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2. Mapping the human genetic architecture of COVID-19

3. Genomewide Association Study of Severe Covid-19 with Respiratory Failure

4. The largest monocentric study on sex distribution, penetrance, incidence, and association with dementia of GBA mutations in Parkinson's disease

5. The soluble glycoprotein NMB (GPNMB) produced by macrophages induces cancer stemness and metastasis via CD44 and IL-33

8. A ‘Multiomic’ Approach of Saliva Metabolomics, Microbiota, and Serum Biomarkers to Assess the Need of Hospitalization in Coronavirus Disease 2019

11. Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis

16. Detailed stratified GWAS analysis for severe COVID-19 in four European populations

17. MEDTEC Students against Coronavirus: Investigating the Role of Hemostatic Genes in the Predisposition to COVID-19 Severity

18. Metagenomic analysis of intestinal mucosa revealed a specific eukaryotic gut virome signature in early-diagnosed inflammatory bowel disease

19. The oxytocin receptor antagonist atosiban inhibits cell growth via a 'biased agonist' mechanism

20. Low-grade parental gonosomal mosaicism in CHD2 siblings with Smith-Magenis-like syndrome.

22. Genetic susceptibility to severe COVID-19.

23. The circular RNA landscape in multiple sclerosis: Disease-specific associated variants and exon methylation shape circular RNA expression profile.

24. Detailed stratified GWAS analysis for severe COVID-19 in four European populations.

25. Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk.

26. MEDTEC Students against Coronavirus: Investigating the Role of Hemostatic Genes in the Predisposition to COVID-19 Severity.

27. Screening of LRP10 mutations in Parkinson's disease patients from Italy.

28. A rapid and low-cost test for screening the most common Parkinson's disease-related GBA variants.

29. The SPID-GBA study: Sex distribution, Penetrance, Incidence, and Dementia in GBA-PD.

32. Metagenomic analysis of intestinal mucosa revealed a specific eukaryotic gut virome signature in early-diagnosed inflammatory bowel disease.

33. First Replication of the Involvement of OTUD6B in Intellectual Disability Syndrome With Seizures and Dysmorphic Features.

34. The GBAP1 pseudogene acts as a ceRNA for the glucocerebrosidase gene GBA by sponging miR-22-3p.

35. DNAJC12 and dopa-responsive nonprogressive parkinsonism.

36. Exploring the global landscape of genetic variation in coagulation factor XI deficiency.

37. miR-634 is a Pol III-dependent intronic microRNA regulating alternative-polyadenylated isoforms of its host gene PRKCA.

38. The Characterization of GSDMB Splicing and Backsplicing Profiles Identifies Novel Isoforms and a Circular RNA That Are Dysregulated in Multiple Sclerosis.

39. Meta-Analysis of Multiple Sclerosis Microarray Data Reveals Dysregulation in RNA Splicing Regulatory Genes.

40. Two novel splicing mutations in the SLC45A2 gene cause Oculocutaneous Albinism Type IV by unmasking cryptic splice sites.

41. Congenital hypofibrinogenemia associated with novel homozygous fibrinogen Aα and heterozygous Bβ chain mutations.

42. Evidence of liquid crystal-assisted abiotic ligation of nucleic acids.

43. Glucocerebrosidase mutations in primary parkinsonism.

44. Functional characterization of two novel splicing mutations in the OCA2 gene associated with oculocutaneous albinism type II.

45. Dual role of G-runs and hnRNP F in the regulation of a mutation-activated pseudoexon in the fibrinogen gamma-chain transcript.

46. Mutational screening and zebrafish functional analysis of GIGYF2 as a Parkinson-disease gene.

47. Oxytocin-induced cell growth proliferation in human myometrial cells and leiomyomas.

48. Molecular characterization of in-frame and out-of-frame alternative splicings in coagulation factor XI pre-mRNA.

49. Analysis of the structural effects of four novel and a previously known mutations causing factor XI deficiency.

50. Association and functional analyses of MEF2A as a susceptibility gene for premature myocardial infarction and coronary artery disease.

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