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 *

168 related articles for article (PubMed ID: 20595515)

  • 1. Sickle cell disease resulting from uniparental disomy in a child who inherited sickle cell trait.
    Swensen JJ; Agarwal AM; Esquilin JM; Swierczek S; Perumbeti A; Hussey D; Lee M; Joiner CH; Pont-Kingdon G; Lyon E; Prchal JT
    Blood; 2010 Oct; 116(15):2822-5. PubMed ID: 20595515
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Modification of hemoglobin H disease by sickle trait.
    Matthay KK; Mentzer WC; Dozy AM; Kan YW; Bainton DF
    J Clin Invest; 1979 Oct; 64(4):1024-32. PubMed ID: 479366
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A late onset sickle cell disease reveals a mosaic segmental uniparental isodisomy of chromosome 11p15.
    Vinatier I; Martin X; Costa JM; Bazin A; Giraudier S; Joly P
    Blood Cells Mol Dis; 2015 Jan; 54(1):53-5. PubMed ID: 25159120
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Evaluation of high performance liquid chromatography (HPLC) pattern and prevalence of beta-thalassaemia trait among sickle cell disease patients in Lagos, Nigeria.
    Adeyemo T; Ojewunmi O; Oyetunji A
    Pan Afr Med J; 2014; 18():71. PubMed ID: 25400838
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Sickle cell anemia associated with alpha-thalassemia in Malaysian Indians.
    Lie-Injo LE; Hassan K; Joishy SK; Lim ML
    Am J Hematol; 1986 Jul; 22(3):265-74. PubMed ID: 2424302
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic model for observed distributions of proportions of haemoglobin in sickle-cell trait.
    Brittenham G
    Nature; 1977 Aug; 268(5621):635-6. PubMed ID: 895858
    [No Abstract]   [Full Text] [Related]  

  • 8. Optimal haematocrit in subjects with normal haemoglobin genotype (HbAA), sickle cell trait (HbAS), and homozygous sickle cell disease (HbSS).
    Bowers AS; Pepple DJ; Reid HL
    Clin Hemorheol Microcirc; 2011; 47(4):253-60. PubMed ID: 21654054
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease.
    Raffield LM; Ulirsch JC; Naik RP; Lessard S; Handsaker RE; Jain D; Kang HM; Pankratz N; Auer PL; Bao EL; Smith JD; Lange LA; Lange EM; Li Y; Thornton TA; Young BA; Abecasis GR; Laurie CC; Nickerson DA; McCarroll SA; Correa A; Wilson JG; ; Lettre G; Sankaran VG; Reiner AP
    PLoS Genet; 2018 Mar; 14(3):e1007293. PubMed ID: 29590102
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Cellular function reinstitution of offspring red blood cells cloned from the sickle cell disease patient blood post CRISPR genome editing.
    Wen J; Tao W; Hao S; Zu Y
    J Hematol Oncol; 2017 Jun; 10(1):119. PubMed ID: 28610635
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Sickle cell traits in Canada. Trimodal distribution of Hb S as a result of interaction with alpha-thalassaemia gene.
    Wong SC; Ali MA; Boyadjian SE
    Acta Haematol; 1981; 65(3):157-63. PubMed ID: 6165216
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hemoglobin synthesis studies of a family with alpha-thalassemia trait and sickle cell trait.
    Shaeffer JR; DeSimone J; Kleve LJ
    Biochem Genet; 1975 Dec; 13(11-12):783-8. PubMed ID: 1200978
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Production of Gene-Corrected Adult Beta Globin Protein in Human Erythrocytes Differentiated from Patient iPSCs After Genome Editing of the Sickle Point Mutation.
    Huang X; Wang Y; Yan W; Smith C; Ye Z; Wang J; Gao Y; Mendelsohn L; Cheng L
    Stem Cells; 2015 May; 33(5):1470-9. PubMed ID: 25702619
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Efficacy of Rapamycin as Inducer of Hb F in Primary Erythroid Cultures from Sickle Cell Disease and β-Thalassemia Patients.
    Pecoraro A; Troia A; Calzolari R; Scazzone C; Rigano P; Martorana A; Sacco M; Maggio A; Di Marzo R
    Hemoglobin; 2015; 39(4):225-9. PubMed ID: 26016899
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical and molecular correlations in the sickle/beta+-thalassemia syndrome.
    Atweh GF; Forget BG
    Am J Hematol; 1987 Jan; 24(1):31-6. PubMed ID: 3799593
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spontaneous erythroid colony formation in Brazilian patients with sickle cell disease.
    Perlingeiro RC; Costa FF; Saad ST; Arruda VR; Queiroz ML
    Am J Hematol; 1999 May; 61(1):40-5. PubMed ID: 10331510
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sickle cell-Hb Lepore Boston syndrome. Uncommon differential diagnosis to homozygous sickle cell disease.
    Stevens MC; Lehmann H; Mason KP; Serjeant BE; Serjeant GR
    Am J Dis Child; 1982 Jan; 136(1):19-22. PubMed ID: 7055103
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Textural differences between AA and SS blood specimens as detected by image analysis.
    Robinson RD; Benjamin LJ; Cosgriff JM; Cox C; Lapets OP; Rowley PT; Yatco E; Wheeless LL
    Cytometry; 1994 Oct; 17(2):167-72. PubMed ID: 7835167
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Abnormal haemoglobins in the Sudan savanna of Nigeria. I. Prevalence of haemoglobins and relationships between sickle cell trait, malaria and survival.
    Fleming AF; Storey J; Molineaux L; Iroko EA; Attai ED
    Ann Trop Med Parasitol; 1979 Apr; 73(2):161-72. PubMed ID: 315211
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.