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Keyword [COL1A2]
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1. Sporadic Intracranial Ruptured Aneurysm: Study Of Epidemiology And Association Analysis With SNP Of COL1A2,COL4A1,TNFRSF13B Genes And Microsatellite DNA Marker D7S2421
2. Establishment And Evaluation Of The High Throughput Screening System For Antagonistic Agents Of Scar Hypertrophy Based On Smad3
3. Investigating The Prevalence Of Endemic Fluorosis In Shanxi Province And The Influencing Factors About Skeletal Fluorosis
4. Detection Of Gene Mutation And Relationship Between Phenotype And Genotype In Four Chinese Families With Osteogenesis Imperfecta
5. Study On Clinical And Identification Of Molecular Mutation Of Osteogenesis Imperfecta And Genetic Variation Of SOST Gene
6. Mutation Spectrum And Genotype-phenotype Correlation In Chinese OI Patients
7. The Preliminary Analysis Of The Role Of MiR-29a-3p In Occurrence And Development Of Hypertension Stroke
8. Pathogenic Gene Mutations And Methylation Analysis Of Collagen Type Ⅰ Genes In Chinese Patients With Osteogenesis Imperfecta
9. Circulating Inflammatory MRNA (KLF4 And MMP9) Associated With Occurrence And Development Of Acute Hypertensive Stroke
10. Application Of High Resolution Melting Analysis In Screening COL1A1/COL1A2 Mutations For Osteogenesis Imperfecta
11. Mechanism Research Of COL1A2 Interact With Dna Methylation Enzyme For Cell Proliferation, Migration, And Invasion In Colorectal Cancer
12. Using Bioinformatics To Perform Gene Priorization And Using Zebrafish Model To Study The Role Of COL1A2 In Intracerebral Hemorrhage With CRISPR/Cas9 Technology
13. Analysis And Validation Of GEO Data Of Obesity-related Genes In Postmenopausal Breast Cancer Patients With Estrogen Receptor Positive
14. Influence Of The Polymorphisms In COL1A2 And MIF On Sudden Cardiac Death In Chinese Populations
15. Carnosic Acid Protects Against Hepatic Fibrosis Through SIRT1-mediated Deacetylation Of Smad3 In Rats
16. Detection And Bioinformatics Analysis Of Osteogenesis Imperfecta Gene Mutation
17. The role of genetic background on the phenotypic severity of the osteogenesis imperfecta murine (oim) COL1A2 gene mutation throughout postnatal development
18. Diverse mechanisms of human genetic disease: Splice order determination in the COL1A2 gene. Effects that influence splice site mutations in osteogenesis imperfecta and a translocation disrupting SNRPN gene causes Prader-Willi syndrome
19. Prediction And Preliminary Verification Of Prognostic-related Genes In Gastric Adenocarcinoma
20. Gene And Histomorphological Analysis Of 1 Case Of Dentinogenesis Imperfecta-?
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