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Journal Articles

Two Distinct Mechanisms Are Responsible for Regulation of Ribosomal Protein S19 Expression Level in Diamond-Blackfan Anemia by NF-κB Pathway.

Corinne Hurtaud, PhD, Aurore Cretien, PhD, Valerie Clayette, PhD, Didier Pisani, PhD, Stephane Giraudier, MD, PhD, Thierry Leblanc, MD, Jean Delaunay, MD, PhD, Gil Tchernia, MD, Narla Mohandas, PhD, Lydie Da Costa, MD, PhD

Blood (2007) 110 (11): 1684.

https://doi.org/10.1182/blood.V110.11.1684.1684

Published: 2007

Journal Articles

Induction of GLUT1 during Erythropoiesis Triggers a Switch from Glucose to DHA Uptake in Vitamin C-Defective Mammals.

Amelie Montel-Hagen, Sandrina Kinet, PhD, Nicolas Manel, PhD, Cedric Mongellaz, Rainer Prohaska, PhD, Jean-Luc Battini, PhD, Jean Delaunay, MD PhD, Marc Sitbon, PhD, Naomi Taylor, MD PhD

Blood (2007) 110 (11): 1705.

https://doi.org/10.1182/blood.V110.11.1705.1705

Published: 2007

Journal Articles

Band 3 Courcouronne: Homozygous Mutation Ser667Phe Causes Severe Hereditary Spherocytosis and Incomplete Distal Renal Tubular Acidosis.

Jean Delaunay, MD, PhD, Ashley Toye, BSc PhD, Rosalind Williamson, BSc, Moudji Khanfar, MD, Brigitte Bader-Meunier, MD, Thérèse Cynober, MD, Madeleine Thibault, Gilbert Jean Tchernia, MD, Michèle Déchaux, MD, Lesley Bruce, BSc PhD

Blood (2006) 108 (11): 1563.

https://doi.org/10.1182/blood.V108.11.1563.1563

Published: 2006

Journal Articles

Proteasome Inhibitors Restore to Normal the Decreased Levels of Protein Expression and Nucleolar Localization of Various Mutant Ribosomal S19 Proteins Identified in DBA Patients.

Aurore Cretien, Alexis Proust, Hanna Gazda, MD, PhD, Jorg Meerpohl, MD, Charlotte Marie Niemeyer, MD, PhD, Jean Delaunay, MD, PhD, Gil Tchernia, MD, Mohandas Narla, MD, PhD, Lydie Da Costa, MD, PhD

Blood (2005) 106 (11): 185.

https://doi.org/10.1182/blood.V106.11.185.185

Published: 2005

Journal Articles

Two New Human DMT1 Mutations in a Compound Heterozygous Patient with Microcytic Anemia and Low Iron Stores.

Carole Beaumont, PhD, Jean Delaunay, MD, PhD, Gilles Hetet, Mariane de Montalembert, MD, Bernard Grandchamp, MD, PhD, Gilbert J. Tchernia, MD, PhD

Blood (2005) 106 (11): 3540.

https://doi.org/10.1182/blood.V106.11.3540.3540

Published: 2005

Journal Articles

The First Homozygous RPS19 Mutation Identified in a Diamond-Blackfan Anemia Patient Is Not Deleterious.

Aurore Cretien, Patricia Rince, Thierry Leblanc, MD, Rolande Ducrocq, MD, Alexis Proust, Isabelle Marie, Jean Delaunay, MD, PhD, Mohandas Narla, MD, PhD, Gil Tchernia, MD, Lydie Da Costa, MD, PhD

Blood (2005) 106 (11): 3548.

https://doi.org/10.1182/blood.V106.11.3548.3548

Published: 2005

NARROW

Two Distinct Mechanisms Are Responsible for Regulation of Ribosomal Protein S19 Expression Level in Diamond-Blackfan Anemia by NF-κB Pathway.

Induction of GLUT1 during Erythropoiesis Triggers a Switch from Glucose to DHA Uptake in Vitamin C-Defective Mammals.

Band 3 Courcouronne: Homozygous Mutation Ser667Phe Causes Severe Hereditary Spherocytosis and Incomplete Distal Renal Tubular Acidosis.

Proteasome Inhibitors Restore to Normal the Decreased Levels of Protein Expression and Nucleolar Localization of Various Mutant Ribosomal S19 Proteins Identified in DBA Patients.

Two New Human DMT1 Mutations in a Compound Heterozygous Patient with Microcytic Anemia and Low Iron Stores.

The First Homozygous RPS19 Mutation Identified in a Diamond-Blackfan Anemia Patient Is Not Deleterious.

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ASH Publications

American Society of Hematology

Two Distinct Mechanisms Are Responsible for Regulation of Ribosomal Protein S19 Expression Level in Diamond-Blackfan Anemia by NF-κB Pathway.

Induction of GLUT1 during Erythropoiesis Triggers a Switch from Glucose to DHA Uptake in Vitamin C-Defective Mammals.

Band 3 Courcouronne: Homozygous Mutation Ser667Phe Causes Severe Hereditary Spherocytosis and Incomplete Distal Renal Tubular Acidosis.

Proteasome Inhibitors Restore to Normal the Decreased Levels of Protein Expression and Nucleolar Localization of Various Mutant Ribosomal S19 Proteins Identified in DBA Patients.

Two New Human DMT1 Mutations in a Compound Heterozygous Patient with Microcytic Anemia and Low Iron Stores.

The First Homozygous RPS19 Mutation Identified in a Diamond-Blackfan Anemia Patient Is Not Deleterious.

Email alerts

ASH Publications

American Society of Hematology

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