Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Erick E. Nasser"'
Autor:
Nicholas Lea, Ghulam J. Mufti, Azim M Mohamedali, Konstantinos Mitsopoulos, Thomas Seidl, Erick E. Nasser, Aytug Kizilors, Austin G. Kulasekararaj, Kevin G. Ford, Syed A Mian, Alexander E. Smith
Publikováno v:
Haematologica. 98:1058-1066
The recent identification of acquired mutations in key components of the spliceosome machinery strongly implicates abnormalities of mRNA splicing in the pathogenesis of myelodysplastic syndromes. However, questions remain as to how these aberrations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5474b4d5b521ddf080a6ee9621c60af2
https://doi.org/10.3324/haematol.2012.075325
https://doi.org/10.3324/haematol.2012.075325
Autor:
Bartlomiej Przychodzen, Nicholas Lea, Alexander E. Smith, Jaroslaw P. Maciejewski, Norbert Gattermann, Ulrich Germing, Joop Gaken, Erick E. Nasser, ZiYi Lim, Syed A Mian, Austin G. Kulasekararaj, Azim M Mohamedali, Claire Shooter, Nigel Westwood, Corinna Strupp, Ghulam J. Mufti
Publikováno v:
Blood. 116:3923-3932
Mutations in the TET2 gene are frequent in myeloid disease, although their biologic and prognostic significance remains unclear. We analyzed 355 patients with myelodysplastic syndromes using “next-generation” sequencing for TET2 aberrations, 91 o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e0a8fd6d5934bc7bc680a2e0b98b8e1
https://doi.org/10.1182/blood-2010-03-274704
https://doi.org/10.1182/blood-2010-03-274704
Autor:
Ghulam J. Mufti, Alan Kenneth Burnett, Nicholas Lea, Azim M Mohamedali, Robert Kerrin Hills, Amanda F. Gilkes, Erick E. Nasser, Atiyeh M Abdallah, Sneha Shinde, Austin G. Kulasekararaj
Publikováno v:
Blood. 118:411-411
Abstract 411 The herald of next generation sequencing has ushered an era for the discovery of frequent novel mutations such as DNMT3a, IDH1/2 and ASXL1 in acute myeloid leukaemia with a normal karyotype (AML-NK). The frequency of these mutations has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::977de696accd63b6a728b8a632f31106
https://doi.org/10.1182/blood.v118.21.411.411
https://doi.org/10.1182/blood.v118.21.411.411
Autor:
Nicholas Lea, Azim M Mohamedali, Alan Kenneth Burnett, Atiyeh M Abdallah, Austin G. Kulasekararaj, Amanda F. Gilkes, Erick E. Nasser, Ghulam J. Mufti, Robert Kerrin Hills
Publikováno v:
Blood. 116:2729-2729
Abstract 2729 Acute myeloid leukaemia with a normal karyotype (AML-NK) is a heterogeneous clonal disorder of haematopoietic progenitor cells with an intermediate prognosis. Acquired mutations of FLT3, NPM1 and CEBPA as well as gene expression profile
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9c0aa7be30a38b705aeaa1a658bc909
https://doi.org/10.1182/blood.v116.21.2729.2729
https://doi.org/10.1182/blood.v116.21.2729.2729
Autor:
Mian SA; King's College London School of Medicine, Department of Haematological Medicine, London, UK., Smith AE, Kulasekararaj AG, Kizilors A, Mohamedali AM, Lea NC, Mitsopoulos K, Ford K, Nasser E, Seidl T, Mufti GJ
Publikováno v:
Haematologica [Haematologica] 2013 Jul; Vol. 98 (7), pp. 1058-66. Date of Electronic Publication: 2013 Jan 08.