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...

ER and oxidative stresses are common mediators of apoptosis in both neurodegenerative and non-neurodegenerative lysosomal storage disorders and are alleviated by chemical chaperones

Human molecular genetics, 2008-02, Vol.17 (4), p.469-477

2008

Volltextzugriff (PDF)

Current State of Clinical and Morphological Features in Human NCL

Brain pathology (Zurich, Switzerland), 2004-01, Vol.14 (1), p.61-69

2004

Volltextzugriff (PDF)

Disruption of PPT1 or PPT2 Causes Neuronal Ceroid Lipofuscinosis in Knockout Mice

Proceedings of the National Academy of Sciences - PNAS, 2001-11, Vol.98 (24), p.13566-13571

2001

Volltextzugriff (PDF)

N-Glycosylation Is Crucial for Folding, Trafficking, and Stability of Human Tripeptidyl-peptidase I

The Journal of biological chemistry, 2004-03, Vol.279 (13), p.12827-12839

2004

Volltextzugriff (PDF)

Carbonic Anhydrase II in the Developing and Adult Human Brain

Journal of neuropathology and experimental neurology, 2006-07, Vol.65 (7), p.664-674

2006

Volltextzugriff (PDF)

Prosegment of Tripeptidyl Peptidase I Is a Potent, Slow-binding Inhibitor of Its Cognate Enzyme

The Journal of biological chemistry, 2008-06, Vol.283 (24), p.16497-16504

2008

Volltextzugriff (PDF)

Increased levels of carbonic anhydrase II in the developing Down syndrome brain

Brain research, 2008-01, Vol.1190, p.193-205

2008

Volltextzugriff (PDF)

Maturation of Human Tripeptidyl-peptidase I in Vitro

The Journal of biological chemistry, 2004-07, Vol.279 (30), p.31058-31067

2004

Volltextzugriff (PDF)

Glycosaminoglycans Modulate Activation, Activity, and Stability of Tripeptidyl-peptidase I in Vitro and in Vivo

The Journal of biological chemistry, 2005-03, Vol.280 (9), p.7550-7561

2005

Volltextzugriff (PDF)

Disruption of PPT2 in Mice Causes an Unusual Lysosomal Storage Disorder with Neurovisceral Features

Proceedings of the National Academy of Sciences - PNAS, 2003-10, Vol.100 (21), p.12325-12330

2003

Volltextzugriff (PDF)

Distribution of Tripeptidyl Peptidase I in Human Tissues Under Normal and Pathological Conditions

Journal of neuropathology and experimental neurology, 2001-03, Vol.60 (3), p.280-292

2001

Volltextzugriff (PDF)

Pheno/genotypic correlations of neuronal ceroid lipofuscinoses

Neurology, 2001-08, Vol.57 (4), p.576-581

2001

Volltextzugriff (PDF)

2 Cellular pathology and pathogenic aspects of neuronal ceroid lipofuscinoses

Advances in Genetics, 2001, Vol.45, p.35-68

2001

Volltextzugriff (PDF)

Biosynthesis, glycosylation, and enzymatic processing in vivo of human tripeptidyl-peptidase I

The Journal of biological chemistry, 2003-02, Vol.278 (9), p.7135

2003

Volltextzugriff (PDF)

Ser475, Glu272, Asp276, Asp327, and Asp360 are involved in catalytic activity of human tripeptidyl-peptidase I

FEBS letters, 2005-02, Vol.579 (6), p.1383-1388

2005

Volltextzugriff (PDF)

Lysosomal ceroid depletion by drugs: Therapeutic implications for a hereditary neurodegenerative disease of childhood

Nature medicine, 2001-04, Vol.7 (4), p.478-484

2001

Volltextzugriff (PDF)

Confronting the issues of therapeutic misconception, enrollment decisions, and personal motives in genetic medicine-based clinical research studies for fatal disorders

Human gene therapy, 2005-09, Vol.16 (9), p.1028-1036

2005

Volltextzugriff (PDF)

Batten Disease

1, 2001

Volltextzugriff (PDF)

Batten disease: diagnosis, treatment, and research

2001

Volltextzugriff (PDF)

Biosynthesis, Glycosylation, and Enzymatic Processingin Vivo of Human Tripeptidyl-peptidase I

The Journal of biological chemistry, 2003-02, Vol.278 (9), p.7135-7145

2003

Volltextzugriff (PDF)

Identification of three novel mutations of the palmitoyl-protein thioesterase-1 (PPT1) gene in children with neuronal ceroid-lipofuscinosis

