UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 326

Sortiert nach

Genome‐wide association study of early ischaemic stroke risk in Brazilian individuals with sickle cell disease implicates ADAMTS2 and CDK18 and uncovers novel loci

British journal of haematology, 2023-04, Vol.201 (2), p.343-352

2023

Volltextzugriff (PDF)

Organ-on-chips made of blood: endothelial progenitor cells from blood reconstitute vascular thromboinflammation in vessel-chips

Lab on a chip, 2019-07, Vol.19 (15), p.25-2511

2019

Volltextzugriff (PDF)

The NLRP3 inflammasome fires up heme-induced inflammation in hemolytic conditions

Translational research : the journal of laboratory and clinical medicine, 2023-02, Vol.252, p.34-44

2023

Volltextzugriff (PDF)

Genetic Modifiers of White Blood Cell Count, Albuminuria and Glomerular Filtration Rate in Children with Sickle Cell Anemia

PloS one, 2016-10, Vol.11 (10), p.e0164364-e0164364

2016

Volltextzugriff (PDF)

Noncanonical Roles of Caspase-4 and Caspase-5 in Heme-Driven IL-1β Release and Cell Death

The Journal of immunology (1950), 2021-04, Vol.206 (8), p.1878-1889

2021

Volltextzugriff (PDF)

Tripartite collaboration of blood‐derived endothelial cells, next generation RNA sequencing and bioengineered vessel‐chip may distinguish vasculopathy and thrombosis among sickle cell disease patients

Bioengineering & translational medicine, 2021-09, Vol.6 (3), p.e10211-n/a

2021

Volltextzugriff (PDF)

Whole exome sequencing identifies novel genes for fetal hemoglobin response to hydroxyurea in children with sickle cell anemia

PloS one, 2014-10, Vol.9 (10), p.e110740

2014

Volltextzugriff (PDF)

Pharmacokinetics, pharmacodynamics, and pharmacogenetics of hydroxyurea treatment for children with sickle cell anemia

Blood, 2011-11, Vol.118 (18), p.4985-4991

2011

Volltextzugriff (PDF)

Characterization of Cytoplasmic Caspase-2 Activation by Induced Proximity

Molecular cell, 2009-09, Vol.35 (6), p.830-840

2009

Volltextzugriff (PDF)

Genetic predictors for stroke in children with sickle cell anemia

Blood, 2011-06, Vol.117 (24), p.6681-6684

2011

Volltextzugriff (PDF)

Vascular Transcriptomics: Investigating Endothelial Activation and Vascular Dysfunction Using Blood Outgrowth Endothelial Cells, Organ‐Chips, and RNA Sequencing

Current protocols, 2022-10, Vol.2 (10), p.e582-n/a

2022

Volltextzugriff (PDF)

Genetic modifiers of sickle cell anemia in the BABY HUG cohort: influence on laboratory and clinical phenotypes

American journal of hematology, 2013-07, Vol.88 (7), p.571-576

2013

Volltextzugriff (PDF)

Genetic variants in toll‐like receptor 4 are associated with lack of steroid‐responsiveness in pediatric ITP patients

American journal of hematology, 2020-04, Vol.95 (4), p.395-400

2020

Volltextzugriff (PDF)

Genetic mapping and exome sequencing identify 2 mutations associated with stroke protection in pediatric patients with sickle cell anemia

Blood, 2013-04, Vol.121 (16), p.3237-3245

2013

Volltextzugriff (PDF)

Whole-exome sequencing for RH genotyping and alloimmunization risk in children with sickle cell anemia

Blood advances, 2017-08, Vol.1 (18), p.1414-1422

2017

Volltextzugriff (PDF)

The Genetic Landscape of Cerebral Steno-Occlusive Arteriopathy and Stroke in Sickle Cell Anemia

Journal of stroke and cerebrovascular diseases, 2018-11, Vol.27 (11), p.2897-2904

2018

Volltextzugriff (PDF)

The fatty acid amide hydrolase 385 A/A (P129T) variant : haplotype analysis of an ancient missense mutation and validation of risk for drug addiction

Human genetics, 2006-11, Vol.120 (4), p.581-588

2006

Volltextzugriff (PDF)

The role of BCL11A and HMIP-2 polymorphisms on endogenous and hydroxyurea induced levels of fetal hemoglobin in sickle cell anemia patients from southern Brazil

Blood cells, molecules, & diseases, 2016-11, Vol.62, p.32-37

2016

Volltextzugriff (PDF)

A novel algorithm comprehensively characterizes human RH genes using whole-genome sequencing data

