1 - 25 of
40
results
for author:"Cui B."
in Literature Citations
| Multiple synostoses syndrome is due to a missense mutation in exon 2 of FGF9 gene. Wu X.L., Gu M.M., Huang L., Liu X.S., Zhang H.X., Ding X.Y., Xu J.Q., Cui B., Wang L., Lu S.Y. et al. Am. J. Hum. Genet. 85:53-63(2009) · Mapped (1) |
| Increased serum HMGB1 is related to the severity of coronary artery stenosis. Hu X., Jiang H., Bai Q., Zhou X., Xu C., Lu Z., Cui B., Wen H. Clin. Chim. Acta 406:139-142(2009) · Mapped (8) |
| PPAR gamma protects cardiomyocytes against oxidative stress and apoptosis via Bcl-2 upregulation. Ren Y., Sun C., Sun Y., Tan H., Wu Y., Cui B., Wu Z. Vascul. Pharmacol. 51:169-174(2009) · Mapped (14) |
| AMP-activated protein kinase and pancreatic/duodenal homeobox-1 involved in insulin secretion under high leucine exposure in rat insulinoma beta-cells. Zhang X., Sun N., Wang L., Guo H., Guan Q., Cui B., Tian L., Gao L., Zhao J. J. Cell. Mol. Med. 13:758-770(2009) · Mapped (2) |
| Gain-of-function mutation of KIT ligand on melanin synthesis causes familial progressive hyperpigmentation. Wang Z.Q., Si L., Tang Q., Lin D., Fu Z., Zhang J., Cui B., Zhu Y., Kong X., Deng M. et al. Am. J. Hum. Genet. 84:672-677(2009) · Mapped (1) |
| Removal of Hsf4 leads to cataract development in mice through down-regulation of gamma S-crystallin and Bfsp expression. Shi X., Cui B., Wang Z., Weng L., Xu Z., Ma J., Xu G., Kong X., Hu L. BMC Mol. Biol. 10:10-10(2009) · Mapped (6) |
| Mutation of PIK3CA: possible risk factor for cervical carcinogenesis in older women. Cui B., Zheng B., Zhang X., Stendahl U., Andersson S., Wallin K.L. Int. J. Oncol. 34:409-416(2009) · Mapped (6) |
| Targeting TLR2 attenuates pulmonary inflammation and fibrosis by reversion of suppressive immune microenvironment. Yang H.Z., Cui B., Liu H.Z., Chen Z.R., Yan H.M., Hua F., Hu Z.W. J. Immunol. 182:692-702(2009) · Mapped (3) |
| Insulin-like growth factor-1 promotes cell cycle progression via upregulation of cyclin D1 expression through the phosphatidylinositol 3-kinase/nuclear factor-kappaB signaling pathway in FRTL thyroid cells. Ren M., Zhong X., Ma C.Y., Sun Y., Guan Q.B., Cui B., Guo J., Wang H., Gao L., Zhao J.J. Acta Pharmacol. Sin. 30:113-119(2009) · Mapped (5) |
| A patient with pseudohypoaldosteronism type II caused by a novel mutation in WNK4 gene. Gong H., Tang Z., Yang Y., Sun L., Zhang W., Wang W., Cui B., Ning G. Endocrine 33:230-234(2008) · Mapped (3) |
| The association of TAAAAn repeat polymorphism in sex hormone-binding protein gene with polycystic ovary syndrome in Chinese population. Liu Q., Gu W., Cui B., Hong J., Zhang Y., Chi Z., Su Y., Ning G. Endocrine 34:62-67(2008) · Mapped (8) |
| The matrix protein CCN1 (CYR61) promotes proliferation, migration and tube formation of endothelial progenitor cells. Yu Y., Gao Y., Wang H., Huang L., Qin J., Guo R., Song M., Yu S., Chen J., Cui B. et al. Exp. Cell Res. 314:3198-3208(2008) · Mapped (1) |
| NMDA enhances stretching-induced differentiation of osteoblasts through the ERK1/2 signaling pathway. Li J.L., Cui B., Qi L., Li X.Y., Deng L.F., Ning G., Liu J.M. Bone 43:469-475(2008) · Mapped (2) |
