Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ileana Cantú"'
Autor:
Anne Korporaal, Nynke Gillemans, Steven Heshusius, Ileana Cantú, Emile van den Akker, Thamar B. van Dijk, Marieke von Lindern, Sjaak Philipsen
Publikováno v:
Haematologica, Vol 106, Iss 2 (2020)
Haploinsufficiency for transcription factor KLF1 causes a variety of human erythroid phenotypes, such as the In(Lu) blood type, increased HbA2 levels, and hereditary persistence of fetal hemoglobin. Severe dominant congenital dyserythropoietic anemia
Externí odkaz:
https://doaj.org/article/be271501667a4190b60d587d61ed3c5a
Autor:
Ileana Cantú, Harmen J G van de Werken, Nynke Gillemans, Ralph Stadhouders, Steven Heshusius, Alex Maas, Fatemehsadat Esteghamat, Zeliha Ozgur, Wilfred F J van IJcken, Frank Grosveld, Marieke von Lindern, Sjaak Philipsen, Thamar B van Dijk
Publikováno v:
PLoS ONE, Vol 14, Iss 3, p e0208659 (2019)
Krüppel-like factor 1 (KLF1) is an essential transcription factor for erythroid development, as demonstrated by Klf1 knockout mice which die around E14 due to severe anemia. In humans, >140 KLF1 variants, causing different erythroid phenotypes, have
Externí odkaz:
https://doaj.org/article/a036d268167f4395a300831947ef3990
Autor:
Ileana Cantú, Sjaak Philipsen
Publikováno v:
Haematologica, Vol 99, Iss 11 (2014)
Externí odkaz:
https://doaj.org/article/1290ae320a65430d9b192a88fca8ca2f
Autor:
Steven Heshusius, Frank Grosveld, Ralph Stadhouders, Marieke von Lindern, Sjaak Philipsen, Alex Maas, Nynke Gillemans, Wilfred F. J. van IJcken, Harmen J.G. van de Werken, Thamar B. van Dijk, Zeliha Ozgur, Fatemehsadat Esteghamat, Ileana Cantú
Publikováno v:
PLoS ONE
PLoS ONE, 14(3):e0208659. Public Library of Science
PLoS One (online), 14(3):e0208659. Public Library of Science
PLoS ONE, Vol 14, Iss 3, p e0208659 (2019)
PLoS ONE, 14(3):e0208659. Public Library of Science
PLoS One (online), 14(3):e0208659. Public Library of Science
PLoS ONE, Vol 14, Iss 3, p e0208659 (2019)
Krüppel-like factor 1 (KLF1) is an essential transcription factor for erythroid development, as demonstrated by Klf1 knockout mice which die around E14 due to severe anemia. In humans, >140 KLF1 variants, causing different erythroid phenotypes, have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::492dd1d517b628ed98595503933f7fd9
http://europepmc.org/articles/PMC6438607
http://europepmc.org/articles/PMC6438607
Autor:
Marieke von Lindern, Ralph Stadhouders, Steven Heshusius, Frank Grosveld, Sjaak Philipsen, Wilfred F. J. van IJcken, Alex Maas, Zeliha Ozgur, Thamar B. van Dijk, Harmen J.G. van de Werken, Ileana Cantú, Nynke Gillemans
Krüppel-like factor 1 (KLF1) is an essential transcription factor for erythroid development, as demonstrated by Klf1 knockout mice which die around E14 due to severe anemia. In humans, >65 KLF1 variants, causing different erythroid phenotypes, have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4eaadd8624adc3d435bffacfe0a38f1
Autor:
Kirsten van Lom, Cornelis L. Harteveld, Ileana Cantú, Rianne Schaap, Sjaak Philipsen, Abdelhafid Natiq, Bella Banjanin, Nynke Gillemans, Abdelaziz Sefiani, Saaid Amzazi, Siham Chafai Elalaoui, Philippe A. Lysy
Publikováno v:
American Journal of Hematology, 92(1), E2-E3. Wiley-Liss Inc.
American Journal of Hematology, 92(1), E2-E3
American Journal of Hematology, 92(1), E2-E3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac277a1810549759ef463109ca4f48f5
https://pure.eur.nl/en/publications/ba8db83e-8f52-4b1e-b58c-af96dd1bc4e0
https://pure.eur.nl/en/publications/ba8db83e-8f52-4b1e-b58c-af96dd1bc4e0
Autor:
Steven Heshusius, Anne Korporaal, Ileana Cantú, Sjaak Philipsen, Nynke Gillemans, Thamar B. van Dijk, Marieke von Lindern, Emile van den Akker
Publikováno v:
Haematologica, 106(2), 464-473. Ferrata Storti Foundation
Haematologica
Haematologica
Haploinsufficiency for transcription factor KLF1 causes a variety of human erythroid phenotypes, such as the In(Lu) blood type, increased HbA2 levels, and hereditary persistence of fetal hemoglobin. Severe dominant congenital dyserythropoietic anemia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8b27c1619cba6202544ac02532dc84c
http://www.scopus.com/inward/record.url?scp=85093095179&partnerID=8YFLogxK
http://www.scopus.com/inward/record.url?scp=85093095179&partnerID=8YFLogxK
Autor:
Claudio Cantù, Francesca Bosè, Paola Bianchi, Eva Reali, Maria Teresa Colzani, Ileana Cantù, Gloria Barbarani, Sergio Ottolenghi, Walter Witke, Laura Spinardi, Antonella Ellena Ronchi
Publikováno v:
Haematologica, Vol 97, Iss 7 (2012)
Background During late differentiation, erythroid cells undergo profound changes involving actin filament remodeling. One of the proteins controlling actin dynamics is gelsolin, a calcium-activated actin filament severing and capping protein. Gelsoli
Externí odkaz:
https://doaj.org/article/0b88213da96547828ac97e199912ac29