Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Qingying Lin"'
Publikováno v:
BMJ Open, Vol 11, Iss 7 (2021)
Objective To develop and internally validate a prediction model for 6-year risk of stroke and its primary subtypes in middle-aged and elderly Chinese population.Design This is a retrospective cohort study from a prospectively collected database.Parti
Externí odkaz:
https://doaj.org/article/6e90241aa7af45a79588ece040ce05aa
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 2, Pp n/a-n/a (2021)
Abstract Background Rare studies focused on the tandem mass spectrometry (MS/MS) findings for the primary carnitine deficiency (PCD) in the neonates in China mainland. In this study, we aim to analyze the gene mutation spectrum of PCD in Fujian Provi
Externí odkaz:
https://doaj.org/article/834a665074a24f94a3e3892a364af641
Publikováno v:
European Journal of Remote Sensing, Vol 51, Iss 1, Pp 1036-1048 (2018)
Weihai's urban development model is representative of coastal cities in China. Landsat MSS/TM/OLI images were used to extract the land use types of Weihai from 1985–2015 using the object-oriented support vector machine (SVM) classification method.
Externí odkaz:
https://doaj.org/article/5d78e76806384bcd84337f1bd6f5fdfc
Autor:
Qingying Lin, Muhua Wang, Diqun Chen, Jiani Wu, Ying Lan, Lijin Wang, Qingdong Jin, Yanqing Chen, Zhihui Chen
Background A significant increasing trend in the prevalence of thyroid nodules has resulted in shining a spotlight on whether thyroid nodules are related to the level of iodine nutrition. In this study, a 1:1 matched case-control study is conducted t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d6fb0b22a4688a096e945984476f0da
https://doi.org/10.21203/rs.3.rs-2990755/v1
https://doi.org/10.21203/rs.3.rs-2990755/v1
Preparation of ultra-high temperature SiC–TiB2 nanocomposites from a single-source polymer precursor
Publikováno v:
Ceramics International. 46:19928-19934
SiC–TiB2 ceramic nanocomposites are valuable ultra-high temperature materials, which are rarely prepared from preceramic polymers. In this work, we synthesized SiC–TiB2 nanocomposites from a new preceramic polymer called titanium- and boron-modif
Phenylalanine hydroxylase deficiency (PAHD) is the most prevalent inborn error of amino acid metabolism in China, has a complex phenotype with many variants and genotypes among different populations. Here, we analyzed the phenylalanine hydroxylase(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6a4277b03107fd1fad72f4e97f6c68f
https://doi.org/10.21203/rs.3.rs-1096859/v1
https://doi.org/10.21203/rs.3.rs-1096859/v1
Publikováno v:
Molecular biology reports. 49(11)
Background Phenylalanine hydroxylase deficiency (PAHD) is the most prevalent inherited disorder of amino acid metabolism in China. Its complex phenotype includes many variants and genotypes among different populations. Methods and results In this stu
Autor:
Yao Chen, Yinglin Zeng, Xiaolong Qiu, Feng Lin, Hong Zhao, Honghua Zhang, Weifen Chen, Qingying Lin, Guanghua Liu, Wenbin Zhu
Background: We aim to explore the realization of 16 quality control indices of neonatal disease screening in neonatal disease management information system, and to establish the multi-center management evaluation model under the framework of the whol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7dc24b46fb25a0a83f8f8f1350f12791
https://doi.org/10.21203/rs.3.rs-520651/v1
https://doi.org/10.21203/rs.3.rs-520651/v1
Gene diagnosis and pedigree analysis of two Han ethnicity families with propionic acidemia in Fujian
Publikováno v:
Medicine
Propionic acidemia is associated with pathogenic variants in PCCA or PCCB gene. We investigated the potential pathogenic variants in PCCA or PCCB genes in Fujian Han population. Two probands and their families of Han ethnicity containing two generati
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 2, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine, Vol 9, Iss 2, Pp n/a-n/a (2021)
Background Rare studies focused on the tandem mass spectrometry (MS/MS) findings for the primary carnitine deficiency (PCD) in the neonates in China mainland. In this study, we aim to analyze the gene mutation spectrum of PCD in Fujian Province in Ch