Zobrazeno 1 - 10
of 218
pro vyhledávání: '"Mark Gower"'
Autor:
Mark Gower, Anastasia N. Tikhonova
Publikováno v:
Haematologica, Vol 108, Iss 5 (2022)
Externí odkaz:
https://doaj.org/article/4ee6e6ddfe2245d9949d9c6108d6dd5f
Autor:
Arvind Singh Mer, Emily M. Heath, Seyed Ali Madani Tonekaboni, Nergiz Dogan-Artun, Sisira Kadambat Nair, Alex Murison, Laura Garcia-Prat, Liran Shlush, Rose Hurren, Veronique Voisin, Gary D. Bader, Corey Nislow, Mattias Rantalainen, Soren Lehmann, Mark Gower, Cynthia J. Guidos, Mathieu Lupien, John E. Dick, Mark D. Minden, Aaron D. Schimmer, Benjamin Haibe-Kains
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-13 (2021)
Molecular heterogeneity of acute myeloid leukaemia (AML) across patients is a major challenge for prognosis and therapy. Here, the authors show that NPM1 mutated AML is a heterogeneous class, consisting of two subtypes which exhibit distinct molecula
Externí odkaz:
https://doaj.org/article/a1a1fb4ad66d4a54b1ec1c09785a2551
Autor:
Mark Gower, Minerva Fernandez, Andrea Aruda, Mark Minden, Johann Hitzler, Anastasia Tikhonova
Publikováno v:
Cancer Research. 83:NG14-NG14
T-cell acute lymphoblastic leukemia (T-ALL) represents a particularly aggressive subtype of leukemia with no targeted therapies or immune interventions. Currently, in response to intensive chemotherapy, ~25% of pediatric and 50% of adult patients und
Autor:
Mark, Gower, Anastasia N, Tikhonova
Publikováno v:
Haematologica.
Not available.
Autor:
Corey Nislow, Sören Lehmann, Alex Murison, Gary D. Bader, Mark Gower, Liran I. Shlush, Benjamin Haibe-Kains, Nergiz Dogan-Artun, Rose Hurren, John E. Dick, Veronique Voisin, Cynthia J. Guidos, Sisira Kadambat Nair, Seyed Ali Madani Tonekaboni, Mathieu Lupien, Emily Heath, Mark D. Minden, Aaron D. Schimmer, Laura García-Prat, Arvind Singh Mer, Mattias Rantalainen
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-13 (2021)
Nature Communications
Nature Communications
In acute myeloid leukemia (AML), molecular heterogeneity across patients constitutes a major challenge for prognosis and therapy. AML with NPM1 mutation is a distinct genetic entity in the revised World Health Organization classification. However, di
Autor:
Anastasia Tikhonova, Mark Gower
Publikováno v:
Blood. 140:3-4
Publikováno v:
Nature Immunology. 22:396-397
Riok2 haploinsufficiency leads to aberrant TH22 skewing and interleukin-22-mediated erythroid dysfunction.
Autor:
Jeffrey Hornung, David Fouse, Tetsuo Kotani, Teruhiko Fukushima, Mark Gower, Nozomu Yoshitomi, Paul Barnes, Noboru Yamaguchi, Jessica Ear
On March 11 2011, a 9.0 magnitude earthquake struck Northeastern Japan followed shortly after by a powerful tsunami. The disaster caused devastating damage along the Pacific coastline and more than 20,000 people were declared killed, injured or missi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32ccecc5170b2f94e46861fead16582a
https://doi.org/10.21236/ada585861
https://doi.org/10.21236/ada585861
Autor:
Journal Record Staff
Publikováno v:
Journal Record, The (Oklahoma City, OK). 07/25/2022.