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    Results: 1 to 20 of 135

    1.

    Molecular genetics of human hemoglobin synthesis.

    Forget BG.

    Ann Intern Med. 1979 Oct;91(4):605-16. Review.PMID: 384860 [PubMed - indexed for MEDLINE]Related articles

    2.

    The alpha / beta and alpha 2 / alpha 1-globin mRNA ratios in different forms of alpha-thalassemia.

    Smetanina NS, Leonova JY, Levy N, Huisman TH.

    Biochim Biophys Acta. 1996 Apr 12;1315(3):188-92.PMID: 8611658 [PubMed - indexed for MEDLINE]Related articles

    3.

    Disorders of the synthesis of human fetal hemoglobin.

    Manca L, Masala B.

    IUBMB Life. 2008 Feb;60(2):94-111. Review.PMID: 18379999 [PubMed - indexed for MEDLINE]Related articles

    4.

    Molecular analysis of Hb Q-H disease and Hb Q-Hb E in a Singaporean family.

    Tan J, Tay JS, Wong YC, Kham SK, Bte Abd Aziz N, Teo SH, Wong HB.

    Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:252-6.PMID: 8629117 [PubMed - indexed for MEDLINE]Related articles

    5.

    Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area?

    Ottolenghi S, Giglioni B, Taramelli R, Comi P, Mazza U, Saglio G, Camaschella C, Izzo P, Cao A, Galanello R, Gimferrer E, Baiget M, Gianni AM.

    Proc Natl Acad Sci U S A. 1982 Apr;79(7):2347-51.PMID: 6179097 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Disorders of human hemoglobin.

    Bank A, Mears JG, Ramirez F.

    Science. 1980 Feb 1;207(4430):486-93.PMID: 7352255 [PubMed - indexed for MEDLINE]Related articles

    7.

    Identification of a nondeletion defect in alpha-thalassemia.

    Kan YW, Dozy AM, Trecartin R, Todd D.

    N Engl J Med. 1977 Nov 17;297(20):1081-4.PMID: 909565 [PubMed - indexed for MEDLINE]Related articles

    8.

    Genetic disorders of human haemoglobin as models for analysing gene regulation.

    Weatherall DJ, Higgs DH, Wood WG, Clegg JB.

    Philos Trans R Soc Lond B Biol Sci. 1984 Dec 4;307(1132):247-59.PMID: 6084252 [PubMed - indexed for MEDLINE]Related articles

    9.

    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 11;610(2):339-51.PMID: 7213630 [PubMed - indexed for MEDLINE]Related articles

    10.

    Molecular basis for alpha-thalassemia associated with the structural mutant hemoglobin Suan-Dok (alpha 2 109leu----arg)

    Weiss I, Cash FE, Coleman MB, Pressley A, Adams JG, Sanguansermsri T, Liebhaber SA, Steinberg MH.

    Blood. 1990 Dec 15;76(12):2630-6. Erratum in: Blood 1991 Mar 15;77(6):1404. PMID: 2265255 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    Hemoglobin constitution of double heterozygotes for alpha or beta-thalassemia and Hb J Sardegna.

    Maccioni L, Galanello R, Melis MA, Cao A.

    Hemoglobin. 1984;8(5):497-507.PMID: 6548732 [PubMed - indexed for MEDLINE]Related articles

    12.

    Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies.

    Traeger-Synodinos J, Papassotiriou I, Metaxotou-Mavrommati A, Vrettou C, Stamoulakatou A, Kanavakis E.

    Blood Cells Mol Dis. 2000 Aug;26(4):276-84.PMID: 11042028 [PubMed - indexed for MEDLINE]Related articles

    13.

    Molecular pathology of alpha-thalassemia.

    Kan YW.

    Ann N Y Acad Sci. 1985;445:28-36.PMID: 3860131 [PubMed - indexed for MEDLINE]Related articles

    14.

    Thalassemic hemoglobinopathies.

    Steinberg MH, Adams JG.

    Am J Pathol. 1983 Dec;113(3):396-409. Review.PMID: 6359893 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    Beta-thalassemia intermedia with exceptionally high hemoglobin A2: relationship to mutations in the beta-gene promoter.

    Coleman MB, Adams JG 3rd, Plonczynski MW, Harrell AH, Walker AM, Fairbanks V, Steinberg MH.

    Am J Med Sci. 1992 Aug;304(2):73-8.PMID: 1380206 [PubMed - indexed for MEDLINE]Related articles

    16.

    A rare 33 bp in-frame deletion (alpha63-74 or alpha64-74 or alpha65-75) in the alpha1-globin gene causing alpha(+)-thalassemia: a second observation.

    Dimisianos G, Traeger-Synodinos J, Vrettou C, Papassotiriou I, Kanavakis E.

    Hemoglobin. 2004 May;28(2):137-43.PMID: 15182056 [PubMed - indexed for MEDLINE]Related articles

    17.

    Laboratory investigation of hemoglobinopathies and thalassemias: review and update.

    Clarke GM, Higgins TN.

    Clin Chem. 2000 Aug;46(8 Pt 2):1284-90. Review.PMID: 10926923 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Molecular basis of hereditary persistence of fetal hemoglobin.

    Forget BG.

    Ann N Y Acad Sci. 1998 Jun 30;850:38-44. Review.PMID: 9668525 [PubMed - indexed for MEDLINE]Related articles

    19.

    Thalassemia: recent insights into molecular mechanisms.

    Steinberg MH, Adams JG 3rd.

    Am J Hematol. 1982 Feb;12(1):81-92. Review.PMID: 6278929 [PubMed - indexed for MEDLINE]Related articles

    20.

    Linkage of alpha G-Philadelphia to alpha-thalassemia in African-Americans .

    Surrey S, Ohene-Frempong K, Rappaport E, Atwater J, Schwartz E.

    Proc Natl Acad Sci U S A. 1980 Aug;77(8):4885-9.PMID: 6933536 [PubMed - indexed for MEDLINE]Related articlesFree article

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