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Keyword [β-thalassemia]
Result: 41 - 60 | Page: 3 of 4
41. Association GT Gene Promoter-158C/T Polymorphism With Methylation Status In B-thalassemia Major
42. Association Between Gene Polymorphism Of BCL11A And Fetal Hemoglobin In β-Thalassemia Major In Guangxi Province
43. The Research About Prevalence Rate Of Diabetes And The Pathogenesis Of Diabetesin The β-Thalassemia Major Patients
44. Detection Of β-thalassemia Mutations By Proofreading Polymerase-mediated Mutation-sensitive On/off Switch
45. Study Of BMD In Patients With β-Thalassemia Major
46. Study On HLA-haploidentical Allogenic Hematopoietic Stem Cell Transplantation In Treatment Ofβ-thalassemia Major
47. Analysis Of Clinical Manifestations Of101Patients With Beta-thalassemia Major
48. Establish β- Thalassemia Embryonic Stem Cell Line - (a) Three Kinds Of Broth System To Establish Embryonic Stem Cell Lines To Compare
49. The Efficacy And Molecular Mechanisms Of Astragalus Membranaceus And Its Formula Medicine As A Treatment For Children With β-thalassemia
50. Basic Gene Research Of Beta Thalassemia For Translating Human Beta-Globin Gene And Rna Interference Of Alpha-Globin Gene Expression By Lentivirus Vectors
51. Identification Of Two Novel Large Segmental Rearrangements Involvingα-globin Gene Cluster From The Telomere Of Chromosome16Causing Thalassemia In Two Chinese Families
52. Expression Of MicroRNA-144/451in Normal And β-thalassemic Erythropoiesis
53. Use Of Free Fetal DNA In Maternal Plasma To Noninvasive Prenatal Diagnosis β-thalassemia Methods Research
54. Studies On Interaction Between DNMT3A And Symmetric Methylation Of Histone H4Arginine3(H4R3Me2s)
55. Application Study Of High-resolution Melting Analysis In Genetic And Prenatal Diagnosis Of Thalassemia
56. Combined Use Of Astragalus Polysaccharide With Sodium Butyrate In The Induction Of HbF Synthesis On K562 Cells And Human Erthroid Progenitor Cells
57. The Body Development, Growth And Iron Overload In Child With β-Thalassemia Major In The Western Of Guangxi
58. The Clinical Researching On The B Thalassemia Mutation IVS-â…¡-5 Gâ†'C
59. The Clinical Study Of Qi And Jing Supplement Formula For Children With β-thalassemia Intermedia And "Weakness Of Spleen And Kidney"
60. Development Of An Electrochemical DNA Sensor For The Detection Of α-thalassemia And β-thalassemia
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