Search Results - "Cantú, Ileana"

Flicking the switch: adult hemoglobin expression in erythroid cells derived from cord blood and human induced pluripotent stem cells by Cantú, Ileana, Philipsen, Sjaak

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The mouse KLF1 Nan variant impairs nuclear condensation and erythroid maturation by Cantú, Ileana, van de Werken, Harmen J G, Gillemans, Nynke, Stadhouders, Ralph, Heshusius, Steven, Maas, Alex, Esteghamat, Fatemehsadat, Ozgur, Zeliha, van IJcken, Wilfred F J, Grosveld, Frank, von Lindern, Marieke, Philipsen, Sjaak, van Dijk, Thamar B

“…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…”
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Hemoglobin switching in mice carrying the Klf1Nan variant by Korporaal, Anne, Gillemans, Nynke, Heshusius, Steven, Cantú, Ileana, van den Akker, Emile, van Dijk, Thamar B, von Lindern, Marieke, Philipsen, Sjaak

“…Haploinsufficiency for transcription factor KLF1 causes a variety of human erythroid phenotypes, such as the In(Lu) blood type, increased HbA2 levels, and…”
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Erythropoiesis and globin switching in compound Klf1::Bcl11a mutant mice by Esteghamat, Fatemehsadat, Gillemans, Nynke, Bilic, Ivan, van den Akker, Emile, Cantù, Ileana, van Gent, Teus, Klingmüller, Ursula, van Lom, Kirsten, von Lindern, Marieke, Grosveld, Frank, Bryn van Dijk, Thamar, Busslinger, Meinrad, Philipsen, Sjaak

“…B-cell lymphoma 11A (BCL11A) downregulation in human primary adult erythroid progenitors results in elevated expression of fetal γ-globin. Recent reports…”
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highly conserved SOX6 double binding site mediates SOX6 gene downregulation in erythroid cells by Cantu', Claudio, Grande, Vito, Alborelli, Ilaria, Cassinelli, Letizia, Cantu', Ileana, Colzani, Maria Teresa, Ierardi, Rossella, Ronzoni, Luisa, Cappellini, Maria Domenica, Ferrari, Giuliana, Ottolenghi, Sergio, Ronchi, Antonella

“…The Sox6 transcription factor plays critical roles in various cell types, including erythroid cells. Sox6-deficient mice are anemic due to impaired red cell…”
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Hereditary persistence of fetal hemoglobin in two patients with KLF1 haploinsufficiency due to 19p13.2–p13.12/13 deletion by Natiq, Abdelhafid, Lysy, Philippe A., Gillemans, Nynke, Schaap, Rianne, Sefiani, Abdelaziz, Amzazi, Saaid, Chafai El‐Alaoui, Siham, Cantú, Ileana, Banjanin, Bella, van Lom, Kirsten, Harteveld, Cornelis L., Philipsen, Sjaak

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Defective erythroid maturation in gelsolin mutant mice by CANTU, Claudio, BOSE, Francesca, RONCHIL, Antonella Ellena, BIANCHI, Paola, REALI, Eva, COLZANI, Maria Teresa, CANTU, Ileana, BARBARANI, Gloria, OTTOLENGHI, Sergio, WITKE, Walter, SPINARDI, Laura

“…During late differentiation, erythroid cells undergo profound changes involving actin filament remodeling. One of the proteins controlling actin dynamics is…”
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Hemoglobin switching in mice carrying the Klf1 Nan variant by Korporaal, Anne, Gillemans, Nynke, Heshusius, Steven, Cantú, Ileana, van den Akker, Emile, van Dijk, Thamar B, von Lindern, Marieke, Philipsen, Sjaak

“…Haploinsufficiency for transcription factor KLF1 causes a variety of human erythroid phenotypes, such as the In(Lu) blood type, increased HbA2 levels, and…”
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Erythropoiesis and Globin Switching in Compound Klf1::Bcl11a mutant mice by Esteghamat, Fatemehsadat, Gillemans, Nynke, Bilic, Ivan, van den Akker, Emile, Cantu', Ileana, van Gent, Teus, Klingmuller, Ursula, van Lom, Kirsten, von Lindern, Marieke, Grosveld, Frank, van Dijk, Thamar, Busslinger, Meinrad, Philipsen, Sjaak

“…Abstract 1019 Reactivation of fetal γ-globin is of outstanding demand in patients with β-hemoglobinopathies. B-Cell/Lymphoma 11A (BCL11A) is a well-known…”
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Hereditary persistence of fetal hemoglobin in two patients with KLF1 haploinsufficiency due to 19p13.2-p13.12/13 deletion by Natiq, Abdelhafid, Lysy, Philippe A, Gillemans, Nynke, Schaap, Rianne, Sefiani, Abdelaziz, Amzazi, Saaid, Chafai El-Alaoui, Siham, Cantú, Ileana, Banjanin, Bella, van Lom, Kirsten, Harteveld, Cornelis L, Philipsen, Sjaak

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