These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
197 related articles for article (PubMed ID: 18477769)
1. Vascular dysfunction in a murine model of severe hemolysis. Frei AC; Guo Y; Jones DW; Pritchard KA; Fagan KA; Hogg N; Wandersee NJ Blood; 2008 Jul; 112(2):398-405. PubMed ID: 18477769 [TBL] [Abstract][Full Text] [Related]
2. Mutations in the murine erythroid alpha-spectrin gene alter spectrin mRNA and protein levels and spectrin incorporation into the red blood cell membrane skeleton. Wandersee NJ; Birkenmeier CS; Bodine DM; Mohandas N; Barker JE Blood; 2003 Jan; 101(1):325-30. PubMed ID: 12393645 [TBL] [Abstract][Full Text] [Related]
3. Murine recessive hereditary spherocytosis, sph/sph, is caused by a mutation in the erythroid alpha-spectrin gene. Wandersee NJ; Birkenmeier CS; Gifford EJ; Mohandas N; Barker JE Hematol J; 2000; 1(4):235-42. PubMed ID: 11920196 [TBL] [Abstract][Full Text] [Related]
4. Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis. Wandersee NJ; Roesch AN; Hamblen NR; de Moes J; van der Valk MA; Bronson RT; Gimm JA; Mohandas N; Demant P; Barker JE Blood; 2001 Jan; 97(2):543-50. PubMed ID: 11154235 [TBL] [Abstract][Full Text] [Related]
6. Hematopoietic cells from -spectrin-deficient mice are sufficient to induce thrombotic events in hematopoietically ablated recipients. Wandersee NJ; Lee JC; Kaysser TM; Bronson RT; Barker JE Blood; 1998 Dec; 92(12):4856-63. PubMed ID: 9845553 [TBL] [Abstract][Full Text] [Related]
7. Sickle cell anemia and vascular dysfunction: the nitric oxide connection. Akinsheye I; Klings ES J Cell Physiol; 2010 Sep; 224(3):620-5. PubMed ID: 20578237 [TBL] [Abstract][Full Text] [Related]
8. Hemolysis in sickle cell mice causes pulmonary hypertension due to global impairment in nitric oxide bioavailability. Hsu LL; Champion HC; Campbell-Lee SA; Bivalacqua TJ; Manci EA; Diwan BA; Schimel DM; Cochard AE; Wang X; Schechter AN; Noguchi CT; Gladwin MT Blood; 2007 Apr; 109(7):3088-98. PubMed ID: 17158223 [TBL] [Abstract][Full Text] [Related]
9. Reduced incidence of thrombosis in mice with hereditary spherocytosis following neonatal treatment with normal hematopoietic cells. Wandersee NJ; Lee JC; Deveau SA; Barker JE Blood; 2001 Jun; 97(12):3972-5. PubMed ID: 11389042 [TBL] [Abstract][Full Text] [Related]
10. Nitrite reductase activity of hemoglobin as a systemic nitric oxide generator mechanism to detoxify plasma hemoglobin produced during hemolysis. Minneci PC; Deans KJ; Shiva S; Zhi H; Banks SM; Kern S; Natanson C; Solomon SB; Gladwin MT Am J Physiol Heart Circ Physiol; 2008 Aug; 295(2):H743-54. PubMed ID: 18552166 [TBL] [Abstract][Full Text] [Related]
11. Increased erythrocyte adhesion in mice and humans with hereditary spherocytosis and hereditary elliptocytosis. Wandersee NJ; Olson SC; Holzhauer SL; Hoffmann RG; Barker JE; Hillery CA Blood; 2004 Jan; 103(2):710-6. PubMed ID: 12947004 [TBL] [Abstract][Full Text] [Related]
12. The clinical sequelae of intravascular hemolysis and extracellular plasma hemoglobin: a novel mechanism of human disease. Rother RP; Bell L; Hillmen P; Gladwin MT JAMA; 2005 Apr; 293(13):1653-62. PubMed ID: 15811985 [TBL] [Abstract][Full Text] [Related]
13. Erythropoiesis in ha/ha and sph/sph mice, mutants which produce spectrin-deficient erythrocytes. Brookoff D; Maggio-Price L; Bernstein S; Weiss L Blood; 1982 Mar; 59(3):646-51. PubMed ID: 7059672 [TBL] [Abstract][Full Text] [Related]
14. Role of the red blood cell in nitric oxide homeostasis and hypoxic vasodilation. Gladwin MT Adv Exp Med Biol; 2006; 588():189-205. PubMed ID: 17089890 [TBL] [Abstract][Full Text] [Related]
16. Impairment of Nitric Oxide Pathway by Intravascular Hemolysis Plays a Major Role in Mice Esophageal Hypercontractility: Reversion by Soluble Guanylyl Cyclase Stimulator. Henrique Silva F; Yotsumoto Fertrin K; Costa Alexandre E; Beraldi Calmasini F; Fernanda Franco-Penteado C; Ferreira Costa F J Pharmacol Exp Ther; 2018 Nov; 367(2):194-202. PubMed ID: 30108160 [TBL] [Abstract][Full Text] [Related]
17. Spectrin deficient inherited hemolytic anemias in the mouse: characterization by spectrin synthesis and mRNA activity in reticulocytes. Bodine DM; Birkenmeier CS; Barker JE Cell; 1984 Jul; 37(3):721-9. PubMed ID: 6234993 [TBL] [Abstract][Full Text] [Related]
18. Identification of quantitative trait loci that modify the severity of hereditary spherocytosis in wan, a new mouse model of band-3 deficiency. Peters LL; Swearingen RA; Andersen SG; Gwynn B; Lambert AJ; Li R; Lux SE; Churchill GA Blood; 2004 Apr; 103(8):3233-40. PubMed ID: 15070709 [TBL] [Abstract][Full Text] [Related]
19. Abnormal oxidant sensitivity and beta-chain structure of spectrin in hereditary spherocytosis associated with defective spectrin-protein 4.1 binding. Becker PS; Morrow JS; Lux SE J Clin Invest; 1987 Aug; 80(2):557-65. PubMed ID: 3611357 [TBL] [Abstract][Full Text] [Related]