Arndt Rolfs

Albrecht-Kossel-Institute for Neuroregeneration, University of Rostock

Affiliated withUniversity of Rostock School of Medicine University of Rostock University Rostock Medical Center

Research Area

BioengineeringBiologyMedicine

Biography

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JoVE Journal Publications

ArticleTotal : 3	Year
Publication title	2012
Publication title	2012
Publication title	2017

Other Publications

Article	Year
NPC1: Complete genomic sequence, mutation analysis, and characterization of haplotypes. Human mutation\| PubMed ID: 11754101	2002
Residual galactosylsphingosine (psychosine) beta-galactosidase activities and associated GALC mutations in late and very late onset Krabbe disease. Clinica chimica acta; international journal of clinical chemistry\| PubMed ID: 11814461	2002
Disorganization of the desmin cytoskeleton and mitochondrial dysfunction in plectin-related epidermolysis bullosa simplex with muscular dystrophy. Journal of neuropathology and experimental neurology\| PubMed ID: 12071635	2002
Trinucleotide repeat expansions in the junctophilin-3 gene are not found in Caucasian patients with a Huntington's disease-like phenotype. Annals of neurology\| PubMed ID: 12112122	2002
Ciliary neurotrophic factor overexpression in neural progenitor cells (ST14A) increases proliferation, metabolic activity, and resistance to stress during differentiation. Journal of neuroscience research\| PubMed ID: 12503085	2003
Gene expression profiling of ciliary neurotrophic factor-overexpressing rat striatal progenitor cells (ST14A) indicates improved stress response during the early stage of differentiation. Journal of neuroscience research\| PubMed ID: 12815707	2003
Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17). Annals of neurology\| PubMed ID: 12953269	2003
Lymphocyte subpopulations, oxidative burst and apoptosis in peripheral blood cells of patients with multiple sclerosis-effect of interferon-beta. Autoimmunity\| PubMed ID: 14567559	2003
Gene-expression profiling of the early stages of MOG-induced EAE proves EAE-resistance as an active process. Journal of neuroimmunology\| PubMed ID: 15145614	2004
An impaired neocortical Ih is associated with enhanced excitability and absence epilepsy. The European journal of neuroscience\| PubMed ID: 15182313	2004
Overexpression of glial cell line-derived neurotrophic factor induces genes regulating migration and differentiation of neuronal progenitor cells. Experimental cell research\| PubMed ID: 15212950	2004
Wnt-5a expression in the rat neuronal progenitor cell line ST14A. Experimental brain research. Experimentelle Hirnforschung. ExpÃ©rimentation cÃ©rÃ©brale\| PubMed ID: 15309358	2004
Neuromodulation by a cytokine: interferon-beta differentially augments neocortical neuronal activity and excitability. Journal of neurophysiology\| PubMed ID: 15385586	2005
Dopamine exerts no acute effects on Kv1.3 in activated encephalitogenic T cells. Neuroimmunomodulation\| PubMed ID: 15756052	2005
Identification of quantitative trait loci controlling cortical motor evoked potentials in experimental autoimmune encephalomyelitis: correlation with incidence, onset and severity of disease... Human molecular genetics\| PubMed ID: 15917267	2005
Representation of individual gene expression in completely pooled mRNA samples. Bioscience, biotechnology, and biochemistry\| PubMed ID: 15973040	2005
Functional significance of HCN2/3-mediated I(h) in striatal cells at early developmental stages. Journal of neuroscience research\| PubMed ID: 16175581	2005
Prevalence of Fabry disease in patients with cryptogenic stroke: a prospective study. Lancet\| PubMed ID: 16298216	2005
2-DE proteome analysis of a proliferating and differentiating human neuronal stem cell line (ReNcell VM). Proteomics\| PubMed ID: 16475233	2006
Ih is maturing: implications for neuronal development. Neuro-degenerative diseases\| PubMed ID: 16909033	2006
Wnt signal pathways and neural stem cell differentiation. Neuro-degenerative diseases\| PubMed ID: 16909041	2006
2-DE proteomic profiling of neuronal stem cells. Neuro-degenerative diseases\| PubMed ID: 16909046	2006
Repeat expansion in spinocerebellar ataxia type 17 alleles of the TATA-box binding protein gene: an evolutionary approach. European journal of human genetics : EJHG\| PubMed ID: 17033685	2007
3-Hydroxy-3-methylglutaryl coenzyme A reductase inhibitor Atorvastatin mediated effects depend on the activation status of target cells in PLP-EAE. Journal of autoimmunity\| PubMed ID: 17085013	2006
