Zobrazeno 1 - 10
of 421
pro vyhledávání: '"Can Liao"'
Autor:
Fang Fu, Xin Yang, Ru Li, Yingsi Li, Hang Zhou, Ken Cheng, Ruibin Huang, You Wang, Fei Guo, Lina Zhang, Min Pan, Jin Han, Li Zhen, Lushan Li, Tingying Lei, Dongzhi Li, Can Liao
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-10 (2024)
Abstract Background The molecular mechanism of fetal cystic hygroma (CH) is still unclear, and no study has previously reported the transcriptome changes of single cells in CH. In this study, single-cell transcriptome sequencing (scRNA-seq) was used
Externí odkaz:
https://doaj.org/article/9b455270797844668b3ce0cf8eaa49ad
Publikováno v:
Molecular Cytogenetics, Vol 16, Iss 1, Pp 1-9 (2023)
Abstract Objective To assess prenatal diagnosis and pregnancy outcomes in twin pregnancies where one fetus has nuchal translucency (NT) above the 95th percentile. Method In this retrospective analysis, 130 twin pregnancies (260 fetuses) in which one
Externí odkaz:
https://doaj.org/article/87dec569f539449aad604cf9dd6415c8
Autor:
Dazhen Jiang, Di Deng, Yu Xiong, Dajiang Wang, Jian Gong, Hongli Zhao, Zhirong Bao, Yongchang Wei, Conghua Xie, Lecheng Jia, Can Liao, Shuo Liu, Hui Liu, Xiaoyong Wang
Publikováno v:
European Journal of Medical Research, Vol 28, Iss 1, Pp 1-10 (2023)
Abstract Background A novel CT-linac (kilovolt fan-beam CT-linac) has been introduced into total marrow and lymphoid irradiation (TMLI) treatment. Its integrated kilovolt fan-beam CT (kV FBCT) can be used not only for image guidance (IGRT) but also t
Externí odkaz:
https://doaj.org/article/525c4b37f11c4e429561d6a6809a3a84
Publikováno v:
Molecular Cytogenetics, Vol 16, Iss 1, Pp 1-5 (2023)
Abstract Objective To evaluate the prenatal and perinatal outcome of fetuses with extremely large nuchal translucency (eNT) thickness (≥ 6.5 mm). Methods 193 (0.61%) singleton fetuses with eNT were retrospectively included. Anomaly scan, echocardio
Externí odkaz:
https://doaj.org/article/7ab56e25936a474abbd6f7084254d24e
Autor:
Fucheng Li, Liya He, Guilan Chen, Yan Lu, Ru Li, Yongling Zhang, Xiangyi Jing, Rujuan Ling, Dongzhi Li, Can Liao
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Hemophilia, an X-linked recessive disorder, is characterized by spontaneous or trauma-induced prolonged bleeding. It is classified as hemophilia A when caused by variants in the F8 gene, and hemophilia B when caused by F9 variants. Few studies have d
Externí odkaz:
https://doaj.org/article/bdfde4a3a4c144b2a7410ad4757da7d6
Publikováno v:
Batteries, Vol 10, Iss 4, p 117 (2024)
Graphite anode materials and carbonate electrolyte have been the top choices for commercial lithium-ion batteries (LIBS) for a long time. However, the uneven deposition and stripping of lithium cause irreversible damage to the graphite structure, and
Externí odkaz:
https://doaj.org/article/52b490e4ab704bda8782d090b56f0ba8
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Objective: In the study, we investigated the genetic etiology of the ventricular septal defect (VSD) and comprehensively evaluated the diagnosis rate of prenatal chromosomal microarray analysis (CMA) and exome sequencing (ES) for VSD to provide evide
Externí odkaz:
https://doaj.org/article/f89a89f7f3d04dbd9c501ec7a8e2a845
Publikováno v:
Skin Health and Disease, Vol 3, Iss 5, Pp n/a-n/a (2023)
Externí odkaz:
https://doaj.org/article/d4871ee793ed4cb981fabee174a1586f
Autor:
Shujuan Yan, Fang Fu, Ru Li, Qiuxia Yu, Fucheng Li, Hang Zhou, You Wang, Ruibin Huang, Chunling Ma, Fei Guo, Dan Wang, Xin Yang, Jin Han, Tingyin Lei, Dongzhi Li, Can Liao
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Objective: This retrospective study aims to evaluate the utility of exome sequencing (ES) in identifying genetic causes of congenital orofacial clefts (OFCs) in fetuses with or without other structural abnormalities, and to further explore congenital
Externí odkaz:
https://doaj.org/article/eb235abb0a124b3a8ae35f0aeb03a221
Autor:
Zequn Liu, Yanmin Jiang, Fu Fang, Ru Li, Jin Han, Xin Yang, Qiong Deng, Lu-Shan Li, Ting-ying Lei, Dong-Zhi Li, Can Liao
Publikováno v:
Biochemistry and Biophysics Reports, Vol 35, Iss , Pp 101505- (2023)
Congenital heart disease (CHD) is a serious condition with unknown etiology. In a recent study, a compound heterozygous mutation (c.3526C > T [p.Arg1176Trp] and c.4643A > G [p.Asp1548Gly]) in the ASXL3 gene was identified, which is associated with CH
Externí odkaz:
https://doaj.org/article/14adc19cfe79437fadd4053acadf00a9