Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Yanting Kong"'
Publikováno v:
IEEE Photonics Journal, Vol 14, Iss 6, Pp 1-4 (2022)
The thickness detection of quantum well has always been the research focus, especially for InxGa1-xAs-based indium-rich cluster (IRC) structure, which has a thickness fluctuation of normal and indium-deficient InGaAs layers caused by IRC effect. In t
Externí odkaz:
https://doaj.org/article/ca4823b05744491f80b078855610be98
Autor:
Xiuxia Ye, Shumei Dong, Yujiao Deng, Chuan Jiang, Yanting Kong, Lili Tang, Yanlin Wang, Fei Bei, Haifa Hong
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
The relationship between vitamin D and cardiovascular health in children remains unclear. Vitamin D deficiency (VDD) is supposed to be a potential risk factor associated with poorer outcomes after congenital heart disease (CHD) surgery. The maximum v
Externí odkaz:
https://doaj.org/article/592a07035e6d410ba847e93023595cba
Autor:
Yanting Kong, Kai Yan, Liyuan Hu, Mingbang Wang, Xinran Dong, Yulan Lu, Bingbing Wu, Huijun Wang, Lin Yang, Wenhao Zhou
Publikováno v:
Data in Brief, Vol 22, Iss , Pp 492-501 (2019)
Mutations in SCN1A and SCN2A are associated with a wide spectrum of epilepsy related disorders in human. This dataset presented variants and clinical features of SCN1A and SCN2A genes. A total of 48 cases were presented, including 33 SCN1A mutations
Externí odkaz:
https://doaj.org/article/56fcae5df5bd4a3c81da7deb74324613
Autor:
Chengxiang Lin, Feifan Xiao, Liping Wang, Chunmei Lu, Jian Zhou, Wenhao Zhou, Zhongwei Qiao, Yu-Wei Jiang, Guoqiang Cheng, Dajiang Zhang, Kai Yan, Haowei Yang, Junbo Wang, Yanting Kong, Yong Zhang, Qian Qin
Publikováno v:
Transl Pediatr
BACKGROUND: Acute bilirubin encephalopathy or kernicterus is the worst consequence of brain damage caused by the elevation of total unbound serum bilirubin (TSB) in neonates. The present study aimed to visualize the characteristic brain regions of ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::525565e8438f89a97726f6be52554476
https://doi.org/10.21037/tp-20-447
https://doi.org/10.21037/tp-20-447
Autor:
Liu Liu, Xinran Dong, Yulan Lu, Lin Yang, Xia Tian, Xiaomin Peng, Zejun Wei, Huijun Wang, Jing Zhang, Yun Cao, Wenhao Zhou, Guoqiang Cheng, Fang Ping, Yanting Kong, Qi Ni, Chao Chen, Chunmei Lu, Jin Wang, Wesley You, Katia Meirelles, Sha Tang, Changhua Li, Xiang Chen, Liyuan Hu, Laishuan Wang, Fengqi Chang, Bingbing Wu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::749202850cf0258ddb67461944b84a15
https://doi.org/10.1111/cge.14075/v2/response1
https://doi.org/10.1111/cge.14075/v2/response1
Autor:
Liu Liu, Chao Chen, Huijun Wang, Yanting Kong, Jin Wang, Jing Zhang, Guoqiang Cheng, Yun Cao, Xiang Chen, Katia Meirelles, Wenhao Zhou, Chunmei Lu, Yulan Lu, Xinran Dong, Sha Tang, Changhua Li, Qi Ni, Xia Tian, Xiaomin Peng, Lin Yang, Fengqi Chang, Wesley You, Bingbing Wu, Laishuan Wang, Zejun Wei, Liyuan Hu, Ping Fang
Publikováno v:
Clinical geneticsREFERENCES. 101(1)
Emerging evidence demonstrates the clinical utility of genomic applications in newborn intensive care unit (NICU) patients with strong indications of Mendelian etiology. However, such applications' diagnostic yield and utility remain unclear for NICU
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::784d7efe55b2b1285323768997ff3554
https://pubmed.ncbi.nlm.nih.gov/34671977
https://pubmed.ncbi.nlm.nih.gov/34671977
Autor:
Liyuan Hu, Xiang Chen, Lin Yang, Q. Richard Lu, Bingbing Wu, Yifeng Lin, Qi Ni, Huijun Wang, Xinran Dong, Yanting Kong, Wenhao Zhou, Yulan Lu
Publikováno v:
Genetics in Medicine. 21:564-571
PURPOSE: Genetic diagnosis for children suffering from epilepsy has important implications for treatment, prognosis, and development of precision medicine strategies. METHODS: We performed exome sequencing (ES) or targeted sequencing on 733 children
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13ddd717637ef864a3baa24897b6cad2
https://doi.org/10.1038/s41436-018-0091-8
https://doi.org/10.1038/s41436-018-0091-8
Autor:
Mingbang Wang, Kai Yan, Liyuan Hu, Wenhao Zhou, Bingbing Wu, Yulan Lu, Lin Yang, Xinran Dong, Yanting Kong, Huijun Wang
Publikováno v:
Data in Brief, Vol 22, Iss, Pp 492-501 (2019)
Data in Brief
Data in Brief
Mutations in SCN1A and SCN2A are associated with a wide spectrum of epilepsy related disorders in human. This dataset presented variants and clinical features of SCN1A and SCN2A genes. A total of 48 cases were presented, including 33 SCN1A mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec8b471ca3e6fd4e76b85ba054044b3e
http://www.sciencedirect.com/science/article/pii/S2352340918309740
http://www.sciencedirect.com/science/article/pii/S2352340918309740
Autor:
Chunmei Lu, Xiaomin Peng, Liu Liu, Chen Xiang, Yulan Lu, Zejun Wei, Chao Chen, Guoqiang Cheng, Katia Meirelles, Xia Tian, Qi Ni, Yanting Kong, Wesley You, Liyuan Hu, Wenhao Zhou, Jing Zhang, Yun Cao, Sha Tang, Ping Fang, Laishuan Wang, Jin Wang, Fengqi Chang, Lin Yang, Bingbing Wu, Xinran Dong, Changhua Li, Yan Dou, Huijun Wang
Publikováno v:
SSRN Electronic Journal.
Background: Rare genetic diseases underlie a significant portion of congenital anomalies and contribute to neonatal intensive care unit (NICU) admissions. A timely genetic diagnosis is important for medical decision making. Emerging evidence demonstr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d974ed7940bde550b691347348f7582
https://doi.org/10.2139/ssrn.3517402
https://doi.org/10.2139/ssrn.3517402
Autor:
Huijun Wang, Lin Yang, Wenhao Zhou, Yulan Lu, Liyuan Hu, Xinran Dong, Bingbing Wu, Kai Yan, Mingbang Wang, Yanting Kong
Publikováno v:
Clinica Chimica Acta. 483:14-19
Background We investigated the association between SCN1A and SCN2A mutations and clinical phenotype and electroencephalography (EEG) features. Methods In this study, 48 patients suffered from epilepsy or severe seizures with SCN1A and SCN2A mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4f70ee24765fddc576ff973e8c89940
https://doi.org/10.1016/j.cca.2018.03.027
https://doi.org/10.1016/j.cca.2018.03.027