Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Nicola Bienz"'
Publikováno v:
HemaSphere, Vol 7, p e651337a (2023)
Externí odkaz:
https://doaj.org/article/0f5564f75d7f4ac698cbf95f910a6df3
Publikováno v:
British Journal of Haematology. 201:640-644
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::136dcb11864ab846e39084597ba4a1a4
https://doi.org/10.1111/bjh.18700
https://doi.org/10.1111/bjh.18700
Publikováno v:
British Journal of Haematology. 197
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ac059d9dce1ef0a19d53072166a9bb2
https://doi.org/10.1111/bjh.18010
https://doi.org/10.1111/bjh.18010
Publikováno v:
British Journal of Haematology. 193:269-270
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d2f6051ba9f864f9c0615090388172a
https://doi.org/10.1111/bjh.17358
https://doi.org/10.1111/bjh.17358
Autor:
Mark Lloyd, Jenny Bosworth, Timothy Wang, Hapinder Dhillon, Laura To, Nicola Bienz, Steve Gosling
Publikováno v:
Rheumatology. 58
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aed0be648d6ad121d15e800e3f3f3b67
https://doi.org/10.1093/rheumatology/kez110.008
https://doi.org/10.1093/rheumatology/kez110.008
Autor:
Simon Moule, Ruth Clifford, Adam J. Mead, Michelle Rugless, Petter S. Woll, D Atkinson, Shirley Henderson, Anna Schuh, Nicola Bienz, Sten Eirik W. Jacobsen, James S. Wainscoat, Paresh Vyas
Abstract 1738 Since the initial description of V617F somatic mutation in patients with Philadelphia chromosome negative myeloproliferative neoplasms (MPNs), a remarkable association between alterations in the JAK2 gene and MPNs has emerged. In additi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b034e86919a36d0925b6caf2016f5d25
https://ora.ox.ac.uk/objects/uuid:e50e82ac-2ead-4101-b5f6-fdc100960634
https://ora.ox.ac.uk/objects/uuid:e50e82ac-2ead-4101-b5f6-fdc100960634
Autor:
Orly Dgany, Nili Avidan, Ali Shamseddine, Paresh Vyas, Laila Zahed, Anne-Marie O'Hea, Aref Chehal, Hannah Tamary, Nicola Bienz, William G. Wood, Jacqui S. Beckmann, Joud H. Haidar, Momin Ahmed, Sunitha N. Wickramasinghe, Ali T. Taher, Douglas R. Higgs
The congenital dyserythropoietic anemias (CDAs) are a heterogeneous group of genetic disorders of erythropoiesis characterized by anemia secondary to ineffective erythropoiesis and striking morphologic abnormalities of erythroblasts (reviewed in Wick
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2470a98478a3168f56dc493093f58b73
https://ora.ox.ac.uk/objects/uuid:7d196392-4918-4b4e-88c1-85221bc91fcd
https://ora.ox.ac.uk/objects/uuid:7d196392-4918-4b4e-88c1-85221bc91fcd
Autor:
R Clifford, Sten Eirik W. Jacobsen, Simon Moule, Alexandra Dusa, Adam Burns, Shirley Henderson, Nicholas C.P. Cross, Petter S. Woll, Rosemary E. Gale, Michelle Rugless, Paresh Vyas, Stefan N. Constantinescu, Nicola Bienz, Adam J. Mead, Joannah Score, Deborah Atkinson, Christian Pecquet, Onima Chowdhury, Anna Schuh
Publikováno v:
Blood. 121(20)
The association between somatic JAK2 mutation and myeloproliferative neoplasms (MPNs) is now well established. However, because JAK2 mutations are associated with heterogeneous clinical phenotypes and often occur as secondary genetic events, some asp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da5e39c5573aa309dfdd759cf6aee679
http://ora.ox.ac.uk/objects/uuid:2d21ab33-f03b-4d0c-8eeb-f20aa678bf87
http://ora.ox.ac.uk/objects/uuid:2d21ab33-f03b-4d0c-8eeb-f20aa678bf87