Zobrazeno 1 - 10
of 69
pro vyhledávání: '"Anton Parker"'
Autor:
Eloy F. Robles, Maria Mena-Varas, Laura Barrio, Sara V. Merino-Cortes, Péter Balogh, Ming-Qing Du, Takashi Akasaka, Anton Parker, Sergio Roa, Carlos Panizo, Idoia Martin-Guerrero, Reiner Siebert, Victor Segura, Xabier Agirre, Laura Macri-Pellizeri, Beatriz Aldaz, Amaia Vilas-Zornoza, Shaowei Zhang, Sarah Moody, Maria Jose Calasanz, Thomas Tousseyn, Cyril Broccardo, Pierre Brousset, Elena Campos-Sanchez, Cesar Cobaleda, Isidro Sanchez-Garcia, Jose Luis Fernandez-Luna, Ricardo Garcia-Muñoz, Esther Pena, Beatriz Bellosillo, Antonio Salar, Maria Joao Baptista, Jesús Maria Hernandez-Rivas, Marcos Gonzalez, Maria Jose Terol, Joan Climent, Antonio Ferrandez, Xavier Sagaert, Ari M. Melnick, Felipe Prosper, David G. Oscier, Yolanda R. Carrasco, Martin J. S. Dyer, Jose A. Martinez-Climent
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-16 (2016)
The homeobox NKX2 family of transcriptional factors has been shown to regulate fundamental developmental processes. Here, the authors show that NKX2-3 is a bona fideoncogenic driver in marginal-zone B-cell lymphoma and that it promotes lymphomagenesi
Externí odkaz:
https://doaj.org/article/8577d51efbf14e6384756140937ba872
Autor:
Nils Winkelmann, Matthew Rose-Zerilli, Jade Forster, Marina Parry, Anton Parker, Anne Gardiner, Zadie Davies, Andrew J. Steele, Helen Parker, Nicholas C.P. Cross, David G. Oscier, Jonathan C. Strefford
Publikováno v:
Haematologica, Vol 100, Iss 6 (2015)
Externí odkaz:
https://doaj.org/article/f538c1b9bd6b48c89081f542513d78eb
Autor:
Axel Benner, Larry Mansouri, Davide Rossi, Aneela Majid, Kerstin Willander, Anton Parker, Gareth Bond, Sarka Pavlova, Holger Nückel, Olaf Merkel, Paolo Ghia, Emili Montserrat, Mohd Arifin Kaderi, Richard Rosenquist, Gianluca Gaidano, Martin J.S. Dyer, Peter Söderkvist, Mats Linderholm, David Oscier, Zuzana Tvaruzkova, Sarka Pospisilova, Ulrich Dührsen, Richard Greil, Hartmut Döhner, Stephan Stilgenbauer, Thorsten Zenz
Publikováno v:
Haematologica, Vol 99, Iss 8 (2014)
A number of single nucleotide polymorphisms have been associated with disease predisposition in chronic lymphocytic leukemia. A single nucleotide polymorphism in the MDM2 promotor region, MDM2SNP309, was shown to soothe the p53 pathway. In the curren
Externí odkaz:
https://doaj.org/article/4c66616d07e24363aff3f1ae2d78014c
Autor:
Matthew J.J. Rose-Zerilli, Jade Forster, Helen Parker, Anton Parker, Ana E. Rodríguez, Tracy Chaplin, Anne Gardiner, Andrew J. Steele, Andrew Collins, Bryan D. Young, Anna Skowronska, Daniel Catovsky, Tatjana Stankovic, David G. Oscier, Jonathan C. Strefford
Publikováno v:
Haematologica, Vol 99, Iss 4 (2014)
ATM mutation and BIRC3 deletion and/or mutation have independently been shown to have prognostic significance in chronic lymphocytic leukemia. However, the relative clinical importance of these abnormalities in patients with a deletion of 11q encompa
Externí odkaz:
https://doaj.org/article/66caa2d4337b42a0aed41826a722d99f
Autor:
David Gonzalez, Monica Else, Dorte Wren, Monica Usai, Anne Mette Buhl, Anton Parker, David Oscier, Gareth Morgan, Daniel Catovsky
Publikováno v:
Haematologica, Vol 98, Iss 2 (2013)
CLLU1, located at chromosome 12q22, encodes a transcript specific to chronic lymphocytic leukemia and has potential prognostic value. We assessed the value of CLLU1 expression in the LRF CLL4 randomized trial. Samples from 515 patients with chronic l
Externí odkaz:
