Zobrazeno 1 - 10
of 66
pro vyhledávání: '"N. Foot"'
Autor:
Martyn J Hiscox, Alexandra Wasmuth, Chris L Williams, Jaelle N Foot, Guy E Wiedermann, Valeria Fadda, Sara Boiani, Terri V Cornforth, Karolina A Wikiert, Shaun Bruton, Neil Cartwright, Victoria Elizabeth Anderson, Christopher S Barnes, Joao V Vieira, Ian Birch-Machin, Andrew B Gerry, Karen Miller, Nicholas J Pumphrey
Publikováno v:
PLoS ONE, Vol 19, Iss 4, p e0301175 (2024)
BackgroundCanonical α/β T-cell receptors (TCRs) bind to human leukocyte antigen (HLA) displaying antigenic peptides to elicit T cell-mediated cytotoxicity. TCR-engineered T-cell immunotherapies targeting cancer-specific peptide-HLA complexes (pHLA)
Externí odkaz:
https://doaj.org/article/45b738a8ccec4feaa6830e4837506529
Autor:
Mikael Feracci, Jaelle N. Foot, Sushma N. Grellscheid, Marina Danilenko, Ralf Stehle, Oksana Gonchar, Hyun-Seo Kang, Caroline Dalgliesh, N. Helge Meyer, Yilei Liu, Albert Lahat, Michael Sattler, Ian C. Eperon, David J. Elliott, Cyril Dominguez
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-12 (2016)
Sam68 and T-STAR are members of the STAR family of proteins, which regulate various aspects of RNA metabolism. Here, the authors reveal structural features required for alternative splicing regulation by these proteins.
Externí odkaz:
https://doaj.org/article/b392828e149940d59b95a44e32da32fa
Autor:
D. Repana, T. Shanmugalingam, G. Gerrard, N. Foot, A. Kulkarni, K. Naidoo, S. Talukdar, K. Snape, H. Hanson, K. Quigley, K. Mokretar, P. Du Parcq, B. Ferguson, D. Sarker, N. Murugaesu
Publikováno v:
Annals of Oncology. 33:S1393
Akademický článek
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Publikováno v:
Methods (San Diego, Calif.)
In the past few years, RNA molecules have been revealed to be at the center of numerous biological processes. Long considered as passive molecules transferring genetic information from DNA to proteins, it is now well established that RNA molecules pl
Autor:
R. Dillon, R. Hills, S. Freeman, N. Potter, J. Jovanovic, A. Kanda, M. Runglall, N. Foot, M. Valganon, K. Raj, A. Khwaja, J. Cavenagh, R. Spearing, H.B. Ommen, U.M. Overgaard, A. Burnett, N. Russell, D. Grimwade
Publikováno v:
HemaSphere. 3:743
Autor:
Oksana Gonchar, Marina Danilenko, Sushma Nagaraja Grellscheid, David J. Elliott, Ralf Stehle, Michael Sattler, Albert Lahat, N. Helge Meyer, Yilei Liu, Cyril Dominguez, Jaelle N. Foot, Hyun-Seo Kang, Ian C. Eperon, Caroline Dalgliesh, Mikael Feracci
Publikováno v:
Nat. Commun. 7:10355 (2016)
Nature Communications
Nature Communications, Vol 7, Iss 1, Pp 1-12 (2016)
Nature communications, 2016, Vol.7, pp.10355 [Peer Reviewed Journal]
Nature Communications
Nature Communications, Vol 7, Iss 1, Pp 1-12 (2016)
Nature communications, 2016, Vol.7, pp.10355 [Peer Reviewed Journal]
Sam68 and T-STAR are members of the STAR family of proteins that directly link signal transduction with post-transcriptional gene regulation. Sam68 controls the alternative splicing of many oncogenic proteins. T-STAR is a tissue-specific paralogue th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccbc7cf6b97fcb4f1450fcb62967c9df
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=47783
https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=47783
Publikováno v:
Biochemical Society transactions. 42(4)
STAR (signal transduction and activation of RNA) proteins are a family of RNA-binding proteins that regulate post-transcriptional gene regulation events at various levels, such as pre-mRNA alternative splicing, RNA export, translation and stability.
