1,429 results on '"Rolfs, Arndt"'
Search Results
202. Overexpression of glial cell line-derived neurotrophic factor induces genes regulating migration and differentiation of neuronal progenitor cells
203. An impaired neocortical Ih is associated with enhanced excitability and absence epilepsy
204. Disorganization of the Desmin Cytoskeleton and Mitochondrial Dysfunction in Plectin-Related Epidermolysis Bullosa Simplex with Muscular Dystrophy
205. In vitro enzyme measurement to test pharmacological chaperone responsiveness in fabry and pompe disease
206. Gene expression profiling of the nervous system in murine experimental autoimmune encephalomyelitis
207. Biallelic loss‐of‐function HACD1 variants are a bona fide cause of congenital myopathy.
208. Hepatosplenomegalic lipidosis: what unless Gaucher? Adult cholesteryl ester storage disease (CESD) with anemia, mesenteric lipodystrophy, increased plasma chitotriosidase activity and a homozygous lysosomal acid lipase −1 exon 8 splice junction mutation
209. Monitoring the Effectiveness of Anticoagulative Therapy in Left Atrial Spontaneous Echo Contrast by Cerebral Microemboli Detection
210. Evaluation of Two Liver Treatment Strategies in a Mouse Model of Niemann–Pick-Disease Type C1
211. De Novo Variants in TAOK1 Cause Neurodevelopmental Disorders
212. Glucosylsphingosine (lyso-Gb1) as a Biomarker for Monitoring Treated and Untreated Children with Gaucher Disease
213. Genotype–Phenotype Correlation in a New Fabry-Disease-Causing Mutation
214. A hexanucleotide repeat modifies expressivity of X‐linked dystonia parkinsonism
215. Clinical Exome Sequencing unravels new disease-causing mutations in the myeloproliferative neoplasms: A pilot study in patients from the state of Qatar
216. A homozygous frameshift variant in an alternatively spliced exon of DLG5 causes hydrocephalus and renal dysplasia
217. Assessment of Cardiac Involvement in Fabry Disease (FD) with Native T1 Mapping
218. Long-term follow-up of 103 untreated adult patients with type 1 Gaucher disease
219. Longitudinal follow-up (4 years) of lyso-Gb1 in children with Gaucher disease in a single center cohort
220. Clinical, biomarker and genetic spectrum of Niemann-Pick type C in Egypt: The detection of nine novel NPC1 mutations
221. A call for considering biochemical concepts in clinical genetics research
222. Persistent increase in cardiac troponin I in Fabry disease: a case report
223. Erythropoietin and the effect of oxygen during proliferation and differentiation of human neural progenitor cells
224. Effect of 3D-scaffold formation on differentiation and survival in human neural progenitor cells
225. Isolation of DNA from Cells and Tissue for PCR
226. Restriction Fragment Analysis
227. Review of Different Heat-Stable DNA Polymerases
228. Oligonucleotides in the Field of PCR
229. PCR Contamination and Falsely Interpreted Results
230. Substances Affecting PCR: Inhibition or Enhancement
231. Alternative Methods to PCR
232. General Applications of PCR
233. In-Situ Polymerase Chain Reaction
234. Cloning Methods Using PCR
235. Addendum: Methodological examples for the application of the Polymerase chain reaction
236. Quantification of PCR Products
237. Optimization Strategies
238. Reverse Transcription/PCR (RT-PCR)
239. Application of PCR to Analyze Unknown Sequences
240. PCR: Clinical Diagnostics and Research
241. Biological Material Amenable to PCR
242. Isolation of RNA from Cells and Tissue for PCR
243. Multiplex PCR
244. Site-Directed Mutagenesis Using the PCR
245. Detection of Single Base Changes Using PCR
246. Methods for Identification of Amplified PCR Products
247. Physical Features of Thermocyclers and Their Influence on the Efficiency of PCR Amplification
248. PCR Principles and Reaction Components
249. Non-Radioactive, Direct, Solid-Phase Sequencing of Genomic DNA Obtained from Polymerase Chain Reaction
250. Residual galactosylsphingosine (psychosine) β-galactosidase activities and associated GALC mutations in late and very late onset Krabbe disease
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.