Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Meijiao, Cai"'
Autor:
Yunsheng Ge, Jiayan Chen, Yanru Huang, Di Shao, Wenbo Wang, Meijiao Cai, Meihua Tan, Jian Zhang
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Fetal chromosomal abnormalities are the main cause of adverse pregnancy outcomes and are the focus of invasive prenatal diagnosis. Recent studies have demonstrated that various techniques have distinct advantages. Achieving high-resolution and effect
Externí odkaz:
https://doaj.org/article/81aee62e5a1c4754b05a2e0eb128a48f
Autor:
Yanru Huang, Libin Mei, Yangdan Wang, Huiming Ye, Xiaomin Ma, Jian Zhang, Meijiao Cai, Ping Li, Yunsheng Ge, Yulin Zhou
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
ObjectiveGlobal developmental delay has markedly high phenotypic and genetic heterogeneity, and is a great challenge for clinical diagnosis. Hypotonia, ataxia, and delayed development syndrome (HADDS), first reported in 2017, is one type of global de
Externí odkaz:
https://doaj.org/article/0077f7668c884639a5f4153518a43d81
Publikováno v:
Journal of Biomaterials and Tissue Engineering. 12:2307-2311
A high density lipoprotein (HDL) based protein delivery system composed of HDL, polyethyleneimine (PEI) and vascular endothelial growth factor (VEGF) protein was constructed (HDL/PEI/VEGF) was fabricated as an advanced system for myocardial ischemia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6761c62b9856e3104121073b8a25b5aa
https://doi.org/10.1166/jbt.2022.3166
https://doi.org/10.1166/jbt.2022.3166
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 38(8)
To carry out prenatal diagnosis for a fetus with absent nasal bone by using cytogenetic and molecular techniques.Chromosomal karyotyping, single nucleotide polymorphism array (SNP-array) and fluorescence in situ hybridization (FISH) assays were appli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a6f16cc35587413813fc4fbab3dfe130
https://pubmed.ncbi.nlm.nih.gov/34365625
https://pubmed.ncbi.nlm.nih.gov/34365625
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 37(10)
To explore the nature of chromosomal abnormality in a fetus with nasal bone dysplasia and clarify its clinical effect.Fetal chromosome karyotype was analyzed by G-banding. Single nucleotide polymorphism array (SNP-array) was used to detect the chromo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4405731a5e687670acbe789b2676e10a
https://pubmed.ncbi.nlm.nih.gov/32924128
https://pubmed.ncbi.nlm.nih.gov/32924128
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 37(9)
To carry out prenatal diagnosis for a fetus with increased nuchal translucency (NT) and another fetus with non-invasive prenatal testing (NIPT) suggested reduced sex chromosomes by cytogenetic and molecular techniques.Chromosomal karyotyping, single
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::440705f30f09b1ca022313eb9dad677f
https://pubmed.ncbi.nlm.nih.gov/32820525
https://pubmed.ncbi.nlm.nih.gov/32820525
Publikováno v:
Andrologia. 52
Sex chromosome abnormality (SCA) is one of the major causes of male spermatogenesis dysfunction. In our study, we sought to investigate the novel X chromosome inversion leading to severe oligozoospermia. Here, we report two brothers with severe oligo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83cb7a0d7d714514629bcc6b7f95600d
https://doi.org/10.1111/and.13602
https://doi.org/10.1111/and.13602
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 37(4)
To carry out genetic testing for 3 fetuses with abnormal prenatal screening.Fetal ultrasound, karyotype analysis, single nucleotide polymorphism (SNP) array and fluorescence in situ hybridization were performed.Abnormalities of chromosome 22 were fou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d3809ef37b697c4a15f5ee43cf44b4eb
https://pubmed.ncbi.nlm.nih.gov/32219823
https://pubmed.ncbi.nlm.nih.gov/32219823
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 36(12)
To explore the clinical significance of a prenatal case with two small supernumerary marker chromosomes (sSMC) through identification of their origins.G-banding chromosomal karyotyping analysis were carried out on fetal amniotic fluid sample and peri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7650aaf6d33f6cd2d56e1c72614ab25c
https://pubmed.ncbi.nlm.nih.gov/31813153
https://pubmed.ncbi.nlm.nih.gov/31813153
Publikováno v:
The Analyst. 143(21)
A portable electrochemical immunosensing protocol was designed for the sensitive detection of a disease-related tumor biomarker (carcinoembryonic antigen, CEA, used in this case) on a pH meter using glucose oxidase (GOx)-encapsulated gold hollow micr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa0794c47ef9220fc96f5bb8b0223b48
https://pubmed.ncbi.nlm.nih.gov/30280731
https://pubmed.ncbi.nlm.nih.gov/30280731