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)

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)

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)

High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia

Neurology, 2006-12, Vol.67 (11), p.1926-1930

2006

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)

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)

Ataxien und hereditäre spastische Spinalparalysen

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

2017

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)

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)

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)

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)

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)

Factor XIII Val34Leu polymorphism is associated with increased factor XIII activation and decreased transcutaneous oxygen readings in patients with diabetic foot ulcers

Diabetic medicine, 2012-12, Vol.29 (12), p.1596-1599

2012

Volltextzugriff (PDF)

Second primary tumor in anti-Ma1/2-positive paraneoplastic limbic encephalitis

Journal of neuro-oncology, 2006-05, Vol.78 (1), p.49-51

2006

Volltextzugriff (PDF)

P159 - The histone methyltransferase KMT9 regulates proliferation and migration of bladder cancer cells and is a novel target for treatment of Muscle Invasive Bladder Cancer (MIBC)

European urology, 2024-03, Vol.85, p.S227-S227

2024

Volltextzugriff (PDF)

The histone methyltransferase KMT9 regulates proliferation and migration of bladder cancer cells and is a novel target for treatment of Muscle Invasive Bladder Cancer (MIBC)

European urology, 2024-03, Vol.85, p.S227

2024

Volltextzugriff (PDF)

A novel clinical syndrome revealing a deficiency of the muscarinic M3 receptor

Neurology, 2011-02, Vol.76 (5), p.451-455

2011

Volltextzugriff (PDF)

“Pseudodominant inheritance” of ataxia with ocular apraxia type 2 (AOA2)

Journal of neurology, 2008-04, Vol.255 (4), p.495-501

2008

Volltextzugriff (PDF)

Bone-related role of the lim-only protein FHL2 in fish

Bone (New York, N.Y.), 2009-06, Vol.44, p.S311-S312

2009

Volltextzugriff (PDF)

TISSUE-SPECIFIC DELETION OF LSD-1 IN MICE TO INVESTIGATE ITS ROLE IN THE ARTICULAR CARTILAGE HOMEOSTASIS

Osteoarthritis and cartilage, 2022-04, Vol.30, p.S160-S160

2022

Volltextzugriff (PDF)

Correlations between serum and CSF pNfH levels in ALS, FTD and controls: a comparison of three analytical approaches

Clinical chemistry and laboratory medicine, 2019-09, Vol.57 (10), p.1556-1564

2019

Volltextzugriff (PDF)

1 – 25 von 549

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(375)
Mit Volltextzugriff
(467)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(232)
Life Sciences & Biomedicine
(173)
Humans
(169)
Male
(100)
Female
(96)
Adult
(81)
Biological And Medical Sciences
(81)
Middle Aged
(73)
Neurosciences & Neurology
(67)
Medical Sciences
(62)
Animals
(60)
Psychiatry
(52)
Neurosciences
(49)
Aged
(45)
Physical Sciences
(43)
Biochemistry & Molecular Biology
(36)
Clinical Neurology
(34)
Mice
(33)
Psychology. Psychoanalysis. Psychiatry
(32)
Fundamental And Applied Biological Sciences. Psychology
(31)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

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

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

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

High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia

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

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

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

Ataxien und hereditäre spastische Spinalparalysen

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

Disease severity affects quality of life of hereditary spastic paraplegia patients

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

SPG10 is a rare cause of spastic paraplegia in European families

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

Factor XIII Val34Leu polymorphism is associated with increased factor XIII activation and decreased transcutaneous oxygen readings in patients with diabetic foot ulcers

Second primary tumor in anti-Ma1/2-positive paraneoplastic limbic encephalitis

P159 - The histone methyltransferase KMT9 regulates proliferation and migration of bladder cancer cells and is a novel target for treatment of Muscle Invasive Bladder Cancer (MIBC)

The histone methyltransferase KMT9 regulates proliferation and migration of bladder cancer cells and is a novel target for treatment of Muscle Invasive Bladder Cancer (MIBC)

A novel clinical syndrome revealing a deficiency of the muscarinic M3 receptor

“Pseudodominant inheritance” of ataxia with ocular apraxia type 2 (AOA2)

Bone-related role of the lim-only protein FHL2 in fish

TISSUE-SPECIFIC DELETION OF LSD-1 IN MICE TO INVESTIGATE ITS ROLE IN THE ARTICULAR CARTILAGE HOMEOSTASIS

Correlations between serum and CSF pNfH levels in ALS, FTD and controls: a comparison of three analytical approaches

Suchergebnisse filtern