| Androgen receptor gene CAG(n) trinucleotide repeats polymorphism in Chinese women with polycystic ovary syndrome. Liu Q., Hong J., Cui B., Zhang Y., Gu W., Chi Z., Su Y., Ning G. Endocrine 33:165-170(2008) · Mapped (8) |
| Association of the interleukin (IL)-16 gene polymorphisms with Graves' disease. Gu X.J., Cui B., Zhao Z.F., Chen H.Y., Li X.Y., Wang S., Ning G., Zhao Y.J. Clin. Immunol. 127:298-302(2008) · Mapped (12) |
| Cloning, in vitro expression and bioactivity of duck interleukin-18. Chen H.Y., Cui B.A., Xia P.A., Li X.S., Hu G.Z., Yang M.F., Zhang H.Y., Wang X.B., Cao S.F., Zhang L.X. et al. Vet. Immunol. Immunopathol. 123:205-214(2008) · UniProtKB (1) |
| Overexpression of ERBB-2 was more frequently detected in malignant than benign pheochromocytomas by multiplex ligation-dependent probe amplification and immunohistochemistry. Yuan W., Wang W., Cui B., Su T., Ge Y., Jiang L., Zhou W., Ning G. Endocr. Relat. Cancer 15:343-350(2008) · Mapped (8) |
| Polymorphisms of KIRs gene and HLA-C alleles in patients with ankylosing spondylitis: possible association with susceptibility to the disease. Jiao Y.L., Ma C.Y., Wang L.C., Cui B., Zhang J., You L., Chen Z.J., Li J.F., Zhao Y.R. J. Clin. Immunol. 28:343-349(2008) · Mapped (383) |
| The common variants of E-selectin gene in Graves' disease. Chen H., Cui B., Wang S., Zhao Z., Sun H., Gu X., Zhao Y., Li X., Ning G. Genes Immun. 9:182-186(2008) · Mapped (8) |
| MEN1 mutation analysis in Chinese patients with multiple endocrine neoplasia type 1. Jiang X.H., Lu J.L., Cui B., Zhao Y.J., Wang W.Q., Liu J.M., Fang W.Q., Cao Y.N., Ge Y., Zhang C.X. et al. Endocr. Relat. Cancer 14:1073-1079(2007) · Mapped (12) |
| The A946T polymorphism in the interferon induced helicase gene does not confer susceptibility to Graves' disease in Chinese population. Zhao Z.F., Cui B., Chen H.Y., Wang S., Li I., Gu X.J., Qi L., Li X.Y., Ning G., Zhao Y.J. Endocrine 32:143-147(2007) · Mapped (4) |
| Clinical and genetic analysis for a Chinese family with hereditary fructose intolerance. Chi Z.N., Hong J., Yang J., Zhang H.J., Dai M., Cui B., Zhang Y., Gu W.Q., Zhang Y.F., Liu Q.R. et al. Endocrine 32:122-126(2007) · Mapped (4) |
| Intercellular adhesion molecule 1 gene polymorphisms do not contribute to Graves' disease in Chinese patients. Wang S., Sun H., Chen H.Y., Zhao Z.F., Yang Y., Zhao Y.J., Cui B., Ning G. Endocrine 31:114-118(2007) · Mapped (9) |
| A functional dynein-microtubule network is required for NGF signaling through the Rap1/MAPK pathway. Wu C., Ramirez A., Cui B., Ding J., Delcroix J.D., Valletta J.S., Liu J.J., Yang Y., Chu S., Mobley W.C. Traffic 8:1503-1520(2007) · Mapped (3) |
| Increased activating killer immunoglobulin-like receptor genes and decreased specific HLA-C alleles in couples with recurrent spontaneous abortion. Wang S., Zhao Y.R., Jiao Y.L., Wang L.C., Li J.F., Cui B., Xu C.Y., Shi Y.H., Chen Z.J. Biochem. Biophys. Res. Commun. 360:696-701(2007) · Mapped (374) |
