BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

117 related articles for article (PubMed ID: 37194736)

  • 1. Hb Ryazan: An Elongated C-Terminal β-Chain Due to a New Frameshift Mutation, HBB: c.396delG p.Val133Trpfs*25.
    Demidova E; Salomashkina V; Selivanova D; Litvin E; Karamyan N; Mann S; Dvirnyk V; Maryina S; Petrova N; Gorgidze L; Peredel'skaya A; Tsvetaeva N; Smetanina N; Surin V
    Hemoglobin; 2023 Nov; 47(2):97-101. PubMed ID: 37194736
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical Genotyping by Next Generation Sequencing Reveals a Novel, De Novo β-Globin Gene Mutation Causing Hemolytic Anemia in a Chinese Individual.
    Pu J; Zhang L; Wei X; Xu X
    Hemoglobin; 2018 May; 42(3):184-188. PubMed ID: 30277086
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hb Wilde and Hb Patagonia: two novel elongated beta-globin variants causing dominant beta-thalassemia.
    Scheps KG; Hasenahuer MA; Parisi G; Fornasari MS; Pennesi SP; Erramouspe B; Basack FN; Veber ES; Aversa L; Elena G; Varela V
    Eur J Haematol; 2015 Jun; 94(6):498-503. PubMed ID: 25284604
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Compound Heterozygote for a Novel Elongated C-Terminal β-Globin Variant (
    Nuinoon M; Thipthara O; Fucharoen S
    Hemoglobin; 2019 Jan; 43(1):52-55. PubMed ID: 31106603
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hb Filottrano [codon 120 (-A)]: a novel frameshift mutation in exon 3 of the β-globin gene causing dominantly inherited β-thalassemia intermedia.
    Amato A; Cappabianca MP; Perri M; Zaghis I; Mastropietro F; Ponzini D; Di Biagio P; Piscitelli R
    Hemoglobin; 2012; 36(5):480-4. PubMed ID: 22992010
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. A Coincidental Discovery of a New Stable Variant (Hb Hachioji or HBB: c.187C>T) in a Patient with Chronic Hemolytic Anemia of Unexplained Origin.
    Mella F; Yamashiro Y; Adhiyanto C; Tanaka T; Nitta T; Amao Y; Kimoto M
    Hemoglobin; 2018 Jan; 42(1):1-6. PubMed ID: 29513125
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular and phenotype characterization of an elongated β-globin variant produced by HBB:C.313delA.
    Lin W; Zhang Q; Shen Z; Qu X; Wang Q; Wei L; Qiu Y; Yang J; Xu X; Lao J
    Int J Lab Hematol; 2021 Dec; 43(6):1620-1627. PubMed ID: 34271589
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The Effect of Nonsense Mediated Decay on Transcriptional Activity Within the Novel β-Thalassemia Mutation HBB: c.129delT.
    Forster L; Ardakani RM; Qadah T; Finlayson J; Ghassemifar R
    Hemoglobin; 2015; 39(5):334-9. PubMed ID: 26207313
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hb Wanjiang: A New β-Globin Chain Variant with Two Amino Acid Substitutions (
    Wu SM; Jiang F; Li C; Guo ZT; Huang SR; Li DZ
    Hemoglobin; 2022 Mar; 46(2):129-131. PubMed ID: 35950878
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Hb Feilding [β12(A9)Thr → Pro; HBB: c.37A>C]: a novel unstable β-globin chain variant.
    Ghallyan N; Donald T; Broad D; Johnson S; Browett P; Van de Water N
    Hemoglobin; 2015; 39(1):49-51. PubMed ID: 25572184
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A Novel β-Globin Gene Mutation: Hb Shenzhen [β90(F6)Glu→Ala, HBB: c.272A>C].
    Xu AP; Li J; Chen WD; Zhou Y; Zheng RY; Ji L
    Hemoglobin; 2018 May; 42(3):196-198. PubMed ID: 30277097
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Dominantly Inherited β-Thalassemia Caused by a Single Nucleotide Deletion in Exon 3 of the β-Globin Gene: Hb Xiangyang (
    Lin XM; Jiang F; Li J; Li DZ
    Hemoglobin; 2022 Jul; 46(4):253-255. PubMed ID: 35686459
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Hb Trento: an elongated C-terminal beta chain due to a new frameshift mutation [beta144 (-A)].
    Ivaldi G; David O; Baffico M; Leone D; Baldi M; Parodi MI; Scimè-Degani V; Piga A; Scagni P; Rabino-Massa E; Ricco G
    Hemoglobin; 2003 Feb; 27(1):15-25. PubMed ID: 12603089
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hb Penang [β78(EF2)Leu→Pro, HBB: c.236T>C]: a Novel β-Globin Variant.
    Hsu CH; Langdown J; Lynn R; Fisher C; Rose A; Proven M; Eglinton J; Besser MW
    Hemoglobin; 2018 May; 42(3):199-202. PubMed ID: 30328734
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new hemoglobin variant: Hb Izmir [β86(F2)Ala→Val, GCC>GTC; HBB:c.260C>T].
    Çelebiler A; Aksoy D; Ocakcı S; Karaca B
    Hemoglobin; 2012; 36(5):474-9. PubMed ID: 22946749
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A new hemoglobin variant: Hb Henan [β90(F6)Glu → Gln; HBB: c.271G < C].
    Cai WJ; Xie XM; Zhang YL; Li R; Liao C; Li DZ
    Hemoglobin; 2014; 38(2):127-9. PubMed ID: 24471793
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hb Grand Junction (HBB: c.348_349delinsG; p.His117IlefsX42): a new hyperunstable hemoglobin variant.
    Kent MW; Oliveira JL; Hoyer JD; Swanson KC; Kluge ML; Dawson DB; Liang X; Winkler TJ; Breaux CW; LaCount R; Silliman CC
    Hemoglobin; 2014; 38(1):8-12. PubMed ID: 24432801
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.