270 results on '"Farinha, Carlos M."'
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2. Fundamental and translational research in Cystic Fibrosis – why we still need it
3. Severity of the S1251N allele in cystic fibrosis is affected by the presence of the F508C variant in cis
4. Comparison of Cas9 and Cas12a CRISPR editing methods to correct the W1282X-CFTR mutation
5. LMTK2 switches on canonical TGF-β1 signaling in human bronchial epithelial cells.
6. Organoids as a personalized medicine tool for ultra-rare mutations in cystic fibrosis: The case of S955P and 1717-2A>G
7. Cell type-specific regulation of CFTR trafficking—on the verge of progress
8. CFTR and Cystic Fibrosis
9. CyFi-MAP: an interactive pathway-based resource for cystic fibrosis
10. R560S: A class II CFTR mutation that is not rescued by current modulators
11. Protein and lipid interactions – Modulating CFTR trafficking and rescue
12. The bidirectional relationship between CFTR and lipids
13. Proteomic interaction profiling reveals KIFC1 as a factor involved in early targeting of F508del-CFTR to degradation
14. Use of adenine base editing and homology-independent targeted integration strategies to correct the cystic fibrosis causing variant, W1282X
15. Personalized medicine: Function of CFTR variant p.Arg334Trp is rescued by currently available CFTR modulators
16. Measurements of Functional Responses in Human Primary Lung Cells as a Basis for Personalized Therapy for Cystic Fibrosis
17. Rescue of Rare CFTR Trafficking Mutants Highlights a Structural Location-Dependent Pattern for Correction
18. Fundamental and translational research in Cystic Fibrosis – why we still need it
19. LMTK2-mediated Phosphorylation Regulates CFTR Endocytosis in Human Airway Epithelial Cells
20. CFTR and Cystic Fibrosis
21. CFTR and Cystic Fibrosis
22. From the endoplasmic reticulum to the plasma membrane: mechanisms of CFTR folding and trafficking
23. Revertants, Low Temperature, and Correctors Reveal the Mechanism of F508del-CFTR Rescue by VX-809 and Suggest Multiple Agents for Full Correction
24. Absence of EPAC1 Signaling to Stabilize CFTR in Intestinal Organoids
25. Molecular mechanisms of cystic fibrosis – how mutations lead to misfunction and guide therapy
26. Investigating Alternative Transport of Integral Plasma Membrane Proteins from the ER to the Golgi: Lessons from the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)
27. Rescue of Mutant CFTR Trafficking Defect by the Investigational Compound MCG1516A
28. Rare Trafficking CFTR Mutations Involve Distinct Cellular Retention Machineries and Require Different Rescuing Strategies
29. Revisiting CFTR Interactions: Old Partners and New Players
30. Repairing the basic defect in cystic fibrosis – one approach is not enough
31. Integrity and Stability of PTC Bearing CFTR mRNA and Relevance to Future Modulator Therapies in Cystic Fibrosis
32. Solubilizing Mutations Used to Crystallize One CFTR Domain Attenuate the Trafficking and Channel Defects Caused by the Major Cystic Fibrosis Mutation
33. Teaching Biochemistry at Lisbon University--Facing the Challenge of the Bologna Declaration in the 25th Anniversary of the Biochemistry Course
34. Revertant mutants modify, but do not rescue, the gating defect of the cystic fibrosis mutant G551D-CFTR
35. Disrupting the TGF-β–Wnt Balance to Control the Polarity of the Cystic Fibrosis Airway Epithelium.
36. Differential Gene Expression Analysis Reveals Global LMTK2 Regulatory Network and Its Role in TGF-β1 Signaling
37. Control of cystic fibrosis transmembrane conductance regulator membrane trafficking: not just from the endoplasmic reticulum to the Golgi
38. Post-translational modifications of CFTR: insight into protein trafficking and cystic fibrosis disease
39. In Vivo Pretargeting Based on Cysteine-Selective Antibody Modification with IEDDA Bioorthogonal Handles for Click Chemistry
40. From disease mechanisms to novel therapies and back
41. Cytoskeleton regulators CAPZA2 and INF2 associate with CFTR to control its plasma membrane levels under EPAC1 activation
42. Full Rescue of F508del-CFTR Processing and Function by CFTR Modulators Can Be Achieved by Removal of Two Regulatory Regions
43. Improved Fmoc‐solid‐phase peptide synthesis of an extracellular loop of CFTR for antibody selection by the phage display technology
44. Mechanical Properties of Human Bronchial Epithelial Cells Expressing Wt- and Mutant CFTR
45. Exploring the basic mechanisms in Cystic Fibrosis: Promoting data presentation and discussion at the 16th ECFS Basic Science Conference
46. Biochemical methods to assess CFTR expression and membrane localization
47. Antibodies for CFTR studies
48. Methods for RNA extraction, cDNA preparation and analysis of CFTR transcripts
49. Non-PCR methods for the analysis of CFTR transcripts
50. Analysis of genomic CFTR DNA
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