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151. High-Throughput Synergy Screening Identifies Microbial Metabolites as Combination Agents for the Treatment of Fungal Infections

152. Granulosa cell mevalonate pathway abnormalities contribute to oocyte meiotic defects

155. Temporal and spatial dynamics mapping reveals follicle development regulated by different stromal cell populations

157. Monocarboxylate transporter 4 inhibition potentiates hepatocellular carcinoma immunotherapy through enhancing T cell infiltration and immune attack

160. Additional file 1 of Effect of recombinant LH supplementation timing on clinical pregnancy outcome in long-acting GnRHa downregulated cycles

165. Mst1-Mediated Phosphorylation of Nur77 is Required for Embryo Implantation

167. Functional Differentiation of Luminal Epithelial Cells Regulated by Maternal and Embryonic Signaling and Its Relationship With Receptivity Establishment

169. Calpain7 Negatively Regulates Human Endometrial Stromal Cell Decidualization in Endometriosis by Promoting FoxO1’s Phosphorylation and Nuclear Exclusion via Hydrolyzing AKT1

173. Spatially-resolved transcriptomics analyses of invasive fronts in solid tumors

181. Machine Learning-Guided Noninvasive Embryo Selection for Clinical in Vitro Fertilization Treatment to Avoid Wasting Potentially Qualified Embryos

184. circPTPN12/miR-21–5 p/∆Np63α pathway contributes to human endometrial fibrosis

187. Author response: circPTPN12/miR-21–5 p/∆Np63α pathway contributes to human endometrial fibrosis

189. Targeting circPTPN12/miR-21-5p/ΔNp63α pathway as a therapeutic strategy for human endometrial fibrosis

192. An elective single cleavage embryo transfer strategy to minimize twin live birth rate based on a prediction model from double cleavage embryos transfer patients.

197. Calpain7 Negatively Regulates Human Endometrial Stromal Cell Decidualization in EMS by Promoting Foxo1 Nuclear Exclusion by Increasing the Phosphorylation of AKT1

198. The Mitochondrial Protease Lonp1 Maintains Oocyte Development and Survival by Suppressing Nuclear Translocation of AIFM1 in Mammals

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