UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 126

Sortiert nach

Hepcidin agonists as therapeutic tools

Blood, 2018-04, Vol.131 (16), p.1790-1794

2018

Volltextzugriff (PDF)

Structure-function analysis of ferroportin defines the binding site and an alternative mechanism of action of hepcidin

Blood, 2018-02, Vol.131 (8), p.899-910

2018

Volltextzugriff (PDF)

DNA binding to TLR9 expressed by red blood cells promotes innate immune activation and anemia

Science translational medicine, 2021-10, Vol.13 (616), p.eabj1008

2021

Volltextzugriff (PDF)

FGF-23 Is a Negative Regulator of Prenatal and Postnatal Erythropoiesis

The Journal of biological chemistry, 2014-04, Vol.289 (14), p.9795-9810

2014

Volltextzugriff (PDF)

Minihepcidins improve ineffective erythropoiesis and splenomegaly in a new mouse model of adult β-thalassemia major

Haematologica (Roma), 2020-07, Vol.105 (7), p.1835

2020

Volltextzugriff (PDF)

Combination of Tmprss6- ASO and the iron chelator deferiprone improves erythropoiesis and reduces iron overload in a mouse model of beta-thalassemia intermedia

Haematologica (Roma), 2016-01, Vol.101 (1), p.e8

2016

Volltextzugriff (PDF)

Tmprss6-ASO as a tool for the treatment of Polycythemia Vera mice

PloS one, 2021-12, Vol.16 (12), p.e0251995-e0251995

2021

Volltextzugriff (PDF)

Short-term administration of JAK2 inhibitors reduces splenomegaly in mouse models of β-thalassemia intermedia and major

Haematologica (Roma), 2018-02, Vol.103 (2), p.e46

2018

Volltextzugriff (PDF)

Klotho Deficiency Disrupts Hematopoietic Stem Cell Development and Erythropoiesis

The American journal of pathology, 2014-03, Vol.184 (3), p.827-841

2014

Volltextzugriff (PDF)

The murine growth differentiation factor 15 is not essential for systemic iron homeostasis in phlebotomized mice

Haematologica (Roma), 2013-03, Vol.98 (3), p.444-447

2013

Volltextzugriff (PDF)

Tropomodulin 1 controls erythroblast enucleation via regulation of F-actin in the enucleosome

Blood, 2017-08, Vol.130 (9), p.1144-1155

2017

Volltextzugriff (PDF)

Hepcidin is regulated by promoter-associated histone acetylation and HDAC3

Nature communications, 2017-09, Vol.8 (1), p.403-15, Article 403

2017

Volltextzugriff (PDF)

The hepcidin regulator erythroferrone is a new member of the erythropoiesis-iron-bone circuitry

eLife, 2021-05, Vol.10

2021

Volltextzugriff (PDF)

Therapeutic hemoglobin levels after gene transfer in β-thalassemia mice and in hematopoietic cells of β-thalassemia and sickle cells disease patients

PloS one, 2012-03, Vol.7 (3), p.e32345-e32345

2012

Volltextzugriff (PDF)

Enhanced erythropoiesis in Hfe-KO mice indicates a role for Hfe in the modulation of erythroid iron homeostasis

Blood, 2011-01, Vol.117 (4), p.1379-1389

2011

Volltextzugriff (PDF)

In vivo activation of the human δ-globin gene: the therapeutic potential in β-thalassemic mice

Haematologica (Roma), 2014-01, Vol.99 (1), p.76

2014

Volltextzugriff (PDF)

Pleckstrin-2 is essential for erythropoiesis in β-thalassemic mice, reducing apoptosis and enhancing enucleation

Communications biology, 2021-05, Vol.4 (1), p.517-517, Article 517

2021

Volltextzugriff (PDF)

New strategies to target iron metabolism for the treatment of beta thalassemia

Annals of the New York Academy of Sciences, 2016-03, Vol.1368 (1), p.162-168

2016

Volltextzugriff (PDF)

Iron age: novel targets for iron overload

Hematology, 2014-12, Vol.2014 (1), p.216-221

2014

Volltextzugriff (PDF)

Heparanase Level and Procoagulant Activity Are Increased in Thalassemia and Attenuated by Janus Kinase 2 Inhibition

