Showing 1 - 15 results of 15 for search 'Tian G', query time: 0.05s
Refine Results
-
1
-
2
-
3
-
4
Carriage of β-lactamase-producing Enterobacteriaceae by Chinese travellers by Zhong, L, Stoesser, N, Doi, Y, Shen, C, Huang, X, Tian, G
Published 2017Journal article -
5
-
6
-
7
-
8
-
9
High rates of human fecal carriage of mcr-1-positive multi-drug resistant Enterobacteriaceae isolates emerge in China in association with successful plasmid families by 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
Published 2017Journal article -
10
Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans. by 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
Published 2007Journal article -
11
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes. by 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
Published 2013Journal article -
12
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes by 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
Published 2012Journal article -
13
Mutations in the β-Tubulin Gene TUBB5 Cause Microcephaly with Structural Brain Abnormalities by 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
Published 2012Journal article -
14
Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria. by 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
Published 2009Journal article -
15
Mutations in MAST1 cause mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations by 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
Published 2018Journal article