UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 28

Sortiert nach

Overexpression of human wildtype torsinA and human ΔGAG torsinA in a transgenic mouse model causes phenotypic abnormalities

Neurobiology of disease, 2007-08, Vol.27 (2), p.190-206

2007

Link zum Volltext

Verfügbarkeit prüfen

Impaired olfactory bulb neurogenesis depends on the presence of human wild-type alpha-synuclein

Neuroscience, 2012-10, Vol.222, p.343-355

2012

Link zum Volltext

Verfügbarkeit prüfen

DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease

Neurology, 2004-02, Vol.62 (3), p.389

2004

Link zum Volltext

Verfügbarkeit prüfen

Ceruloplasmin gene variations and substantia nigra hyperechogenicity in Parkinson disease

Neurology, 2004-11, Vol.63 (10), p.1912

2004

Link zum Volltext

Verfügbarkeit prüfen

Collaboration in NeurOmics: Enabling effective data-sharing and maximising impact in neuromuscular disease

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S298-S298

2015

Link zum Volltext

Verfügbarkeit prüfen

NeurOmics: EU-funded-omics research for diagnosis and therapy in rare neuromuscular and neurodegenerative diseases

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S298-S299

2015

Link zum Volltext

Verfügbarkeit prüfen

3.309 THE GUANINE NUCLEOTIDE EXCHANGE FACTOR KALIRIN-7 IS A NOVEL SYNPHILIN-1 INTERACTING PROTEIN

Parkinsonism & related disorders, 2012, Vol.18, p.S221-S221

2012

Link zum Volltext

Verfügbarkeit prüfen

Sleep disturbance in spinocerebellar ataxias: is the SCA3 mutation a cause of restless legs syndrome?

Neurology, 1998-12, Vol.51 (6), p.1603

1998

Link zum Volltext

Verfügbarkeit prüfen

Expression profiling in peripheral blood reveals signature for penetrance in DYT1 dystonia

Neurobiology of disease, 2010-05, Vol.38 (2), p.192-200

2010

Link zum Volltext

Verfügbarkeit prüfen

Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriers

Neurology, 2001-05, Vol.56 (10), p.1355

2001

Link zum Volltext

Verfügbarkeit prüfen

Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease

Neurology, 2004-04, Vol.62 (7), p.1231

2004

Link zum Volltext

Verfügbarkeit prüfen

3.002 PD: Genetics

Parkinsonism & related disorders, 2007, Vol.13, p.S147-S147

2007

Link zum Volltext

Verfügbarkeit prüfen

DNA analysis of Huntington's disease: five years of experience in Germany, Austria, and Switzerland

Neurology, 1999-09, Vol.53 (4), p.801

1999

Link zum Volltext

Verfügbarkeit prüfen

Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6

Neurology, 1997-09, Vol.49 (3), p.842

1997

Link zum Volltext

Verfügbarkeit prüfen

2.018 Neuropathology of conditional alpha-synuclein transgenic mouse models of Parkinson's disease

Parkinsonism & related disorders, 2007, Vol.13, p.S90-S90

2007

Link zum Volltext

Verfügbarkeit prüfen

2.304 Neuropathology of conditional alpha-synuclein transgenic mouse models of Parkinson's disease

Parkinsonism & related disorders, 2007, Vol.13, p.S122-S122

2007

Link zum Volltext

Verfügbarkeit prüfen

Spinocerebellar ataxia type 6: evidence for a strong founder effect among German families

Neurology, 1999-03, Vol.52 (4), p.849

1999

Link zum Volltext

Verfügbarkeit prüfen

Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12

Nature genetics, 1999-12, Vol.23 (4), p.391-392

1999

Link zum Volltext

Verfügbarkeit prüfen

Regional and subtype selective changes of neurotransmitter receptor density in a rat transgenic for the Huntington's disease mutation

Journal of neurochemistry, 2005-08, Vol.94 (3), p.639-650

2005

Link zum Volltext

Verfügbarkeit prüfen

Adult neural precursor cells unaffected in animal models of DYT1 dystonia

Neuroreport, 2009-11, Vol.20 (17), p.1529-1533

2009

Link zum Volltext

Verfügbarkeit prüfen

Microarray expression analysis of human dopaminergic neuroblastoma cells after RNA interference of SNCA — A key player in the pathogenesis of Parkinson's disease

Brain research, 2009-02, Vol.1256, p.19-33

2009

Link zum Volltext

Verfügbarkeit prüfen

Neurofilament L gene is not a genetic factor of sporadic and familial Parkinson’s disease

Brain research, 2002-09, Vol.951 (1), p.82-86

2002

Link zum Volltext

Verfügbarkeit prüfen

Isolation and characterization of new highly polymorphic DNA markers from the Huntington disease region

American journal of human genetics, 1992-02, Vol.50 (2), p.382-393

1992

Link zum Volltext

Verfügbarkeit prüfen

Mutation analysis and association studies of the UCHLI gene in German Parkinson's disease patients

Neuroreport, 2000, Vol.11 (10), p.2079-2082

2000

Link zum Volltext

Verfügbarkeit prüfen

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study

Lancet neurology, 2011-10, Vol.10 (10), p.898-908

2011

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 28

Suche als RSS-Feed

Aktive Filter

Zeitschrift / SerieHuman Molecular Genetics

ThemaGenetics

KollektionIngentaConnect Journals

ThemaNeurology

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(28)
Mit Volltextzugriff
(18)

Publikationsform

Artikel
(28)

Sprache

Englisch
(28)
Japanisch
(2)

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Overexpression of human wildtype torsinA and human ΔGAG torsinA in a transgenic mouse model causes phenotypic abnormalities

Impaired olfactory bulb neurogenesis depends on the presence of human wild-type alpha-synuclein

DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease

Ceruloplasmin gene variations and substantia nigra hyperechogenicity in Parkinson disease

Collaboration in NeurOmics: Enabling effective data-sharing and maximising impact in neuromuscular disease

NeurOmics: EU-funded-omics research for diagnosis and therapy in rare neuromuscular and neurodegenerative diseases

3.309 THE GUANINE NUCLEOTIDE EXCHANGE FACTOR KALIRIN-7 IS A NOVEL SYNPHILIN-1 INTERACTING PROTEIN

Sleep disturbance in spinocerebellar ataxias: is the SCA3 mutation a cause of restless legs syndrome?

Expression profiling in peripheral blood reveals signature for penetrance in DYT1 dystonia

Familial parkinsonism with synuclein pathology: clinical and PET studies of A30P mutation carriers

Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease

3.002 PD: Genetics

DNA analysis of Huntington's disease: five years of experience in Germany, Austria, and Switzerland

Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6

2.018 Neuropathology of conditional alpha-synuclein transgenic mouse models of Parkinson's disease

2.304 Neuropathology of conditional alpha-synuclein transgenic mouse models of Parkinson's disease

Spinocerebellar ataxia type 6: evidence for a strong founder effect among German families

Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12

Regional and subtype selective changes of neurotransmitter receptor density in a rat transgenic for the Huntington's disease mutation

Adult neural precursor cells unaffected in animal models of DYT1 dystonia

Microarray expression analysis of human dopaminergic neuroblastoma cells after RNA interference of SNCA — A key player in the pathogenesis of Parkinson's disease

Neurofilament L gene is not a genetic factor of sporadic and familial Parkinson’s disease

Isolation and characterization of new highly polymorphic DNA markers from the Huntington disease region

Mutation analysis and association studies of the UCHLI gene in German Parkinson's disease patients

Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study

Aktive Filter

Suchergebnisse filtern