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...

Lysine-specific demethylase 1 restricts hematopoietic progenitor proliferation and is essential for terminal differentiation

Leukemia, 2012-09, Vol.26 (9), p.2039-2051

2012

Volltextzugriff (PDF)

Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect

Neurology, 2011-09, Vol.77 (10), p.959-964

2011

Volltextzugriff (PDF)

Leukodystrophies underlying cryptic spastic paraparesis: frequency and phenotype in 76 patients

European journal of neurology, 2014-07, Vol.21 (7), p.983-988

2014

Volltextzugriff (PDF)

Disease severity affects quality of life of hereditary spastic paraplegia patients

European journal of neurology, 2012-01, Vol.19 (1), p.168-171

2012

Volltextzugriff (PDF)

Amplicon-based high-throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patients

Clinical genetics, 2011-08, Vol.80 (2), p.148-160

2011

Volltextzugriff (PDF)

SPG10 is a rare cause of spastic paraplegia in European families

Journal of neurology, neurosurgery and psychiatry, 2008-05, Vol.79 (5), p.584-587

2008

Volltextzugriff (PDF)

Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24

Neurology, 2009-06, Vol.72 (22), p.1893-1898

2009

Volltextzugriff (PDF)

Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia

The New England journal of medicine, 2023-01, Vol.388 (2), p.128-141

2023

Volltextzugriff (PDF)

GEnomes Management Application (GEM.app): A New Software Tool for Large-Scale Collaborative Genome Analysis

Human mutation, 2013-06, Vol.34 (6), p.842-846

2013

Volltextzugriff (PDF)

Ataxias and hereditary spastic paraplegias

Nervenarzt, 2017-07, Vol.88 (7), p.720-727

2017

Volltextzugriff (PDF)

V28. KCNA2 mutations cause epileptic encephalopathy by gain- or loss-of channel function

Clinical neurophysiology, 2015-08, Vol.126 (8), p.e80-e80

2015

Volltextzugriff (PDF)

Target-Based Approach to Inhibitors of Histone Arginine Methyltransferases

Journal of medicinal chemistry, 2007-05, Vol.50 (10), p.2319-2325

2007

Volltextzugriff (PDF)

The Spastic Paraplegia Rating Scale (SPRS): a reliable and valid measure of disease severity

Neurology, 2006-08, Vol.67 (3), p.430-434

2006

Volltextzugriff (PDF)

RECESSION ODE

The Wilson quarterly (Washington), 2012-03, Vol.36 (2), p.7-7

Schuele, William R.

2012

Volltextzugriff (PDF)

L’inhibition de Lsd1 dans le cartilage articulaire révèle le rôle potentiel d’une déméthylase d’histones au cours de l’arthrose

Revue du rhumatisme (Ed. française : 1993), 2021-12, Vol.88, p.A156

2021

Volltextzugriff (PDF)

PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia

Clinical genetics, 2017-11, Vol.92 (5), p.534-539

2017

Volltextzugriff (PDF)

Do Not Trust the Pedigree: Reduced and Sex-Dependent Penetrance at a Novel Mutation Hotspot in ATL1 Blurs Autosomal Dominant Inheritance of Spastic Paraplegia

Human mutation, 2013-06, Vol.34 (6), p.860-863

2013

Volltextzugriff (PDF)

CYP2U1 Mutations in Two Iranian Patients with Activity Induced Dystonia, Motor Regression and Spastic Paraplegia

European journal of paediatric neurology, 2016-09, Vol.20 (5), p.782-787

2016

Volltextzugriff (PDF)

All- trans retinoic acid is a ligand for the orphan nuclear receptor RORβ

Nature structural & molecular biology, 2003-10, Vol.10 (10), p.820-825

2003

Volltextzugriff (PDF)

LSD1 controls metastasis of androgen-independent prostate cancer cells through PXN and LPAR6

Oncogenesis (New York, NY), 2014-10, Vol.3 (10), p.e120-e120

2014

Volltextzugriff (PDF)

Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia

Journal of neurology, neurosurgery and psychiatry, 2009-12, Vol.80 (12), p.1402-1404

2009

Volltextzugriff (PDF)

Development of a NanoBRET assay to validate inhibitors of Sirt2-mediated lysine deacetylation and defatty-acylation that block prostate cancer cell migration

RSC chemical biology, 2022-04, Vol.3 (4), p.468-485

2022

Volltextzugriff (PDF)

FHL2, a novel tissue-specific coactivator of the androgen receptor

The EMBO journal, 2000-02, Vol.19 (3), p.359-369

2000

Volltextzugriff (PDF)

Extracellular Signal-Regulated Kinase 2 Interacts with and Is Negatively Regulated by the LIM-Only Protein FHL2 in Cardiomyocytes

Molecular and Cellular Biology, 2004-02, Vol.24 (3), p.1081-1095

2004

Volltextzugriff (PDF)

The transcriptional coactivator FHL2 transmits Rho signals from the cell membrane into the nucleus

The EMBO journal, 2002-02, Vol.21 (4), p.736-748

2002

Volltextzugriff (PDF)

1 – 25 von 387

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(228)
Mit Volltextzugriff
(309)

Publikationsform

Sprache

Englisch
(229)
Deutsch
(159)
Französisch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Lysine-specific demethylase 1 restricts hematopoietic progenitor proliferation and is essential for terminal differentiation

Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect

Leukodystrophies underlying cryptic spastic paraparesis: frequency and phenotype in 76 patients

Disease severity affects quality of life of hereditary spastic paraplegia patients

Amplicon-based high-throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patients

SPG10 is a rare cause of spastic paraplegia in European families

Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24

Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia

GEnomes Management Application (GEM.app): A New Software Tool for Large-Scale Collaborative Genome Analysis

Ataxias and hereditary spastic paraplegias

V28. KCNA2 mutations cause epileptic encephalopathy by gain- or loss-of channel function

Target-Based Approach to Inhibitors of Histone Arginine Methyltransferases

The Spastic Paraplegia Rating Scale (SPRS): a reliable and valid measure of disease severity

RECESSION ODE

L’inhibition de Lsd1 dans le cartilage articulaire révèle le rôle potentiel d’une déméthylase d’histones au cours de l’arthrose

PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia

Do Not Trust the Pedigree: Reduced and Sex-Dependent Penetrance at a Novel Mutation Hotspot in ATL1 Blurs Autosomal Dominant Inheritance of Spastic Paraplegia

CYP2U1 Mutations in Two Iranian Patients with Activity Induced Dystonia, Motor Regression and Spastic Paraplegia

All- trans retinoic acid is a ligand for the orphan nuclear receptor RORβ

LSD1 controls metastasis of androgen-independent prostate cancer cells through PXN and LPAR6

Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia

Development of a NanoBRET assay to validate inhibitors of Sirt2-mediated lysine deacetylation and defatty-acylation that block prostate cancer cell migration

FHL2, a novel tissue-specific coactivator of the androgen receptor

Extracellular Signal-Regulated Kinase 2 Interacts with and Is Negatively Regulated by the LIM-Only Protein FHL2 in Cardiomyocytes

The transcriptional coactivator FHL2 transmits Rho signals from the cell membrane into the nucleus

Suchergebnisse filtern