Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Taoli Ding"'
Autor:
Jiandong Shen, Taoli Ding, Xueping Sun, Ji Yang, Yue Zhang, Jing Wang, Mengdi Ge, Heng Xu, Jiazi Xie, Fei Wang, Feiyang Diao
Publikováno v:
BMC Genomics, Vol 25, Iss 1, Pp 1-10 (2024)
Abstract Background Dystrophinopathies are the most common X-linked inherited muscle diseases, and the disease-causing gene is DMD. Exonic duplications are a common type of pathogenic variants in the DMD gene, however, 5’ end exonic duplications co
Externí odkaz:
https://doaj.org/article/7c2e136828244e9d98c21c38f97d1f51
Autor:
Qiuping Xia, Taoli Ding, Tianli Chang, Jiangxing Ruan, Ji Yang, Menglin Ma, Jiaqi Liu, Zhen Liu, Shujing Jiao, Jian Wu, Jun Ren, Sijia Lu, Yanping Li, Zhongyuan Yao
Publikováno v:
Clinical and Translational Medicine, Vol 14, Iss 3, Pp n/a-n/a (2024)
Abstract Background Structural rearrangements in highly repetitive heterochromatin regions can result in miscarriage or foetal malformations; however, detecting and preventing the transmission of these rearrangements has been challenging. Recently, t
Externí odkaz:
https://doaj.org/article/15959df55b844ed88fcb466a9eefd18a
Autor:
Cuiting Peng, Han Chen, Jun Ren, Fan Zhou, Yutong Li, Yuezhi Keqie, Taoli Ding, Jiangxing Ruan, He Wang, Xinlian Chen, Shanling Liu
Publikováno v:
BMC Genomics, Vol 24, Iss 1, Pp 1-9 (2023)
Abstract The autosomal dominant form of polycystic kidney disease (ADPKD) is the most common hereditary disease that causes late-onset renal cyst development and end-stage renal disease. Preimplantation genetic testing for monogenic disease (PGT-M) h
Externí odkaz:
https://doaj.org/article/1815035dc77944bdb97c87e064efe7a1
Autor:
Qiuping Xia, Shenglan Li, Taoli Ding, Zhen Liu, Jiaqi Liu, Yanping Li, Huimin Zhu, Zhongyuan Yao
Publikováno v:
BMC Genomics, Vol 24, Iss 1, Pp 1-10 (2023)
Abstract Background Balanced reciprocal translocation (BRT) is one of the most common chromosomal abnormalities that causes infertility, recurrent miscarriage, and birth defects. Preimplantation genetic testing (PGT) is widely used to select euploid
Externí odkaz:
https://doaj.org/article/acb6a3057e0c45568f7ee5fa6d7ae392
Autor:
Taoli Ding
The autosomal dominant form of polycystic kidney disease (ADPKD) is the most common hereditary disease that causes late-onset renal cyst development and end-stage renal disease. Preimplantation genetic testing for monogenic disease (PGT-M) has emerge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::933a53668a0f1f6ebf1b7b803dbb040e
Autor:
Qiuping Xia, Shenglan Li, Taoli Ding, Zhen Liu, Jiaqi Liu, Yanping Li, Huimin Zhu, Zhongyuan Yao
Publikováno v:
BMC genomics. 24(1)
Background Balanced reciprocal translocation (BRT) is one of the most common chromosomal abnormalities that causes infertility, recurrent miscarriage, and birth defects. Preimplantation genetic testing (PGT) is widely used to select euploid embryos f
Publikováno v:
Nucleic Acids Research
Nanopore technology is a promising label-free detection method. However, challenges exist for its further application in sequencing, clinical diagnostics and ultra-sensitive single molecule detection. The development of DNA nanotechnology nonetheless
Autor:
Taoli Ding
Nanopore sequencing for detecting reciprocal translocation carrier status in preimplantation genetic testing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f85bbd5b724e4c8d846ed93b4ed42bc
Publikováno v:
Biosensorsbioelectronics. 195
DNA origami is widely used as a translocation carrier to assist solid-state nanopore analysis, e.g., soft linear origami carrier and special-shaped origami structures. In the linear origami carriers based nanopore sensing, molecular modifications ind
Publikováno v:
Science Bulletin. 64:1456-1467
Nanopores are a label-free platform with the ability to detect subtle changes in the activities of individual biomolecules under physiological conditions. Here, we comprehensively review the technological development of nanopores, focusing on their a