The American journal of pathology, 2020-10, Vol.190 (10), p.2146-2154

2020

Volltextzugriff (PDF)

Reducing TMPRSS6 ameliorates hemochromatosis and β-thalassemia in mice

The Journal of clinical investigation, 2013-04, Vol.123 (4), p.1531-1541

2013

Volltextzugriff (PDF)

Minihepcidin peptides as disease modifiers in mice affected by β-thalassemia and polycythemia vera

Blood, 2016-07, Vol.128 (2), p.265-276

2016

Volltextzugriff (PDF)

Lack of Gdf11 does not improve anemia or prevent the activity of RAP-536 in a mouse model of β-thalassemia

Blood, 2019-08, Vol.134 (6), p.568-572

2019

Volltextzugriff (PDF)

Lobe specificity of iron binding to transferrin modulates murine erythropoiesis and iron homeostasis

Blood, 2019-10, Vol.134 (17), p.1373-1384

2019

Volltextzugriff (PDF)

Combination of a Luspatercept-like Drug (RAP-GRL) and Tmprss6-ASO Is Superior to Either Drug Alone for Correcting β-Thalassemia

Blood, 2021-11, Vol.138 (Supplement 1), p.2013-2013

2021

Volltextzugriff (PDF)

1 – 25 von 126

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(118)
Mit Volltextzugriff
(114)

Publikationsform

Sprache

Englisch
(126)
Japanisch
(10)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Blood
(46)
Haematologica
(5)
Annals Of The New York Academy Of Sciences
(4)
Plos One
(4)
Brain Research
(3)
Epilepsia
(3)
Isrn Hematology
(3)
Journal Of Materials Chemistry
(3)
Biophysical Journal
(2)
Chemistry Of Materials
(2)

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Hepcidin agonists as therapeutic tools

Structure-function analysis of ferroportin defines the binding site and an alternative mechanism of action of hepcidin

DNA binding to TLR9 expressed by red blood cells promotes innate immune activation and anemia

FGF-23 Is a Negative Regulator of Prenatal and Postnatal Erythropoiesis

Minihepcidins improve ineffective erythropoiesis and splenomegaly in a new mouse model of adult β-thalassemia major

Combination of Tmprss6- ASO and the iron chelator deferiprone improves erythropoiesis and reduces iron overload in a mouse model of beta-thalassemia intermedia

Tmprss6-ASO as a tool for the treatment of Polycythemia Vera mice

Short-term administration of JAK2 inhibitors reduces splenomegaly in mouse models of β-thalassemia intermedia and major

Klotho Deficiency Disrupts Hematopoietic Stem Cell Development and Erythropoiesis

The murine growth differentiation factor 15 is not essential for systemic iron homeostasis in phlebotomized mice

Tropomodulin 1 controls erythroblast enucleation via regulation of F-actin in the enucleosome

Hepcidin is regulated by promoter-associated histone acetylation and HDAC3

The hepcidin regulator erythroferrone is a new member of the erythropoiesis-iron-bone circuitry

Therapeutic hemoglobin levels after gene transfer in β-thalassemia mice and in hematopoietic cells of β-thalassemia and sickle cells disease patients

Enhanced erythropoiesis in Hfe-KO mice indicates a role for Hfe in the modulation of erythroid iron homeostasis

In vivo activation of the human δ-globin gene: the therapeutic potential in β-thalassemic mice

Pleckstrin-2 is essential for erythropoiesis in β-thalassemic mice, reducing apoptosis and enhancing enucleation

New strategies to target iron metabolism for the treatment of beta thalassemia

Iron age: novel targets for iron overload

Heparanase Level and Procoagulant Activity Are Increased in Thalassemia and Attenuated by Janus Kinase 2 Inhibition

Reducing TMPRSS6 ameliorates hemochromatosis and β-thalassemia in mice

Minihepcidin peptides as disease modifiers in mice affected by β-thalassemia and polycythemia vera

Lack of Gdf11 does not improve anemia or prevent the activity of RAP-536 in a mouse model of β-thalassemia

Lobe specificity of iron binding to transferrin modulates murine erythropoiesis and iron homeostasis

Combination of a Luspatercept-like Drug (RAP-GRL) and Tmprss6-ASO Is Superior to Either Drug Alone for Correcting β-Thalassemia

Suchergebnisse filtern