Autor:
B. Rosenbusch, M.-T. Bihoreau, J. Satrústegui, J. Browne, B.P. Morgan, C. Niehrs, V.A. Valentine, L.Z. Topol, K. Rader, S.-Y. Li, S. Seino, T. Ono, M.L. Ramírez-Dueñas, K.C Arden, T.-H. Hsu, M. Schmid, S. Rensen, S.H. Park, M.J. Pettenati, H. Yano, W. Van Hul, J.L Vernon, K. Ellington, S. Yonezawa, M.A. Sims, A. Dutra, G. Kandala, S. Paradisi, N.A. Jenkins, F. Gruetzner, C. Dixkens, A.I. Protopopov, N.G. Copeland, A. Glinka, L. Ferretti, H.-U.G. Weier, S. Zabel, Y.-C. Li, S. Sonta, R.A. White, E. Roessler, C. Von Kap-Herr, D. Incarnato, M. Osaki, A. Solans, A.V. Zelenin, E. Petek, G.P. Zambetti, K. Wagner, D.S. Holt, P.M. Richardson, N.D. Rendtorff, T.A. Lister, D. Taruscio, L. Iannuzzi, A. Buck, N.A. Jensen, M.G. Foti, M.A. Hyatt, I. Nanda, M.R. James, P. Doevendans, L. Cai, Y. Du, C.X. George, S. Doerr, M. Athanasiou, G.J.J.M. van Eys, Y. Yokoyama, M.R. Barnes, C.E. Samuel, W. Wuyts, R.S. Bora, M.G. Farquhar, F. Sablitzky, L. Archangelo, M.-G. Mattéi, E.R. Zabarovsky, Q. Zhang, M.-J. Pébusque, M.L. Ayala-Madrigal, L.M. Pasztor, M.-C. Hernandez, R.A. Lersch, S. Yamashita, N. Spurr, G.K. Zoraqi, Y.M. Heng, P.M. Kroisel, M.J. Neat, P. Zambonelli, S. Comincini, R.K. Gupta, G.P. Di Meo, P. Musilová, H. Vissing, Z. Shan, E. Kalm, X. Estivill, S.S. Mann, C. Hansen, I. Hansmann, V. Setaluri, A. Stratil, V.I. Kashuba, R. Davoli, M. Fox, C.C. Lin, H. Egger, J.E. Wiley, Y. Wang, Z. Gu, A. Oohira, A.S. Hill, R. Sanz, V. Falbo, J. Fitzgibbon, P.D. Thomsen, A. Perucatti, J.B. Rattner, G. Merkx, H. Kim, S. Masaki, S. de la Luna, T.L. Harboe, L. Schibler, M.A. Israel, S. Paul, O. Bögler, R.Z. Gizatullin, O.V. Muravenko, B. Brenig, S. Ichikawa, M. Muenke, M.B. Powell, J.-F. Cheng, J. Rubeš, C. Looft, A. Vortkamp, P.C. Burr, T.C. Hart, C. Ramos, N. Tommerup, D.A. Campbell, C.M. Owczarek, B.U. Koelsch, L. Jones, Y. Hirabayashi, K.J. Portbury, S. Aono, C.-Z. Wang, S.D. Field, V. Russo, T. Haaf, P.J. Andres-Barquin, W. Emberger, S. Hirano, C. Lee, A. Kindler-Röhrborn, C. Ayuso, T. Tsukasaki, C. Windpassinger, P.J. Hertzog, A. Kanamori, C. Popovici, A.D. Boyer, M.A. Farwell, N. Foot, L.I. Zon, S. Cepica, D. Birnbaum, A. Silahtaroglu, I. Kola, B. Castiglioni, J. Kohlhase, A. Geurts van Kessel, D.J. Gilbert, M. Yerle, V.W. Sykes, K.E. Murphy, A. del Arco, M. Schneider, E.P. Cribiu, N.K. Rushmere, S.T. Suzuki, S. Breitweser, D.G. Blair, Y.K. Jung, N. Shaikh, Z. Tümer, N. Yokoi, K. Lindpaintner, D.G. Jo
Publikováno v:
Cytogenetic and Genome Research. 89:287-289
Publikováno v:
Clinical and laboratory haematology. 25(3)
We describe two cases of recurrent autoimmune cytopenias, which were subsequently diagnosed with a 22q11.2 deletion/DiGeorge syndrome. The cases are of particular interest as both possessed limited clinical features of this syndrome, and the investig