Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Cuiting Peng"'
Autor:
Fan Zhou, Jun Ren, Yutong Li, Yuezhi Keqie, Cuiting Peng, Han Chen, Xinlian Chen, Shanling Liu
Publikováno v:
BMC Pregnancy and Childbirth, Vol 24, Iss 1, Pp 1-10 (2024)
Abstract Background Couples with balanced chromosome rearrangement (BCR) are at high risk of recurrent miscarriages or birth defects due to chromosomally abnormal embryos. This study aimed to provide real-world evidence of the euploidy rate of blasto
Externí odkaz:
https://doaj.org/article/c160050c68a2419ba1b9466408022f5e
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:
Cuiting Peng, Haixia Zhang, Jun Ren, Han Chen, Ze Du, Tong Zhao, Aiping Mao, Ruofan Xu, Yulin Lu, He Wang, Xinlian Chen, Shanling Liu
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-9 (2022)
Abstract Thalassemia is a group of common hereditary anemias that cause significant morbidity and mortality worldwide. However, precisely diagnosing thalassemia, especially rare thalassemia variants, is still challenging. Long-range PCR and long-mole
Externí odkaz:
https://doaj.org/article/c43ac6845daa4781bdaad4ccd8bb067e
Autor:
Jun Ren, Yuezhi Keqie, Yutong Li, Lingping Li, Min Luo, Meng Gao, Cuiting Peng, Han Chen, Ting Hu, Xinlian Chen, Shanling Liu
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Chromosome rearrangement is one of the main causes of abortion. In individuals with double chromosomal rearrangements, the abortion rate and the risk of producing abnormal chromosomal embryos are increased. In our study, preimplantation genetic testi
Externí odkaz:
https://doaj.org/article/19e0ad4815ff46b98b746efb6fcfa518
Autor:
Yongxia Zhu, Tinghong Ye, Xi Yu, Qian Lei, Fangfang Yang, Yong Xia, Xuejiao Song, Li Liu, Hongxia Deng, Tiantao Gao, Cuiting Peng, Weiqiong Zuo, Ying Xiong, Lidan Zhang, Ningyu Wang, Lifeng Zhao, Yongmei Xie, Luoting Yu, Yuquan Wei
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-3 (2022)
Externí odkaz:
https://doaj.org/article/71980e2cc3a54010b98ba4437228d7db
Autor:
Jun Ren, Cuiting Peng, Fan Zhou, Yutong Li, Yuezhi Keqie, Han Chen, Hongmei Zhu, Xinlian Chen, Shanling Liu
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Preimplantation genetic testing (PGT) has been increasingly used to prevent rare inherited diseases. In this study, we report a case where PGT was used to prevent the transmission of disease-caused variant in a SCID-X1 (OMIM:300400) family. SCID-X1 i
Externí odkaz:
https://doaj.org/article/41f8d401a0bc474592b58185aa68e85d
Publikováno v:
In Annals of Nuclear Energy July 2024 202
Publikováno v:
Proceedings of the 23rd Pacific Basin Nuclear Conference, Volume 2 ISBN: 9789811987793
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::106996bc22c2ebab8d08a7d74150a3aa
https://doi.org/10.1007/978-981-19-8780-9_49
https://doi.org/10.1007/978-981-19-8780-9_49
Publikováno v:
Annals of Nuclear Energy. 183:109635
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::821662974970eadd2203d70618b56745
https://doi.org/10.1016/j.anucene.2022.109635
https://doi.org/10.1016/j.anucene.2022.109635
Autor:
Xinlian Chen, Yuezhi Keqie, Ting Hu, He Wang, Hongmei Zhu, Fan Zhou, Xuemei Zhang, Cuiting Peng, Shanling Liu, Yutong Li, Jun Ren
Publikováno v:
Reproductive sciences (Thousand Oaks, Calif.). 28(12)
Methylmalonic acidemia combined with homocysteinemia and cobalamin C type (MMA-CblC, MIM # 277400) is a rare inherited disease with cobalamin metabolic disorder, which are caused by deficiency in the MMACHC gene. A couple with a proband child carried
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::299766bf315932242ba43faa999bd1d2
https://pubmed.ncbi.nlm.nih.gov/34076870
https://pubmed.ncbi.nlm.nih.gov/34076870