254 results on '"Zhao, Shidou"'
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2. Novel compound heterozygous variants in FANCI cause premature ovarian insufficiency
3. FAAP100 is required for the resolution of transcription-replication conflicts in primordial germ cells
4. Next-generation sequencing of 500 POI patients identified novel responsible monogenic and oligogenic variants
5. NLRP14 deficiency causes female infertility with oocyte maturation defects and early embryonic arrest by impairing cytoplasmic UHRF1 abundance
6. Landscape of pathogenic mutations in premature ovarian insufficiency
7. Contributors
8. Premature ovarian insufficiency
9. UBE2T resolves transcription-replication conflicts and protects common fragile sites in primordial germ cells
10. HGF Secreted by Mesenchymal Stromal Cells Promotes Primordial Follicle Activation by Increasing the Activity of the PI3K-AKT Signaling Pathway
11. Mesenchymal stem cells combined with autocrosslinked hyaluronic acid improve mouse ovarian function by activating the PI3K-AKT pathway in a paracrine manner
12. TP63 gain-of-function mutations cause premature ovarian insufficiency by inducing oocyte apoptosis
13. lncRNA GCAT1 is involved in premature ovarian insufficiency by regulating p27 translation in GCs via competitive binding to PTBP1
14. New theca-cell marker insulin-like factor 3 is associated with premature ovarian insufficiency
15. Novel pathogenic mutations in minichromosome maintenance complex component 9 (MCM9) responsible for premature ovarian insufficiency
16. Analysis of STAG3 variants in Chinese non-obstructive azoospermia patients with germ cell maturation arrest
17. A novel FOXL2 mutation in two infertile patients with blepharophimosis–ptosis–epicanthus inversus syndrome
18. Correction: FANCI plays an essential role in spermatogenesis and regulates meiotic histone methylation
19. FANCI plays an essential role in spermatogenesis and regulates meiotic histone methylation
20. LncRNA ZNF674-AS1 regulates granulosa cell glycolysis and proliferation by interacting with ALDOA
21. Homozygous missense variant in MEIOSIN causes premature ovarian insufficiency
22. Analysis of CDK2 mutations in Chinese men with non-obstructive azoospermia who underwent testis biopsy
23. TMEM150B is dispensable for oocyte maturation and female fertility in mouse
24. CPEB1 deletion is not a common explanation for premature ovarian insufficiency in a Chinese cohort
25. Variation analysis of PUM1 gene in Chinese women with primary ovarian insufficiency
26. DNA repair protein FANCD2 has both ubiquitination-dependent and ubiquitination-independent functions during germ cell development
27. Variation analysis of PRIM1 gene in Chinese patients with primary ovarian insufficiency
28. Variation analysis of EXO1 gene in Chinese patients with premature ovarian failure
29. The screening of HELQ gene in Chinese patients with premature ovarian failure
30. MicroRNA-379-5p is associated with biochemical premature ovarian insufficiency through PARP1 and XRCC6
31. Metabolic actions of insulin in ovarian granulosa cells were unaffected by hyperandrogenism
32. Transcription–replication conflicts in primordial germ cells necessitate the Fanconi anemia pathway to safeguard genome stability
33. Palmitic acid increases apoptosis of neural stem cells via activating c-Jun N-terminal kinase
34. Additional file 1 of Mesenchymal stem cells combined with autocrosslinked hyaluronic acid improve mouse ovarian function by activating the PI3K-AKT pathway in a paracrine manner
35. Autophagy regulates differentiation of ovarian granulosa cells through degradation of WT1
36. lncRNA DDGC participates in premature ovarian insufficiency through regulating RAD51 and WT1
37. T reg deficiency‐mediated T H 1 response causes human premature ovarian insufficiency through apoptosis and steroidogenesis dysfunction of granulosa cells
38. Stem Cell Transplantation Improves Ovarian Function through Paracrine Mechanisms
39. Melatonin suppresses migration and invasion via inhibition of oxidative stress pathway in glioma cells
40. Downregulation of GRIM-19 promotes growth and migration of human glioma cells
41. Expression profile of embryonic stem cell-associated genes Oct4, Sox2 and Nanog in human gliomas
42. Expression of OCT4 pseudogenes in human tumours: lessons from glioma and breast carcinoma
43. In vivo and in vitro activation of dormant primordial follicles by EGF treatment in mouse and human
44. Response to “Should FANCL heterozygous pathogenic variants be considered as potentially causative of primary ovarian insufficiency?”
45. Analysis of STAG3 Mutations in Chinese Non-Obstructive Azoospermia Patients with Germ Cell Maturation Arrest
46. Variants in Homologous Recombination Genes EXO1 and RAD51 Related with Premature Ovarian Insufficiency
47. Dysregulated cytokine profile associated with biochemical premature ovarian insufficiency
48. MicroRNA‐127‐5p impairs function of granulosa cells via HMGB2 gene in premature ovarian insufficiency
49. Variation analysis of SOX8 gene in Chinese men with non‐obstructive azoospermia or oligozoospermia
50. Front Cover, Volume 41, Issue 5
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