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.
6. Remarks on the hemoglobin molecule, thalassemia and unstable hemoglobins. Lehmann H Humangenetik; 1970; 9(3):224-6. PubMed ID: 5451686 [No Abstract] [Full Text] [Related]
7. [The unstable hemoglobins]. Labie D Ann Biol Clin (Paris); 1970; 28(4):283-5. PubMed ID: 5491549 [No Abstract] [Full Text] [Related]
8. Denaturation of the normal and abnormal hemoglobin molecule. Rachmilewitz EA Semin Hematol; 1974 Oct; 11(4):441-62. PubMed ID: 4371697 [No Abstract] [Full Text] [Related]
9. Altered sulfhydryl reactivity of hemoglobins and red blood cell membranes in congenital Heinz body hemolytic anemia. Jacob HS; Brain MC; Dacie JV J Clin Invest; 1968 Dec; 47(12):2664-77. PubMed ID: 5725279 [TBL] [Abstract][Full Text] [Related]
10. Mechanisms of hemoglobin precipitation into Heinz bodies: possible relevance to cataract formation. Jacob HS Exp Eye Res; 1971 May; 11(3):356-64. PubMed ID: 4941677 [No Abstract] [Full Text] [Related]
12. The unstable hemoglobins--molecular and clinical features. White JM; Dacie JV Prog Hematol; 1971; 7(0):69-109. PubMed ID: 4950839 [No Abstract] [Full Text] [Related]
13. Mechanisms of Heinz body formation and attachment to red cell membrane. Jacob HS Semin Hematol; 1970 Jul; 7(3):341-54. PubMed ID: 5425759 [No Abstract] [Full Text] [Related]
14. Alterations of red cell membrane proteins and hemoglobin under natural and experimental oxidant stress. Alloisio N; Michelon D; Bannier E; Revol A; Beuzard Y; Delaunay J Biochim Biophys Acta; 1982 Oct; 691(2):300-8. PubMed ID: 7138863 [No Abstract] [Full Text] [Related]
16. The role of hemoglobin heme loss in Heinz body formation: studies with a partially heme-deficient hemoglobin and with genetically unstable hemoglobins. Jacob HS; Winterhalter KH J Clin Invest; 1970 Nov; 49(11):2008-16. PubMed ID: 5475984 [TBL] [Abstract][Full Text] [Related]
19. [Anomalous unstable hemoglobins, a special group of hereditary hemolytic anemias (survey of the literature and the authors' own data]. Didkovskiĭ NA; Filippova AV; Idel'son LI Probl Gematol Pereliv Krovi; 1972 Nov; 17(11):38-46. PubMed ID: 4356586 [No Abstract] [Full Text] [Related]
20. A novel silent posttranslational mechanism converts methionine to aspartate in hemoglobin Bristol (beta 67[E11] Val-Met->Asp). Rees DC; Rochette J; Schofield C; Green B; Morris M; Parker NE; Sasaki H; Tanaka A; Ohba Y; Clegg JB Blood; 1996 Jul; 88(1):341-8. PubMed ID: 8704193 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]