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Keyword [CYP17A1]
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1. Clinical Analysis Of Autoantibodies Against AT1-receptor And Cardiac Remodeling In Patients With Hypertension
2. The Cyp17a1 Gene Sequence Analysis And Function Prediction Of Two Sisters And Their Parents With 17a-hydroxylase Deficiency
3. Prevalence Of Common Mutations In The Cyp17A1 Gene In Chinese Han Population
4. A New Compound Heterozygous Mutation In CYP17A1 Gene Causes 17α-hydroxylase Deficiency And Pedigree Study
5. Association Of The CYP17A1 Gene Polymorphism With Coronary Artery Disease And Hypertension And A Meta Analysis
6. The Association Study Between CYP17A1, CYP19 Gene Polymorphisms And Male Infertility In Henan Han Chinese Population
7. Clinical And Genetic Analysis Of Two Patients With 17?-hydroxylase/17,20- Lyase Deficiency
8. Analysis Of The Relationships Of CYP17A1 Gene And Famine Exposure With Essential Hypertension In She Population With Metabolic Syndrome In Fujian Province
9. Biological Significance Of CYP17A1 In Glioma
10. Expression Of CYP17A1 In Glioma Cell Lines And Effects Of Its Inhibitor On Proliferation Of Glioma Cells
11. Environmental Factors,maternal CYP1A1 And CYP17A1 Polymorphisms,and Their Interaction In Hypospadias In Offspring
12. CYP17A1 Gene Polymorphism And Coronary Heart Disease Research
13. Clinical And Molecular Genetic Studies Of 17-hydroxylase/17,20-lyase Deficiency
14. Clinical Study And Literature Review On 23 Cases With 17?-hydroxylase/17,20-lyase Deficiency
15. A Case Report And Literature Review Of 17OHD With Hypertension
16. Mechanism Of Autocrine Testosterone In Androgen Receptor-dependent Glioblastoma
17. Effect Of Protecting Spermatogenesis And Regulating The Expression Of CYP17A1 On The Tests Of BPA-infected Mice By LBP Gavage
18. Correlation Analysis Of Hypertension And Mild Cognitive Impairment Combined With Metabolic Syndrome In Elderly Patients And The Relationship Between Hypertension And CYP17A1 Gene
19. Molecular Etiology And Clinical Study Of7Cases Of Female Phenotypic 46,XY Disorders Of Sex Development
20. Clinical And Genetic Analysis Of 8 Patients With 17alpha-hydroxylase/17,20-lyase Deficiency
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