Carriage of β-lactamase-producing Enterobacteriaceae by Chinese travellers od Zhong, L, Stoesser, N, Doi, Y, Shen, C, Huang, X, Tian, G

Inhibition of alpha-glucosidases I and II increases the cell surface expression of functional class A macrophage scavenger receptor (SR-A) by extending its half-life. od Tian, G, Wilcockson, D, Perry, V, Rudd, P, Dwek, R, Platt, F, Platt, N

Enhancing the Inhibition of Breast Cancer Growth Through Synergistic Modulation of the Tumor Microenvironment Using Combined Nano-Delivery Systems od Wu J, Lu Q, Zhao J, Wu W, Wang Z, Yu G, Tian G, Gao Z, Wang Q

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The Public’s Self-Avoidance and Other-Reliance in the Reporting of Medical Insurance Fraud: A Cross-Sectional Survey in China od Xu J, Tian G, He J, Deng F, Chen F, Shi Q, Liu J, Zhang H, Zhang T, Wu Q, Kang Z

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Immunogenicity and protective efficacy of a live attenuated H5N1 vaccine in nonhuman primates. od Fan, S, Gao, Y, Shinya, K, Li, C, Li, Y, Shi, J, Jiang, Y, Suo, Y, Tong, T, Zhong, G, Song, J, Zhang, Y, Tian, G, Guan, Y, Xu, X, Bu, Z, Kawaoka, Y, Chen, H, Xu, X

High rates of human fecal carriage of mcr-1-positive multi-drug resistant Enterobacteriaceae isolates emerge in China in association with successful plasmid families od Zhong, L, Phan, H, Shen, C, Vihta, K, Sheppard, A, Huang, X, Zeng, K, Li, H, Zhang, X, Patil, S, Crook, D, Walker, A, Zing, Y, Lin, J, Feng, L, Doi, Y, Xia, Y, Stoesser, N, Tian, G

Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans. od Keays, D, Tian, G, Poirier, K, Huang, G, Siebold, C, Cleak, J, Oliver, P, Fray, M, Harvey, R, Molnár, Z, Piñon, M, Dear, N, Valdar, W, Brown, S, Davies, K, Rawlins, J, Cowan, N, Nolan, P, Chelly, J, Flint, J

Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes. od Albrechtsen, A, Grarup, N, Li, Y, Sparsø, T, Tian, G, Cao, H, Jiang, T, Kim, S, Korneliussen, T, Li, Q, Nie, C, Wu, R, Skotte, L, Morris, A, Ladenvall, C, Cauchi, S, Stančáková, A, Andersen, G, Astrup, A, Banasik, K, Bennett, A, Bolund, L, Charpentier, G, Chen, Y, Dekker, J

Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes od Albrechtsen, A, Grarup, N, Li, Y, Sparsø, T, Tian, G, Cao, H, Jiang, T, Kim, S, Korneliussen, T, Li, Q, Nie, C, Wu, R, Skotte, L, Morris, A, Ladenvall, C, Cauchi, S, Stančáková, A, Andersen, G, Astrup, A, Banasik, K, Bennett, A, Bolund, L, Charpentier, G, Chen, Y, Dekker, J

Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities od Breuss, M, Heng, J, Poirier, K, Tian, G, Jaglin, X, Qu, Z, Braun, A, Gstrein, T, Ngo, L, Haas, M, Bahi-Buisson, N, Moutard, M, Passemard, S, Verloes, A, Gressens, P, Xie, Y, Robson, K, Rani, D, Thangaraj, K, Clausen, T, Chelly, J, Cowan, N, Keays, D

Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria. od Jaglin, X, Poirier, K, Saillour, Y, Buhler, E, Tian, G, Bahi-Buisson, N, Fallet-Bianco, C, Phan-Dinh-Tuy, F, Kong, X, Bomont, P, Castelnau-Ptakhine, L, Odent, S, Loget, P, Kossorotoff, M, Snoeck, I, Plessis, G, Parent, P, Beldjord, C, Cardoso, C, Represa, A, Flint, J, Keays, D, Cowan, N, Chelly, J

Mutations in MAST1 cause mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations od Tripathy, R, Leca, I, Van Dijk, T, Weiss, J, Van Bon, B, Sergaki, M, Gstrein, T, Breuss, M, Tian, G, Bahi-Buisson, N, Paciorkowski, A, Pagnamenta, A, Wenninger-Weinzierl, A, Martinez-Reza, M, Landler, L, Lise, S, Taylor, J, Terrone, G, Vitiello, G, Del Giudice, E, Brunetti-Pierri, N, D'Amico, A, Reymond, A, Voisin, N, Bernstein, J, Farrelly, E, Kini, U, Leonard, T, Valence, S, Burglen, L, Armstrong, L, Hiatt, S, Cooper, G, Aldinger, K, Dobyns, W, Mirzaa, G, Pierson, T, Baas, F, Chelly, J, Cowan, N, Keays, D