BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

409 related articles for article (PubMed ID: 3965046)

  • 1. Hemoglobin S polymerization: primary determinant of the hemolytic and clinical severity of the sickling syndromes.
    Brittenham GM; Schechter AN; Noguchi CT
    Blood; 1985 Jan; 65(1):183-9. PubMed ID: 3965046
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Intracellular polymerization of sickle hemoglobin: disease severity and therapeutic goals.
    Noguchi CT; Rodgers GP; Schechter AN
    Prog Clin Biol Res; 1987; 240():381-91. PubMed ID: 3615501
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Non-uniformity of intracellular polymer formation in sickle erythrocytes: possible correlation with severity of hemolytic anemia.
    Noguchi CT; Schechter AN
    Am J Pediatr Hematol Oncol; 1984; 6(1):46-50. PubMed ID: 6711762
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Overview of pathophysiology and rationale for treatment of sickle cell anemia.
    Rodgers GP
    Semin Hematol; 1997 Jul; 34(3 Suppl 3):2-7. PubMed ID: 9317195
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The interaction of coexistent alpha-thalassemia and sickle cell anemia: a model for the clinical and cellular results of diminished polymerization?
    Embury SH
    Ann N Y Acad Sci; 1985; 445():37-44. PubMed ID: 3893275
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Hemoglobin S as the cause of primary hyperviscosity of the blood].
    Mosca A; Samaja M; Niggeler M; Rossi-Bernardi L
    Ric Clin Lab; 1983; 13 Suppl 3():115-20. PubMed ID: 6672990
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Rapid and reproducible characterization of sickling during automated deoxygenation in sickle cell disease patients.
    Rab MAE; van Oirschot BA; Bos J; Merkx TH; van Wesel ACW; Abdulmalik O; Safo MK; Versluijs BA; Houwing ME; Cnossen MH; Riedl J; Schutgens REG; Pasterkamp G; Bartels M; van Beers EJ; van Wijk R
    Am J Hematol; 2019 May; 94(5):575-584. PubMed ID: 30784099
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Quantitative prediction of erythrocyte sickling for the development of advanced sickle cell therapies.
    Lu L; Li Z; Li H; Li X; Vekilov PG; Karniadakis GE
    Sci Adv; 2019 Aug; 5(8):eaax3905. PubMed ID: 31457104
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Intracellular polymerization of sickle hemoglobin. Effects of cell heterogeneity.
    Noguchi CT; Torchia DA; Schechter AN
    J Clin Invest; 1983 Sep; 72(3):846-52. PubMed ID: 6886006
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Intracellular polymerization. Disease severity and therapeutic predictions.
    Noguchi CT; Rodgers GP; Schechter AN
    Ann N Y Acad Sci; 1989; 565():75-82. PubMed ID: 2476066
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Determination of deoxyhemoglobin S polymer in sickle erythrocytes upon deoxygenation.
    Noguchi CT; Torchia DA; Schechter AN
    Proc Natl Acad Sci U S A; 1980 Sep; 77(9):5487-91. PubMed ID: 6933568
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Solidity of sickle hemoglobin gels: relevance to pathophysiology of sickling disorders.
    Danish EH; Harris JW; Oh K
    Cleve Clin J Med; 1989; 56(8):793-800. PubMed ID: 2605778
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian Prospective Study on Sickle Cell Disease.
    Maier-Redelsperger M; Noguchi CT; de Montalembert M; Rodgers GP; Schechter AN; Gourbil A; Blanchard D; Jais JP; Ducrocq R; Peltier JY
    Blood; 1994 Nov; 84(9):3182-8. PubMed ID: 7524767
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rate of deoxygenation modulates rheologic behavior of sickle red blood cells at a given mean corpuscular hemoglobin concentration.
    Kaul DK; Liu XD
    Clin Hemorheol Microcirc; 1999; 21(2):125-35. PubMed ID: 10599596
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Effects of a single sickling event on the mechanical fragility of sickle cell trait erythrocytes.
    Presley TD; Perlegas AS; Bain LE; Ballas SK; Nichols JS; Sabio H; Gladwin MT; Kato GJ; Kim-Shapiro DB
    Hemoglobin; 2010; 34(1):24-36. PubMed ID: 20113285
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Determination of sickle hemoglobin polymer in SS and AS erythrocytes.
    Noguchi CT; Torchia DA; Schechter AN
    Blood Cells; 1982; 8(2):225-35. PubMed ID: 7159747
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Intracellular hemoglobin S polymerization and the clinical severity of sickle cell anemia.
    Poillon WN; Kim BC; Castro O
    Blood; 1998 Mar; 91(5):1777-83. PubMed ID: 9473246
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sickle cell syndromes. I. Hemoglobin SC-alpha-thalassemia.
    Honig GR; Gunay U; Mason RG; Vida LN; Ferenc C
    Pediatr Res; 1976 Jun; 10(6):613-20. PubMed ID: 1272638
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Characterization of Sickling During Controlled Automated Deoxygenation with Oxygen Gradient Ektacytometry.
    Rab MAE; van Oirschot BA; Bos J; Kanne CK; Sheehan VA; van Beers EJ; van Wijk R
    J Vis Exp; 2019 Nov; (153):. PubMed ID: 31762454
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Effects of carbon dioxide and pH variations in vitro on blood respiratory functions, red blood cell volume, transmembrane pH gradients, and sickling in sickle cell anemia.
    Ueda Y; Bookchin RM
    J Lab Clin Med; 1984 Aug; 104(2):146-59. PubMed ID: 6431043
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.