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Keyword [nonsense mutation]
Result: 1 - 20 | Page: 1 of 2
1. Study On The Clinic And Molecular Mechanism Of Hereditary Bleeding Disorders
2. Targeted Correction Of Point Mutations In Low Density Lipoprotein Receptor Gene Mediated By Modified Single Stranded Oligonucleotides In Mouse Liver In Vivo
3. Aminoglycosides Saved A Nonsense Mutation In The Herg Channel Drug
4. Four New Genetic Mutations Lead To The Molecular Pathogenesis Of Research And Read Through The Therapy Of Hemophilia B Nonsense Mutation Hemophilia Treatment Due To The Initial Research
5. Molecular Epidemiology Investigation Of Enlarged Vestibular Aqueduct Associated With SLC26A4 Gene
6. Study On Clinical And Pathologic Mechanism Of Hereditary Antithrombin Deficiency
7. Investigation Of SLC26A4 Gene In Patients Associated With Sensorineural Hearing Loss In Northwest China
8. Rapid Analysis Of RB1 Gene Mutation By RT-PCR In A Southern Chinese Retinoblastoma Pedigree
9. Mucolipidosis Type Ⅲ Alpha/Beta In A Chinese Family Is Associated With GNPTAB
10. Mucolipidosis Type Ⅲ Alpha/beta In A Chinese Family Is Associated With Gnptab
11. Molecular Mechanism Of Severe Hemophilia Caused By Nonsense Mutation In F9Gene
12. Molecular Genetics Study Of Congenital Cataract
13. Whole-exome Sequencing Identifies A Causative Gene Of X-linked Dominant High Myopia And The Establishment Of Human Gene Variant Database-LOVD
14. Nonsense Mutation Of XPF Gene Is Associated With Carcinogenesis
15. Research On The Translation Control Of F9 And MEN1 Gene With Nonsense Mutation And Gene Readthrough
16. The Etiopathogenisis Analysis Of Madelung Deformity Pedigree、Achondroplasia Pedigress And A Norrie Disease Pedigree
17. Mechanism And Impact Factors Of HERG Gene Nonsense Mutation Drug Salvation
18. Localization Of The Disease-associated Gene Of Autosomal Dominant Congenital Y-suture Cataract
19. Translational Control And Readthrough Of Tumor Suppress Gene RB1 And MEN1 With Nonsense Mutation
20. Phenotypic Analysis Of Dhtkd1Tyr486* Knock-in Mouse Model And Pathogenic Mechanism Of Hereditary Protein C Deficiency
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