Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mandy Y. Boontanrart"'
Autor:
Mandy Y. Boontanrart, Markus S. Schröder, Gautier M. Stehli, Marija Banović, Stacia K. Wyman, Rachel J. Lew, Matteo Bordi, Benjamin G. Gowen, Mark A. DeWitt, Jacob E. Corn
Publikováno v:
Cell Reports, Vol 32, Iss 5, Pp 107993- (2020)
Summary: β-Hemoglobinopathies can trigger rapid production of red blood cells in a process known as stress erythropoiesis. Cellular stress prompts differentiating erythroid precursors to express high levels of fetal γ-globin. However, the mechanism
Externí odkaz:
https://doaj.org/article/3fe47469212244e8974cbf8b70ce5d59
Autor:
Mandy Y Boontanrart, Elia Mächler, Simone Ponta, Jan C Nelis, Viviana G Preiano, Jacob E Corn
Publikováno v:
eLife, Vol 12 (2023)
The β-hemoglobinopathies, such as sickle cell disease and β-thalassemia, are one of the most common genetic diseases worldwide and are caused by mutations affecting the structure or production of β-globin subunits in adult hemoglobin. Many gene ed
Externí odkaz:
https://doaj.org/article/e0ff0c9f59204524b6452950d77ab453
Autor:
Mandy Y. Boontanrart, Elia Mächler, Simone Ponta, Jan C. Nelis, Viviana G. Preiano, Jacob E. Corn
The β-hemoglobinopathies, such as sickle cell disease and β-thalassemia, are one of the most common genetic diseases worldwide and are caused by mutations affecting the structure or production of β-globin subunits in adult hemoglobin. Many gene ed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d566fd1fdcd0cae9b732f9bc529ec33
https://doi.org/10.1101/2022.12.19.521003
https://doi.org/10.1101/2022.12.19.521003
