447 results on '"Strom, Roberto"'
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2. The Impact on Genetic Testing of Mutational Patterns of CFTR Gene in Different Clinical Macrocategories of Cystic Fibrosis
3. A Genotypic-Oriented View of CFTR Genetics Highlights Specific Mutational Patterns Underlying Clinical Macrocategories of Cystic Fibrosis
4. A new complex allele of the CFTR gene partially explains the variable phenotype of the L997F mutation
5. Differentiation of Myoblast Cell Lines and Biological Methylation: 3-deazaadenosine Stimulates Formation of Multinucleated Myofibers
6. Antibody‐mediated enzyme formation: Its legacy at age fifty‐four
7. Fluorometric Quantitation of Fluorescein-Coupled Antibodies Attached to the Cell Membrane
8. The Genetics of CFTR: Genotype - Phenotype Relationship, Diagnostic Challenge and Therapeutic Implications
9. A 96-well formatted method for exon and exon/intron boundary full sequencing of the CFTR gene
10. A reassessment of semiquantitative analytical procedures for DNA methylation: Comparison of bisulfite- and HpaII polymerase-chain-reaction-based methods
11. A template for mutational data analysis of the CFTR gene
12. In vitro induction of H1-H1 histone cross-linking by adenosine diphosphate-ribose polymers
13. Autoantibodies in Patients with Monoclonal Gammopathies
14. Influence of pre-existing methylation on the de novo activity of eukaryotic DNA methyltransferase
15. Zidovudine Inhibits Protein Kinase C Activity in Human Chronic Myeloid (K562) Cells
16. Does poly(ADP-ribosyl)ation regulate the DNA methylation pattern?
17. Different effects of histone H1 on de novo DNA methylation in vitro depend on both the DNA base composition and the DNA methyltransferase
18. High frequency of (TG) mT n variant tracts in the cystic fibrosis transmembrane conductance regulator gene in men with high semen viscosity
19. Expression of OP4 (ORL1, NOP1) receptors in vascular endothelium
20. Two-step formation of 1H NMR visible mobile lipids during apoptosis of paclitaxel-treated K562 cells
21. Inhibitory effect of somatostatin on neutral amino acid transport in isolated brain microvessels
22. Triacsin C inhibits the formation of 1H NMR-visible mobile lipids and lipid bodies in HuT 78 apoptotic cells
23. Expression of OP4 (ORL1, NOP 1) receptors in vascular endothelium
24. Effects of different oxidizing agents on neutral amino acid transport systems in isolated bovine brain microvessels
25. The expression of native and oxidized LDL receptors in brain microvessels is specifically enhanced by astrocytes-derived soluble factor(s)
26. Structural Aspects of the Binding of Melittin to Phospholipid Bilayers, as a Model for Protein-Lipid Interactions in Membranes
27. On the Structure of in Melittin in Aqueous Solutions and upon Interaction with Membrane Model Systems
28. The Dynamics of Myogenin Site-specific Demethylation Is Strongly Correlated with Its Expression and with Muscle Differentiation
29. 1H NMR-visible mobile lipid domains correlate with cytoplasmic lipid bodies in apoptotic T-lymphoblastoid cells
30. Nicotine Regulates Basic Fibroblastic Growth Factor and Transforming Growth Factor β1Production in Endothelial Cells
31. Biophysical and structural characterization of 1H-NMR-detectable mobile lipid domains in NIH-3T3 fibroblasts
32. Is There a Preferential Pathway for Antibody-Mediated Enzyme Activation?
33. MOESM1 of A Genotypic-Oriented View of CFTR Genetics Highlights Specific Mutational Patterns Underlying Clinical Macrocategories of Cystic Fibrosis
34. Emergence of blaKPC-3–Tn4401a in Klebsiella pneumoniae ST512 in the municipal wastewater treatment plant and in the university hospital of a town in central Italy
35. Enzyme defense against reactive oxygen derivatives. II. Erythrocytes and tumor cells
36. Influenza del pattern mutazionale del gene CFTR sul test genetico e sulla relazione genotipo-fenotipo in diverse forme di fibrosi cistica
37. GENETIC BASIS OF ALCOHOL DEPENDENCE: TRIALLELIC POLYMORPHISM OF THE SEROTONIN TRANSPORTER GENE IN A POPULATION OF ALCOHOL DEPENDENT SUBJECTS FROM ITALY
38. Genetica della dipendenza da alcol: studio dei polimorfismi 5HTTLPR e RS25531 del gene codificante per il trasportatore della serotonina (5-HTT)
39. Analisi mutazionale dei geni ApoA1 e LPL nella dislipidemia aterogena in età pediatrica
40. Correction: Atherogenic Dyslipidemia in Children: Evaluation of Clinical, Biochemical and Genetic Aspects
41. Atherogenic Dyslipidemia in Children: Evaluation of Clinical, Biochemical and Genetic Aspects
42. Homocyste(e)ine and Endothelial Dysfunction in Uncomplicated IDDM Patients
43. Occurrence of complex alleles, revealed by extensive mutational analysis, can account for high sweat test variability
44. The variable phenotype of the (TG)12T5 or L997F compound heterozygotes
45. High-throughput mutational analysis, complex alleles and genotype – phenotype relationship in Cystic Fibrosis
46. Automation of CFTR re-sequencing: time and cost analysis
47. Does male fertility impairment due to idiopathic semen hyperviscosity depend on CFTR gene mutations?
48. ELUCIDATION, BY LOW ANGLE X-RAY AND NEUTRON DIFFRACTION AND BY HIGH RESOLUTION NUCLEAR MAGNETIC RESONANCE, OF SOME STRUCTURAL ASPECTS OF THE INTERACTION OF BEE VENOM MELITTIN WITH PHOSPHOLIPIDS
49. Progettazione e validazione di un metodo semiautomatizzato di ricerca mutazionale nel CFTR, basato su multiplex mini-sequencing, integrato in una procedura a tre step ad elevata sensibilità diagnostica (detection rate)
50. Extensive CFTR mutational analysis in patients with CBAVD
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