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Keyword [Nonsense]
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21. A Critical Role Of RBM8a In Proliferation And Differentiation Of Embryonic Neural Progenitors
22. The Etiopathogenisis Analysis Of Madelung Deformity Pedigree、Achondroplasia Pedigress And A Norrie Disease Pedigree
23. The Impacts Of Two Nonsense Mutations And Six Missense Mutations On Enzymatic Activity Of USP26
24. Mechanism And Impact Factors Of HERG Gene Nonsense Mutation Drug Salvation
25. Localization Of The Disease-associated Gene Of Autosomal Dominant Congenital Y-suture Cataract
26. Translational Control And Readthrough Of Tumor Suppress Gene RB1 And MEN1 With Nonsense Mutation
27. Phenotypic Analysis Of Dhtkd1Tyr486* Knock-in Mouse Model And Pathogenic Mechanism Of Hereditary Protein C Deficiency
28. KISS1R Gene Mutation Analysis In A Chinese Family With IHH
29. Association Of Mutations In BRCA2 Domains And Acquired Platinum Resistance After Neoadjuvant Chemotherapy In Patients With Advanced Ovarian Cancer
30. The Molecular Basis Of Venous Thromboembolism Caused By Hereditary Anticoagulant Protein Deficiency
31. Characteristics Of Corneal Opacity And Its Modified Gene In RAX Nonsense Mutant Mice
32. Genetic Sequencing And Analysis Of The Mutation In A Chinese Family With Congenital Aniridia
33. Novel Assays For CtDNA Enrichment And Analysis With The Employment Of Ccdb Reporter Genes
34. Clinical Heterogeneity Analysis Of Glanzmann’s Thrombasthenia And A Pilot Study Of Gene Editing
35. Loss Of PTPN4 Activates STAT3 To Promote The Tumor Tumorigenesis In Rectal Cancer
36. The Function And Mechanism Of CPA1 Variants And Splice Donor Site Mutations In Chronic Pancreatitis
37. Generation Of Non-integration Induced Pluripotent Stem Cells From Chorionic Villi Cells Of A Duchenne Muscular Dystrophy Fetus
38. Correction Of PTC124 On In Vitro Expression Of Nonsense Mutated PAH Protein
39. Study On Dhtkd1Tyr486* Knock-in Mouse Model And Gene Diagnosis Of A Cone-Rod Dystrophy Family
40. Genetic Analysis And Literature Review Of 6 Cases Of Hereditary Spherocytosis
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