Search Results - "Ou, Zhanhui"
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Activation of the p62‐Keap1‐NRF2 pathway protects against ferroptosis in hepatocellular carcinoma cells
Published in Hepatology (Baltimore, Md.) (01-01-2016)“…Ferroptosis is a recently recognized form of regulated cell death caused by an iron‐dependent accumulation of lipid reactive oxygen species. However, the…”
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Improved hematopoietic differentiation efficiency of gene-corrected beta-thalassemia induced pluripotent stem cells by CRISPR/Cas9 system
Published in Stem cells and development (01-05-2015)“…The generation of beta-thalassemia (β-Thal) patient-specific induced pluripotent stem cells (iPSCs), subsequent homologous recombination-based gene correction…”
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3
Cigarette smoking is associated with high level of ferroptosis in seminal plasma and affects semen quality
Published in Reproductive biology and endocrinology (27-05-2020)“…The effects of cigarette smoking on male semen quality are controversial, and the molecular mechanisms underlying how cigarette smoking affects semen quality…”
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4
Using affected embryos to establish linkage phase in preimplantation genetic testing for thalassemia
Published in Reproductive biology and endocrinology (30-04-2022)“…This study aimed to evaluate the ability of next-generation sequencing (NGS) to conduct preimplantation genetic testing (PGT) for thalassemia using affected…”
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5
Day 3 Embryo Morphology is a Significant Predictor of Blastocyst Euploidy
Published in Clinical and experimental obstetrics & gynecology (01-11-2023)“…Background: This retrospective cohort study aims to determine the relationship between morphologic grading of day 1 or 3 embryos and euploid blastocyst rate in…”
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6
Effects of reduced follicle-stimulating hormone dosage before human chorionic gonadotropin trigger on in vitro fertilization outcomes
Published in BMC pregnancy and childbirth (25-08-2023)“…ObjectiveTo determine whether a reduced dose of follicle-stimulating hormone (FSH) before human chorionic gonadotropin (hCG) trigger during ovarian stimulation…”
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Improved Non-Invasive Preimplantation Genetic Testing for Beta-Thalassemia Using Spent Embryo Culture Medium Containing Blastocoelic Fluid
Published in Frontiers in endocrinology (Lausanne) (20-01-2022)“…To compare successful beta-thalassemia (β-thalassemia) detection rates obtained using spent culture medium and spent culture medium containing blastocoelic…”
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High concordance between next-generation sequencing and single-nucleotide polymorphism array in preimplantation genetic testing for aneuploidy
Published in Clinical and experimental obstetrics & gynecology (01-01-2022)“…Background: This study aimed to compare the use of next-generation sequencing (NGS) and single-nucleotide polymorphism (SNP) array in preimplantation genetic…”
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9
Does current ovarian endometrioma increase the time for DOR patients to reach live birth in IVF?
Published in BMC pregnancy and childbirth (15-04-2022)“…The contents of ovarian endometrioma (OMA) such as inflammatory mediators, reactive oxygen species, and iron may disrupt normal folliculogenesis and result in…”
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Feasibility of preimplantation genetic testing for aneuploidy on frozen-thawed embryos following conventional IVF insemination
Published in Frontiers in endocrinology (Lausanne) (01-10-2024)“…Intracytoplasmic sperm injection (ICSI) is commonly employed in preimplantation genetic testing (PGT) to minimize the risk of foreign sperm DNA contamination…”
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11
The impact of low oocyte maturity ratio on blastocyst euploidy rate: a matched retrospective cohort study
Published in Contraception and reproductive medicine (26-08-2024)“…To investigate the association between a low oocyte maturity ratio from in vitro fertilization cycle and blastocyst euploidy. A total of 563 preimplantation…”
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12
Re-analysis of whole blastocysts after trophectoderm biopsy indicated chromosome aneuploidy
Published in Human genomics (13-01-2020)“…To compare the concordance between trophectoderm (TE) analysis and whole blastocyst analysis of embryos from chromosomal structural rearrangement (SR)…”
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13
Case report: Preimplantation genetic testing for X-linked alport syndrome caused by variation in the COL4A5 gene
Published in Frontiers in pediatrics (10-08-2023)“…X-Linked Alport Syndrome (XLAS) is an X-linked, dominant, hereditary nephropathy mainly caused by mutations in the COL4A5 gene, found on chromosome Xq22. In…”
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14
The safety and effectiveness of genetically corrected iPSCs derived from β-thalassaemia patients in nonmyeloablative β-thalassaemic mice
Published in Stem cell research & therapy (16-07-2020)“…Background β-Thalassaemia is a clinically common cause of hereditary haemolytic anaemia stemming from mutations in important functional regions of the β-globin…”
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15
Autophagy Promoted the Degradation of Mutant ATXN3 in Neurally Differentiated Spinocerebellar Ataxia-3 Human Induced Pluripotent Stem Cells
Published in BioMed research international (01-01-2016)“…Spinocerebellar ataxia-3 (SCA3) is the most common dominant inherited ataxia worldwide and is caused by an unstable CAG trinucleotide expansion mutation within…”
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Elevated Hemoglobin A2 as a Marker for β-Thalassemia Trait in Pregnant Women
Published in The Tohoku Journal of Experimental Medicine (2011)“…β-thalassemia is one of the most prevalent inherited hemoglobin disorders. Compound heterozygotes or homozygous mutations of the β-globin chain gene account…”
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Generation of integration-free induced pluripotent stem cells (GZHMUi001-A) by reprogramming peripheral blood mononuclear cells from a 47, XXX syndrome patient
Published in Stem cell research (01-08-2017)“…47, XXX syndrome is one of several sex-chromosomal aneuploidies, and it has an incidence of approximately 1/1000 in newborn females. Because of heterogeneity…”
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Duchenne Muscular Dystrophy in a Female Patient with a Karyotype of 46,X,i(X)(q10)
Published in The Tohoku Journal of Experimental Medicine (01-10-2010)“…Duchenne muscular dystrophy (DMD) is a severe recessive X-linked form of muscular dystrophy caused by mutations in the dystrophin gene and it affects males…”
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Combining Single Strand Oligodeoxynucleotides and CRISPR/Cas9 to Correct Gene Mutations in β-Thalassemia-induced Pluripotent Stem Cells
Published in The Journal of biological chemistry (05-08-2016)“…β-Thalassemia (β-Thal) is one of the most common genetic diseases in the world. The generation of patient-specific β-Thal-induced pluripotent stem cells…”
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20
HSPB1 as a novel regulator of ferroptotic cancer cell death
Published in Oncogene (05-11-2015)“…Ferroptosis is an iron-dependent form of non-apoptotic cell death, but its molecular mechanism remains largely unknown. Here, we demonstrate that heat shock…”
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