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Nature Medicine|November 5, 1999
Requirement for T-cell apoptosis in the induction of peripheral transplantation toleranceA D Wells, X C Li, Y Li, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|January 20, 2018
A mutational signature associated with alcohol consumption and prognostically significantly mutated driver genes in esophageal squamous cell carcinomaX C Li, M Y Wang, M Yang, et al.
American Journal of Medical Genetics|May 26, 1999
Maternally inherited nonsyndromic hearing lossR A Friedman, Y Bykhovskaya, C M Sue, et al.
European Review for Medical and Pharmacological Sciences|October 20, 2022
Lung cancer screening study from a smoking population in KunmingQ Cao, Q Zhang, K-X Zhou, et al.
Zhonghua Liu Xing Bing Xue Za Zhi = Zhonghua Liuxingbingxue Zazhi|August 29, 2017
[Study on the classification of dominant pathogens related to febrile respiratory syndrome, based on the method of Bayes discriminant analysis]X C Li, J S Li, L Meng, et al.
The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|November 9, 2013
Development and validation of a chronic obstructive pulmonary disease screening questionnaire in ChinaY-M Zhou, S-Y Chen, J Tian, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|October 19, 2016
Age-Dependent Metabolic and Immunosuppressive Effects of TacrolimusF Krenzien, M Quante, T Heinbokel, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|March 28, 2019
Genomic and transcriptional heterogeneity of multifocal hepatocellular carcinomaL X Xu, M H He, Z H Dai, et al.
Zhonghua Wai Ke Za Zhi [Chinese Journal of Surgery]|March 9, 2025
[Surgical treatment and survival analyses of intrahepatic cholangiocarcinoma]H Zhang, C Y Jiao, C X Li, et al.
European Journal of Human Genetics : EJHG|December 25, 2008
Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15Lance Doucette, Nancy D Merner, Sandra Cooke, et al.
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