BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

126 related articles for article (PubMed ID: 30578720)

  • 1. Identification of a novel hemoglobin variant Hb Jilin [α139(HC1)Lys>Gln; HBA2:C.418 A>C] in a Chinese family.
    Xu A; Li J; Chen W; Ji L
    Int J Lab Hematol; 2019 Jun; 41(3):e73-e75. PubMed ID: 30578720
    [No Abstract]   [Full Text] [Related]  

  • 2. Hb Sichuan [α67(E16)Thr→Ile, HBA2: c.203C>T]: A Novel Hemoglobin Variant That Can Be Detected by Glycated Hemoglobin Electrophoresis.
    Xu AP; Chen WD; Li J; Zhou Y; Zheng RY; Li X; Ji L
    Hemoglobin; 2018; 42(5-6):330-332. PubMed ID: 30612495
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hb Dapu (HBA2: c.52G > T): A Novel Nondeletional α-Thalassemia Mutation.
    Yang Y; Li DZ; He P
    Hemoglobin; 2016 Aug; 40(4):264-6. PubMed ID: 27258683
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A New α Chain Variant, Hb Heilongjiang (
    Xu A; Chen W; Xie W; Ji L; Wang Y; Xu M
    Hemoglobin; 2020 Mar; 44(2):143-145. PubMed ID: 32425076
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical presentation and molecular identification of four uncommon alpha globin variants in Thailand. Initiation codon mutation of α2-globin Gene (HBA2:c.1delA), donor splice site mutation of α1-globin gene (IVSI-1, HBA1:c.95 + 1G>A), hemoglobin Queens Park/Chao Pra Ya (HBA1:c.98T>A) and hemoglobin Westmead (HBA2:c.369C>G).
    Viprakasit V; Ekwattanakit S; Chalaow N; Riolueang S; Wijit S; Tanyut P; Chat-Uthai N; Tachavanich K
    Acta Haematol; 2014; 131(2):88-94. PubMed ID: 24081251
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hb Hubei [α114(GH2)Pro→His, HBA1: c.344C>A]: A Novel Hemoglobin Variant of the α1-Globin Chain.
    Xu AP; Li J; Chen WD; Zhou Y; Ji L
    Hemoglobin; 2018 May; 42(3):206-208. PubMed ID: 30277418
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
    Henderson SJ; Timbs AT; McCarthy J; Gallienne AE; Proven M; Rugless MJ; Lopez H; Eglinton J; Dziedzic D; Beardsall M; Khalil MS; Old JM
    Hemoglobin; 2016; 40(2):75-84. PubMed ID: 26635043
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hb Papanui [α99(G8)Lys→Arg; HBA2: c.299A>G]: a novel silent substitution interfering in Hb A1c determination.
    Brennan SO; Chan T
    Hemoglobin; 2013; 37(6):589-92. PubMed ID: 23806116
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hb Lake Tapawingo [α46(CE4)Phe→Ser; HBA2:c.140T>C]: a new unstable α chain hemoglobin variant associated with low systemic arterial saturation.
    Guest EM; Neville KA; Hoyer JD; Safo MK; Garg U; Saunders CJ; Abdulmalik O; Zwick DL
    Hemoglobin; 2011; 35(4):411-6. PubMed ID: 21797707
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A new hemoglobin variant, Hb Fukui [alpha139(HC1)Lys --> Asn (AAA --> AAC) (alpha2)].
    Harano T; Suetsugu Y; Harano K; Than AM; Hong YF; Kuroda A
    Hemoglobin; 2003 May; 27(2):117-21. PubMed ID: 12779274
    [No Abstract]   [Full Text] [Related]  

  • 11. Hb Stanleyville II [alpha 78(EF7) Asn→Lys] occurrence in combination with Hb Constant Spring.
    Lin M; Huang Y; Yang LY; Wang Q; Zheng L
    Blood Cells Mol Dis; 2011 Feb; 46(2):145-6. PubMed ID: 21093326
    [No Abstract]   [Full Text] [Related]  

  • 12. Hb Kalavasos [HBA2: c.275T > A; p.Leu92His]: a Novel α Chain Hemoglobin Variant.
    Kelany M; Pickersgill JS; Al Hasso N; Viljoen A; van Bijlen N; Besser MW
    Hemoglobin; 2016 Sep; 40(5):345-348. PubMed ID: 27624082
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A new α1-globin mutation, Hb Brugg [α20(B1)His→Gln].
    Rizzi M; Zurbriggen K; Schmid M; Goede JS; Nardi MA; Schmugge M; Speer O
    Hemoglobin; 2011; 35(4):417-22. PubMed ID: 21797708
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Homozygous Hb Stanleyville-II [alpha2 78(EF7) Asn>Lys; HBA2:c.237C>A, not C>G] associated with genotype -α 3.7/-α 3.7 in two Brazilian families.
    Pimentel FS; Silva MR; Ferraz MH; Carvalho NO; Perone C; del Castillo DM; Januario JN; Viana MB
    Int J Lab Hematol; 2011 Dec; 33(6):566-9. PubMed ID: 21470372
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Characterization of Homozygous Hb Setif (HBA2: c.283G>T) in the Iranian Population.
    Farashi S; Garous NF; Vakili S; Ashki M; Imanian H; Azarkeivan A; Najmabadi H
    Hemoglobin; 2016; 40(1):53-5. PubMed ID: 26574177
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A New Hemoglobin Variant: Hb Jiujiang [α18(A16)Gly→Cys,
    Lei YL; Liang YM; Cao Q; Sui H; Li DZ
    Hemoglobin; 2021 Jul; 45(4):254-255. PubMed ID: 34547968
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hb St. Truiden [α68(E17)Asn→His] and Hb Westeinde [α125(H8)Leu→Gln]: two new abnormalities of the α2-globin gene.
    Kaufmann JO; Phylipsen M; Neven C; Huisman W; van Delft P; Bakker-Verweij M; Arkesteijn SG; Harteveld CL; Giordano PC
    Hemoglobin; 2010; 34(5):439-44. PubMed ID: 20854117
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A Novel Mutation of the α2-Globin Gene Causing α
    Chen B; Lin L; Yi S; Chen Q; Wei H; Li G; Zheng C; He S; Qiu X
    Hemoglobin; 2017 Jan; 41(1):56-58. PubMed ID: 28395547
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Complex interaction of hemoglobin (Hb) Nakhon Ratchasima [α63(E12)Ala→Val], a novel α2-globin chain variant with Hb E [β26(B8)Glu→Lys] and a deletional α(+)-thalassemia.
    Srivorakun H; Fucharoen G; Puangplruk R; Kheawon N; Fucharoen S
    Eur J Haematol; 2011 Jul; 87(1):68-72. PubMed ID: 21447006
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Compound Heterozygosity for an Unstable Novel Hemoglobin Variant, Hb Dongguan [α52(E1)Ser→Cys (T
    Chen WD; Ren YX; Wang YJ; Xie WJ; Li J; Xu AP; Ji L
    Hemoglobin; 2019; 43(4-5):286-288. PubMed ID: 31650882
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.