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101. Transcriptional characterization of subcutaneous adipose tissue in obesity affected women highlights metabolic dysfunction and implications for lncRNAs

103. COVID-19 patients and Dementia: Frontal cortex transcriptomic data

104. Clinical Pregenetic Screening for Stroke Monogenic Diseases: Results From Lombardia GENS Registry

106. TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations

108. Neural Precursor Cells Expanded Inside the 3D Micro-Scaffold Nichoid Present Different Non-Coding RNAs Profiles and Transcript Isoforms Expression: Possible Epigenetic Modulation by 3D Growth

109. Plasmatic Hippuric Acid as a Hallmark of Frailty in an Italian Cohort: The Mediation Effect of Fruit–Vegetable Intake

115. Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1

116. RNA-seq Characterization of Sex-Differences in Adipose Tissue of Obesity Affected Patients: Computational Analysis of Differentially Expressed Coding and Non-Coding RNAs

117. Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

118. Drug treatments and interactions, disease progression and quality of life in ALS patients.

120. COVID‐19‐related neuropathology and microglial activation in elderly with and without dementia

121. Diagnostic Yield and Cost-Effectiveness of “Dynamic” Exome Analysis in Epilepsy with Neurodevelopmental Disorders: A Tertiary-Center Experience in Northern Italy

122. RNA-seq Characterization of Sex-Differences in Adipose Tissue of Obesity Affected Patients: Computational Analysis of Differentially Expressed Coding and Non-Coding RNAs

123. Case Report: Novel Compound Heterozygous RNASEH2B Mutations Cause Aicardi–Goutières Syndrome

124. PSEN1 Compound Heterozygous Mutations Associated with Cerebral Amyloid Angiopathy and Cognitive Decline Phenotype

126. Archaeogenomic distinctiveness of the Isthmo-Colombian area

127. Transcriptome Analysis of Subcutaneous Adipose Tissue from Severely Obese Patients Highlights Deregulation Profiles in Coding and Non-Coding Oncogenes

128. Hsp90‐mediated regulation of DYRK3 couples stress granule disassembly and growth via mTORC1 signaling

132. A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis

133. Mitogenome Relationships and Phylogeography of Barn Swallows (Hirundo rustica).

134. Hsp90‐mediated regulation of DYRK3 couples stress granule disassembly and growth via mTORC1 signaling

135. Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

136. Different miRNA Profiles in Plasma Derived Small and Large Extracellular Vesicles from Patients with Neurodegenerative Diseases

137. Transcriptome Analysis of Subcutaneous Adipose Tissue from Severely Obese Patients Highlights Deregulation Profiles in Coding and Non-Coding Oncogenes

138. Ruxolitinib in Aicardi-Goutières Syndrome

139. Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

142. Neural precursors cells expanded in a 3D micro-engineered niche present enhanced therapeutic efficacy in vivo

144. Alzheimer’s, Parkinson’s Disease and Amyotrophic Lateral Sclerosis Gene Expression Patterns Divergence Reveals Different Grade of RNA Metabolism Involvement

149. Different RNA profiles in plasma derived small and large extracellular vesicles of Neurodegenerative diseases patients

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