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...

InFUSing antisense oligonucleotides for treating ALS

Trends in molecular medicine, 2022-04, Vol.28 (4), p.253-254

2022

Volltextzugriff (PDF)

TDP43 aggregates: the 'Schrödinger's cat' in amyotrophic lateral sclerosis

Nature reviews. Neuroscience, 2021-08, Vol.22 (8), p.514-514

2021

Volltextzugriff (PDF)

GC-MS-based urine metabolic profiling of autism spectrum disorders

Analytical and bioanalytical chemistry, 2013-06, Vol.405 (15), p.5291-5300

2013

Volltextzugriff (PDF)

Post-Translational Variants of Major Proteins in Amyotrophic Lateral Sclerosis Provide New Insights into the Pathophysiology of the Disease

International journal of molecular sciences, 2024-08, Vol.25 (16), p.8664

2024

Volltextzugriff (PDF)

The Roles of NEDD4 Subfamily of HECT E3 Ubiquitin Ligases in Neurodevelopment and Neurodegeneration

International journal of molecular sciences, 2022-03, Vol.23 (7), p.3882

2022

Volltextzugriff (PDF)

Deep sequencing is an appropriate tool for the selection of unique Hepatitis C virus (HCV) variants after single genomic amplification

PloS one, 2017-03, Vol.12 (3), p.e0174852-e0174852

2017

Volltextzugriff (PDF)

What Was the Set of Ubiquitin and Ubiquitin-Like Conjugating Enzymes in the Eukaryote Common Ancestor?

Journal of molecular evolution, 2009-06, Vol.68 (6), p.616-628

2009

Volltextzugriff (PDF)

Study of Ubiquitin Pathway Genes in a French Population with Amyotrophic Lateral Sclerosis: Focus on HECW1 Encoding the E3 Ligase NEDL1

International journal of molecular sciences, 2023-01, Vol.24 (2), p.1268

2023

Volltextzugriff (PDF)

Dysregulations of Expression of Genes of the Ubiquitin/SUMO Pathways in an In Vitro Model of Amyotrophic Lateral Sclerosis Combining Oxidative Stress and SOD1 Gene Mutation

International journal of molecular sciences, 2021-02, Vol.22 (4), p.1796

2021

Volltextzugriff (PDF)

Behavior and serotonergic disorders in rats exposed prenatally to valproate: A model for autism

Neuroscience letters, 2010-02, Vol.470 (1), p.55-59

2010

Volltextzugriff (PDF)

Metabolic Profile and Pathological Alterations in the Muscle of Patients with Early-Stage Amyotrophic Lateral Sclerosis

Biomedicines, 2022-06, Vol.10 (6), p.1307

2022

Volltextzugriff (PDF)

TAR DNA-binding protein of 43 kDa (TDP-43) and amyotrophic lateral sclerosis (ALS): a promising therapeutic target

Expert opinion on therapeutic targets, 2022-06, Vol.26 (6), p.575-592

2022

Volltextzugriff (PDF)

Genes containing hexanucleotide repeats resembling C9ORF72 and expressed in the central nervous system are frequent in the human genome

Neurobiology of aging, 2021-01, Vol.97, p.148.e1-148.e7

2021

Volltextzugriff (PDF)

LIMK2-1, a new isoform of human LIMK2, regulates actin cytoskeleton remodeling via a different signaling pathway than that of its two homologs, LIMK2a and LIMK2b

Biochemical journal, 2018-12, Vol.475 (23), p.3745-3761

2018

Volltextzugriff (PDF)

The effect of pH alterations on TDP-43 in a cellular model of amyotrophic lateral sclerosis

Biochemistry and biophysics reports, 2024-07, Vol.38, p.101664, Article 101664

2024

Volltextzugriff (PDF)

A novel mutation of the C-terminal amino acid of FUS (Y526C) strengthens FUS gene as the most frequent genetic factor in aggressive juvenile ALS

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2017-05, Vol.18 (3-4), p.298-301

2017

Volltextzugriff (PDF)

Post hoc analysis of plasma amino acid profiles: towards a specific pattern in autism spectrum disorder and intellectual disability

Annals of clinical biochemistry, 2018-09, Vol.55 (5), p.543-552

2018

Volltextzugriff (PDF)

Some CSF Kynurenine Pathway Intermediates Associated with Disease Evolution in Amyotrophic Lateral Sclerosis

Biomolecules (Basel, Switzerland), 2021-05, Vol.11 (5), p.691

2021

Volltextzugriff (PDF)

Inflammatory mediators, lipoproteins and apolipoproteins in early diagnosis of amyotrophic lateral sclerosis

SLAS technology, 2022-10, Vol.27 (5), p.327-334

2022

Volltextzugriff (PDF)

NSC-34 Motor Neuron-Like Cells Are Unsuitable as Experimental Model for Glutamate-Mediated Excitotoxicity

Frontiers in cellular neuroscience, 2016-05, Vol.10, p.118-118

2016

Volltextzugriff (PDF)

