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 *

139 related articles for article (PubMed ID: 9886340)

  • 1. The Fy(x) phenotype is associated with a missense mutation in the Fy(b) allele predicting Arg89Cys in the Duffy glycoprotein.
    Olsson ML; Smythe JS; Hansson C; Poole J; Mallinson G; Jones J; Avent ND; Daniels G
    Br J Haematol; 1998 Dec; 103(4):1184-91. PubMed ID: 9886340
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular mechanisms that lead to reduced expression of duffy antigens.
    Yazdanbakhsh K; Rios M; Storry JR; Kosower N; Parasol N; Chaudhuri A; Reid ME
    Transfusion; 2000 Mar; 40(3):310-20. PubMed ID: 10738032
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Duffy blood group antigens: structure, serological properties and function].
    Łukasik E; Waśniowska K
    Postepy Hig Med Dosw (Online); 2016 Mar; 70():143-61. PubMed ID: 26943312
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Arg89Cys substitution results in very low membrane expression of the Duffy antigen/receptor for chemokines in Fy(x) individuals.
    Tournamille C; Le Van Kim C; Gane P; Le Pennec PY; Roubinet F; Babinet J; Cartron JP; Colin Y
    Blood; 1998 Sep; 92(6):2147-56. PubMed ID: 9731074
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Duffy blood group phenotype-genotype correlations using high-resolution melting analysis PCR and microarray reveal complex cases including a new null FY*A allele: the role for sequencing in genotyping algorithms.
    Lopez GH; Morrison J; Condon JA; Wilson B; Martin JR; Liew YW; Flower RL; Hyland CA
    Vox Sang; 2015 Oct; 109(3):296-303. PubMed ID: 25900316
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fyx is associated with two missense point mutations in its gene and can be detected by PCR-SSP.
    Gassner C; Kraus RL; Dovc T; Kilga-Nogler S; Utz I; Mueller TH; Schunter F; Schoenitzer D
    Immunohematology; 2000; 16(2):61-7. PubMed ID: 15373620
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A clinically applicable method for determining the three major alleles at the Duffy (FY) blood group locus using polymerase chain reaction with allele-specific primers.
    Olsson ML; Hansson C; Avent ND; Akesson IE; Green CA; Daniels GL
    Transfusion; 1998 Feb; 38(2):168-73. PubMed ID: 9531948
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The Duffy blood group system: a review.
    Meny GM
    Immunohematology; 2010; 26(2):51-6. PubMed ID: 20932074
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Duffy blood group genotyping in Thai blood donors.
    Nathalang O; Intharanut K; Siriphanthong K; Nathalang S; Kupatawintu P
    Ann Lab Med; 2015 Nov; 35(6):618-23. PubMed ID: 26354350
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular basis of the Duffy blood group system.
    Höher G; Fiegenbaum M; Almeida S
    Blood Transfus; 2018 Jan; 16(1):93-100. PubMed ID: 28151395
    [TBL] [Abstract][Full Text] [Related]  

  • 11. FY*X real-time polymerase chain reaction with melting curve analysis associated with a complete one-step real-time FY genotyping.
    Ansart-Pirenne H; Martin-Blanc S; Le Pennec PY; Rouger P; Cartron JP; Tournamille C
    Vox Sang; 2007 Feb; 92(2):142-7. PubMed ID: 17298577
    [TBL] [Abstract][Full Text] [Related]  

  • 12. First example of an FY*01 allele associated with weakened expression of Fya on red blood cells.
    Arndt PA; Horn T; Keller JA; Heri SM; Keller MA
    Immunohematology; 2015; 31(3):103-7. PubMed ID: 26829175
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular identification of rare FY*Null and FY*X alleles in Caucasian thalassemic family from Sardinia.
    Manfroi S; Scarcello A; Pagliaro P
    Transfus Apher Sci; 2015 Oct; 53(2):225-7. PubMed ID: 25921504
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular characterization of the Fy(a-b-) phenotype in a Polish family.
    Karolak E; Grodecka M; Suchanowska A; Klausa E; Bochenek S; Majorczyk E; Czerwiński M; Waśniowska K
    Transfus Apher Sci; 2013 Oct; 49(2):313-7. PubMed ID: 23820435
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel FY*A allele with the 265T and 298A SNPs formerly associated exclusively with the FY*B allele and weak Fy(b) antigen expression: implication for genotyping interpretative algorithms.
    Lopez GH; Condon JA; Wilson B; Martin JR; Liew YW; Flower RL; Hyland CA
    Vox Sang; 2015 Jan; 108(1):52-7. PubMed ID: 25092430
    [TBL] [Abstract][Full Text] [Related]  

  • 16. New genotypes in Fy(a-b-) individuals: nonsense mutations (Trp to stop) in the coding sequence of either FY A or FY B.
    Rios M; Chaudhuri A; Mallinson G; Sausais L; Gomensoro-Garcia AE; Hannon J; Rosenberger S; Poole J; Burgess G; Pogo O; Reid M
    Br J Haematol; 2000 Feb; 108(2):448-54. PubMed ID: 10691880
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Duffy genotyping facilitates transfusion therapy.
    Cotorruelo C; Biondi C; Racca L; Borrás SG; Racca A
    Clin Exp Med; 2009 Sep; 9(3):249-51. PubMed ID: 19225719
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Diversity of variant alleles encoding Kidd, Duffy, and Kell antigens in individuals with sickle cell disease using whole genome sequencing data from the NHLBI TOPMed Program.
    Dinardo CL; Oliveira TGM; Kelly S; Ashley-Koch A; Telen M; Schmidt LC; Castilho S; Melo K; Dezan MR; Wheeler MM; Johnsen JM; Nickerson DA; Jain D; Custer B; Pereira AC; Sabino EC;
    Transfusion; 2021 Feb; 61(2):603-616. PubMed ID: 33231305
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Duffy blood group system - the frequency of Duffy antigen polymorphisms and novel mutations in the Polish population.
    Łukasik E; Nowak I; Czerwinski M; Waśniowska K
    Transfus Apher Sci; 2019 Apr; 58(2):156-161. PubMed ID: 30639084
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.