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Keyword [site mutation]
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1. The Studies On LG1-3 Module Of Human Laminin α4
2. The Effect Of HNF3 Binding Site Mutation In The Inhibition Role Of Hepatocyte Nuclear Factor 3β On HBV Transcription And Replication
3. Development Of Highly Glycosylated Erythropoietin
4. The C-Terminus Of α Subunit Determines The Activity Of AMP-Activated Protein Kinase
5. Clinical And Molecular Analysis Of Primary Immunodeficiency Disease
6. Study On Signal Transduction Of Transmembrane Co - Protein CBP And Its Palmitoylation Site Mutation In CD59 - Mediated T - Line Leukemia
7. Molecular Epidemiology Investigation Of Enlarged Vestibular Aqueduct Associated With SLC26A4 Gene
8. The Etiopathogenisis Analysis And Prenatal Testing Of A Piebaldism Family The Etiopathogenisis Analysis Of A Hereditay Multiple Exostose
9. Next Generation Sequencing Reveals A Novel Splice Donor Site Mutation In2B Domain Of KRT1Underlies Diffuse Palmoplantar Keratoderm In A Four Generation Chinese Family
10. One Novel5’Splice Site Mutation Of ACTC1Gene Might Play A Important Role In Ventricular Septal Defect (VSD)
11. Molecular Dynamics Simulation On The Effect Of Site Mutation On The Structure And Aggregation Properties Of Cystatin
12. A Novel Splice Site Mutation In DFNA5 Gene Causing Autosomal Dominant Non-syndromic Hearing Loss
13. Isolation And Identification Of HEV71 Strains From Mild Or Severe Children With Hand-foot-and-mouth Disease And Analysis Of Their VP1 Genotypes
14. Localization Of The Disease-associated Gene Of A Congenital Cataract Family
15. In Vitro Splicing Assay Of NMDAR Subunit Mutations With Idiopathic Epilepsy
16. Correlation And Clinical Intervention Between Recurrent Acute Pancreatitis And Chronic Pancreatitis
17. Molecular Dynamics Simulation To Investigate The Impact Of Disulfide Bond Formation On Structure Stability Of Cystatin Mononer
18. Relationship Between Ala746Thr Site And Gly49Ser Site Mutation Of ATP13A2 Gene And Parkinson's Disease
19. Study On The Molecular Pathogenesis Of Hemophilia A Caused By Two Splice Site Mutations Of F8 And Hemophilia B Caused By Two Large Duplications Of F9
20. Roles Of PAG1 Of Palmitoylation Site Mutation In Skin Squamous Cell Carcinoma
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