203 results on '"Brown, Kristy J."'
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2. Microdystrophin Expression as a Surrogate Endpoint for Duchenne Muscular Dystrophy Clinical Trials
3. Clinical potential of microdystrophin as a surrogate endpoint
4. Creation and characterization of an immortalized canine myoblast cell line: Myok9
5. Biomarkers for Muscle Disease Gene Therapy
6. Histological and Biochemical Evaluation of Muscle Gene Therapy
7. Membrane recruitment of nNOSµ in microdystrophin gene transfer to enhance durability
8. Chapter 6 - The use of proteomic analysis to study trafficking defects in axons
9. TNF-α-Induced microRNAs Control Dystrophin Expression in Becker Muscular Dystrophy
10. The use of urinary and kidney SILAM proteomics to monitor kidney response to high dose morpholino oligonucleotides in the mdx mouse
11. Assessment of systemic AAV-microdystrophin gene therapy in the GRMD model of Duchenne muscular dystrophy
12. Proteomic analysis of Medulloblastoma reveals functional biology with translational potential
13. The human secretome atlas initiative: Implications in health and disease conditions
14. Sparing of the Dystrophin-Deficient Cranial Sartorius Muscle Is Associated with Classical and Novel Hypertrophy Pathways in GRMD Dogs
15. Interlaboratory Study on Differential Analysis of Protein Glycosylation by Mass Spectrometry: The ABRF Glycoprotein Research Multi-Institutional Study 2012
16. Identification of Disease Specific Pathways Using in Vivo SILAC Proteomics in Dystrophin Deficient mdx Mouse
17. The Involvement of Acidic Nucleoplasmic DNA-binding Protein (And-1) in the Regulation of Prereplicative Complex (pre-RC) Assembly in Human Cells
18. Use of Quantitative Membrane Proteomics Identifies a Novel Role of Mitochondria in Healing Injured Muscles
19. Characterization of transferrin glycopeptide structures in human cerebrospinal fluid
20. Quantitative Proteomic Analyses of Human Cytomegalovirus-Induced Restructuring of Endoplasmic Reticulum-Mitochondrial Contacts at Late Times of Infection
21. The use of proteomic analysis to study trafficking defects in axons
22. The Effect of Immunomodulatory Treatments on Anti-Dystrophin Immune Response After AAV Gene Therapy in Dystrophin Deficient mdx Mice
23. Interrogation of Dystrophin and Dystroglycan Complex Protein Turnover After Exon Skipping Therapy
24. Aicardi–Goutières syndrome harbours abundant systemic and brain-reactive autoantibodies
25. Quantitative Proteomics Reveals an Altered Cystic Fibrosis In Vitro Bronchial Epithelial Secretome
26. Dystrophin deficiency leads to disturbance of LAMP1-vesicle-associated protein secretion
27. Discovery of serum protein biomarkers in the mdx mouse model and cross-species comparison to Duchenne muscular dystrophy patients
28. Directional Secretomes Reflect Polarity-Specific Functions in an In Vitro Model of Human Bronchial Epithelium
29. Activation of the Ubiquitin Proteasome Pathway in a Mouse Model of Inflammatory Myopathy: A Potential Therapeutic Target
30. Propranolol-Mediated Attenuation of MMP-9 Excretion in Infants With Hemangiomas
31. Current Proteome Profiling Methods
32. Time Series Proteome Profiling
33. Advances in the proteomic investigation of the cell secretome
34. Integrated genomics and proteomics of the Torpedo californica electric organ: concordance with the mammalian neuromuscular junction
35. Pathological Issues in Dystrophinopathy in the Age of Genetic Therapies
36. Effect of endurance exercise on microRNAs in myositis skeletal muscle—A randomized controlled study
37. First patients treated with a 1.5 T MRI-Linac : Clinical proof of concept of a high-precision, high-field MRI guided radiotherapy treatment
38. First patients treated with a 1.5 T MRI-Linac: Clinical proof of concept of a high-precision, high-field MRI guided radiotherapy treatment
39. Mitochondria mediate cell membrane repair and contribute to Duchenne muscular dystrophy
40. Serum pharmacodynamic biomarkers for chronic corticosteroid treatment of children
41. Clinical utility of serum biomarkers in Duchenne muscular dystrophy
42. Somatic mosaicism due to a reversion variant causing hemi-atrophy: a novel variant of dystrophinopathy
43. SuperSILAC Quantitative Proteome Profiling of Murine Middle Ear Epithelial Cell Remodeling with NTHi
44. Aicardi-Goutières syndrome harbours abundant systemic and brain-reactive autoantibodies
45. Elusive sources of variability of dystrophin rescue by exon skipping
46. Extraordinary Diversity of Immune Response Proteins among Sea Urchins: Nickel-Isolated Sp185/333 Proteins Show Broad Variations in Size and Charge
47. Proteomic profiling of high risk medulloblastoma reveals functional biology
48. Mechanism of Ca2+-triggered ESCRT assembly and regulation of cell membrane repair
49. Proteomic analysis of pediatric sinonasal secretions shows increased MUC5B mucin in CRS
50. Aicardi–Goutières syndrome harbours abundant systemic and brain-reactive autoantibodies
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