2-DE profiling of GDNF overexpression-related proteome changes in differentiating ST14A rat progenitor cells. Proteomics\| PubMed ID: 17146836	2007
Efferent connections of the parabigeminal nucleus to the amygdala and the superior colliculus in the rat: a double-labeling fluorescent retrograde tracing study. Brain research\| PubMed ID: 17196559	2007
Deep brain stimulation in a rat model modulates TH, CaMKIIa and Homer1 gene expression. The European journal of neuroscience\| PubMed ID: 17241285	2007
A rare manifestation of Fabry's disease. Swiss medical weekly\| PubMed ID: 17370152	2007
Neurological and brain MRS findings in patients with Gaucher disease type 1. Molecular genetics and metabolism\| PubMed ID: 17560820	2007
Long-term course and mutational spectrum of spatacsin-linked spastic paraplegia. Annals of neurology\| PubMed ID: 18067136	2007
Efficient palladium-catalyzed synthesis of 3-aryl-4-indolylmaleimides. Organic & biomolecular chemistry\| PubMed ID: 18327323	2008
Increasing extracellular potassium results in subthalamic neuron activity resembling that seen in a 6-hydroxydopamine lesion. Journal of neurophysiology\| PubMed ID: 18385482	2008
Heterozygous S44L missense change of the spastin gene in amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases\| PubMed ID: 18608088	2008
New aspects of liver abnormalities as part of the systemic mast cell activation syndrome. Liver international : official journal of the International Association for the Study of the Liver\| PubMed ID: 18662284	2009
Specific properties of sodium currents in multipotent striatal progenitor cells. The European journal of neuroscience\| PubMed ID: 18783365	2008
Differential astroglial activation in 6-hydroxydopamine models of Parkinson's disease. Neuroscience research\| PubMed ID: 18824050	2008
In vitro characterization of embryionic ST14A-cells. The International journal of neuroscience\| PubMed ID: 18853328	2008
The microstructure of cornea verticillata in Fabry disease and amiodarone-induced keratopathy: a confocal laser-scanning microscopy study. Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fÃ¼r klinische und experimentelle Ophthalmologie\| PubMed ID: 18931853	2009
Cadherin-20 expression by motor neurons is regulated by Sonic hedgehog during spinal cord development. Neuroreport\| PubMed ID: 19218874	2009
Efferent projections of the anterior and posterodorsal regions of the medial nucleus of the amygdala in the mouse. Cells, tissues, organs\| PubMed ID: 19287129	2009
Ataxia oculomotor apraxia type 2: course over 27 years and a novel stop mutation in the senataxin gene. Journal of neurology\| PubMed ID: 19377860	2009
Leukodystrophies and other genetic metabolic leukoencephalopathies in children and adults. Brain & development\| PubMed ID: 19427149	2010
Interferon-beta modulates protein synthesis in the central nervous system. Journal of neuroimmunology\| PubMed ID: 19541371	2009
Protection of neurons derived from human neural progenitor cells by veratridine. Neuroreport\| PubMed ID: 19617853	2009
Structural changes associated with progression of motor deficits in spinocerebellar ataxia 17. Cerebellum (London, England)\| PubMed ID: 20016963	2010
A new facile synthesis of 3-amidoindole derivatives and their evaluation as potential GSK-3beta inhibitors. Organic & biomolecular chemistry\| PubMed ID: 20165807	2010
Expression of seven members of the ADAM family in developing chicken spinal cord. Developmental dynamics : an official publication of the American Association of Anatomists\| PubMed ID: 20235233	2010
Design and validation of a metabolic disorder resequencing microarray (BRUM1). Human mutation\| PubMed ID: 20578233	2010
Regional expression of the ADAMs in developing chicken cochlea. Developmental dynamics : an official publication of the American Association of Anatomists\| PubMed ID: 20658692	2010
Novel indolylmaleimide acts as GSK-3beta inhibitor in human neural progenitor cells. Bioorganic & medicinal chemistry\| PubMed ID: 20708937	2010
Differentiation of human neural progenitor cells regulated by Wnt-3a. Biochemical and biophysical research communications\| PubMed ID: 20735988	2010
Small molecule GSK-3 inhibitors increase neurogenesis of human neural progenitor cells. Neuroscience letters\| PubMed ID: 21056624	2011
Effect of 3D-scaffold formation on differentiation and survival in human neural progenitor cells. Biomedical engineering online\| PubMed ID: 21070668	2010
Expert opinion on temporary treatment recommendations for Fabry disease during the shortage of enzyme replacement therapy (ERT). Molecular genetics and metabolism\| PubMed ID: 21123099	2011
