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Advances in preimplantation genetic diagnosis/screening.
Science China. Life sciences Jul, 2014 | Pubmed ID: 24907939
Mesenchymal Stem Cells Enhance Angiogenesis and Follicle Survival in Human Cryopreserved Ovarian Cortex Transplantation.
Cell transplantation , 2015 | Pubmed ID: 25353724
Mesenchymal Stem Cells Facilitate In Vitro Development of Human Preantral Follicle.
Reproductive sciences (Thousand Oaks, Calif.) Nov, 2015 | Pubmed ID: 25854744
Mesenchymal stem cell-derived angiogenin promotes primodial follicle survival and angiogenesis in transplanted human ovarian tissue.
Reproductive biology and endocrinology : RB&E Mar, 2017 | Pubmed ID: 28274269
Poly(ADP-ribose) mediates asymmetric division of mouse oocyte.
Cell research Apr, 2018 | Pubmed ID: 29463901
Identifying normal embryos from reciprocal translocation carriers by whole chromosome haplotyping.
Journal of genetics and genomics = Yi chuan xue bao 09, 2018 | Pubmed ID: 30287172
The present and future of whole-exome sequencing in studying and treating human reproductive disorders.
Journal of genetics and genomics = Yi chuan xue bao 10, 2018 | Pubmed ID: 30391409
Transcriptome Landscape of Human Folliculogenesis Reveals Oocyte and Granulosa Cell Interactions.
Molecular cell 12, 2018 | Pubmed ID: 30472193
Fbxo30 regulates chromosome segregation of oocyte meiosis.
Cellular and molecular life sciences : CMLS Jun, 2019 | Pubmed ID: 30980108
Genetic testing and PGD for unexplained recurrent fetal malformations with MAGEL2 gene mutation.
Science China. Life sciences Jul, 2019 | Pubmed ID: 31152388
Genetic analysis and preimplantation genetic diagnosis of Chinese Marfan syndrome patients.
Journal of genetics and genomics = Yi chuan xue bao 06, 2019 | Pubmed ID: 31279624
Trio-whole-exome sequencing and preimplantation genetic diagnosis for unexplained recurrent fetal malformations.
Human mutation 02, 2020 | Pubmed ID: 31680349
scHaplotyper: haplotype construction and visualization for genetic diagnosis using single cell DNA sequencing data.
BMC bioinformatics Feb, 2020 | Pubmed ID: 32007105
Novel PGD strategy based on single sperm linkage analysis for carriers of single gene pathogenic variant and chromosome reciprocal translocation.
Journal of assisted reproduction and genetics May, 2020 | Pubmed ID: 32350783
A strategy using SNP linkage analysis for monogenic diseases PGD combined with HLA typing.
Clinical genetics 08, 2020 | Pubmed ID: 32378203
A novel method for noninvasive diagnosis of monogenic diseases from circulating fetal cells.
Prenatal diagnosis Mar, 2021 | Pubmed ID: 32673403
A novel pathogenic mutation in FBN2 associated with congenital contractural arachnodactyly for preimplantation genetic diagnosis.
Journal of genetics and genomics = Yi chuan xue bao 05, 2020 | Pubmed ID: 32747207
Single-cell multiomics sequencing reveals the functional regulatory landscape of early embryos.
Nature communications 02, 2021 | Pubmed ID: 33623021
Clinical application of an NGS-based method in the preimplantation genetic testing for Duchenne muscular dystrophy.
Journal of assisted reproduction and genetics Mar, 2021 | Pubmed ID: 33719023
A comprehensive PGT-M strategy for ADPKD patients with de novo PKD1 mutations using affected embryo or gametes as proband.
Journal of assisted reproduction and genetics May, 2021 | Pubmed ID: 33939064
Jin Huang*,1,2,3,4,
Yaxin Yao*,5,
Jialin Jia1,2,3,4,
Xiaohui Zhu1,2,3,4,
Jieliang Ma5,
Jing Wang5,
Ping Liu1,2,3,4,
Sijia Lu5
1Centre for Reproductive Medicine, Department of Obstetrics and Gynecology, Peking University Third Hospital,
2, National Clinical Research Center for Obstetrics and Gynecology(Peking University Third Hospital),
3Ministry of Education, Key Laboratory of Assisted Reproduction (Peking University),
4, Beijing Key Laboratory of Reproductive Endocrinology and Assisted Reproductive Technology,
5Department of Clinical Research, Yikon Genomics Co. Ltd.
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