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Keyword [Single nucleotide polymorphisms(SNP)]
Result: 1 - 20 | Page: 1 of 3
1. The Relationship Between The Single Nuleotide Polymorphisms Of Th Cytokine Genes And The Susceptibility Of Oral Lichen Planus
2. Gene Polymorphisms In Toll-like Receptor Signaling Pathway And Their Relationship With The Susceptibility And Prognosis Of Sever Sepsis
3. Brain-derived Neurotrophic Factor And Bipolar Disorder, And Drug Treatment For Acute Mania Efficacy Study
4. The ABCG1 Gene Polymorphism And Coronary Heart Disease Association Studies And ABCG1 Promoter Transcriptional Activity Of Research
5. Genetic Associations Of MiRNA-SNPs With The Common Diseases And Integrative Analysis Of " OMICS" Data Of Hepatocellular Carcinoma
6. The Correlation Between Polymorphism Of TNF-α And IL-10 Gene Promoter And Severe Hepatitis B
7. Influence Of Tumor Necrosis Factor And Interleukin-10 Single Nucletide Polymorphisms On Response To Interferon Therapy In Patients With Chronic Hepatitis B
8. The Polymorphism And Significance Of GRIN2A Gene's Two SNP
9. Association Between The Genes Polymorphisms In BDNF Signal Pathways And Personality
10. Association Between The Genes Polymorphisms In BDNF Signal Pathways And Personality In The Recovered Patients With Depression
11. A Study On Polymorphism And Differentially Methylated Parental Allele Of Rs220030 In Snrpn Gene
12. Associations Of APOA5 Level And APOA5 Gene-1131T/C Single Nucleotide Polymorphism With Metabolic Syndrome Among Elderly Patients
13. Analysis Of Clinicopathological And Survival Changes On 61781 Familial And Sporadic Esophageal Cancer Patients As Well As PLCE1 And RFT2 Polymorphisms
14. A Study On The Association Of Four Single Nucleotide Polymorphisms (SNP) In Chromosome 4 With High Myopia
15. Brca1 Gene Methylation And Snp With Sporadic Breast Cancer Research
16. Associations Between Polymorphisms In Toll-like Receptor4Signaling Pathway Genes And The Susceptibility To Sepsis
17. MiR-146a Rs2910164G/C Polymorphism Is Associated With Gastric Cancer Risk Through Aberrant Exprssion Of MiR-146a
18. The Role Of HOXA Genes In The Pathogenesis Of Human Mullerian Duct Abnormalities (MDAs) And Pregnancy Outcome In Women With MDAs
19. Screening Of Causative Genes In Chinese Patients With Idiopathic Hypogonadotropic Hypogonadism (IHH) And The Reproductive Performance Of Women With IHH During In Vitro Fertilization And Embryo Transfer Treatment
20. A Variant Of CLEC16A Gene Confers Protection For Vogt-Koyanagi-Harada Syndrome But Not For Behcet’s Disease In A Chinese Han Population
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