https://doaj.org/article/2604ec1d4bdc4014b4a6b844755e034f
Autor:
Robert Brown, Richard Soutar, Heather G. Jorgensen, Joanne C. Mountford, Anne M. Dickinson, Tim Eden, Stefan Meyer, Junia V. Melo, David G. Oscier, Anton Parker, Alyson Sim, Tessa L. Holyoake, Gordon Strathdee
Supplementary Table S2 from Inactivation of HOXA Genes by Hypermethylation in Myeloid and Lymphoid Malignancy is Frequent and Associated with Poor Prognosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47270a3ae046c13b679ff7d0ad94e7e4
https://doi.org/10.1158/1078-0432.22440031
https://doi.org/10.1158/1078-0432.22440031
Autor:
Jonathan C. Strefford, David Oscier, Kostas Stamatopoulos, Gerassimos Pangalis, Estella Matutes, Paolo Ghia, Andrew Collins, Francesco Forconi, Margaret Ashton-Key, Richard Rosenquist, Guy Pratt, Claire Dearden, David Gonzalez de Castro, Claudia Fazi, Achilles Anagnostopoulos, Aliki Xochelli, Christina Kalpadakis, Neil McIver-Brown, Anne Gardiner, Zadie Davis, Anton Parker, Helen Parker, Renata Walewska, Jun Wang, Jane Gibson, Viktor Ljungström, Matthew J.J. Rose-Zerilli, Marina Parry
Supplementary Table 4. Haloplex re-sequencing gene mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92a14db39e1d32fdae1b201c82f0cd0d
https://doi.org/10.1158/1078-0432.22456673
https://doi.org/10.1158/1078-0432.22456673
Autor:
Jonathan C. Strefford, David Oscier, Kostas Stamatopoulos, Gerassimos Pangalis, Estella Matutes, Paolo Ghia, Andrew Collins, Francesco Forconi, Margaret Ashton-Key, Richard Rosenquist, Guy Pratt, Claire Dearden, David Gonzalez de Castro, Claudia Fazi, Achilles Anagnostopoulos, Aliki Xochelli, Christina Kalpadakis, Neil McIver-Brown, Anne Gardiner, Zadie Davis, Anton Parker, Helen Parker, Renata Walewska, Jun Wang, Jane Gibson, Viktor Ljungström, Matthew J.J. Rose-Zerilli, Marina Parry
Supplementary Table 5. Sanger screening of NOTCH2 exon 34
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3333dfbaba5c8c250c8c990234d751d2
https://doi.org/10.1158/1078-0432.22456667
https://doi.org/10.1158/1078-0432.22456667
Autor:
Jonathan C. Strefford, David Oscier, Kostas Stamatopoulos, Gerassimos Pangalis, Estella Matutes, Paolo Ghia, Andrew Collins, Francesco Forconi, Margaret Ashton-Key, Richard Rosenquist, Guy Pratt, Claire Dearden, David Gonzalez de Castro, Claudia Fazi, Achilles Anagnostopoulos, Aliki Xochelli, Christina Kalpadakis, Neil McIver-Brown, Anne Gardiner, Zadie Davis, Anton Parker, Helen Parker, Renata Walewska, Jun Wang, Jane Gibson, Viktor Ljungström, Matthew J.J. Rose-Zerilli, Marina Parry
Supplementary Figure 1. Additional gene maps
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e1f2d17eda6455a320e9756f3aff573
https://doi.org/10.1158/1078-0432.22456679
https://doi.org/10.1158/1078-0432.22456679
Autor:
Jonathan C. Strefford, David Oscier, Kostas Stamatopoulos, Gerassimos Pangalis, Estella Matutes, Paolo Ghia, Andrew Collins, Francesco Forconi, Margaret Ashton-Key, Richard Rosenquist, Guy Pratt, Claire Dearden, David Gonzalez de Castro, Claudia Fazi, Achilles Anagnostopoulos, Aliki Xochelli, Christina Kalpadakis, Neil McIver-Brown, Anne Gardiner, Zadie Davis, Anton Parker, Helen Parker, Renata Walewska, Jun Wang, Jane Gibson, Viktor Ljungström, Matthew J.J. Rose-Zerilli, Marina Parry
Supplementary Figure 2. ABSOLUTE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08bf0440de16fa291431d3e9dc343005
https://doi.org/10.1158/1078-0432.22456676
https://doi.org/10.1158/1078-0432.22456676