23,273 results on '"genetics (clinical)"'
Search Results
2. International Society for Cell & Gene Therapy Stem Cell Engineering Committee: Cellular therapies for the treatment of graft-versus-host-disease after hematopoietic stem cell transplant
3. Bone mesenchymal stromal cell-derived small extracellular vesicles inhibit inflammation and ameliorate sepsis via delivery of microRNA-21a-5p
4. Do classical and computerized cognitive tests have equal intrarater reliability in myotonic dystrophy type 1?
5. Pain interference and fatigue in limb-girdle muscular dystrophy R9
6. Associations of granulocyte colony-stimulating factor with toxicities and efficacy of chimeric antigen receptor T-cell therapy in relapsed or refractory multiple myeloma
7. 253rd ENMC international workshop: Striated muscle laminopathies - natural history and clinical trial readiness. 24–26 June 2022, Hoofddorp, the Netherlands
8. Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysis
9. Limb-girdle myopathy and mild intellectual disability: The expanding spectrum of TANGO2-related disease
10. Impact of soluble tumor necrosis factor-related apoptosis-inducing ligand released by engineered adipose mesenchymal stromal cells on white blood cells
11. Safety, tolerability and pharmacokinetics of eteplirsen in young boys aged 6–48 months with Duchenne muscular dystrophy amenable to exon 51 skipping
12. Engineered exosome-mediated messenger RNA and single-chain variable fragment delivery for human chimeric antigen receptor T-cell engineering
13. 254th ENMC international workshop. Formation of a European network to initiate a European data collection, along with development and sharing of treatment guidelines for adult SMA patients. Virtual meeting 28 – 30 January 2022
14. Therapeutic modulation of V Set and Ig domain-containing 4 (VSIG4) signaling in immune and inflammatory diseases
15. Cardiac cell therapies for the treatment of acute myocardial infarction in mice: systematic review and meta-analysis
16. Limitations of the apnea-hypopnea index in children and young adults with neuromuscular disorders
17. Clinical outcomes of therapeutic leukapheresis in acute promyelocytic leukemia: A single-center retrospective cohort study
18. Label-free in vitro assays predict the potency of anti-disialoganglioside chimeric antigen receptor T-cell products
19. Reference gene selection for clinical chimeric antigen receptor T-cell product vector copy number assays
20. The miR-21-5p enriched in the apoptotic bodies of M2 macrophage-derived extracellular vesicles alleviates osteoarthritis by changing macrophage phenotype
21. Regulation mechanism and pathogenic role of lncRNA plasmacytoma variant translocation 1 (PVT1) in human diseases
22. Wnt genes in colonic polyposis predisposition
23. LncRNA MIR31HG controls the proliferation and metastasis of gastric cancer by c-CBL-mediated degradation of β-catenin
24. Molecular and cellular pathophysiology of circulating cardiomyocyte-specific cell free DNA (cfDNA): Biomarkers of heart failure and potential therapeutic targets
25. Modulation of SIRT6 activity acts as an emerging therapeutic implication for pathological disorders in the skeletal system
26. Genetic heritage of the Baphuthi highlights an over-ethnicized notion of 'Bushman' in the Maloti-Drakensberg, southern Africa
27. Altered expression of m1A regulatory genes is associated with oncogenic pathways, overall survival, and infiltration of immune cells in diverse human cancers
28. Mitochondria-derived small RNAs as diagnostic biomarkers in lung cancer patients through a novel ratio-based expression analysis methodology
29. Circulating and non-circulating proteins and nucleic acids as biomarkers and therapeutic molecules in ovarian cancer
30. The emerging role of Arid5a in cancer: A new target for tumors
31. Kurt Hirschhorn (1926–2022)
32. De novo variants implicate chromatin modification, transcriptional regulation, and retinoic acid signaling in syndromic craniosynostosis
33. A pathogenic CTBP1 variant featuring HADDTS with dystrophic myopathology
34. Variations in EXD3 caused congenital cataracts in three Chinese families
35. Prolonged control of insulin-dependent diabetes via intramuscular expression of plasmid-encoded single-strand insulin analogue
36. How a paternal uniparental isodisomy of chromosome 17 leads to autosomal recessive limb-girdle muscular dystrophy R3
37. Long-term outcomes of relmacabtagene autoleucel in Chinese patients with relapsed/refractory large B-cell lymphoma: Updated results of the RELIANCE study
38. Trio RNA sequencing in a cohort of medically complex children
39. Comparison analysis of multiple-omics data between female germline stem cells and spermatogonial stem cells
40. Functional crosstalk and regulation of natural killer cells in tumor microenvironment: Significance and potential therapeutic strategies
41. Novel Alu-mediated deletions of the SMN1 gene were identified by ultra-long read sequencing technology in patients with spinal muscular atrophy
42. A novel aptamer-based small RNA delivery platform and its application to cancer therapy
43. The NK-92 cell line—30 years later: its impact on natural killer cell research and treatment of cancer
44. A patient with glycogen storage disease type IA combined with hepatic adenoma: A case report
45. Amyloid-like IgM deposition neuropathy with multiple mononeuropathies and generalized neuropathy
46. The functional impact of 1,570 individual amino acid substitutions in human OTC
47. Transplanted mesenchymal stromal cells are unable to migrate to the bone surface and subsequently improve osteogenesis in glucocorticoid-induced osteoporosis
48. Parkinson's disease: From genetics to molecular dysfunction and targeted therapeutic approaches
49. Mechanistic insight into lysyl oxidase in vascular remodeling and angiogenesis
50. Cysteine dioxygenase type 1 (CDO1): Its functional role in physiological and pathophysiological processes
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