522 results on '"Ramirez-Alvarado, Marina"'
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2. Biophysical characterization of human-cell-expressed, full-length κI O18/O8, AL-09, λ6a, and Wil immunoglobulin light chains
3. A proteomic atlas of kidney amyloidosis provides insights into disease pathogenesis
4. A BAK subdomain that binds mitochondrial lipids selectively and releases cytochrome C
5. Scientific Societies Fostering Inclusive Scientific Environments through Travel Awards: Current Practices and Recommendations
6. Scientific Societies Fostering Inclusive Scientific Environments through Travel Awards: Current Practices and Recommendations
7. IGVL gene region usage correlates with distinct clinical presentation in IgM vs non-IgM light chain amyloidosis
8. Vesicular Stomatitis Virus Encoding a Destabilized Tumor Antigen Improves Activation of Anti-tumor T Cell Responses
9. A Proteomic Atlas of Cardiac Amyloid Plaques
10. Light chain amyloidosis induced inflammatory changes in cardiomyocytes and adipose-derived mesenchymal stromal cells
11. IgM AL amyloidosis: delineating disease biology and outcomes with clinical, genomic and bone marrow morphological features
12. A proteomic atlas of kidney amyloidosis provides insights into disease pathogenesis
13. Secondary Structure by Circular Dichroism, Experimental Assessment of
14. Human Thiopurine S-Methyltransferase Pharmacogenetics: Variant Allozyme Misfolding and Aggresome Formation
15. Mesenchymal stromal cells protect human cardiomyocytes from amyloid fibril damage
16. Kinetic stability and sequence/structure studies of urine-derived Bence-Jones proteins from multiple myeloma and light chain amyloidosis patients
17. B-type natriuretic peptide overexpression ameliorates hepatorenal fibrocystic disease in a rat model of polycystic kidney disease
18. A Systematic Exploration of the Influence of the Protein Stability on Amyloid Fibril Formation in vitro
19. Clarifying immunoglobulin gene usage in systemic and localized immunoglobulin light-chain amyloidosis by mass spectrometry
20. Assay to rapidly screen for immunoglobulin light chain glycosylation: a potential path to earlier AL diagnosis for a subset of patients
21. Design of a 20-Amino Acid, Three-Stranded β-Sheet Protein
22. Cell Damage in Light Chain Amyloidosis: FIBRIL INTERNALIZATION, TOXICITY AND CELL-MEDIATED SEEDING
23. Assays for Light Chain Amyloidosis Formation and Cytotoxicity
24. Thermodynamic and fibril formation studies of full length immunoglobulin light chain AL-09 and its germline protein using scan rate dependent thermal unfolding
25. Differential Effects on Light Chain Amyloid Formation Depend on Mutations and Type of Glycosaminoglycans
26. Solid-state NMR chemical shift assignments for AL-09 VL immunoglobulin light chain fibrils
27. Professional and Scientific Societies Impacting Diversity, Equity and Inclusion in STEMM
28. A BAK subdomain that binds mitochondrial lipids selectively and releases cytochrome C
29. Fibril Structure and Fibrillogenesis
30. Kinetic Control in Protein Folding for Light Chain Amyloidosis and the Differential Effects of Somatic Mutations
31. Evaluation of the BH3-only Protein Puma as a Direct Bak Activator
32. Immunoglobulin Light Chain and Systemic Light-Chain Amyloidosis
33. Pathologic light chain amyloidosis oligomer detection in urinary extracellular vesicles as a diagnostic tool for response and progression of disease
34. Tyrosine Residues Mediate Fibril Formation in a Dynamic Light Chain Dimer Interface
35. Correction: Assay to rapidly screen for immunoglobulin light chain glycosylation: a potential path to earlier AL diagnosis for a subset of patients
36. Glycosaminoglycans promote fibril formation by amyloidogenic immunoglobulin light chains through a transient interaction
37. Scientific Societies Fostering Inclusivity in the Life Sciences Through Engagement of Undergraduate Scientists
38. Serum immunoglobulin free light-chain measurement in primary amyloidosis: prognostic value and correlations with clinical features
39. Celastrol Inhibits Hsp90 Chaperoning of Steroid Receptors by Inducing Fibrillization of the Co-chaperone p23
40. A Single Mutation Promotes Amyloidogenicity through a Highly Promiscuous Dimer Interface
41. Mutations can cause light chains to be too stable or too unstable to form amyloid fibrils
42. Structural and Functional Studies of Truncated Hemolysin A from Proteus mirabilis
43. Structural Alterations within Native Amyloidogenic Immunoglobulin Light Chains
44. Beyond Ticking Boxes: Holistic Assessment of Travel Award Programs Is Essential for Inclusivity
45. Structural Insights into the Role of Mutations in Amyloidogenesis
46. A Reappraisal of Immunoglobulin Variable Gene Primers and Its Impact on Assessing Clonal Relationships Between PB B Cells and BM Plasma Cells in AL Amyloidosis
47. Biologic and genetic characterization of the novel amyloidogenic lambda light chain–secreting human cell lines, ALMC-1 and ALMC-2
48. Altered Dimer Interface Decreases Stability in an Amyloidogenic Protein
49. Salts enhance both protein stability and amyloid formation of an immunoglobulin light chain
50. Principles of Protein Misfolding
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