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Acta Biochimica Et Biophysica Sinica|March 6, 2013
The structure of prion: is it enough for interpreting the diverse phenotypes of prion diseases?Chan Tian, Xiaoping Dong
Hereditas|May 25, 2020
Identification of a 6-month-old baby with a combination of WAGR and Potocki-Shaffer contiguous deletion syndromes by SNP array testingYan Meng, Jun Yang, Chan Tian, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 9, 2021
[Genetic analysis of an individual with a fragile site at 16q22]Minjie Shao, Yun Wang, Chan Tian, et al.
Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi = Chinese Journal of Cellular and Molecular Immunology|September 11, 2008
[Preparation of the polypeptide antibody against human transcriptional factors TFDP1 and TFDP3]Chan Tian, Yun-yan Li, Huan Qiao, et al.
The American Journal of the Medical Sciences|December 11, 2012
C-reactive protein levels predict bacterial exacerbation in patients with chronic obstructive pulmonary diseaseChunhong Peng, Chan Tian, Yonggang Zhang, et al.
Molecular Cytogenetics|September 8, 2017
A de novo complex chromosome rearrangement associated with multisystematic abnormalities, a case reportChan Tian, Dan Li, Ping Liu, et al.
Ecotoxicology and Environmental Safety|December 17, 2024
Association between alkali and alkaline earth elements in chorionic villus and risk for spontaneous abortionMeng Lin, Yutong Wang, Xiaoye Wang, et al.
Frontiers in Endocrinology|January 18, 2024
Low follistatin level is a causal risk factor for spontaneous abortion: a two-sample mendelian randomization studyChen Gong, Wenzhi Yang, Xue Liu, et al.
Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences|December 27, 2005
[Estimation of an NY-ESO-1 expressing HCC cell line by NY-ESO-1b specific CD8+T cells in vitro induced by HLA-A2 restricted NY-ESO-1b peptide]Huan Qiao, Xiao-ping Qian, Hua-gang Zhang, et al.
BMC Medical Genetics|November 9, 2019
A case report and mechanism analysis of a normal phenotype mosaic 47, XXY complicated by paternal iUPD (9) who had a normal PGD resultDan Li, Yun Wang, Nan Zhao, et al.
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