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Keyword [CRISPR]
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1. Tomoregulin-1 Inhibits Cardiac Hypertrophy Caused By Negative Pressure In The TAK1-JNK Pathway
2. Construction Of ATRX Gene Knockout HeLa Cell Line Based On CRISPR / Cas9 Technique
3. FKBP52 Regulates The Balance Of Estrogen Receptor ER And Androgen Receptor AR By FOXA1
4. Construction Of Hemophilia Model Mice By TALEN And CRISPR / Cas9 Techniques
5. Lipid Accumulation Mechanistic Studies Of Nonalcoholic Fatty Liver Disease Based On CRISPR/Cas9System
6. Creation And Analysis Of Zebrafish Mutants As Models For Human Porphyrias And Anemia
7. The Phenotype And Pathogenic Mechanisms Studies Of The TBX6 Associated Congenital Scoliosis
8. Study On The Effect And Mechanism Of Reprogrammed CRISPR-Cas9 In Proliferation And Apoptosis Of HPV6/11 E7 Genes-transformed Cells
9. Generation Of B Cell-deficient Pigs By Efficient TALENs Or CRISPR/Cas9-mediated Gene Targeting
10. Construction And Characterization Of Congenital Cataracts Mediated By CRISPR/Cas9 In Rabbits
11. The Application Of CRISPR-Cas9 System In Animal Model Building And Treatment Of Hemophilia B
12. The Protective Effect To MN And Mechanism Of ScAAV9-hIGF1 In ALS Mice Model Via Intrathecal Injection
13. Therapeutic Effect And Mechanism Of ScAAV9-hIGF1 Retrograde Axonal Targeting Motor Neurons In ALS Mouse Model
14. The Genetic Polymorphism Of CRISPR System And Its Functions Of Immune And Regulation In Shigella
15. The Role Of C10ORF2 And HELQ,PR1M1 Genes Played In Primary Ovarian Insufficiency
16. Effect Of Long No Coding MALAT1 On Pancreatic Ductal Adenocarcinoma’s Biological Function And Its Mechanism
17. Expression Of FTO Gene In Human Breast Cancer And Its Role On Cell Proliferation, Migration And Invision
18. A Research On Drug-resistant Mutations In HER2-positive Breast Cancer Based On Circulating Tumor DNA And CRISPR/cas9 Technique
19. Androgen/androgen Receptor Axis Effect On Cancer Cells Stemness Through Regulating Pluripotency Factor Nanog
20. The Generation, Gene Correction And Hair Cell Differentiation Of The IPS Cells Derived From The Deafness Patient With Mutations In MYO7A
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