Special communication: China’s first historic efforts to develop a tobacco control advocacy workforce via schools of public health

Por Yang, T, Yang, X, Lv, Q, Zhao, Q, Ke, X
Publicado em 2009

14.5 Rheumatoid Arthritis susceptibility loci; STAT4, TRAF1/C5 and 6q23 region, are also associated with Juvenile Idiopathic Arthritis

Por Hinks A, Barton A, Eyre S, Ke X, Worthington J, Thomson W
Publicado em 2008-09-01

14.5 Rheumatoid Arthritis susceptibility loci; STAT4, TRAF1/C5 and 6q23 region, are also associated with Juvenile Idiopathic Arthritis

Por Hinks, A, Barton, A, Eyre, S, Ke, X, Worthington, J, Thomson, W
Publicado em 2008

Absorption mechanism of three curcumin constituents through in situ intestinal perfusion method

Por Wang, Y.-H., Ke, X.-M., Zhang, C.-H., Yang, R.-P.
Publicado no Braz J Med Biol Res (2017)

Intracellular Na(+) and Ca(2+) Modulation Increases the Tensile Properties of Developing Engineered Articular Cartilage

Por Natoli, Roman M., Skaalure, Stacey, Bijlani, Shweta, Chen, Ke X., Hu, Jerry, Athanasiou, Kyriacos A.
Publicado em 2010

Association of the AFF3 gene and IL2/IL21 gene region with juvenile idiopathic arthritis

Por Hinks, A, Eyre, S, Ke, X, Barton, A, Martin, P, Flynn, E, Packham, J, Worthington, J, Thomson, W
Publicado em 2010

Examining the Overlap Between Genome-Wide Rare Variant Association Signals and Linkage Peaks in Rheumatoid Arthritis

Por Eyre, S., Ke, X., Lawrence, R., Bowes, J., Panoutsopoulou, K., Barton, A., Thomson, W., Worthington, J., Zeggini, E.
Publicado em 2011

Berberine Attenuates Arterial Plaque Formation in Atherosclerotic Rats with Damp-Heat Syndrome via Regulating Autophagy

Por Ke X, Huang Y, Li L, Xin F, Xu L, Zhang Y, Zeng Z, Lin F, Song Y
Publicado em 2020-06-01

Competition Between Antiferromagnetism and Ferromagnetism in Sr(2)RuO(4) Probed by Mn and Co Doping

Por Ortmann, J. E., Liu, J. Y., Hu, J., Zhu, M., Peng, J., Matsuda, M., Ke, X., Mao, Z. Q.
Publicado em 2013

Formononetin, an active compound of Astragalus membranaceus (Fisch) Bunge, inhibits hypoxia-induced retinal neovascularization via the HIF-1α/VEGF signaling pathway

Por Wu J, Ke X, Ma N, Wang W, Fu W, Zhang H, Zhao M, Gao X, Hao X, Zhang Z
Publicado em 2016-09-01

A novel locus for autosomal dominant non‐syndromic deafness, DFNA53, maps to chromosome 14q11.2‐q12

Por Yan, D, Ke, X, Blanton, S H, Ouyang, X M, Pandya, A, Du, L L, Nance, W E, Liu, X Z
Publicado em 2006

The first linkage disequilibrium (LD) maps: Delineation of hot and cold blocks by diplotype analysis

Por Maniatis, N., Collins, A., Xu, C.-F., McCarthy, L. C., Hewett, D. R., Tapper, W., Ennis, S., Ke, X., Morton, N. E.
Publicado em 2002

Temperature- and field-driven spin reorientations in triple-layer ruthenate Sr(4)Ru(3)O(10)

Por Zhu, M., Li, P. G., Wang, Y., Cao, H. B., Tian, W., Zhang, H. D., Phelan, B. D., Mao, Z. Q., Ke, X.
Publicado no Sci Rep (2018)

CTLA4 mediates antigen-specific apoptosis of human T cells.

Por Gribben, J G, Freeman, G J, Boussiotis, V A, Rennert, P, Jellis, C L, Greenfield, E, Barber, M, Restivo, V A, Ke, X, Gray, G S
Publicado em 1995

Polymorphisms in the PTPN22 region are associated with psoriasis of early onset

Por Smith, RhLl, Warren, RB, Eyre, S, Ke, X, Young, HS, Allen, M, Strachan, D, McArdle, W, Gittins, MP, Barker, JNWN, Griffiths, CEM, Worthington, J
Publicado em 2008

Audiological and genetic features of the mtDNA mutations

Por Liu, X.Z., Angeli, S., Ouyang, X.M., Liu, W., Ke, X.M., Liu, Y.H., Liu, S.X., Du, L.L., Deng, X.W., Yuan, H., Yan, D.
Publicado no Acta Otolaryngol (2008)

Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome.

Por Liu, X Z, Hope, C, Walsh, J, Newton, V, Ke, X M, Liang, C Y, Xu, L R, Zhou, J M, Trump, D, Steel, K P, Bundey, S, Brown, S D
Publicado em 1998

Unusual interlayer quantum transport behavior caused by the zeroth Landau level in YbMnBi(2)

Por Liu, J. Y., Hu, J., Graf, D., Zou, T., Zhu, M., Shi, Y., Che, S., Radmanesh, S. M. A., Lau, C. N., Spinu, L., Cao, H. B., Ke, X., Mao, Z. Q.
Publicado no Nat Commun (2017)