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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

78 related articles for article (PubMed ID: 6930874)

  • 1. Proteolysis in thalassemia: studies with protease inhibitors.
    Loukopoulos D; Karoulias A; Fessas P
    Ann N Y Acad Sci; 1980; 344():323-35. PubMed ID: 6930874
    [TBL] [Abstract][Full Text] [Related]  

  • 2. ATP-dependent proteolysis of hemoglobin alpha chains in beta-thalassemic hemolysates is ubiquitin-dependent.
    Shaeffer JR
    J Biol Chem; 1988 Sep; 263(27):13663-9. PubMed ID: 2843527
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Evidence for increased proteolysis in intact beta thalassemia erythroid cells.
    Braverman AS; Lester D
    Hemoglobin; 1981; 5(6):549-64. PubMed ID: 7319826
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Turnover of excess hemoglobin alpha chains in beta-thalassemic cells is ATP-dependent.
    Shaeffer JR
    J Biol Chem; 1983 Nov; 258(21):13172-7. PubMed ID: 6195159
    [TBL] [Abstract][Full Text] [Related]  

  • 5. AMINO ACIDS: INCORPORATION INTO ALPHA- AND BETA-CHAINS OF HEMOGLOBIN BY NORMAL AND THALASSEMIC RETICULOCYTES.
    HEYWOOD JD; KARON M; WEISSMAN S
    Science; 1964 Oct; 146(3643):530-1. PubMed ID: 14190243
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Proteolytic activity in erythrocyte precursors.
    Hanash SM; Rucknagel DL
    Proc Natl Acad Sci U S A; 1978 Jul; 75(7):3427-31. PubMed ID: 277945
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Globin synthesis in fractionated Normoblasts of beta-thalassemia heterozygotes.
    Wood WG; Stamatoyannopoulos G
    J Clin Invest; 1975 Mar; 55(3):567-78. PubMed ID: 1167870
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Absence of functional beta-globin messenger RNA in Kurdish Jews with beta0-thalassemia.
    Di Segni G; Kerem H; Cividalli G; Rachmilewitz EA; Kaempfer R
    Isr J Med Sci; 1978 Nov; 14(11):1116-23. PubMed ID: 750536
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Oxidative denaturation of red blood cells in thalassemia.
    Shinar E; Rachmilewitz EA
    Semin Hematol; 1990 Jan; 27(1):70-82. PubMed ID: 2405497
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cellular and membrane properties of alpha and beta thalassemic erythrocytes are different: implication for differences in clinical manifestations.
    Schrier SL; Rachmilewitz E; Mohandas N
    Blood; 1989 Nov; 74(6):2194-202. PubMed ID: 2804358
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Post-translational control of human hemoglobin synthesis: the role of the differential affinity between globin chains in the control of mutated globin gene expression.
    Mavilio F; Marinucci M; Guerriero R; Cappellozza G; Tentori L
    Biochim Biophys Acta; 1980 Dec; 610(2):339-51. PubMed ID: 7213630
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Abnormal red cell membrane proteolytic activity in severe heterozygous beta-thalassemia.
    Ballas SK; Burka ER; Gill FM
    J Lab Clin Med; 1982 Feb; 99(2):263-74. PubMed ID: 7038010
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fate of alpha-hemoglobin chains and erythrocyte defects in beta-thalassemia.
    Rouyer-Fessard P; Scott MD; Leroy-Viard K; Garel MC; Bachir D; Galacteros F; Beuzard Y
    Ann N Y Acad Sci; 1990; 612():106-17. PubMed ID: 2291540
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Differences in the pathophysiology of hemolysis of alpha- and beta-thalassemic red blood cells.
    Shinar E; Rachmilewitz EA
    Ann N Y Acad Sci; 1990; 612():118-26. PubMed ID: 2291541
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Excess alpha chains are lost from beta-thalassemic reticulocytes by proteolysis.
    Testa U; Hinard N; Beuzard Y; Tsapis A; Galacteros F; Thomopoulos P; Rosa J
    J Lab Clin Med; 1981 Sep; 98(3):352-63. PubMed ID: 7021718
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Erythrocytic proteases: preferential degradation of alpha hemoglobin chains.
    Vettore L; De Matteis MC; Di Iorio EE; Winterhalter KH
    Acta Haematol; 1983; 70(1):35-42. PubMed ID: 6408866
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Excess of alpha-globin synthesis in homozygous beta-thalassemia. Its cytoplasmic molecular forms.
    Conconi F; Bargellesi A; Pontremoli S
    Eur J Biochem; 1968 Aug; 5(3):409-14. PubMed ID: 5680358
    [No Abstract]   [Full Text] [Related]  

  • 18. Hemoglobin Indianapolis (beta 112[G14] arginine). An unstable beta-chain variant producing the phenotype of severe beta-thalassemia.
    Adams JG; Boxer LA; Baehner RL; Forget BG; Tsistrakis GA; Steinberg MH
    J Clin Invest; 1979 May; 63(5):931-8. PubMed ID: 447835
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A soluble ATP-dependent proteolytic system responsible for the degradation of abnormal proteins in reticulocytes.
    Etlinger JD; Goldberg AL
    Proc Natl Acad Sci U S A; 1977 Jan; 74(1):54-8. PubMed ID: 264694
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ubiquitin aldehyde increases adenosine triphosphate-dependent proteolysis of hemoglobin alpha-subunits in beta-thalassemic hemolysates.
    Shaeffer JR; Cohen RE
    Blood; 1997 Aug; 90(3):1300-8. PubMed ID: 9242565
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.