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收藏A role for NANOG in G1 to S transition in human embryonic stem cells through direct binding of CDK6 and CDC25A
Zhang, Xin; Neganova, Irina; Przyborski, Stefan; Yang, Chunbo; Cooke, Michael; Atkinson, Stuart P.; Anyfantis, George; Fenyk, Stefan; Keith, W. Nicol; Hoare, Stacey F.; Hughes, Owen; Strachan, Tom; Stojkovic, Miodrag; Hinds, Philip W.; Armstrong, Lyle; Lako, Majlinda 分享 收藏 Downregulation of NANOG induces differentiation of human embryonic stem cells to extraembryonic lineagesHyslop, L; Stojkovic, M; Armstrong, L; Walter, T; Stojkovic, P; Przyborski, S; Herbert, M; Murdoch, A; Strachan, T; Lako, M 分享 收藏 Derivation of human embryonic stem cells from day-8 blastocysts recovered after three-step in vitro culture从体外三步培养后回收的第8天胚泡中获得人胚胎干细胞Stojkovic, M; Lako, M; Stojkovic, P; Stewart, R; Przyborski, S; Armstrong, L; Evans, J; Herbert, M; Hyslop, L; Ahmad, S; Murdoch, A; Strachan, T 分享 收藏 Modelling, gene expression mapping and post-mapping image analysis in the developing human brainSarma, S; Kerwin, J; Puelles, L; Scott, M; Strachan, T; Feng, GJ; Sharpe, J; Davidson, D; Baldock, R; Lindsay, S 分享 收藏 分享 收藏 分享 收藏 A giant novel gene undergoing extensive alternative splicing is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.3Tonkin, ET; Smith, M; Eichhorn, P; Jones, S; Imamwerdi, B; Lindsay, S; Jackson, M; Wang, TJ; Ireland, M; Burn, J; Krantz, ID; Carr, P; Strachan, T 分享 收藏 分享 收藏 Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determinationOtto, EA; Schermer, B; Obara, T; O'Toole, JF; Hiller, KS; Mueller, AM; Ruf, RG; Hoefele, J; Beekmann, F; Landau, D; Foreman, JW; Goodship, JA; Strachan, T; Kispert, A; Wolf, MT; Gagnadoux, MF; Nivet, H; Antignac, C; Walz, G; Drummond, IA; Benzing, T; Hildebrandt, F 分享 收藏 分享 收藏 分享 收藏 分享 收藏 Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier diseaseSakuntabhai, A; Ruiz-Perez, V; Carter, S; Jacobsen, N; Burge, S; Monk, S; Smith, M; Munro, CS; O'Donovan, M; Craddock, N; Kucherlapati, R; Rees, JL; Owen, M; Lathrop, GM; Monaco, AP; Strachan, T; Hovnanian, A 分享 收藏 Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouseMorgan, D; Turnpenny, L; Goodship, J; Dai, WL; Majumder, K; Matthews, L; Gardner, A; Schuster, G; Vien, L; Harrison, W; Elder, FEB; Penman-Splitt, M; Overbeek, P; Strachan, T 分享 收藏 A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2BBashir, R; Britton, S; Strachan, T; Keers, S; Vafiadaki, E; Lako, M; Richard, I; Marchand, S; Bourg, N; Argov, Z; Sadeh, M; Mahjneh, I; Marconi, G; Passos-Bueno, MR; Moreira, ED; Zatz, M; Beckmann, JS; Bushby, K 分享 收藏 Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactylyVargas, FR; Roessler, E; Gaudenz, K; Belloni, E; Whitehead, AS; Kirke, PN; Mills, JL; Hooper, G; Stevenson, RE; Cordeiro, I; Correia, P; Felix, T; Gereige, R; Cunningham, ML; Canún, S; Antonarakis, SE; Strachan, T; Tsui, LC; Scherer, SW; Muenke, M 分享 收藏 Refined genetic mapping of the Darier locus to a <1-cM region of chromosome 12q24.1, and construction of a complete, high-resolution P1 artificial chromosome bacterial artificial chromosome contig of the critical regionMonk, S; Sakuntabhai, A; Carter, SA; Bryce, SD; Cox, R; Harrington, L; Levy, E; Ruiz-Perez, VL; Katsantoni, E; Kodvawala, A; Munro, CS; Burge, S; Larrègue, M; Nagy, G; Rees, JL; Lathrop, M; Monaco, AP; Strachan, T; Hovnanian, A 分享 收藏 A sequence-ready physical map of a region of 12q24.1Renault, B; Hovnanian, A; Bryce, S; Chang, JJ; Lau, S; Sakuntabhai, A; Monk, S; Carter, S; Ross, CJD; Pang, J; Twells, R; Chamberlain, S; Monaco, AP; Strachan, T; Kucherlapati, R 分享 收藏 分享 收藏 
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