The downstream regulatory sequence of the adenovirus type 2 major late promoter is functionally redundant.

Por Li, X C, Huang, W L, Flint, S J
Publicado em 1992

Novel signaling mechanisms of intracellular angiotensin II-induced NHE3 expression and activation in mouse proximal tubule cells

Por Li, X. C., Hopfer, U., Zhuo, J. L.
Publicado em 2012

The role of peripheral T-cell deletion in transplantation tolerance.

Por Wells, A D, Li, X C, Strom, T B, Turka, L A
Publicado em 2001

Mutational spectrometry without phenotypic selection: human mitochondrial DNA.

Por Khrapko, K, Coller, H, André, P, Li, X C, Foret, F, Belenky, A, Karger, B L, Thilly, W G
Publicado em 1997

Study on Characteristics of Chemokine CXCL10 Gene Cloned from cDNA Expression Library of Ujumqin Sheep

Por Hu, P. F., Li, X. C., Lei, N., Lan, X. Y., Zhao, Q. J., Guan, W. J., Ma, Y. H.
Publicado em 2013

Graft-Infiltrating Macrophages Adopt an M2 Phenotype and Are Inhibited by Purinergic Receptor P2X7 Antagonist in Chronic Rejection

Por Wu, C., Zhao, Y., Xiao, X., Fan, Y., Kloc, M., Liu, W., Ghobrial, R. M., Lan, P., He, X., Li, X. C.
Publicado no Am J Transplant (2016)

Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15

Por Doucette, Lance, Merner, Nancy D, Cooke, Sandra, Ives, Elizabeth, Galutira, Dante, Walsh, Vanessa, Walsh, Tom, MacLaren, Linda, Cater, Tracey, Fernandez, Bridget, Green, Jane S, Wilcox, Edward R, Shotland, Larry, Li, X C, Lee, Ming, King, Mary-Claire, Young, Terry-Lynn
Publicado em 2009

Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15

Por Doucette, Lance, Merner, Nancy D, Cooke, Sandra, Ives, Elizabeth, Galutira, Dante, Walsh, Vanessa, Walsh, Tom, MacLaren, Linda, Cater, Tracey, Fernandez, Bridget, Green, Jane S, Wilcox, Edward R, Shotland, Larry, Li, X C, Lee, Ming, King, Mary-Claire, Young, Terry-Lynn
Publicado em 2009

Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2.

Por Liang, Y, Wang, A, Probst, F J, Arhya, I N, Barber, T D, Chen, K S, Deshmukh, D, Dolan, D F, Hinnant, J T, Carter, L E, Jain, P K, Lalwani, A K, Li, X C, Lupski, J R, Moeljopawiro, S, Morell, R, Negrini, C, Wilcox, E R, Winata, S, Camper, S A, Friedman, T B
Publicado em 1998

Integrative analyses of transcriptome sequencing identify novel functional lncRNAs in esophageal squamous cell carcinoma

Por Li, C-Q, Huang, G-W, Wu, Z-Y, Xu, Y-J, Li, X-C, Xue, Y-J, Zhu, Y, Zhao, J-M, Li, M, Zhang, J, Wu, J-Y, Lei, F, Wang, Q-Y, Li, S, Zheng, C-P, Ai, B, Tang, Z-D, Feng, C-C, Liao, L-D, Wang, S-H, Shen, J-H, Liu, Y-J, Bai, X-F, He, J-Z, Cao, H-H, Wu, B-L, Wang, M-R, Lin, D-C, Koeffler, H P, Wang, L-D, Li, X, Li, E-M, Xu, L-Y
Publicado no Oncogenesis (2017)