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 *

134 related articles for article (PubMed ID: 26035111)

  • 21. Heterozygosity for the Novel
    Forouzesh Pour F; Karimi K; Ghaderi Z; Tavakoli Koudehi A; Najmabadi H
    Hemoglobin; 2020 Nov; 44(6):423-426. PubMed ID: 33054440
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A Wide Spectrum Study of α-Globin Chain Variants: Cases from the UK.
    Khalil MSM; Timbs AT; Henderson SJ; Schuh A; El-Khawanky MM; Old JM
    Hemoglobin; 2020 May; 44(3):195-200. PubMed ID: 32597250
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Molecular and Hematological Analysis of Alpha- and Beta-Thalassemia in a Cohort of Mexican Patients.
    Rizo-de la Torre LDC; Rentería-López VM; Sánchez-López JY; Magaña-Torres MT; Ibarra-Cortés B; Perea-Díaz FJ
    Genet Test Mol Biomarkers; 2021 Mar; 25(3):247-252. PubMed ID: 33734896
    [No Abstract]   [Full Text] [Related]  

  • 24. [Application of mPCR and MLPA in diagnostics of alpha-thalassaemia].
    Splitt A; Mokras U; Windyga J; Kościelak J
    Przegl Lek; 2010; 67(7):460-4. PubMed ID: 21387755
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Hb Milano [α109(G16)Leu→Pro (C
    Curcio C; Giannone V; Benzoni E; Cesaretti C; Ivaldi G
    Hemoglobin; 2019 Jan; 43(1):4-6. PubMed ID: 31084368
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Detection of Hb H disease genotypes common in northern Thailand by quantitative real-time polymerase chain reaction and high resolution melting analyses.
    Seeratanachot T; Sanguansermsri T; Shimbhu D
    Hemoglobin; 2013; 37(6):574-83. PubMed ID: 23957826
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Sequence variations of the alpha-globin genes: scanning of high CG content genes with DHPLC and DG-DGGE.
    Lacerra G; Fiorito M; Musollino G; Di Noce F; Esposito M; Nigro V; Gaudiano C; Carestia C
    Hum Mutat; 2004 Oct; 24(4):338-49. PubMed ID: 15365991
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Development of a High Resolution Melting Curve Analysis for the Detection of Hemoglobin δ-Chain Variants in Thailand and Identification of Hb A2-Walsgrave [codon 52 (GAT>CAT), Asp→His; HBD:c.157G>C] in a Pregnant Woman from Southern Thailand.
    Prajantasen T; Prayalaw P; Panyasai S; Binlee S; Nongnuan S
    Genet Test Mol Biomarkers; 2021 Jun; 25(6):426-433. PubMed ID: 34152843
    [No Abstract]   [Full Text] [Related]  

  • 29. Novel nonsense mutation in the α1-globin gene [HBA1:C.49A>T] is responsible for non-deletion α-thalassemia.
    Ropero P; Villegas A; Nieto JM; González FA; Martínez R
    Clin Biochem; 2019 Jan; 63():139-142. PubMed ID: 30595158
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Eight Cases of Hb Winnipeg [
    Khalil MSM; Timbs AT; Henderson SJ; Schuh A; Old JM
    Hemoglobin; 2021 Jul; 45(4):256-258. PubMed ID: 34496687
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Pedigree Analysis of Nonhomologous Sequence Recombination of
    Luo SQ; Chen XY; Tang N; Huang J; Zhong QY; Cai R; Yan TZ
    Hemoglobin; 2020 Sep; 44(5):329-333. PubMed ID: 32811243
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Simultaneous mutation scanning and genotyping by high-resolution DNA melting analysis.
    Montgomery J; Wittwer CT; Palais R; Zhou L
    Nat Protoc; 2007; 2(1):59-66. PubMed ID: 17401339
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. In vitro characterization of the α-thalassemia point mutation HBA2:c.95+1G>A [IVS-I-1(G>A) (α2)].
    Qadah T; Finlayson J; Ghassemifar R
    Hemoglobin; 2012; 36(1):38-46. PubMed ID: 21967524
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Diagnosis and Prenatal Diagnosis in a Chinese Family Carrying the Rare α-Thalassemia Gene
    Chen X; Luo S; Huang J; Yuan D; Yan T; Cai R; Tang N
    Hemoglobin; 2020 Jan; 44(1):51-54. PubMed ID: 31933393
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].
    Zhu BS; He J; Zhang J; Zeng XH; Su J; Xu XH; Li SY; Chen H; Zhang YH
    Zhonghua Fu Chan Ke Za Zhi; 2012 Feb; 47(2):85-9. PubMed ID: 22455737
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A molecular tool to assess the pathological relevance of alpha-globin DNA variants.
    Qadah T; Finlayson J; Newbound C; Pell N; Jennens M; Holmes P; Grey D; Beilby J; Ghassemifar R
    Pathology; 2012 Jun; 44(4):337-41. PubMed ID: 22531344
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Hb Souli, a 6 bp in-frame deletion on the HBA2 gene (HBA2: c.[41-46delCCTGGG]) leads to α-thalassemia intermedia, when in trans to a single α-globin gene deletion.
    Kattamis A; Delaporta P; Fylaktou I; Vrettou C; Kyriakopoulou D; Stamoulakatou A; Papassotiriou I; Kanavakis E; Traeger-Synodinos J
    Hemoglobin; 2015; 39(1):55-7. PubMed ID: 25476779
    [TBL] [Abstract][Full Text] [Related]  

  • 39. High resolution melting analysis for gene scanning.
    Erali M; Wittwer CT
    Methods; 2010 Apr; 50(4):250-61. PubMed ID: 20085814
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Eleven Cases of Hb J-Paris-I [
    Khalil MSM; Timbs AT; Henderson SJ; Schuh A; Old JM
    Hemoglobin; 2021 Sep; 45(5):322-324. PubMed ID: 34784833
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.