UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 86

Sortiert nach

Immunosuppressive CD71+ erythroid cells compromise neonatal host defence against infection

Nature (London), 2013-12, Vol.504 (7478), p.158-162

2013

Link zum Volltext

Verfügbarkeit prüfen

Characterizing bulk rigidity of rigid red blood cell populations in sickle-cell disease patients

Scientific reports, 2021-04, Vol.11 (1), p.7909-7909, Article 7909

2021

Link zum Volltext

Verfügbarkeit prüfen

Rapid measurement of hemoglobin-oxygen dissociation by leveraging Bohr effect and Soret band bathochromic shift

Analyst (London), 2024-04, Vol.149 (9), p.2561-2572

2024

Link zum Volltext

Verfügbarkeit prüfen

M-CSF supports medullary erythropoiesis and erythroid iron demand following burn injury through its activity on homeostatic iron recycling

Scientific reports, 2022-01, Vol.12 (1), p.1235-1235, Article 1235

2022

Link zum Volltext

Verfügbarkeit prüfen

RGL2 Deficiency Impairs Human Erythropoiesis By Altering Terminal Erythroid Differentiation and Apoptosis

Blood, 2017-12, Vol.130 (Suppl_1), p.8-8

2017

Link zum Volltext

Verfügbarkeit prüfen

Rare Hereditary Hemolytic Anemias

Hematology/oncology clinics of North America, 2019-06, Vol.33 (3), p.373-392

2019

Link zum Volltext

Verfügbarkeit prüfen

801 Overexpression of human TLR8 induces bone marrow dysfunction and severe anemia in lupus- prone mice

Lupus science & medicine, 2024-05, Vol.11 (Suppl 2), p.A67-A69

2024

Link zum Volltext

Verfügbarkeit prüfen

Multicenter, phase 1 study of etavopivat (FT-4202) treatment for up to 12 weeks in patients with sickle cell disease

Blood advances, 2024-04

2024

Link zum Volltext

Verfügbarkeit prüfen

Corrigendum: The Spectrum of SPTA1-Associated Hereditary Spherocytosis

Frontiers in physiology, 2019-10, Vol.10, p.1331-1331

2019

Link zum Volltext

Verfügbarkeit prüfen

Case report: Childhood erythrocytosis due to hypermanganesemia caused by homozygous SLC30A10 mutation

Frontiers in hematology, 2024-03, Vol.3

2024

Link zum Volltext

Verfügbarkeit prüfen

Identification of a murine erythroblast subpopulation enriched in enucleating events by multi-spectral imaging flow cytometry

Journal of visualized experiments, 2014-06 (88)

2014

Link zum Volltext

Verfügbarkeit prüfen

MPN-024 Hypereosinophilic Syndrome: A Catastrophic Pediatric Case

Clinical lymphoma, myeloma and leukemia, 2022-10, Vol.22 Suppl 2, p.S322

2022

Link zum Volltext

Verfügbarkeit prüfen

Poster: MPN-024 Hypereosinophilic Syndrome: A Catastrophic Pediatric Case

Clinical lymphoma, myeloma and leukemia, 2022-10, Vol.22, p.S160

2022

Link zum Volltext

Verfügbarkeit prüfen

Rapid degradation of protein tyrosine phosphatase 1B in sickle cells: Possible contribution to sickle cell membrane weakening

The FASEB journal, 2022-06, Vol.36 (6), p.e22360-n/a

2022

Link zum Volltext

Verfügbarkeit prüfen

eP420: Clinical utility of a 38-gene NGS panel in diagnosing patients with hemolytic anemia: A retrospective review of 435 cases

Genetics in medicine, 2022-03, Vol.24 (3), p.S263-S263

2022

Link zum Volltext

Verfügbarkeit prüfen

Overexpression of Human TLR8 Causes Fatal Anemia in SLE-Prone Mice By Altering the Bone Marrow Erythropoietic Niche

Blood, 2021-11, Vol.138 (Supplement 1), p.1989-1989

2021

Link zum Volltext

Verfügbarkeit prüfen

Novel role(s) for Irf5 in controlling myelopoiesis and erythropoiesis

The Journal of immunology (1950), 2020-05, Vol.204 (1_Supplement), p.63-63.1

2020

Link zum Volltext

Verfügbarkeit prüfen

Dominant-Negative VPS4A Mutations Causing Congenital Dyserythropoietic Anemia Disrupt Iron Trafficking of Terminal Erythropoiesis

Blood, 2022-11, Vol.140 (Supplement 1), p.8190-8191

2022

Link zum Volltext

Verfügbarkeit prüfen

Ex-Vivo FT-4202 Treatment Improves Hemoglobin Oxygen Affinity and Membrane Health in Red Blood Cells of Patients with Hemoglobin SS and Hemoglobin SC Disease Irrespective of Prior Hydroxyurea Use

Blood, 2020-11, Vol.136 (Supplement 1), p.23-24

2020

Link zum Volltext

Verfügbarkeit prüfen

SERF1 Is Required for G-CSF Resistance of Start-Codon Mutant ELANE Granulocytic Precursors

Blood, 2021-11, Vol.138 (Supplement 1), p.433-433

2021

Link zum Volltext

Verfügbarkeit prüfen

Activation of Pyruvate Kinase-R with Etavopivat (FT-4202) Is Well Tolerated, Improves Anemia, and Decreases Intravascular Hemolysis in Patients with Sickle Cell Disease Treated for up to 12 Weeks

