Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Ding, Taoli"'
Autor:
Shen, Jiandong1 (AUTHOR) jiandongsh@njmu.edu.cn, Ding, Taoli2 (AUTHOR), Sun, Xueping1 (AUTHOR), Yang, Ji2 (AUTHOR), Zhang, Yue2 (AUTHOR), Wang, Jing1 (AUTHOR), Ge, Mengdi1 (AUTHOR), Xu, Heng1 (AUTHOR), Xie, Jiazi1 (AUTHOR), Wang, Fei2 (AUTHOR), Diao, Feiyang1 (AUTHOR) phenix_y@163.com
Publikováno v:
BMC Genomics. 3/19/2024, Vol. 25 Issue 1, p1-10. 10p.
Autor:
Xia, Qiuping1 (AUTHOR), Ding, Taoli2 (AUTHOR), Chang, Tianli1 (AUTHOR), Ruan, Jiangxing2 (AUTHOR), Yang, Ji2 (AUTHOR), Ma, Menglin2 (AUTHOR), Liu, Jiaqi2 (AUTHOR), Liu, Zhen2 (AUTHOR), Jiao, Shujing2 (AUTHOR), Wu, Jian2 (AUTHOR), Ren, Jun2 (AUTHOR), Lu, Sijia2 (AUTHOR) lusijia@yikongenomics.com, Li, Yanping1 (AUTHOR) lyp7798@126.com, Yao, Zhongyuan1 (AUTHOR) yaozhongyuan@sklmg.edu.cn
Publikováno v:
Clinical & Translational Medicine. Mar2024, Vol. 14 Issue 3, p1-12. 12p.
Publikováno v:
In Biosensors and Bioelectronics 1 January 2022 195
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
In Science Bulletin 15 October 2019 64(19):1456-1467
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Xia, Qiuping, Li, Shenglan, Ding, Taoli, Liu, Zhen, Liu, Jiaqi, Li, Yanping, Zhu, Huimin, Yao, Zhongyuan
Additional file 7: Fig.S6. Informativesingle-nucleotide polymorphisms (SNPs) flanking the breakpoint in chromosome 17 from pedigree 2 (Family LHY) and embryos based on nanopore sequencing. SNP haplotypes were identified successfully for chromosome 17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4089004d57535912bce9c11fe4b4cf4
Autor:
Xia, Qiuping, Li, Shenglan, Ding, Taoli, Liu, Zhen, Liu, Jiaqi, Li, Yanping, Zhu, Huimin, Yao, Zhongyuan
Additional file 4: Fig.S3. Informative single-nucleotide polymorphisms (SNPs) flanking the breakpoint in chromosome 2 from pedigree 1 (Family LJ) and embryos based on nanopore sequencing. SNP haplotypes were identified successfully for chromosome 2,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d14329a6078db718256c167ecaca04e5
Autor:
Xia, Qiuping, Li, Shenglan, Ding, Taoli, Liu, Zhen, Liu, Jiaqi, Li, Yanping, Zhu, Huimin, Yao, Zhongyuan
Additional file 1: Fig.S1. Chromosomal ploidy results of the embryos (G–K) from patient 1. Embryo J had normal ploidy. Three embryos, G, H, and K, were identified as having abnormal chromosomes 2 and 5 and were used as reference embryos for the ide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::248349951c1959bec20d5818919f9ebc
Autor:
Xia, Qiuping, Li, Shenglan, Ding, Taoli, Liu, Zhen, Liu, Jiaqi, Li, Yanping, Zhu, Huimin, Yao, Zhongyuan
Additional file 6: Fig.S5. Informativesingle-nucleotide polymorphisms (SNPs) flanking the breakpoint in chromosome 13 from pedigree 2 (Family LHY) and embryos based on nanopore sequencing. SNP haplotypes were identified successfully for chromosome 13
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2b73c57db465bda32c42c7914ef00ae