829 results on '"Ghidoni, R"'
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152. DISMETABOLISMO DEI METALLI E STRESS OSSIDATIVOIN PAZIENTI CON IN PARKINSON’S DISEASE DI UN’AREAINDUSTRIALE ESPOSTA AD INQUINAMENTO DA METALLI [Metals and oxidative stress in Parkinson’s Disease from industrial areas with exposure to environmental toxins or metal pollution]
153. Insulin-like growth factor binding protein-3 induces angiogenesis through IGF-I- and SphK1-dependent mechanisms
154. CHANGES IN RABBIT BRAIN CYTOSOLIC AND MEMBRANE BOUND GANGLIOSIDES DURING PRENATAL LIFE
155. Gangliosides and Associated Enzymes at the Nerve-Ending Membranes
156. Effect of the different supramolecular organization on the uptake and metabolization of exogenous GM1 ganglioside by human fibroblasts
157. Metals and oxidative stress in Parkinson’s disease
158. Familial Alzheimer’s Disease presenilin mutants reduce calcium levels of intracellular stores. A critical revaluation of the “calcium overload†hypothesis
159. Genotype and EEG phenotype in Alzheimer disease and mild cognitive impairment subjects
160. Genotipo e fenotipo EEG nella malattia di Alzheimer e in soggetti con lievi deficit cognitivi
161. Lack of association between MnSOD gene polymorphism and sporadic Alzheimer's disease
162. Synthetic hydroxylated aryl-naphthalene derivatives as resveratrol rigid analogues showing ceramide-mediated antiproliferative and pro-apoptotic properties
163. Influence of G1730A polymorphism of estrogen receptor beta gene on brain morphology in postmenopausal women
164. Behavior of gangliosides on dialysis
165. Resveratrol structure and ceramide-associated growth inhibition in prostate cancer cells
166. The Ca2+ overload hypothesis in the familial form of Alzheimer's disease: New light from presenilin 2 mutations
167. Frontotemporal dementia: impact of P301L tau mutation on a healthy carrier
168. Optimization-based nycely nonlinear modelling
169. BACE-2 is overexpressed in Down's syndrome
170. Microglia convert aggregated amyloid-β into neurotoxic forms through the shedding of microvesicles
171. Genetics and expression analysis of the transcription factor Sp4 in patients with Alzheimer’s disease and frontotemporal lobar degeneration.
172. Transcription factor Sp1 is regulated by hsa-miR-29b in peripheral blood mononuclear cells from patients with Alzheimer’s disease
173. Genetics and expression analysis of the specificity protein 4 gene (SP4) in patients with Alzheimer's disease and frontotemporal lobar degeneration
174. BAG1 is a protective factor for sporadic frontotemporal lobar degeneration but not for Alzheimer's disease
175. Causal frontotemporal lobar degeneration mutations: a novel mutation in MAPT associated with non-fluent progressive aphasia phenotype
176. Causal Frontotemporal Lobar Degeneration mutations: a novel MAPT mutation associated with the clinical phenotype of Progressive nonfluent Aphasia
177. Genetics and expression analysis of Sp4 transcription factor in patients with Alzheimer’s disease and frontotemporal lobar degeneration.
178. Role of hnRNP-A1 and miR-590-3p in neuronal death: genetics and expression analysis in patients with Alzheimer disease and frontotemporal lobar degeneration
179. A kibbutz full of lipids. Lipids: Regulatory Functions in Membrane Traffic and Cell Development, Kfar Blum Kibbutz Guest House, Galilee, Israel, May 10-15, 1998
180. C9ORF72 repeat expansions in cases with previously identified pathogenic mutations
181. Pattern of Cortical Thinning in Unaffected at Risk Members of Families with Mutations in Granulin (S34.006)
182. Evidence in Support of the AD Biomarker Dynamic Model from a Memory Clinic Naturalistic Series of Patients with Mild Cognitive Impairment (PD1.009)
183. Frontotemporal dementia: impact of P301L tau mutation on a healthy carrier
184. TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers
185. TheCST3B haplotype is associated with frontotemporal lobar degeneration
186. Longitudinal prognostic value of serum "free" copper in patients with Alzheimer disease
187. The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration
188. Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration
189. Association of Blood Pressure and Genetic Background With White Matter Lesions in Patients With Mild Cognitive Impairment
190. Role of non-canonical Beclin 1-independent autophagy in cell death induced by resveratrol in human breast cancer cells
191. Homocysteine and electroencephalographic rhythms in Alzheimer disease: A multicentric study
192. Topography of glycosyltransferases involved in the initial glycosylation of gangliosides
193. Precursor-product relationship between GM1 and GD1a biosynthesized from exogenous GM2 ganglioside in rat liver
194. Sub-Golgi distribution in rat liver of CMP-NeuAc: GM3- and CMP-NeuAc: GT1b alpha2-8 sialyltransferases and comparison with the distribution the other glycosyltransferase activities involved in ganglioside biosynthesis
195. Resveratrol as an anticancer nutrient: molecular basis, open questions and promises
196. A kibbutz full of lipids. Lipids: Regulatory Functions in Membrane Traffic and Cell Development, Kfar Blum Kibbutz Guest House, Galilee, Israel, May 10-15, 1998
197. Microglia convert aggregated amyloid-β into neurotoxic forms through the shedding of microvesicles.
198. The Metabolic Processing of Glycosphingolipids in HT-29 Cells Is Differentiation-Dependent
199. Estimating the Age of the Most Common Italian GRN Mutation: Walking Back to Canossa Times.
200. Replication Study to Confirm the Role of CYP2D6 Polymorphism rs1080985 on Donepezil Efficacy in Alzheimer's Disease Patients.
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