Human mutation, 2000-02, Vol.15 (2), p.206-207

2000

Volltextzugriff (PDF)

1 Neuronal ceroid lipofuscinoses: Classification and diagnosis

Advances in Genetics, 2001, Vol.45, p.1-34

2001

Volltextzugriff (PDF)

Genotype-phenotype analyses of classic neuronal ceroid lipofuscinosis (NCLs): genetic predictions from clinical and pathological findings

Beijing da xue xue bao. Journal of Peking University. Yi xue ban, 2006-02, Vol.38 (1), p.41

2006

Volltextzugriff (PDF)

Intraneuronal Aβ42 accumulation in Down syndrome brain

Amyloid, 2002, Vol.9 (2), p.88-102

2002

Volltextzugriff (PDF)

Temporal Accrual of Complement Proteins in Amyloid Plaques in Down's Syndrome with Alzheimer's Disease

The American journal of pathology, 2000-02, Vol.156 (2), p.489-499

2000

Volltextzugriff (PDF)

1 – 25 von 91

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(82)
Mit Volltextzugriff
(79)

Publikationsform

Sprache

Englisch
(91)

Erscheinungsjahr

n.n

Thema

Humans
(65)
Science & Technology
(59)
Life Sciences & Biomedicine
(55)
Biological And Medical Sciences
(32)
Medical Sciences
(31)
Child
(26)
Neuronal Ceroid-Lipofuscinoses - Genetics
(21)
Infant
(20)
Neurosciences & Neurology
(20)
Animals
(18)
Genetics & Heredity
(18)
Male
(18)
Adolescent
(17)
Female
(17)
Metabolic Diseases
(16)
Child, Preschool
(15)
Mutation
(15)
Aminopeptidases
(14)
Clinical Neurology
(14)
Dipeptidyl-Peptidases And Tripeptidyl-Peptidases
(14)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

ER and oxidative stresses are common mediators of apoptosis in both neurodegenerative and non-neurodegenerative lysosomal storage disorders and are alleviated by chemical chaperones

Current State of Clinical and Morphological Features in Human NCL

Disruption of PPT1 or PPT2 Causes Neuronal Ceroid Lipofuscinosis in Knockout Mice

N-Glycosylation Is Crucial for Folding, Trafficking, and Stability of Human Tripeptidyl-peptidase I

Carbonic Anhydrase II in the Developing and Adult Human Brain

Prosegment of Tripeptidyl Peptidase I Is a Potent, Slow-binding Inhibitor of Its Cognate Enzyme

Increased levels of carbonic anhydrase II in the developing Down syndrome brain

Maturation of Human Tripeptidyl-peptidase I in Vitro

Glycosaminoglycans Modulate Activation, Activity, and Stability of Tripeptidyl-peptidase I in Vitro and in Vivo

Disruption of PPT2 in Mice Causes an Unusual Lysosomal Storage Disorder with Neurovisceral Features

Distribution of Tripeptidyl Peptidase I in Human Tissues Under Normal and Pathological Conditions

Pheno/genotypic correlations of neuronal ceroid lipofuscinoses

2 Cellular pathology and pathogenic aspects of neuronal ceroid lipofuscinoses

Biosynthesis, glycosylation, and enzymatic processing in vivo of human tripeptidyl-peptidase I

Ser475, Glu272, Asp276, Asp327, and Asp360 are involved in catalytic activity of human tripeptidyl-peptidase I

Lysosomal ceroid depletion by drugs: Therapeutic implications for a hereditary neurodegenerative disease of childhood

Confronting the issues of therapeutic misconception, enrollment decisions, and personal motives in genetic medicine-based clinical research studies for fatal disorders

Batten Disease

Batten disease: diagnosis, treatment, and research

Biosynthesis, Glycosylation, and Enzymatic Processingin Vivo of Human Tripeptidyl-peptidase I

Identification of three novel mutations of the palmitoyl-protein thioesterase-1 (PPT1) gene in children with neuronal ceroid-lipofuscinosis

1 Neuronal ceroid lipofuscinoses: Classification and diagnosis

Genotype-phenotype analyses of classic neuronal ceroid lipofuscinosis (NCLs): genetic predictions from clinical and pathological findings

Intraneuronal Aβ42 accumulation in Down syndrome brain

Temporal Accrual of Complement Proteins in Amyloid Plaques in Down's Syndrome with Alzheimer's Disease

Suchergebnisse filtern