Zobrazeno 1 - 10
of 177
pro vyhledávání: '"P Bray-Ward"'
Autor:
Anthony R Torres, Thayne L Sweeten, Randall C Johnson, Dennis Odell, Jonna B Westover, Patricia Bray-Ward, David C Ward, Christopher J Davies, Aaron J Thomas, Lisa A Croen, Michael Benson
Publikováno v:
Frontiers in Neuroscience, Vol 10 (2016)
The common variant - common disease hypothesis was proposed to explain diseases with strong inheritance. This model suggests that a genetic disease is the result of the combination of several common genetic variants. Common genetic variants are descr
Externí odkaz:
https://doaj.org/article/0857e46ea5f5427fa1293fe9c3717fb4
Autor:
O. Henegariu, L. Grober, W. Haskins, P.N. Bowers, M.W. State, N. Ohmido, P. Bray-Ward, D.C. Ward
Publikováno v:
BioTechniques, Vol 31, Iss 2, Pp 246-250 (2001)
Externí odkaz:
https://doaj.org/article/812701aa08be427fa359808ddf318c22
Publikováno v:
BioTechniques, Vol 28, Iss 3, Pp 518-522 (2000)
Many projects, such as multiplex-fluorescence in situ hybridization (M-FISH) karyotyping, require the use of relatively large amounts of multiple fluor- or hapten-labeled nucleotides for the preparation of DNA probes. Such a requirement makes these e
Externí odkaz:
https://doaj.org/article/d4f1ce01604042ab9f46fdc372ccc3c8
Autor:
Ariel M Pani, Holly H Hobart, Colleen A Morris, Carolyn B Mervis, Patricia Bray-Ward, Kendra W Kimberley, Cecilia M Rios, Robin C Clark, Maricela D Gulbronson, Gordon C Gowans, Ronald G Gregg
Publikováno v:
PLoS ONE, Vol 5, Iss 8, p e12349 (2010)
Intellectual disability (ID) affects 2-3% of the population and may occur with or without multiple congenital anomalies (MCA) or other medical conditions. Established genetic syndromes and visible chromosome abnormalities account for a substantial pe
Externí odkaz:
https://doaj.org/article/3ca61bbe14914e18b2633f5b2005b84b
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
M Ferguson-Smith, KL Cheung, M Gregson, L Kearney, T. J. Butler, B Gibbons, L Dirscherl, P Bray-Ward, FT Yang, CJ Harrison
Publikováno v:
Cytogenetic and Genome Research. 85:154-181
Autor:
D. Birnbaum, N.Z. Parsa, C. Flores, A.G. Shilov, B. Sèle, U. Claussen, M. Gastaldi, J. Zimmer, B. Andréo, A.F. Markham, D.T. Bonthron, H.S. Tenenhouse, H. Lovec, O.I. Olopade, R. Hernandez, D. Adrian, S. Rousseaux, A. Frady, N.B. Rubtsov, M. Goldfarb, J.M. Trent, K.J. Gratton, B.G. Beatty, P. Eydoux, N. Tommerup, M. Schmid, D.R. Lohmann, J. Benet, S.K. Bohlander, N.V. Rubtsova, A. Girardet, P. Mühlig, T.P. Moynihan, D. Stephan, R. Hliscs, M.H. Dreyling, Y. Zhu, J. Torresani, J. Navarro, J.P. Grillasca, X.-Y. Zhang, N.T. Bech-Hansen, W. Jiang, M. Dean, H.H. Quek, G.J. Pappanicolaou, B. Wainwright, J.P. Charlieu, H. Hartung, S.M. Zakian, M.A. Peters, J.L. Coate, M.B. Qumsiyeh, C. Wicking, P. Bray-Ward, S. Taviaux, J. Wirth, G. Valle, M. Ehrlich, T. Muraro, R.A. Gravel, N.J. Lench, F. Yang, R. Zimbello, J.A. Peppers, E. Chevret, I. Garkavtsev, B. Horsthemke, F. Coulier, C. Pressman, X.X. Zhang, T.B. Nesterova, A-S. Verdier, A.A. Isaenko, S. Mori, S. Levanat, K. Riabowol, A. Sahota, G. Lefort, D. Demetrick, M-G. Matté, P.C.M. O’Brien, E.H. Hoffman, J.L VandeBerg, V.T.K. Chow, J. Cozzi, R. Planells, J. Wienberg, I. Parra, H. Satoh, K. Sperling, K. Buiting, K.L. Stoddart, A. León-Del-Rio, J. Weissenbach, A.E. Bale, M.R. Gailani, H.-J. Lüdecke, J.A. Tischfield, N.V. Vorobieva, P.S. Meltzer, G. Scherer, M-G. Mattéi, B. Windle, E.J. Taparowsky, A. Chidambaram, G. Lanfranch, H. Leffers, J.P. Leek, A.S. Hewson, R. Toftgard, E. Back, N. Tiso, M.L. Kennedy, G.A. Danieli, M. Varela, M.R. Martorell, T. Wagner, R. Anwar, P.K. Gupta, C. Shao, F. Pellestor, K.M. Boycott, E.H. McConkey, C. Márquez, J.C. Myers, B.J. Moore, I. Nanda, M. Monteil, J. Egozcue, N.M. Matveeva, P.K. Kennedy, M.A. Ferguson-Smith, B. Roland, R. Pelletier
