Increased levels of endothelin-1 in plasma of sickle cell anemia patients

AC Rybicki, LJ Benjamin - Blood, The Journal of the American …, 1998 - ashpublications.org
AC Rybicki, LJ Benjamin
Blood, The Journal of the American Society of Hematology, 1998ashpublications.org
1. Iolascon A, D'Agostaro G, Perrotta S, Izzo P, Tavano R, Miraglia del Giudice E: Congenital
dyserythropoietic anemia type II: Molecular basis and clinical aspects. Haematologica 81:
543, 1996 2. Wong KY, Hug G, Lampkin BC: Congenital dyserythropoietic anemia type II.
Ultrastructural and radioautographic studies of blood and bone marrow. Blood 39: 23, 1972
3. Alloisio N, Texier P, Denoroy L, Berger C, Miraglia del Giudice E, Perrotta S, Iolascon A,
Gilsanz F, Berger G, Guichard J, Massé JM, Debili N, Breton-Gorlus J, Delaunay J: The …
1. Iolascon A, D’Agostaro G, Perrotta S, Izzo P, Tavano R, Miraglia del Giudice E: Congenital dyserythropoietic anemia type II: Molecular basis and clinical aspects. Haematologica 81: 543, 1996 2. Wong KY, Hug G, Lampkin BC: Congenital dyserythropoietic anemia type II. Ultrastructural and radioautographic studies of blood and bone marrow. Blood 39: 23, 1972 3. Alloisio N, Texier P, Denoroy L, Berger C, Miraglia del Giudice E, Perrotta S, Iolascon A, Gilsanz F, Berger G, Guichard J, Massé JM, Debili N, Breton-Gorlus J, Delaunay J: The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulum. Blood 87: 4433, 1996 4. Iolascon A, Miraglia del Giudice E, Perrotta S, Granatiero M, Zelante L, Gasparini P: Exclusion of three candidate genes as determinants of congenital dyserithropoietic anemia type II (CDA II). Blood 90: 4197, 1997
5. Gasparini P, Miraglia del Giudice E, Delaunay J, Totaro A, Granatiero M, Melchionda S, Zelante L, Iolascon A: Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11. 2 by genomewide search. Am J Hum Genet 61: 1112, 1997 6. Fukuda MN, Dell A, Scartezzini P: Primary defect congenital dyserythropoietic anemia type II: Failure in glycosylation of erythrocyte lactosaminoglycan proteins caused by lowered N acetylglucosaminyltransferase II. J Biol Chem 262: 7195, 1987 7. Fukuda MN, Masri KA, Dell A, Luzzatto L, Moremen KW: Incomplete synthesis of N-glycans in congenital dyserythropoietic anemia type II (HEMPAS) caused by a gene defect encoding a mannosidase II. Proc Natl Acad Sci USA 87: 7443, 1990
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