Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Gerovasilli, A"'
Autor:
Thein, Swee Lay, Menzel, Stephan, Peng, Xu, Best, Steve, Jiang, Jie, Close, James, Silver, Nicholas, Gerovasilli, Ageliki, Ping, Chen, Yamaguchi, Masao, Wahlberg, Karin, Ulug, Pinar, Spector, Tim D., Garner, Chad, Matsuda, Fumihiko, Farrall, Martin, Lathrop, Mark
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2007 Jul 01. 104(27), 11346-11351.
Externí odkaz:
https://www.jstor.org/stable/25436117
Autor:
Thein, SL, Menzel, S, Peng, X, Best, S, Jiang, J, Close, J, Silver, N, Gerovasilli, A, Ping, C, Yamaguchi, M, Wahlberg, K, Muller, H, Spector, TD, Garner, C, Matsuda, F, Farrall, M, Lathrop, M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::feb4abc9d715352a299111e6a1829cf5
https://ora.ox.ac.uk/objects/uuid:7dde1ad1-4411-4e8b-bd8f-4f7d0543008b
https://ora.ox.ac.uk/objects/uuid:7dde1ad1-4411-4e8b-bd8f-4f7d0543008b
Autor:
Martin Farrall, Ageliki Gerovasilli, Stephan Menzel, Xu Peng, James Close, Karin Wahlberg, Masao Yamaguchi, Chad Garner, Pinar Ulug, Fumihiko Matsuda, Tim D. Spector, Steve Best, Chen Ping, Jie Jiang, Swee Lay Thein, Mark Lathrop, Nicholas Silver
Publikováno v:
Proceedings of the National Academy of Sciences. 104:11346-11351
Individual variation in fetal hemoglobin (HbF, α 2 γ 2 ) response underlies the remarkable diversity in phenotypic severity of sickle cell disease and β thalassemia. HbF levels and HbF-associated quantitative traits (e.g., F cell levels) are highl
Autor:
James Paul Close, Xu Peng, Jie Jiang, Martin Farrall, Karin Wahlberg, Nicholas Silver, Chad Garner, Stephan Menzel, Heike Muller, Chen Ping, Fumihiko Matsuda, Swee Lay Thein, Ageliki Gerovasilli, Steve Best, Masao Yamaguchi, Tim D. Spector, Mark Lathrop
Publikováno v:
Blood Cells, Molecules, and Diseases. 38:181
Autor:
Nicholas Silver, Chen Ping, Stephan Menzel, Tim D. Spector, Martin Farrall, Swee Lay Thein, Jie Jiang, James Close, Masao Yamaguchi, Chad Garner, Steve Best, Mark Lathrop, Fumihiko Matsuda, Xu Peng, Karin Wahlberg, Ageliki Gerovasilli, Heike Muller
Publikováno v:
Blood. 108:652-652
Sickle cell disease and β-thalassemia demonstrate a remarkable diversity in phenotypic severity, and the innate ability to produce fetal hemoglobin (HbF, α 2γ 2) is a major ameliorating factor in these β-hemoglobinopathies. HbF and F cells (denot
Autor:
Lay Thein, Swee, Menzel, Stephan, Peng, Xu, Best, Steve, Jiang, Jie, Close, James, Silver, Nicholas, Gerovasilli, Ageliki, Ping, Chen, Yamaguchi, Masao, Wahlberg, Karin, Muller, Heike, Spector, Tim D., Garner, Chad, Matsuda, Fumihiko, Farrall, Martin, Lathrop, Mark
Publikováno v:
In Blood Cells, Molecules and Diseases March-April 2007 38(2):181-181
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