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 *

136 related articles for article (PubMed ID: 26754300)

  • 1. The Codon 35 (A > G) (HBB: c.107A > G) at the α-β Chain Interface of the β-Globin Gene: A Silent Mutation?
    Wu MY; Li DZ
    Hemoglobin; 2016; 40(1):56-8. PubMed ID: 26754300
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Compound Heterozygosity for a Novel Mutation Codon 104 (-A) (
    Qiu Y; Huang Y; Chen P; Wei S; Su Q; Zhang Z; Yang Z; Ye L; Huang J; Shen X; Mo W
    Hemoglobin; 2020 Nov; 44(6):402-405. PubMed ID: 33198537
    [TBL] [Abstract][Full Text] [Related]  

  • 3. First Detection of the -27 (A > G) (HBB: c.-77A > G) Mutation of the β-Globin Gene in a Chinese Family.
    Wu MY; Li DZ
    Hemoglobin; 2016; 40(1):59-60. PubMed ID: 26554738
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel beta-globin mutation (HBB:c.107A>G; or codon 35 beta (A-->G)) at alpha-beta chain interfaces.
    Kumar R; Tamhankar PM; Panigrahi I; Dalal A; Agarwal S
    Ann Hematol; 2009 Dec; 88(12):1269-71. PubMed ID: 19488752
    [No Abstract]   [Full Text] [Related]  

  • 5. Compound Heterozygosity for Silent Cap +1570 (T>C) (HBB: c*96T>C), Codon 39 (C>T) (HBB: c.118C>T) and the Presence of ααα
    Theodoridou S; Vyzantiadis TA; Vlachaki E
    Hemoglobin; 2018 May; 42(3):194-195. PubMed ID: 30205726
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Combination of Hb Heze [β144(HC1)Lys→Arg; HBB: c.434A>G] and β
    Li Y; Yan JM; Zhou JY; Lu YC; Li DZ
    Hemoglobin; 2017 Jan; 41(1):47-49. PubMed ID: 28366026
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. A Novel Frameshift Mutation at Codons 138/139 (HBB: c.417_418insT) on the β-Globin Gene Leads to β-Thalassemia.
    Jiang F; Huang LY; Chen GL; Zhou JY; Xie XM; Li DZ
    Hemoglobin; 2017 Jan; 41(1):59-60. PubMed ID: 28460555
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Novel Frameshift Mutation at Codon 2 (-T) (
    Bayramov B; Aliyeva G; Asadov C; Mammadova T; Karimova N; Eynullazadeh K; Gafarova S; Akbarov S; Farhadova S; Safarzadeh Z; Abbasov M
    Hemoglobin; 2019; 43(4-5):280-282. PubMed ID: 31476942
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of a Novel β-Globin Mutation (HBB: C.189_195delTCATGGC) in a Chinese Family.
    He S; Lin L; Wei Y; Chen B; Yi S; Chen Q; Qiu X; Wei H; Li G; Zheng C
    Hemoglobin; 2016 Aug; 40(4):277-9. PubMed ID: 27492766
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of Two Novel β-Thalassemia Mutations (HBB: c.335-346del and HBB: c.108 C > G) in Han Chinese.
    Wang W; Wang Q; Tao T; Sun A; Ruan C; Chen S
    Hemoglobin; 2015; 39(5):359-61. PubMed ID: 26096710
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Co-heredity of silent CAP + 1570 T>C (HBB:c*96T>C) defect and severe β-thal mutation: a cause of mild β-thalassemia intermedia.
    Vinciguerra M; Passarello C; Cassarà F; Leto F; Cannata M; Calvaruso G; Di Maggio R; Renda D; Maggio A; Giambona A
    Int J Lab Hematol; 2016 Feb; 38(1):17-26. PubMed ID: 26418075
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A rare gene variation cap +1 (A>C) (HBB: c. -50A>C) associated with codon 5 (-CT) (HBB: c.17_18delCT) mutation in Syrian family.
    Murad H; Moassas F; Fakseh NAL
    Mol Genet Genomic Med; 2021 Mar; 9(3):e1602. PubMed ID: 33491330
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. A Novel Mutation in the Promoter Region of the β-Globin Gene: HBB: c.-127G > C.
    Bilgen T; Canatan D; Delibas S; Keser I
    Hemoglobin; 2016 Aug; 40(4):280-2. PubMed ID: 27349616
    [TBL] [Abstract][Full Text] [Related]  

  • 16. First Description of a β-Thalassemia Mutation, -86 (C > G) (HBB: c.-136C > G), in a Chinese Family.
    He S; Qin Q; Yi S; Zhou W; Deng J; Zheng C; Chen B
    Hemoglobin; 2015; 39(6):448-50. PubMed ID: 26291972
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Double Heterozygosity for Hb Durham-N.C. (
    Cannata M; Cassarà F; Vinciguerra M; Licari P; Passarello C; Leto F; Lo Pinto C; Pitrolo L; Ganci R; Maggio A; Giambona A
    Hemoglobin; 2019 May; 43(3):210-213. PubMed ID: 31456457
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A β-Thalassemia Trait with Two Mutations in
    Li J; Jiang F; Zhen L; Tang XW; Li DZ
    Hemoglobin; 2019; 43(4-5):289-291. PubMed ID: 31690135
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel promoter mutation (HBB: c.-75G>T) was identified as a cause of β(+)-thalassemia.
    Li Z; Li L; Yao Y; Li N; Li Y; Zhang Z; Yan F; Qiu H; Wu C; Zhang Z
    Hemoglobin; 2015; 39(2):115-20. PubMed ID: 25657036
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Elevated Hb A₂ Levels in a Patient with a Compound Heterozygosity for the (β⁺) -31 (A > G) and (β⁰) Codon 17 (A > T) Mutations Together with a Single α-Globin Gene.
    Panyasai S; Jaiping K; Pornprasert S
    Hemoglobin; 2015; 39(4):292-5. PubMed ID: 26029792
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.