Combined Metabolomics and Transcriptomics Approaches to Assess the IL-6 Blockade as a Therapeutic of ALS: Deleterious Alteration of Lipid Metabolism

Neurotherapeutics, 2016-10, Vol.13 (4), p.905-917

2016

Volltextzugriff (PDF)

Iron Metabolism Disturbance in a French Cohort of ALS Patients

BioMed research international, 2014-01, Vol.2014 (2014), p.1-6

2014

Volltextzugriff (PDF)

Primary fibroblasts derived from sporadic amyotrophic lateral sclerosis patients do not show ALS cytological lesions

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2018-07, Vol.19 (5-6), p.446-456

2018

Volltextzugriff (PDF)

Effect of the oligodendrocyte myelin glycoprotein (OMgp) on the expansion and neuronal differentiation of rat neural stem cells

Brain research, 2009-08, Vol.1284, p.22-30

2009

Volltextzugriff (PDF)

Ferritin and LDL-cholesterol as biomarkers of fat-free mass loss in ALS

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2019-07, Vol.20 (5-6), p.441-444

2019

Volltextzugriff (PDF)

1 – 25 von 150

Suche als RSS-Feed

Aktive Filter

KollektionWK Lippincott Williams & Wilkins–Connect here FIRST to enable access

KollektionJournals@Ovid Complete

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(128)
Mit Volltextzugriff
(121)

Publikationsform

Artikel
(141)
Berichte
(9)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(107)
Life Sciences & Biomedicine
(97)
Humans
(70)
Life Sciences
(50)
Neurosciences & Neurology
(47)
Amyotrophic Lateral Sclerosis
(45)
Female
(43)
Male
(38)
Animals
(34)
Neurosciences
(29)
Clinical Neurology
(25)
Middle Aged
(25)
Als
(24)
Mutation
(22)
Aged
(20)
Amyotrophic Lateral Sclerosis - Genetics
(20)
Biochemistry & Molecular Biology
(19)
Adult
(18)
France
(17)
Biological And Medical Sciences
(16)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

InFUSing antisense oligonucleotides for treating ALS

TDP43 aggregates: the 'Schrödinger's cat' in amyotrophic lateral sclerosis

GC-MS-based urine metabolic profiling of autism spectrum disorders

Post-Translational Variants of Major Proteins in Amyotrophic Lateral Sclerosis Provide New Insights into the Pathophysiology of the Disease

The Roles of NEDD4 Subfamily of HECT E3 Ubiquitin Ligases in Neurodevelopment and Neurodegeneration

Deep sequencing is an appropriate tool for the selection of unique Hepatitis C virus (HCV) variants after single genomic amplification

What Was the Set of Ubiquitin and Ubiquitin-Like Conjugating Enzymes in the Eukaryote Common Ancestor?

Study of Ubiquitin Pathway Genes in a French Population with Amyotrophic Lateral Sclerosis: Focus on HECW1 Encoding the E3 Ligase NEDL1

Dysregulations of Expression of Genes of the Ubiquitin/SUMO Pathways in an In Vitro Model of Amyotrophic Lateral Sclerosis Combining Oxidative Stress and SOD1 Gene Mutation

Behavior and serotonergic disorders in rats exposed prenatally to valproate: A model for autism

Metabolic Profile and Pathological Alterations in the Muscle of Patients with Early-Stage Amyotrophic Lateral Sclerosis

TAR DNA-binding protein of 43 kDa (TDP-43) and amyotrophic lateral sclerosis (ALS): a promising therapeutic target

Genes containing hexanucleotide repeats resembling C9ORF72 and expressed in the central nervous system are frequent in the human genome

LIMK2-1, a new isoform of human LIMK2, regulates actin cytoskeleton remodeling via a different signaling pathway than that of its two homologs, LIMK2a and LIMK2b

The effect of pH alterations on TDP-43 in a cellular model of amyotrophic lateral sclerosis

A novel mutation of the C-terminal amino acid of FUS (Y526C) strengthens FUS gene as the most frequent genetic factor in aggressive juvenile ALS

Post hoc analysis of plasma amino acid profiles: towards a specific pattern in autism spectrum disorder and intellectual disability

Some CSF Kynurenine Pathway Intermediates Associated with Disease Evolution in Amyotrophic Lateral Sclerosis

Inflammatory mediators, lipoproteins and apolipoproteins in early diagnosis of amyotrophic lateral sclerosis

NSC-34 Motor Neuron-Like Cells Are Unsuitable as Experimental Model for Glutamate-Mediated Excitotoxicity

Combined Metabolomics and Transcriptomics Approaches to Assess the IL-6 Blockade as a Therapeutic of ALS: Deleterious Alteration of Lipid Metabolism

Iron Metabolism Disturbance in a French Cohort of ALS Patients

Primary fibroblasts derived from sporadic amyotrophic lateral sclerosis patients do not show ALS cytological lesions

Effect of the oligodendrocyte myelin glycoprotein (OMgp) on the expansion and neuronal differentiation of rat neural stem cells

Ferritin and LDL-cholesterol as biomarkers of fat-free mass loss in ALS

Aktive Filter

Suchergebnisse filtern