Zobrazeno 1 - 10
of 194
pro vyhledávání: '"Dongzhi, Li"'
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:
Li Xu, Zhenghua Wu, Jingkun Li, Yihao Xu, Feng Zhou, Fulong Zhang, Dongzhi Li, Lin Zhou, Runqiang Liu
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract As an important pest on winter wheat, Rhopalosiphum padi (L.) causes damage to the wheat yield by sucking plant nutrients, transmitting plant viruses and producing mildew. R. padi has been reported to develop resistance to pyrethroids and ne
Externí odkaz:
https://doaj.org/article/bbcadb5a6b364118aa5de739e171c8b1
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:
Frontiers in Genetics, Vol 15 (2024)
ObjectiveThe recurrent 1q21.1 microdeletion syndrome is an autosomal dominant disorder and is characterized by dysmorphic facial features, microcephaly, developmental delay, and congenital defects. However, most studies on the distal deletions in the
Externí odkaz:
https://doaj.org/article/4ba146321c8b48c8b8d33debaca91b9e
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
Publikováno v:
Molecular Plant-Microbe Interactions, Vol 36, Iss 10, Pp 623-635 (2023)
Lipopolysaccharide (LPS) is a ubiquitous microbial-associated molecular pattern. Plants can sense the three components of LPS, including core polysaccharide, lipid A, and O-antigen. LPS biosynthesis is an essential factor for the successful establish
Externí odkaz:
https://doaj.org/article/b6959e695ad64d2a8b0e1367b7e82979
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