Blood, 2021-11, Vol.138 (Supplement 1), p.9-9

2021

Link zum Volltext

Verfügbarkeit prüfen

Trial in Progress: A Phase 2, Open-Label Study Evaluating the Safety and Efficacy of the PKR Activator Etavopivat (FT-4202) in Patients with Thalassemia or Sickle Cell Disease

Blood, 2021-11, Vol.138 (Supplement 1), p.4162-4162

2021

Link zum Volltext

Verfügbarkeit prüfen

De Novo Germline DHX38 Variant Associated with Alternative Splicing of Multiple Transcripts in Iron-Related Pathways in a Patient with Atypical Congenital Dyserythropoietic Anemia with Ring Sideroblasts

Blood, 2022-11, Vol.140 (Supplement 1), p.1234-1235

2022

Link zum Volltext

Verfügbarkeit prüfen

Rapid and Automated Quantitation of Dense Red Blood Cells: A Robust Biomarker of Therapeutic Response to Early Initiation of Hydroxyurea in Young Children with Sickle Cell Anemia

Blood, 2020-11, Vol.136 (Supplement 1), p.16-17

2020

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 86

Suche als RSS-Feed

Aktive Filter

Zeitschrift / SerieBritish Journal Of Haematology

Zeitschrift / SerieProceedings Of The National Academy Of Sciences - Pnas

ThemaLife Sciences & Biomedicine

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(82)
Mit Volltextzugriff
(83)

Publikationsform

Sprache

Englisch
(86)
Japanisch
(2)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Blood
(57)
Nature
(6)
Clinical Lymphoma, Myeloma And Leukemia
(2)
Journal Of Visualized Experiments
(2)
Scientific Reports
(2)
The Journal Of Immunology
(2)
Analyst
(1)
Blood Advances
(1)
Frontiers In Hematology
(1)
Frontiers In Physiology
(1)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Base editing of haematopoietic stem cells rescues sickle cell disease in mice

Immunosuppressive CD71+ erythroid cells compromise neonatal host defence against infection

Characterizing bulk rigidity of rigid red blood cell populations in sickle-cell disease patients

Rapid measurement of hemoglobin-oxygen dissociation by leveraging Bohr effect and Soret band bathochromic shift

M-CSF supports medullary erythropoiesis and erythroid iron demand following burn injury through its activity on homeostatic iron recycling

RGL2 Deficiency Impairs Human Erythropoiesis By Altering Terminal Erythroid Differentiation and Apoptosis

Rare Hereditary Hemolytic Anemias

801 Overexpression of human TLR8 induces bone marrow dysfunction and severe anemia in lupus- prone mice

Multicenter, phase 1 study of etavopivat (FT-4202) treatment for up to 12 weeks in patients with sickle cell disease

Corrigendum: The Spectrum of SPTA1-Associated Hereditary Spherocytosis

Case report: Childhood erythrocytosis due to hypermanganesemia caused by homozygous SLC30A10 mutation

Identification of a murine erythroblast subpopulation enriched in enucleating events by multi-spectral imaging flow cytometry

MPN-024 Hypereosinophilic Syndrome: A Catastrophic Pediatric Case

Poster: MPN-024 Hypereosinophilic Syndrome: A Catastrophic Pediatric Case

Rapid degradation of protein tyrosine phosphatase 1B in sickle cells: Possible contribution to sickle cell membrane weakening

eP420: Clinical utility of a 38-gene NGS panel in diagnosing patients with hemolytic anemia: A retrospective review of 435 cases

Overexpression of Human TLR8 Causes Fatal Anemia in SLE-Prone Mice By Altering the Bone Marrow Erythropoietic Niche

Novel role(s) for Irf5 in controlling myelopoiesis and erythropoiesis

Dominant-Negative VPS4A Mutations Causing Congenital Dyserythropoietic Anemia Disrupt Iron Trafficking of Terminal Erythropoiesis

Ex-Vivo FT-4202 Treatment Improves Hemoglobin Oxygen Affinity and Membrane Health in Red Blood Cells of Patients with Hemoglobin SS and Hemoglobin SC Disease Irrespective of Prior Hydroxyurea Use

SERF1 Is Required for G-CSF Resistance of Start-Codon Mutant ELANE Granulocytic Precursors

Activation of Pyruvate Kinase-R with Etavopivat (FT-4202) Is Well Tolerated, Improves Anemia, and Decreases Intravascular Hemolysis in Patients with Sickle Cell Disease Treated for up to 12 Weeks

Trial in Progress: A Phase 2, Open-Label Study Evaluating the Safety and Efficacy of the PKR Activator Etavopivat (FT-4202) in Patients with Thalassemia or Sickle Cell Disease

De Novo Germline DHX38 Variant Associated with Alternative Splicing of Multiple Transcripts in Iron-Related Pathways in a Patient with Atypical Congenital Dyserythropoietic Anemia with Ring Sideroblasts

Rapid and Automated Quantitation of Dense Red Blood Cells: A Robust Biomarker of Therapeutic Response to Early Initiation of Hydroxyurea in Young Children with Sickle Cell Anemia

Aktive Filter

Suchergebnisse filtern