BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

123 related articles for article (PubMed ID: 31657650)

  • 1. A Kindred with a β-Globin Base Substitution [β89(F5)Ser→Arg (AG
    Shomali W; Brar R; Arekapudi SR; Gotlib JR
    Hemoglobin; 2019; 43(4-5):273-276. PubMed ID: 31657650
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel base change leading to Hb Vanderbilt [β89(F5)Ser→Arg, AGT>AGA].
    Goodyer MJ; Elhassadi EI; Percy MJ; McMullin MF
    Hemoglobin; 2011; 35(4):428-9. PubMed ID: 21797710
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A Novel Hemoglobin Variant Associated with Congenital Erythrocytosis: Hb Seoul [β86(F2)Ala→Thr] (HBB:c.259G>A).
    Shin SY; Bang SM; Kim HJ
    Ann Clin Lab Sci; 2016 May; 46(3):312-4. PubMed ID: 27312559
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hb Nebraska [β86(F2)Ala→Ile (HBB:c.259G>A;260C>T)]: a unique high oxygen affinity hemoglobin variant with a double nucleotide substitution within the same codon.
    Hoyer JD; Wendt PC; Hogan WJ; Oliveira JL
    Hemoglobin; 2011; 35(1):22-7. PubMed ID: 21250878
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Erythrocytosis due to a combination of the high oxygen affinity hemoglobin variant, Hb Olympia [beta20(B2)Val-->Met] with beta- and alpha-thalassemia mutations: first case in the literature.
    Kalotychou V; Tzanetea R; Konstantopoulos K; Papassotiriou I; Rombos I
    Hemoglobin; 2010; 34(4):383-8. PubMed ID: 20642336
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hb Cambridge-MA [β144(HC1)-β146(HC3)Lys-Tyr-His→0 (HBB c.433 A>T)]: a new high oxygen affinity variant.
    Oliveira JL; Swanson K; Wendt P; Caughey TD; Hoyer JD
    Hemoglobin; 2010; 34(6):565-71. PubMed ID: 21077764
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A Clinical Update of the Hb Siirt [β27(B9)Ala→Gly; HBB: c.83C>G] Hemoglobin Variant.
    Cappabianca MP; Colosimo A; Sabatucci A; Dainese E; Di Biagio P; Piscitelli R; Sarra O; Zei D; Amato A
    Hemoglobin; 2017 Jan; 41(1):53-55. PubMed ID: 28391745
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A new high affinity variant Hb Aurillac (β141Leu→Val).
    Boursier G; Trouillier S; Blaizot MG; Igual H; Schved JF; Martinez PA
    Hemoglobin; 2013; 37(6):584-8. PubMed ID: 23859762
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Compound heterozygous Hb Tak/Hb E causes secondary erythrocytosis in a Thai family.
    Teawtrakul N; Sirijirachai C; Chansung G; Fucharoen G
    Hemoglobin; 2010 Jan; 34(2):165-8. PubMed ID: 20353353
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A Novel β-Globin Chain Hemoglobin Variant, Hb Allentown [β137(H15)Val→Trp (GTG>TGG) HBB: c.412_413delinsTG, p.Val138Trp], Associated with Low Oxygen Saturation, Intermittent Aplastic Crises and Splenomegaly.
    Collier AB; Coon LM; Monteleone P; Umaru S; Swanson KC; Hoyer JD; Oliveira JL
    Hemoglobin; 2016; 40(2):130-3. PubMed ID: 26681102
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Hb Bakersfield (HBA1: c.151_152insGGAGCC): The Insertion of Arg-His Between Codons 49 and 50 of the α1-Globin Chain Leads to Increased Oxygen Affinity.
    Brunner-Agten S; von Känel T; Röthlisberger B; Broquet C; Huber AR
    Hemoglobin; 2017 Jan; 41(1):1-5. PubMed ID: 28532286
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hb Grove City [β38(C4)Thr→Ser, ACC>AGC; HBB: c.116C>G]: a new low oxygen affinity β chain variant.
    Taliercio RM; Ashton RW; Horwitz L; Swanson KC; Wendt PC; Hoyer JD; Oliveira JL
    Hemoglobin; 2013; 37(4):396-403. PubMed ID: 23651408
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Familial polycythemia caused by a novel mutation in the beta globin gene: essential role of P50 in evaluation of familial polycythemia.
    Agarwal N; Mojica-Henshaw MP; Simmons ED; Hussey D; Ou CN; Prchal JT
    Int J Med Sci; 2007 Oct; 4(4):232-6. PubMed ID: 17952198
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Severe Thalassemia Caused by Hb Zunyi [β147(HC3)Stop→Gln;
    Su Q; Chen S; Wu L; Tian R; Yang X; Huang X; Chen Y; Peng Z; Chen J
    Hemoglobin; 2019 Jan; 43(1):7-11. PubMed ID: 31084366
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Coinheritance of High Oxygen Affinity Hb Helsinki [HBB: c.248A>T; β82(EF6)Lys→Met] with Hb H Disease.
    Lee SY; Goh JH; Tan KML; Liu TC
    Hemoglobin; 2017 May; 41(3):209-212. PubMed ID: 28791912
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hb KOCHI [beta141(H19)Leu-->Val (g.1404 C-->G); 144-->146(HC1-3)Lys-Tyr-His-->0 (g.1413 A-->T)]: a new variant with increased oxygen affinity.
    Miyazaki A; Nakanishi T; Shimizu A; Mizobuchi M; Yamada Y; Imai K
    Hemoglobin; 2005; 29(1):1-10. PubMed ID: 15768550
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hb Knossos (HBB: c.82G > T), β-globin CD 5 (-CT) (HBB: c.17_18delCT) and δ-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia.
    Moassas F; Nweder MS; Murad H
    BMC Pediatr; 2019 Feb; 19(1):61. PubMed ID: 30777047
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hb Trollhättan [beta 20(B2)Val-->Glu]--a new haemoglobin variant with increased oxygen affinity causing erythrocytosis.
    Landin B; Berglund S; Lindoff B
    Eur J Haematol; 1994 Jul; 53(1):21-5. PubMed ID: 7914875
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hb zoeterwoude [beta23(B5)Val-->Ala)]: a new beta-globin variant found in association with erythrocytosis.
    Harteveld CL; Groeneveld JH; van Dam B; Van Delft P; Akkerman N; Arkesteijn S; Giordano PC
    Hemoglobin; 2005; 29(1):11-7. PubMed ID: 15768551
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A new hemoglobin variant: Hb Meylan [β73(E17)Asp → Phe; HBB: c.220G>T; c.221A>T] with a double base mutation at the same codon.
    Renoux C; Feray C; Joly P; Zanella-Cleon I; Garcia C; Lacan P; Couprie N; Francina A
    Hemoglobin; 2015; 39(1):46-8. PubMed ID: 25476778
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.