Publikováno v:
Cytogenetic and Genome Research. 76:I-IV
Autor:
M Donnelly, S Pendse, Kimberly Stegmaier, Jeffrey Sklar, Carol Reynolds, G. F. Barker, P Bray-Ward, DC Ward, KT Montgomery, KS Krauter
Publikováno v:
Blood. 86:38-44
TEL is a new member of the ETS family of transcription factors which is rearranged in a number of hematologic malignancies with translocations involving chromosome band 12p13. In some cases, both TEL alleles are affected, resulting in loss of wild-ty
Autor:
D. Quincey, Y.-O. Kim, N. Sato, T. Leeb, L.J. Conner, A. Veronese, H. Satoh, C.G. Jakobsen, L. Martins, S.E. Hayes, E. Gentile, Manfred Gessler, F. Hosoda, M. Kinebuchi, C. Lemercier, O. Marcu, K. Hoehn, S.-Y. Park, T. Hardt, G. Barbanti-Brodano, F. Yang, Mariano Rocchi, Masanori Hatakeyama, T. Torii, T. Kitamura, N. Serakıncı, W. Mann, S. Osborne Lawrence, B. Brenig, D.G. Stathakis, H.-J. Koh, E. Verdin, Y. Franke, Masaki Okano, G. Pottier, K. Amimoto, Grant C. Sellar, N. Spieker, P.A. Martin-DeLeon, A. Strub, E. Li, M.-D. Devignes, X. Reveles, C. Roussakis, P. Grossfeld, N. Miyasaka, L.F.M. van Zutphen, S.A.N. Goldstein, M. Lepke, A. Tunnacliffe, G.N. Hendy, N.A. Manjunath, X. Deng, K. Georgas, U. Mahlknecht, K. Kikuchi, U. Sohn, A. Fogli, P.J. Yarowsky, P.C.M. O’Brien, W. Van Hul, T. Kozaki, L. Burridge, W. Wuyts, D. Masson, S. Forbes, J.P. Murnane, J. Stamberg, L. Viggiano, R. Favier, H. Kawakami, N. Katsanis, Matthew Breen, L.E. Stramm, L. Reid, P. Lustenberger, H.-H. Ropers, M. Athanasiou, S. Grimmond, K. Smith, M. Schmid, J.-Å. Gustafsson, D.S. Gerhard, J. Cruces, H. Narimatsu, J.L. Marsh, C-C. Hu, S. Katabami, Katsuzumi Okumura, L.A. Rethy, Y.-J. Kang, C.N. Sprung, B. Zabel, V. Bhide, P. Taschner, M. Trubia, S.-H. Kim, T. Haaf, Teijiro Aso, P.G. Gallagher, Marcel M.A.M. Mannens, T. Shiina, P.A. Ioannou, E. Schuuring, M.A. Ferguson-Smith, K. Yamada, R.J. Peoples, H. Inoko, D. Hoelzer, Y.-K. Wang, S. Stilgenbauer, R. Carrozzo, W. Rens, J. Harris, K. Yuri, E. Karayianni, A. De Paepe, T. Taguchi, H. Iwasaki, K. Krejčí, D. Carbonnelle, M. Hattori, L.A. Pérez Jurado, G. Gaudray, M.C. Yoshida, J. Justesen, G.F. Carle, I. Nanda, H.C. Au, M. Zollo, Veronica van Heyningen, J.T. Mascarello, R. Bucala, S.-H. Park, L.L. Hansen, S. Takai, Y. Shi, T. Kudo, M. Ohki, S. Raynaud, T. Watanabe, C. Turc-Carel, C.L. Pin, R. Korstanje, G. Chenevix-Trench, T. Miyachi, N. Van Roy, D.H. Spathas, C. Jacquot, M. Kaneko, C. Talbot, C. Magnanini, F.A. Ponce de León, Rogier Versteeg, Barbara R. DuPont, Glen A. Evans, R. Koike, R. Taramelli, H.-Z. Chen, N.A. Jenkins, C. Morelli, Shin-ichiro Takebayashi, Franki Speleman, P. Zisimopoulou, H. Hummerich, G.P. Holmes, A. Matsuura, H.A. van Lith, V. Orphanos, T. Kuramoto, P. Gaudray, T.K. Watanabe, T. Iizuka, D.J. Gilbert, S. Nakamura, F. Grummt, I.E. Scheffler, A.A. Bosma, M. Tixier-Boichard, C. Berger, C. Desmaze, H. Maruyama, Melissa H. Little, C. Alberti, F. Parente, G. Arrigo, K. De Boulle, N.G. Copeland, M. Selkirk, T. Mattina, M. Rosati, L. Sabatier, A. Calender, S.F. Konieczny, S. Sabbioni, Jet Bliek, M. James, M. Gordon, S. Giglio, Peter Little, T. Liehr, L. Canaff, N. Saitou, P.J. Willems, M.G. Denis, G.M. Maniatis, Nicoletta Archidiacono, L.V. Debelenko, O. Zuffardi, J.P. Simmer, J.J. Bitgood, K. Ladjali-Mohammedi, T. Thangarajah, B. Gawin, H. Himmelbauer, C. Lo Nigro, U. Francke, T.-L. Huh, M. Horie, C.M. Croce, J. Strovel, C. Staib, P. Bray-Ward, G. Weber, J. Koch, K. Kitada, Giovanna Grimaldi, J. Kalla, T. Serikawa, M. Negrini
Publikováno v:
Cytogenetic and Genome Research. 86:340-342