41 results on '"Zheng, Jiayong"'
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2. Comparison of Chromosomal Microarray Analysis and Noninvasive Prenatal Testing in Pregnant Women with Fetal Ultrasonic Soft Markers
3. Deterministic transition of enterotypes shapes the infant gut microbiome at an early age
4. Fibroblast growth factor 21 protects the heart from angiotensin II-induced cardiac hypertrophy and dysfunction via SIRT1
5. miR-9 knockdown inhibits hypoxia-induced cardiomyocyte apoptosis by targeting Yap1
6. Short-Term and Mid-Term Results of Minimally Invasive Occlusion of Ventricular Septal Defects via a Subaxillary Approach in a Single Center
7. Clinical Biochemical Indicators and Intestinal Microbiota Testing Reveal the Influence of Reproductive Age Extending from the Mother to the Offspring
8. Advances in Latest Application Status, Challenges, and Future Development Direction of Electrospinning Technology in the Biomedical
9. Maternal and neonatal viromes indicate the risk of offspring's gastrointestinal tract exposure to pathogenic viruses of vaginal origin during delivery
10. A novel factor X mutation Cys81 by Arg and a reported factor VII polymorphism Arg353 replaced by Gln co-occured in a patient
11. CRISPRs provide broad and robust protection to oral microbial flora of gingival health against bacteriophage challenge
12. Maternal, umbilical arterial metabolic levels and placental Nrf2/CBR1 expression in pregnancies with and without 25-hydroxyvitamin D deficiency
13. Maternal, umbilical arterial metabolic levels and placental Nrf2/CBR1 expression in pregnancies with and without 25-hydroxyvitamin D deficiency
14. Additional file 1 of Deterministic transition of enterotypes shapes the infant gut microbiome at an early age
15. Additional file 3 of Deterministic transition of enterotypes shapes the infant gut microbiome at an early age
16. Disorder of Sexual Development Males With XYY in Blood Have Exactly X/XY/XYY Mosaicism in Gonad Tissues
17. The oral microbiome of pregnant women facilitates gestational diabetes discrimination
18. FOXD3-AS1 Knockdown Suppresses Hypoxia-Induced Cardiomyocyte Injury by Increasing Cell Survival and Inhibiting Apoptosis via Upregulating Cardioprotective Molecule miR-150-5p In Vitro
19. Maternal 25-Hydroxyvitamin D Deficiency Promoted Metabolic Syndrome and Downregulated Nrf2/CBR1 Pathway in Offspring
20. Identification of Novel Compound Heterozygous Mutations in the GAN Gene of a Chinese Patient Diagnosed With Giant Axonal Neuropathy
21. The Effect of Mitomycin C on Reducing Endometrial Fibrosis for Intrauterine Adhesion
22. Pregnant women with gestational diabetes mellitus exhibit unique features in oral microbiome
23. Comparison of Efficiencies of Non-invasive Prenatal Testing, Karyotyping, and Chromosomal Micro-Array for Diagnosing Fetal Chromosomal Anomalies in the Second and Third Trimesters
24. A Visual Prognostic Model of Delivery Time in Preeclampsia Patients: A Nationwide Retrospective Analysis of 7005 Patients
25. Short-Term and Mid-Term Results of Minimally Invasive Occlusion of Ventricular Septal Defects via a Subaxillary Approach in a Single Center
26. Dysbiosis of maternal and neonatal microbiota associated with gestational diabetes mellitus
27. A Visual Prognostic Model of Delivery Time in Preeclampsia Patients: A Nationwide Retrospective Analysis of 7005 Patients in China
28. Inhibition of 12/15-LO ameliorates CVB3-induced myocarditis by activating Nrf2
29. CRISPR/Cas9- loxP -Mediated Gene Editing as a Novel Site-Specific Genetic Manipulation Tool
30. Associations of GATA4 genetic mutations with the risk of congenital heart disease
31. Anti-tumor effect of cisplatin in human oral squamous cell carcinoma was enhanced by andrographolide via upregulation of phospho-p53 in vitro and in vivo
32. Clinical features and genetic diagnosis of hereditary spinocerebellar ataxia 3
33. Severe female hemophilia A patient caused by a nonsense mutation (p.Gln1686X) of F8 gene combined with skewed X-chromosome inactivation
34. Associations of GATA4 genetic mutations with the risk of congenital heart disease: A meta-analysis.
35. Comparison of non-canonical PAMs for CRISPR/Cas9-mediated DNA cleavage in human cells
36. mirTools 2.0 for non-coding RNA discovery, profiling, and functional annotation based on high-throughput sequencing
37. Severe female hemophilia A patient caused by a nonsense mutation (p.Gln1686X) of F8 genecombined with skewed X-chromosome inactivation
38. [Association of coagulation factor V gene polymorphism with unexplained recurrent spontaneous abortion among ethnic Hans from Wenzhou area].
39. CRISPR/Cas9-loxP-Mediated Gene Editing as a Novel Site-Specific Genetic Manipulation Tool.
40. [Analysis of the association of human leukocyte antigen DQ gene polymorphisms with unexplained recurrent spontaneous abortion among ethnic Han Chinese from Wenzhou region].
41. The changes of platelet and platelet activation markers in acute coronary syndrome patients.
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