14 (2), p.161-173

2008

Volltextzugriff (PDF)

Glypican‐1 as an Aβ binding HSPG in the human brain: Its localization in DIG domains and possible roles in the pathogenesis of Alzheimer's disease

The FASEB journal, 2004-06, Vol.18 (9), p.1013-1015

2004

Volltextzugriff (PDF)

Aprataxin, the causative protein for EAOH is a nuclear protein with a potential role as a DNA repair protein

Annals of neurology, 2004-02, Vol.55 (2), p.241-249

2004

Volltextzugriff (PDF)

Increased Production of β-Amyloid and Vulnerability to Endoplasmic Reticulum Stress by an Aberrant Spliced Form of Presenilin 2

The Journal of biological chemistry, 2001-01, Vol.276 (3), p.2108-2114

2001

Volltextzugriff (PDF)

Systemic mastocytosis and recurrent anaphylactic shock

The Lancet (British edition), 2002-06, Vol.359 (9323), p.2084-2084

2002

Volltextzugriff (PDF)

Ataxin-3 Is Translocated into the Nucleus for the Formation of Intranuclear Inclusions in Normal and Machado–Joseph Disease Brains

Experimental neurology, 2000-10, Vol.165 (2), p.248-256

2000

Volltextzugriff (PDF)

A decrease in interleukin-1 receptor antagonist expression in the prefrontal cortex of schizophrenic patients

Neuroscience research, 2003-07, Vol.46 (3), p.299-307

2003

Volltextzugriff (PDF)

Apoptotic neurons in Alzheimer's disease frequently show intracellular Aβ42 labeling

Journal of Alzheimer's disease, 2001-05, Vol.3 (2), p.231-239

2001

Volltextzugriff (PDF)

A quantitative study on the expression of synapsin II and N-ethylmaleimide-sensitive fusion protein in schizophrenic patients

Neuroscience letters, 2001-06, Vol.305 (3), p.185-188

2001

Volltextzugriff (PDF)

Intracellular A beta 42 activates p53 promoter: a pathway to neurodegeneration in Alzheimer's disease

The FASEB journal, 2005-02, Vol.19 (2), p.255-257

2005

Volltextzugriff (PDF)

Intracellular Ab42 actiavtes p53 promoter: a pathway to neurodegeneration in Alzheimer's disease

The FASEB journal, 2005, Vol.19, p.255-257

2005

Volltextzugriff (PDF)

Distinct Pathological Features of the Gallyas- and Tau-positive Glia in the Parkinsonism-Dementia Complex and Amyotrophic Lateral Sclerosis of Guam

Journal of neuropathology and experimental neurology, 1997-03, Vol.56 (3), p.308-316

1997

Volltextzugriff (PDF)

Both N-terminal and C-terminal fragments of Presenilin 1 colocalize with neurofibrillary tangles in neurons and dystrophic neurites of senile plaques in Alzheimer's disease

Journal of neuroscience research, 1998-07, Vol.53 (1), p.99-106

1998

Volltextzugriff (PDF)

A TOPOGRAPHIC AND QUANTITATIVE STUDY OF NEURONS IN HUMAN SPINAL GRAY MATTER, WITH SPECIAL REFERENCE TO THEIR CHANGES IN AMYOTROPHIC LATERAL SCLEROSIS

Biomedical Research, 1983/04/01, Vol.4(2), pp.211-224

1983

Volltextzugriff (PDF)

1 – 25 von 88

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(75)
Mit Volltextzugriff
(71)

Publikationsform

Sprache

Englisch
(82)
Japanisch
(7)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Cytoplasmic and nuclear polyglutamine aggregates in SCA6 Purkinje cells

Brain hydrogen sulfide is severely decreased in Alzheimer's disease

Corticobasal degeneration: etiopathological significance of the cytoskeletal alterations

Hereditary spastic paraplegia with frontal lobe dysfunction: a clinicopathologic study

A patient with dementia with Lewy bodies and codon 232 mutation of PRNP

Sporadic Creutzfeldt-Jakob disease with MM1-type prion protein and plaques

Prefrontal Abnormality of Schizophrenia Revealed by DNA Microarray: Impact on Glial and Neurotrophic Gene Expression

White matter hyperintensities on MRI in a patient with corticobasal degeneration

Hereditary dentatorubral-pallidoluysian atrophy: clinical and pathologic variants in a family

Wobble modification deficiency in mutant tRNAs in patients with mitochondrial diseases

Selective reduction of a PDZ protein, SAP‐97, in the prefrontal cortex of patients with chronic schizophrenia

Development and characterization of a TAPIR-like mouse monoclonal antibody to amyloid-beta

Glypican‐1 as an Aβ binding HSPG in the human brain: Its localization in DIG domains and possible roles in the pathogenesis of Alzheimer's disease

Aprataxin, the causative protein for EAOH is a nuclear protein with a potential role as a DNA repair protein

Increased Production of β-Amyloid and Vulnerability to Endoplasmic Reticulum Stress by an Aberrant Spliced Form of Presenilin 2

Systemic mastocytosis and recurrent anaphylactic shock

Ataxin-3 Is Translocated into the Nucleus for the Formation of Intranuclear Inclusions in Normal and Machado–Joseph Disease Brains

A decrease in interleukin-1 receptor antagonist expression in the prefrontal cortex of schizophrenic patients

Apoptotic neurons in Alzheimer's disease frequently show intracellular Aβ42 labeling

A quantitative study on the expression of synapsin II and N-ethylmaleimide-sensitive fusion protein in schizophrenic patients

Intracellular A beta 42 activates p53 promoter: a pathway to neurodegeneration in Alzheimer's disease

Intracellular Ab42 actiavtes p53 promoter: a pathway to neurodegeneration in Alzheimer's disease

Distinct Pathological Features of the Gallyas- and Tau-positive Glia in the Parkinsonism-Dementia Complex and Amyotrophic Lateral Sclerosis of Guam

Both N-terminal and C-terminal fragments of Presenilin 1 colocalize with neurofibrillary tangles in neurons and dystrophic neurites of senile plaques in Alzheimer's disease

A TOPOGRAPHIC AND QUANTITATIVE STUDY OF NEURONS IN HUMAN SPINAL GRAY MATTER, WITH SPECIAL REFERENCE TO THEIR CHANGES IN AMYOTROPHIC LATERAL SCLEROSIS

Suchergebnisse filtern