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Results 1-10 of 12 (Search time: 0.002 seconds).
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First PublishedTitleAuthor(s)Type
1-Oct-2008Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal development.Webb, TR; Cross, SH; McKie, L; Edgar, R; Vizor, L; Harrison, J; Peters, J; Jackson, IJJournal Article
30-Nov-2006Radiation-induced transgenerational alterations in genome stability and DNA damage.Barber, RC; Hickenbotham, P; Hatch, T; Kelly, D; Topchiy, N; Almeida, GM; Jones, GD; Johnson, GE; Parry, JM; Rothkamm, K; Dubrova, YEJournal Article
Oct-2001MSY2 and MSY4 bind a conserved sequence in the 3' untranslated region of protamine 1 mRNA in vitro and in vivoGiorgini, Flaviano; Davies, Holly G.; Braun, Robert E.Journal Article
8-Jan-2010Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance.Tischfield, MA; Baris, HN; Wu, C; Rudolph, G; Van Maldergem L; He, W; Chan, WM; Andrews, C; Demer, JL; Robertson, RL; Mackey, DA; Ruddle, JB; Bird, TD; Gottlob, I; Pieh, C; Traboulsi, EI; Pomeroy, SL; Hunter, DG; Soul, JS; Newlin, A; Sabol, LJ; Doherty, EJ; de Uzcátegui CE; de Uzcátegui N; Collins, ML; Sener, EC; Wabbels, B; Hellebrand, H; Meitinger, T; de Berardinis T; Magli, A; Schiavi, C; Pastore-Trossello, M; Koc, F; Wong, AM; Levin, AV; Geraghty, MT; Descartes, M; Flaherty, M; Jamieson, RV; Møller, HU; Meuthen, I; Callen, DF; Kerwin, J; Lindsay, S; Meindl, A; Gupta, ML; Pellman, D; Engle, ECJournal Article
Dec-2000P2X receptor expression in mouse urinary bladder and the requirement of P2X(1) receptors for functional P2X receptor responses in the mouse urinary bladder smooth muscle.Vial, C; Evans, RJJournal Article
23-Sep-1991Spontaneous mutation at the hypervariable mouse minisatellite locus Ms6-hm: flanking DNA sequence and analysis of germline and early somatic mutation events.Kelly, R; Gibbs, M; Collick, A; Jeffreys, AJJournal Article
15-Apr-2000Somatic versus germline mutation processes at minisatellite CEB1 (D2S90) in humans and transgenic mice.Buard, J; Collick, A; Brown, J; Jeffreys, AJJournal Article
15-Mar-2011In vivo cell-autonomous transcriptional abnormalities revealed in mice expressing mutant huntingtin in striatal but not cortical neurons.Thomas, EA; Coppola, G; Tang, B; Kuhn, A; Kim, S; Geschwind, DH; Brown, TB; Luthi-Carter, R; Ehrlich, MEJournal Article
Dec-2010Mutations in the selenocysteine insertion sequence-binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans.Schoenmakers, E; Agostini, M; Mitchell, C; Schoenmakers, N; Papp, L; Rajanayagam, O; Padidela, R; Ceron-Gutierrez, L; Doffinger, R; Prevosto, C; Luan, J; Montano, S; Lu, J; Castanet, M; Clemons, N; Groeneveld, M; Castets, P; Karbaschi, M; Aitken, S; Dixon, A; Williams, J; Campi, I; Blount, M; Burton, H; Muntoni, F; O'Donovan, D; Dean, A; Warren, A; Brierley, C; Baguley, D; Guicheney, P; Fitzgerald, R; Coles, A; Gaston, H; Todd, P; Holmgren, A; Khanna, KK; Cooke, M; Semple, R; Halsall, D; Wareham, N; Schwabe, J; Grasso, L; Beck-Peccoz, P; Ogunko, A; Dattani, M; Gurnell, M; Chatterjee, KJournal Article
Mar-2009Sustained effects of nonallele-specific Huntingtin silencing.Drouet, V; Perrin, V; Hassig, R; Dufour, N; Auregan, G; Alves, S; Bonvento, G; Brouillet, E; Luthi-Carter, R; Hantraye, P; Déglon, NJournal Article