Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Stephanie Pellegrin"'
Publikováno v:
Haematologica, Vol 106, Iss 9 (2021)
Patients with inherited anemia and hemoglobinopathies (such as sickle cell disease and β-thalassemia) are treated with red blood cell (RBC) transfusions to alleviate their symptoms. Some of these patients may have rare blood group types or go on to
Externí odkaz:
https://doaj.org/article/06c7149fe74045e1acea9e3c88e62f0a
Autor:
Timothy J. Satchwell, Amanda J. Bell, Bethan R. Hawley, Stephanie Pellegrin, Kathryn E. Mordue, Cees Th. B. M. van Deursen, Nicole Heitink-ter Braak, Gerwin Huls, Mathie P.G Leers, Eline Overwater, Rienk Y. J. Tamminga, Bert van der Zwaag, Elisa Fermo, Paola Bianchi, Richard van Wijk, Ashley M. Toye
Publikováno v:
Haematologica, Vol 101, Iss 9 (2016)
Ankyrin-R provides a key link between band 3 and the spectrin cytoskeleton that helps to maintain the highly specialized erythrocyte biconcave shape. Ankyrin deficiency results in fragile spherocytic erythrocytes with reduced band 3 and protein 4.2 e
Externí odkaz:
https://doaj.org/article/fd21b983b35844cfb39c72239f261d93
Autor:
Timothy J. Satchwell, Stephanie Pellegrin, Paola Bianchi, Bethan R. Hawley, Alexandra Gampel, Kathryn E. Mordue, Annika Budnik, Elisa Fermo, Wilma Barcellini, David J. Stephens, Emile van den Akker, Ashley M. Toye
Publikováno v:
Haematologica, Vol 98, Iss 11 (2013)
Congenital dyserythropoietic anemia type II is an autosomally recessive form of hereditary anemia caused by SEC23B gene mutations. Patients exhibit characteristic phenotypes including multinucleate erythroblasts, erythrocytes with hypoglycosylated me
Externí odkaz:
https://doaj.org/article/97aa60fa9a4a4428a17ed8516ad0a77a
Autor:
Emile van den Akker, Timothy J. Satchwell, Stephanie Pellegrin, Geoff Daniels, Ashley M. Toye
Publikováno v:
Haematologica, Vol 95, Iss 9 (2010)
The study of human erythropoiesis in health and disease requires a robust culture system that consistently and reliably generates large numbers of immature erythroblasts that can be induced to differentiate synchronously. We describe a culture method
Externí odkaz:
https://doaj.org/article/fa0661345cc74a648abd23d45c72e8cb
Autor:
Emile van den Akker, Timothy J. Satchwell, Stephanie Pellegrin, Joanna F. Flatt, Michel Maigre, Geoff Daniels, Jean Delaunay, Lesley J. Bruce, Ashley M. Toye
Publikováno v:
Haematologica, Vol 95, Iss 8 (2010)
Background Protein 4.2 deficiency caused by mutations in the EPB42 gene results in hereditary spherocytosis with characteristic alterations of CD47, CD44 and RhAG. We decided to investigate at which stage of erythropoiesis these hallmarks of protein
Externí odkaz:
https://doaj.org/article/e6cb6d91cc184560878bfad16c55d634
Autor:
Léa P Wilhelm, Juan Zapata‐Muñoz, Beatriz Villarejo‐Zori, Stephanie Pellegrin, Catarina Martins Freire, Ashley M Toye, Patricia Boya, Ian G Ganley
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Wilhelm, L P, Zapata-Muñoz, J, Villarejo-Zori, B, Pellegrin, S, Freire, C M, Toye, A M, Boya, P & Ganley, I G 2022, ' BNIP3L/NIX regulates both mitophagy and pexophagy ', EMBO Journal, vol. 41, no. 24, e111115 . https://doi.org/10.15252/embj.2022111115
instname
Wilhelm, L P, Zapata-Muñoz, J, Villarejo-Zori, B, Pellegrin, S, Freire, C M, Toye, A M, Boya, P & Ganley, I G 2022, ' BNIP3L/NIX regulates both mitophagy and pexophagy ', EMBO Journal, vol. 41, no. 24, e111115 . https://doi.org/10.15252/embj.2022111115
19 p.-6 fig.
Mitochondria and peroxisomes are closely related metabolic organelles, both in terms of origin and in terms of function. Mitochondria and peroxisomes can also be turned over by autophagy, in processes termed mitophagy and pexophagy,
Mitochondria and peroxisomes are closely related metabolic organelles, both in terms of origin and in terms of function. Mitochondria and peroxisomes can also be turned over by autophagy, in processes termed mitophagy and pexophagy,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4eba8cfeadbb0c827b1bf4375338ff8c
http://hdl.handle.net/10261/281336
http://hdl.handle.net/10261/281336
Autor:
Emile van den Akker, Bethan R. Hawley, Stephanie Pellegrin, Ashley M. Toye, Paola Bianchi, Elisa Fermo, Timothy J. Satchwell, David J. Stephens, Annika Budnik, Alexandra Gampel, Wilma Barcellini, Kathryn E. Mordue
Publikováno v:
Haematologica. 98:1788-1796
Congenital dyserythropoietic anemia type II is an autosomally recessive form of hereditary anemia caused by SEC23B gene mutations. Patients exhibit characteristic phenotypes including multinucleate erythroblasts, erythrocytes with hypoglycosylated me
Publikováno v:
Journal of Cell Science. 123:1247-1252
Actin stress fibers are fundamental components of the actin cytoskeleton that produce contractile force in non-muscle cells. The formation of stress fibers is controlled by the small GTPase RhoA and two highly related proteins, RhoB and RhoC. Togethe
Autor:
Geoff Daniels, Jean Delaunay, Emile van den Akker, Timothy J. Satchwell, Michel Maigre, Joanna F. Flatt, Lesley J. Bruce, Ashley M. Toye, Stephanie Pellegrin
Publikováno v:
Haematologica. 95:1278-1286
Background Protein 4.2 deficiency caused by mutations in the EPB42 gene results in hereditary spherocytosis with characteristic alterations of CD47, CD44 and RhAG. We decided to investigate at which stage of erythropoiesis these hallmarks of protein
Publikováno v:
Neuroscience letters. 590
The small GTPase Rif is required for the early stages of dendritic spine formation in neurons, acting through the formin mDia2 to control actin polymerization. Rif is expressed at high levels in the brain, suggesting broader roles in neuronal functio