Zobrazeno 1 - 10
of 188
pro vyhledávání: '"Yuanzhen Zhang"'
Autor:
Yuqi Shao, Saisai Yang, Lin Cheng, Jie Duan, Jin Li, Jiawei Kang, Fang Wang, Juan Liu, Fang Zheng, Jianhong Ma, Yuanzhen Zhang
Publikováno v:
Molecular Cytogenetics, Vol 17, Iss 1, Pp 1-10 (2024)
Abstract Objective The primary object of this study is to analyze chromosomal abnormalities in miscarriages detected by copy number variants sequencing (CNV-Seq), establish potential pathways or genes related to miscarriages, and provide guidance for
Externí odkaz:
https://doaj.org/article/72384a310523490db2d181319683c33a
Publikováno v:
Journal of Translational Medicine, Vol 21, Iss 1, Pp 1-16 (2023)
Abstract Background Congenital heart defect (CHD) is the most common congenital abnormality, and it has long been a clinical and public health concern. Our previous findings have found Periostin (POSTN) and Pappalysin-1 (PAPPA) as potential biomarker
Externí odkaz:
https://doaj.org/article/2f71e35505304956a8d3a5dc0336082e
Autor:
Yuqi Shao, Saisai Yang, Jiafu Li, Lin Cheng, Jiawei Kang, Juan Liu, Jianhong Ma, Jie Duan, Yuanzhen Zhang
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Objective: The article aims to provide genetic counseling to a family with two children who were experiencing growth and developmental delays.Methods: Clinical information of the proband was collected. Peripheral blood was collected from core family
Externí odkaz:
https://doaj.org/article/eeb6893c99df476f9ebfdf205f056caa
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 172, Iss , Pp 116246- (2024)
Azithromycin, a commonly used macrolide antibiotic for treating chlamydial infections during pregnancy, has sparked investigations into its potential effects on offspring development. Despite these inquiries, there remains uncertainty about the speci
Externí odkaz:
https://doaj.org/article/d8ae8b670c804ee593a89154a89f6972
Autor:
Huanhuan Yang, Jun Huang, Hao Zheng, Yunfan Zhang, Yuanzhen Zhang, Wei Liu, Jinrong Wu, Xiaobin Chen, Jinfeng Lin, Yanna Ni, Xiaojing Nie
Publikováno v:
BMC Medical Genomics, Vol 16, Iss 1, Pp 1-6 (2023)
Abstract Background 1P36 deletion syndrome is recognized as the most common terminal microdeletion syndrome in humans, characterized by early developmental delay and consequent intellectual disability, seizure disorder, and distinctive facial feature
Externí odkaz:
https://doaj.org/article/a1428a035fcb4ac7bffc25753ea03e30
Publikováno v:
Reproductive Biology and Endocrinology, Vol 21, Iss 1, Pp 1-11 (2023)
Abstract Background Diminished ovarian reserve (DOR) is a common cause of female infertility, with genetic factors being a significant contributor. However, due to high genetic heterogeneity, the etiology of DOR in many cases remains unknown. In this
Externí odkaz:
https://doaj.org/article/51768fca391f461594795bd040b9eb85
Publikováno v:
Journal of Ovarian Research, Vol 16, Iss 1, Pp 1-12 (2023)
Abstract Background Prednisone is one of the most used synthetic glucocorticoids during pregnancy. Epidemiological investigations suggested that prenatal prednisone therapy could affect fetal development, but systematic studies on its effects on ovar
Externí odkaz:
https://doaj.org/article/230db391ace84228b0e97ee4536a6265
Autor:
Yi Chen, Yuanzhen Zhang, Jun Huang, Yugui Zeng, Yifang Qian, Junyan Chen, Guangming Chen, Guizhi Xia, Chengfeng Wang, Ai Feng, Zheng Li, Li Chen, Sirui Zheng, Fenrong Li, Zengfeng Weng, Chuanyin Zhang, Yuen Yang, Jinfeng Lin, Jinrong Wu, Hannan Zhang, Wenhua Ouyang, Xiaojing Nie
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 7, Pp n/a-n/a (2023)
Abstract Background Kidney disease of children markedly affects their health and development. Limited clinical data of early‐stage kidney disease render a tremendous challenge for the accurate diagnosis. Trio whole‐exome sequencing (Trio‐WES) i
Externí odkaz:
https://doaj.org/article/6c4cf3b4bca143b487d1db016238d665
Publikováno v:
Cell & Bioscience, Vol 12, Iss 1, Pp 1-18 (2022)
Abstract Background As a member of RNA-binding protein, CDKN2AIP has been shown to play a critical role in stem cell pluripotency and somatic differentiation. Recent studies indicate that Cdkn2aip is essential for spermatogonial self-renewal and prol
Externí odkaz:
https://doaj.org/article/d85ce58c771648048e8e716d1cf645b7
Publikováno v:
Orthopaedic Surgery, Vol 14, Iss 6, Pp 1251-1259 (2022)
Background Osteonecrosis of the femoral head (ONFH) is a multifactorial disease, and agnogenic ONFH, otherwise known as idiopathic ONFH, is rare in clinic. Idiopathic ONFH that exhibits severe necrosis and progresses extremely rapidly is called rapid
Externí odkaz:
https://doaj.org/article/4b793a52ba6c4ddba2ce583500a1f0ea