Zobrazeno 1 - 10
of 1 810
pro vyhledávání: '"Fang Fu"'
Autor:
Yuhan Tian, Xia Wu, Songhao Luo, Dan Xiong, Rong Liu, Lanqi Hu, Yuchen Yuan, Guowei Shi, Junjie Yao, Zhiwei Huang, Fang Fu, Xin Yang, Zhonghui Tang, Jiajun Zhang, Kunhua Hu
Publikováno v:
Computational and Structural Biotechnology Journal, Vol 23, Iss , Pp 2173-2189 (2024)
The vast neuronal diversity in the human neocortex is vital for high-order brain functions, necessitating elucidation of the regulatory mechanisms underlying such unparalleled diversity. However, recent studies have yet to comprehensively reveal the
Externí odkaz:
https://doaj.org/article/73c7f4a2770f448ba2736defc3f3527e
Autor:
Lu Zhang, Ruibin Huang, Hang Zhou, Xiaomei Lin, Fei Guo, Xiangyi Jing, Yongling Zhang, Fucheng Li, Fatao Li, Qiuxia Yu, Dan Wang, Guilan Chen, Fang Fu, Min Pan, Jin Han, Dongzhi Li, Ru Li
Publikováno v:
Molecular Cytogenetics, Vol 17, Iss 1, Pp 1-14 (2024)
Abstract Background Right aortic arch (RAA) is a common congenital aortic arch abnormality. Fetuses with RAA frequently have good outcomes after birth. However, chromosomal abnormalities and genetic syndromes suggest poor prognosis for these patients
Externí odkaz:
https://doaj.org/article/c78cbe666ef74978b379f36ab48f0a27
Autor:
Shujuan Yan, Qiuxia Yu, Hang Zhou, Ruibin Huang, You Wang, Chunling Ma, Fei Guo, Fang Fu, Ru Li, Fucheng Li, Xiangyi Jin, Li Zhen, Min Pan, Dongzhi Li, Can Liao
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-9 (2024)
Abstract Backgroud A systematic analysis was conducted to investigate the molecular etiology of fetal cleft lip and/or palate (CL/P) and the association between various types of CL/P and copy number variations (CNVs), as well as their impact on birth
Externí odkaz:
https://doaj.org/article/d77a68af9f074d7eac5fb93c7065bc2a
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
Autor:
Ruibin Huang, Chunling Ma, Huanyi Chen, Fang Fu, Jin Han, Liyuan Liu, Lushan Li, Shujuan Yan, Jianqin Lu, Hang Zhou, You Wang, Fei Guo, Xiangyi Jing, Fucheng Li, Li Zhen, Dongzhi Li, Ru Li, Can Liao
Publikováno v:
Heliyon, Vol 10, Iss 17, Pp e36558- (2024)
Purpose: 17q12 copy number variants (CNVs) have variable presentations and incomplete penetrance, challenging prenatal counseling and management. This study aims to investigate the intrauterine phenotype. Methods: We included 48 fetuses diagnosed wit
Externí odkaz:
https://doaj.org/article/944f4e88ca6540fab02971bb4b0ad44a
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
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
Autor:
Fang Fu, Ru Li, Qiuxia Yu, Dan Wang, Qiong Deng, Lushan Li, Tingying Lei, Guilan Chen, Zhiqiang Nie, Xin Yang, Jin Han, Min Pan, Li Zhen, Yongling Zhang, Xiangyi Jing, Fucheng Li, Fatao Li, Lina Zhang, Cuixing Yi, Yingsi Li, Yan Lu, Hang Zhou, Ken Cheng, Jian Li, Lina Xiang, Jing Zhang, Sha Tang, Ping Fang, Dongzhi Li, Can Liao
Publikováno v:
Genome Medicine, Vol 14, Iss 1, Pp 1-20 (2022)
Abstract Background Exome sequencing (ES) is becoming more widely available in prenatal diagnosis. However, data on its clinical utility and integration into clinical management remain limited in practice. Herein, we report our experience implementin
Externí odkaz:
https://doaj.org/article/9017e03aca3941f79ba8d55459ae1e83
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
Publikováno v:
Biomimetics, Vol 9, Iss 3, p 183 (2024)
Insects produce a variety of highly acrobatic maneuvers in flight owing to their ability to achieve various wing-stroke trajectories. Among them, beetles can quickly change their flight velocities and make agile turns. In this work, we report a newly
Externí odkaz:
https://doaj.org/article/16f29a4bf0da4d4abaefc2d69bb59350