Jean Delaunay

Étude des proteines ribosomales des eukaryotes / (1974)

Delaunay, Jean.

Thesis (doctoral)--Université de Paris VII, 1974.

Characterization of a rat liver factor that inhibits initiation of protein synthesis in rabbit reticulocyte lysates

Delaunay, Jean, Ranu, Rajinder Singh, Levin, Daniel H., Ernst, Vivian, London, Irving M.

Protein synthesis in rabbit reticulocytes and their lysates is regulated by heme. In heme-deficient reticulocyte lysates, protein synthesis proceeds at the initial rate for several minutes and then...

Congenital Dyserythropoietic Anemia Type I Is Caused by Mutations in Codanin-1

Dgany, Orly, Avidan, Nili, Delaunay, Jean, Krasnov, Tatyana, Shalmon, Lea, Shalev, Hanna, ...

Congenital dyserythropoietic anemias (CDAs) constitute a rare group of inherited red-blood-cell disorders associated with dysplastic changes in late erythroid precursors. CDA type I (CDAI [MIM...

Characterization of a rat liver factor that inhibits initiation of protein synthesis in rabbit reticulocyte lysates

Delaunay, Jean, Ranu, Rajinder Singh, Levin, Daniel H., Ernst, Vivian, London, Irving M.

Protein synthesis in rabbit reticulocytes and their lysates is regulated by heme. In heme-deficient reticulocyte lysates, protein synthesis proceeds at the initial rate for several minutes and then...

Band 3 Courcouronnes (Ser667Phe): a trafficking mutant differentially rescued by wild-type band 3 and glycophorin A

Toye, Ashley M., Williamson, Rosalind C., Khanfar, Moudji, Bader-Meunier, Brigitte, Cynober, Thérèse, Thibault, Madeleine, ...

We describe a mutation in human erythrocyte band 3 (anion exchanger 1; SLC4A1) causing both hereditary spherocytosis and distal renal tubular acidosis. The proband developed a transfusion-dependent,...

Close to unraveling the secrets of congenital dyserythropoietic anemia types I and II

Iolascon, Achille, Delaunay, Jean

The congenital dyserythropoietic anemias are rare recessive disorders characterized by erythroblast multinuclearity, ineffective erythropoiesis, anemia and iron overload. In this perspective article,...

4.1R-deficient human red blood cells have altered phosphatidylserine exposure pathways and are deficient in CD44 and CD47 glycoproteins

Jeremy, Kris P., Plummer, Zoe E., Head, David J., Madgett, Tracey E., Sanders, Kelly L., Wallington, Amanda, ...

Phosphatidylserine exposure on the surface of the red cell membrane initiates the process of eryptosis, the red cell death program. The 4.1R protein is a phosphatidylserine binding protein. In this...