Erythropoietin and the effect of oxygen during proliferation and differentiation of human neural progenitor cells. BMC cell biology\| PubMed ID: 21126346	2010
Neuroproteomics in stem cell differentiation. Proteomics. Clinical applications\| PubMed ID: 21136647	2007
Protocol and methodology of the Stroke in Young Fabry Patients (sifap1) study: a prospective multicenter European study of 5,024 young stroke patients aged 18-55 years. Cerebrovascular diseases (Basel, Switzerland)\| PubMed ID: 21178350	2011
Basilar artery diameter is a potential screening tool for Fabry disease in young stroke patients. Cerebrovascular diseases (Basel, Switzerland)\| PubMed ID: 21196729	2011
Persistent increase in cardiac troponin I in Fabry disease: a case report. BMC cardiovascular disorders\| PubMed ID: 21281467	2011
CAG repeats determine brain atrophy in spinocerebellar ataxia 17: a VBM study. PloS one\| PubMed ID: 21311576	2011
Juvenile parkinsonism associated with heterozygous frameshift ATP13A2 gene mutation. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society\| PubMed ID: 21316993	2011
Morphological alterations of the cornea in the mouse model of niemann-pick disease type c1. Cornea\| PubMed ID: 21317782	2011
Hereditary spastic paraplegia associated with axonal neuropathy: a novel mutation of SPG3A in a large family. Journal of clinical neuromuscular disease\| PubMed ID: 21321493	2011
Amygdalotrigeminal projection in the rat: An anterograde tracing study. Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft\| PubMed ID: 21333509	2011
Vocal cord paralysis and rapid progressive motor neuron disease by the I113F mutation in SOD1 gene. Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases\| PubMed ID: 21413851	2011
Regional expression of ADAM19 during chicken embryonic development. Development, growth & differentiation\| PubMed ID: 21492148	2011
Differential expression of the ADAMs in developing chicken retina. Development, growth & differentiation\| PubMed ID: 21671920	2011
Quantitative and dynamic expression profile of premature and active forms of the regional ADAM proteins during chicken brain development. Cellular & molecular biology letters\| PubMed ID: 21786032	2011
Quantitative and kinetic profile of Wnt/Î²-catenin signaling components during human neural progenitor cell differentiation. Cellular & molecular biology letters\| PubMed ID: 21805133	2011
Human Neural Progenitor Cells Show Functional Neuronal Differentiation and Regional Preference After Engraftment onto Hippocampal Slice Cultures. Stem cells and development\| PubMed ID: 21867424	2011
Orexinergic innervation of the extended amygdala and basal ganglia in the rat. Brain structure & function\| PubMed ID: 21935673	2011
Decreased expression of myelin gene regulatory factor in Niemann-Pick type C 1 mouse. Metabolic brain disease\| PubMed ID: 21938520	2011
An unusual neurological syndrome of crawling gait, dystonia, pyramidal signs, and limited speech. Movement disorders : official journal of the Movement Disorder Society\| PubMed ID: 21953512	2011
A novel SGCE gene mutation causing myoclonus dystonia in a family with an unusual phenotype. Acta paediatrica (Oslo, Norway : 1992)\| PubMed ID: 22026499	2012
Corneal alterations during combined therapy with cyclodextrin/allopregnanolone and miglustat in a knock-out mouse model of NPC1 disease. PloS one\| PubMed ID: 22163015	2011
Expression patterns of ADAMs in the developing chicken lens. Journal of molecular histology\| PubMed ID: 22246534	2012
ADAM17 overexpression promotes angiogenesis by increasing blood vessel sprouting and pericyte number during brain microvessel development. The International journal of developmental biology\| PubMed ID: 22252493	2011
Increased excitability and compromised long-term potentiation in the neocortex of NPC1(-/-) mice. Brain research\| PubMed ID: 22325094	2012
Journal of nuclear medicine : official publication, Society of Nuclear Medicine\| PubMed ID: 22653791	2012
NeuroImage\| PubMed ID: 22659444	2012
Kidney function and white matter disease in young stroke patients: analysis of the stroke in young fabry patients study population. Stroke; a journal of cerebral circulation\| PubMed ID: 22723456	2012
Rett-like onset in late-infantile neuronal ceroid lipofuscinosis (CLN7) caused by compound heterozygous mutation in the MFSD8 gene and review of the literature data on clinical onset signs. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society\| PubMed ID: 25439737	2015