[1] Wu L, Zhou X, Xiao Z, et al. Functional expression, characterization, and application of human S100B[J]. Oncol Rep, 2017, 38(4): 2309-2316.
[2] Gulen B, Serinken M, Eken C, et al. Serum S100B as a surrogate biomarker in the diagnoses of burnout and depression in emergency medicine residents[J]. Acad Emerg Med, 2016, 23(7): 786-789.
[3] Liu J, Zheng F, Long Y, et al. Preliminary analysis of parkinson-like motor coordination abnormityin brain-specific hS100B transgenic mice[J]. Acta Academiae Medicinae Sinicae, 2017, 39(2): 240-246.
[4] Chen S, Tian L, Chen N, et al. Cognitive dysfunction correlates with elevated serum S100B concentration in drug-free acutely relapsed patients with schizophrenia[J]. Psychiatry Res, 2017, 247: 6-11.
[5] Gebhardt C, Lichtenberger R, Utikal J. Biomarker value and pitfalls of serum S100B in the follow-up of high-risk melanoma patients[J]. J Dtsch Dermatol Ges, 2016, 14(2): 158-164.
[6] Shimizu A, Sakai Y, Ohno K, et al. A molecular genetic linkage map of mouse chromosome 10, including the Myb, S100b, Pah, Sl, and Ifg genes[J]. Biochem Genet, 1992, 30(9-10): 529-535.
[7] Diaz-Romero J, Nesic D. S100A1 and S100B: calcium sensors at the cross-roads of multiple chondrogenic pathways[J]. J Cell Physiol, 2017, 232(8): 1979-1987.
[8] Jensen JL, Indurthi VS, Neau DB, et al. Structural insights into the binding of the human receptor for advanced glycation end products (RAGE) by S100B, as revealed by an S100B-RAGE-derived peptide complex[J]. Acta Crystallogr D Biol Crystallogr, 2015, 71(Pt 5): 1176-1183.
[9] Zhai J, Cheng L, Dong J, et al. S100B gene polymorphisms predict prefrontal spatial function in both schizophrenia patients and healthy individuals[J]. Schizophr Res, 2012, 134(1): 89-94.
[10]Matsson H, Huss M, Persson H, et al. Polymorphisms in DCDC2 and S100B associate with developmental dyslexia[J]. J Hum Genet, 2015, 60(7): 399-401.
[11]Luo X, Mo ShN, Kong R, et al. Polymorphisms of S100BGene in children with developmental dyslexia in China[J]. Acta Medicinae Universitatis Scientiae et Technologiae Huazhong, 2016, (4): 394-397. (in Chinese)
罗秀, 莫胜男, 孔锐, 等. 汉语阅读障碍儿童S100B基因多态性研究[J]. 华中科技大学学报(医学版), 2016, (4): 394-397.
[12]Fardell C, Zettergren A, Ran C, et al. S100B polymorphisms are associated with age of onset of Parkinson’s disease[J]. BMC Med Genet, 2018, 19(1): 42.
[13]Huang HT, Lu YL, Wang R, et al. Polymorphisms of rs3819024 and rs1974226 in interleukin-17A gene in Guangxi populations[J]. Acta Anatomica Sinica,2018, 49(2): 246-250. (in Chinese)
黄华佗, 陆玉兰, 王荣,等. 广西人群白细胞介素17A基因rs3819024和rs1974226的多态性[J]. 解剖学报, 2018, 49(2): 246-250.
[14]Wang XL, Zhao DX, Zhuang WT, et al. Correlation between genetic polymorphism and hypertensive disorder complicating pregnancy in Qinghai[J]. Acta Anatomica Sinica, 2018, 49(3): 379-386. (in Chinese)
王香林, 赵得雄, 庄文婷,等. 基因多态性与青海妊娠高血压疾病的相关性[J]. 解剖学报, 2018, 49(3): 379-386.
|