Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Tony Todd"'
Autor:
Hemanth Tummala, Amanda J Walne, Mohsin Badat, Manthan Patel, Abigail M Walne, Jenna Alnajar, Chi Ching Chow, Ibtehal Albursan, Jennifer M Frost, David Ballard, Sally Killick, Peter Szitányi, Anne M Kelly, Manoj Raghavan, Corrina Powell, Reinier Raymakers, Tony Todd, Elpis Mantadakis, Sophia Polychronopoulou, Nikolas Pontikos, Tianyi Liao, Pradeep Madapura, Upal Hossain, Tom Vulliamy, Inderjeet Dokal
Publikováno v:
EMBO Molecular Medicine, Vol 16, Iss 10, Pp 2560-2582 (2024)
Abstract Dyskeratosis congenita (DC) is a rare inherited bone marrow failure syndrome, caused by genetic mutations that principally affect telomere biology. Approximately 35% of cases remain uncharacterised at the genetic level. To explore the geneti
Externí odkaz:
https://doaj.org/article/a5c1a71362e94f24b64c6893fb53d636
Autor:
Tony Todd
Publikováno v:
Film-Philosophy, Vol 13, Iss 1, Pp 68-89 (2009)
Externí odkaz:
https://doaj.org/article/7cd41c9ce1984b599204358ff9673281
Autor:
David A Enoch, Jenny I.O. Craig, James S Cargill, Emma Gudgin, Sandra Young Min, Hugo A. Ludlam, Robert E. Marcus, Charles Crawley, Tony Todd, George A. Follows, Pat Sartori, Martin Besser
Publikováno v:
Journal of Infection. 56:156-158
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58db083e3326f9550a5d1dbaef04f9ee
https://doi.org/10.1016/j.jinf.2007.11.002
https://doi.org/10.1016/j.jinf.2007.11.002
Autor:
Tony, Todd, Tim, Caroe
Publikováno v:
Praxis. 97(13)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::492825f4764b54d48ebf8bfb39452da8
https://pubmed.ncbi.nlm.nih.gov/18770926
https://pubmed.ncbi.nlm.nih.gov/18770926
Autor:
Wendy N. Erber, Tony Todd
Publikováno v:
British journal of haematology. 134(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::469db5126953c8c3e742384dd280de99
https://pubmed.ncbi.nlm.nih.gov/16764685
https://pubmed.ncbi.nlm.nih.gov/16764685
Publikováno v:
Praxis. 97:735-736
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e7e2fad35230946c4582b18a1d34051
https://doi.org/10.1024/1661-8157.97.13.735
https://doi.org/10.1024/1661-8157.97.13.735
Autor:
Peter J. Campbell, Anthony R. Green, E. Joanna Baxter, Tony Todd, Linda M. Scott, Michael R. Stratton, Philip J. Stephens, P. Andrew Futreal, Richard Wooster, Sarah Edkins
Publikováno v:
Blood. 106:2920-2921
Four groups recently reported the existence of an activating mutation of JAK2 in many patients with one of the classic myeloproliferative disorders (MPDs).[1][1]-[4][2] Mutant Janus kinase 2 (JAK2) has increased kinase activity, renders BaF3 cells cy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e26b4a8d17a4230e3e40b51ff137d24
https://doi.org/10.1182/blood-2005-05-2087
https://doi.org/10.1182/blood-2005-05-2087
Publikováno v:
BMJ. 334:259-259
A 40 year old woman with persistent fatigue has come back to you for the results of blood tests. The results show a hypochromic, microcytic anaemia with a haemoglobin concentration of 100 g/l and a ferritin concentration of 5 µg/l, the classic featu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33dfaa9bb6a3bde279a144f4dbd8bb0b
https://doi.org/10.1136/bmj.39003.602338.94
https://doi.org/10.1136/bmj.39003.602338.94
Autor:
Joanna Baxter, Anthony R. Green, Michael R. Stratton, Philip J. Stephens, Andrew Futreal, Linda M. Scott, Richard Wooster, Tony Todd, Sarah Edkins, Peter J. Campbell
Publikováno v:
Blood. 106:2598-2598
The JAK2 V617F mutation is present in 97% patients with polycythemia vera (PV) and approximately 50% of patients with essential thrombocythemia (ET) and idiopathic myelofibrosis (IMF). JAK2 is widely expressed and is a critical component of signaling
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f2d71e7e15e373babff1fd721b1eb4a
https://doi.org/10.1182/blood.v106.11.2598.2598
https://doi.org/10.1182/blood.v106.11.2598.2598