Font Size: a A A
Keyword [Nonsense]
Result: 1 - 20 | Page: 1 of 4
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. Identification And Functional Analylsis Of A De Novo NKX2.5 Mutation And Translational Readthrough Analysis Of NKX2.5 Nonsense Mutations By Aminoglycosides
4. The Role Of Nonsense Mrna Decay In Human Breast Cancer Research
5. Aminoglycosides Saved A Nonsense Mutation In The Herg Channel Drug
6. 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
7. Molecular Epidemiology Investigation Of Enlarged Vestibular Aqueduct Associated With SLC26A4 Gene
8. Study On Clinical And Pathologic Mechanism Of Hereditary Antithrombin Deficiency
9. Identification Of A Novel Frameshift Mutation At Codon 53 (-T) In The β Globin Gene Causing Dominantly Inherited β Thalassemia In A Chinese Miao Family
10. Investigation Of SLC26A4 Gene In Patients Associated With Sensorineural Hearing Loss In Northwest China
11. Rapid Analysis Of RB1 Gene Mutation By RT-PCR In A Southern Chinese Retinoblastoma Pedigree
12. Mucolipidosis Type Ⅲ Alpha/Beta In A Chinese Family Is Associated With GNPTAB
13. Mucolipidosis Type Ⅲ Alpha/beta In A Chinese Family Is Associated With Gnptab
14. Study On The PTC124Treatment For Pseudoxanthoma Elasticum
15. Molecular Mechanism Of Severe Hemophilia Caused By Nonsense Mutation In F9Gene
16. Molecular Genetics Study Of Congenital Cataract
17. Whole-exome Sequencing Identifies A Causative Gene Of X-linked Dominant High Myopia And The Establishment Of Human Gene Variant Database-LOVD
18. Nonsense Mutation Of XPF Gene Is Associated With Carcinogenesis
19. Research On The Translation Control Of F9 And MEN1 Gene With Nonsense Mutation And Gene Readthrough
20. Research On Isolated FSH Deficiency Caused By Arg97X Mutation In FSHβ Subunit
  <<First  <Prev  Next>  Last>>  Jump to