Blood advances, 2020-09, Vol.4 (18), p.4347-4357

2020

Volltextzugriff (PDF)

Genotoxicity associated with hydroxyurea exposure in infants with sickle cell anemia: Results from the BABY-HUG phase III clinical trial

Pediatric blood & cancer, 2012-08, Vol.59 (2), p.254-257

2012

Volltextzugriff (PDF)

GSTM1 and Liver Iron Content in Children with Sickle Cell Anemia and Iron Overload

Journal of clinical medicine, 2019-11, Vol.8 (11), p.1878

2019

Volltextzugriff (PDF)

Chromosome damage and repair in children with sickle cell anaemia and long‐term hydroxycarbamide exposure

British journal of haematology, 2011-07, Vol.154 (1), p.134-140

2011

Volltextzugriff (PDF)

Hydroxycarbamide alters erythroid gene expression in children with sickle cell anaemia

British journal of haematology, 2012-04, Vol.157 (2), p.240-248

2012

Volltextzugriff (PDF)

Assessment of genotoxicity associated with hydroxyurea therapy in children with sickle cell anemia

Mutation research, 2010-04, Vol.698 (1), p.38-42

2010

Volltextzugriff (PDF)

Effects of Alcohol Consumption on Iron Metabolism in Mice with Hemochromatosis Mutations

Alcoholism, clinical and experimental research, 2007-01, Vol.31 (1), p.138-143

2007

Volltextzugriff (PDF)

1 – 25 von 326

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(307)
Mit Volltextzugriff
(287)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 7 Tagen
(2)
... seit 90 Tagen
(5)

Menü

Weitere Dienste

Einstellungen

Genome‐wide association study of early ischaemic stroke risk in Brazilian individuals with sickle cell disease implicates ADAMTS2 and CDK18 and uncovers novel loci

Organ-on-chips made of blood: endothelial progenitor cells from blood reconstitute vascular thromboinflammation in vessel-chips

The NLRP3 inflammasome fires up heme-induced inflammation in hemolytic conditions

Genetic Modifiers of White Blood Cell Count, Albuminuria and Glomerular Filtration Rate in Children with Sickle Cell Anemia

Noncanonical Roles of Caspase-4 and Caspase-5 in Heme-Driven IL-1β Release and Cell Death

Tripartite collaboration of blood‐derived endothelial cells, next generation RNA sequencing and bioengineered vessel‐chip may distinguish vasculopathy and thrombosis among sickle cell disease patients

Whole exome sequencing identifies novel genes for fetal hemoglobin response to hydroxyurea in children with sickle cell anemia

Pharmacokinetics, pharmacodynamics, and pharmacogenetics of hydroxyurea treatment for children with sickle cell anemia

Characterization of Cytoplasmic Caspase-2 Activation by Induced Proximity

Genetic predictors for stroke in children with sickle cell anemia

Vascular Transcriptomics: Investigating Endothelial Activation and Vascular Dysfunction Using Blood Outgrowth Endothelial Cells, Organ‐Chips, and RNA Sequencing

Genetic modifiers of sickle cell anemia in the BABY HUG cohort: influence on laboratory and clinical phenotypes

Genetic variants in toll‐like receptor 4 are associated with lack of steroid‐responsiveness in pediatric ITP patients

Genetic mapping and exome sequencing identify 2 mutations associated with stroke protection in pediatric patients with sickle cell anemia

Whole-exome sequencing for RH genotyping and alloimmunization risk in children with sickle cell anemia

The Genetic Landscape of Cerebral Steno-Occlusive Arteriopathy and Stroke in Sickle Cell Anemia

The fatty acid amide hydrolase 385 A/A (P129T) variant : haplotype analysis of an ancient missense mutation and validation of risk for drug addiction

The role of BCL11A and HMIP-2 polymorphisms on endogenous and hydroxyurea induced levels of fetal hemoglobin in sickle cell anemia patients from southern Brazil

A novel algorithm comprehensively characterizes human RH genes using whole-genome sequencing data

Genotoxicity associated with hydroxyurea exposure in infants with sickle cell anemia: Results from the BABY-HUG phase III clinical trial

GSTM1 and Liver Iron Content in Children with Sickle Cell Anemia and Iron Overload

Chromosome damage and repair in children with sickle cell anaemia and long‐term hydroxycarbamide exposure

Hydroxycarbamide alters erythroid gene expression in children with sickle cell anaemia

Assessment of genotoxicity associated with hydroxyurea therapy in children with sickle cell anemia

Effects of Alcohol Consumption on Iron Metabolism in Mice with Hemochromatosis Mutations

Suchergebnisse filtern