Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Chang Shun Yu"'
Publikováno v:
In Journal of Alloys and Compounds 25 March 2017 698:814-818
Autor:
Jing LI, Cheng ZHANG, Yi⁃xin ZHANG, Shan⁃wei FENG, Juan YANG, Ji⁃qing CAO, Chang⁃shun YU, Ya⁃qin LI, Yan⁃yun WANG, Fei CHEN, Jie KONG, Min⁃ying ZHENG, Ling LIAO
Publikováno v:
Chinese Journal of Contemporary Neurology and Neurosurgery, Vol 12, Iss 3, Pp 282-287 (2012)
Objective To explore the clinical features, genetic characters and the importance of prenatal diagnosis in spinocerebellar ataxia 3 (SCA3) patients. Methods SCA3/ATXN3 gene was determined by using PCR and segmental analysis techniques in 2 patients a
Externí odkaz:
https://doaj.org/article/8976d63864d64f41bb273f938c0e28a5
Autor:
Chang,Shun-Yu, 張舜裕
105
In this paper, the physical properties and microwave dielectric properties of LaM2VO6 (M = Mg, Co, Cu, Ni, Ca) dielectric ceramics are studied. experiment result shows, LaMg2VO6 has the best result (εr value is 14.26, Q×f is 14,600 GHz and
In this paper, the physical properties and microwave dielectric properties of LaM2VO6 (M = Mg, Co, Cu, Ni, Ca) dielectric ceramics are studied. experiment result shows, LaMg2VO6 has the best result (εr value is 14.26, Q×f is 14,600 GHz and
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/13130309892349501669
Akademický článek
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Publikováno v:
Advanced Materials Research. :2240-2244
Nanosized TiO2 particles were synthesized by sol-gel method using ionic liquid as assistant. The samples were characterized by UV-vis diffuse reflectance spectra, X-ray diffraction (XRD), transmission electron microscopy (TEM). It was shown that the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a629d6794b7da83339e44c9ca9a8b0b
https://doi.org/10.4028/www.scientific.net/amr.535-537.2240
https://doi.org/10.4028/www.scientific.net/amr.535-537.2240
Publikováno v:
Journal of Materials Science: Materials in Electronics; Sep2018, Vol. 29 Issue 17, p14835-14841, 7p
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 24(9-10)
Fanconi-Bickel syndrome (FBS) is a rare inherited disease caused by mutations in the glucose transporter 2 gene, SLC2A2. We reported the first two Chinese cases of FBS. Both cases presented typical clinical features of hepatomegaly, hypophosphatemic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd6bd863432ee08a0f912ad02d97f8ba
https://pubmed.ncbi.nlm.nih.gov/22145468
https://pubmed.ncbi.nlm.nih.gov/22145468
Autor:
Gui Ling Mo, Wenli Feng, Yi Xin Zhan, Ya Juan Li, Zong Ping Mo, Zheng Yu Zeng, Chaohui Hu, Chang Shun Yu, Wei Xi Cao
Publikováno v:
Clinical chemistry and laboratory medicine. 50(4)
Background The aim of this study was to establish a sensitive method that can detect the presence of not only the common but also the unusual or unknown α-globin gene deletions for screening of α-thalassemia. We used quantitative multiplex PCR of s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cb72ecec6cd3dfcaed7ccf9892ce496
https://pubmed.ncbi.nlm.nih.gov/22505528
https://pubmed.ncbi.nlm.nih.gov/22505528
Publikováno v:
Nan fang yi ke da xue xue bao = Journal of Southern Medical University. 29(12)
To screen the proteins interacting with FXR1P for functional investigation of FXR1P.The yeast strain AH109 transformed with the recombinant expression vector pGBKT7/FXR1 was mated with the yeast strain Y187 pretransformed with human fetal brain cDNA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c3dd8975085c7c26557fad75c3889b99
https://pubmed.ncbi.nlm.nih.gov/20034884
https://pubmed.ncbi.nlm.nih.gov/20034884
Publikováno v:
Zhongguo shi yan xue ye xue za zhi. 17(6)
The aim of this study was to investigate the polymorphism of microsatellite repeats DXS15, CA13, CA22 tightly linked to FVIII gene in Guangdong population and its practical value in genetic diagnosis for hemophilia A. The polymerase chain reaction (P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::517c33e6981b9faff12e8ebb82f94bb5
https://pubmed.ncbi.nlm.nih.gov/20030949
https://pubmed.ncbi.nlm.nih.gov/20030949