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 *

148 related articles for article (PubMed ID: 21950494)

  • 1. Variant screening of the RHD gene in a large cohort of subjects with D phenotype ambiguity: report of 17 novel rare alleles.
    Fichou Y; Le Maréchal C; Bryckaert L; Guerry C; Bénech C; Dupont I; Jamet D; Férec C; Chen JM
    Transfusion; 2012 Apr; 52(4):759-64. PubMed ID: 21950494
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of 12 novel RHD alleles in western France by denaturing high-performance liquid chromatography analysis.
    Le Maréchal C; Guerry C; Benech C; Burlot L; Cavelier B; Porra V; Delamaire M; Férec C; Chen JM
    Transfusion; 2007 May; 47(5):858-63. PubMed ID: 17465951
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Establishment of a medium-throughput approach for the genotyping of RHD variants and report of nine novel rare alleles.
    Fichou Y; Le Maréchal C; Jamet D; Bryckaert L; Ka C; Audrézet MP; Le Gac G; Dupont I; Chen JM; Férec C
    Transfusion; 2013 Aug; 53(8):1821-8. PubMed ID: 23228153
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Identification of RHD alleles with the potential of anti-D immunization among seemingly D- blood donors in Upper Austria.
    Polin H; Danzer M; Gaszner W; Broda D; St-Louis M; Pröll J; Hofer K; Gabriel C
    Transfusion; 2009 Apr; 49(4):676-81. PubMed ID: 19170995
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Partial D, weak D types, and novel RHD alleles among 33,864 multiethnic patients: implications for anti-D alloimmunization and prevention.
    Denomme GA; Wagner FF; Fernandes BJ; Li W; Flegel WA
    Transfusion; 2005 Oct; 45(10):1554-60. PubMed ID: 16181204
    [TBL] [Abstract][Full Text] [Related]  

  • 6. RHD alleles in Brazilian blood donors with weak D or D-negative phenotypes.
    Cruz BR; Chiba AK; Moritz E; Bordin JO
    Transfus Med; 2012 Apr; 22(2):84-9. PubMed ID: 22211984
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Weak D phenotypes caused by intronic mutations in the RHD gene: four novel weak D alleles identified in the Chinese population.
    Ye L; He Y; Gao H; Guo Z; Zhu Z
    Transfusion; 2013 Aug; 53(8):1829-33. PubMed ID: 23216299
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Characterization of novel RHD alleles: relationship between phenotype, genotype, and trimeric architecture.
    Silvy M; Chapel-Fernandes S; Callebaut I; Beley S; Durousseau C; Simon S; Lauroua P; Dubosc-Marchenay N; Babault C; Mouchet C; Ferrera V; Chiaroni J; Bailly P
    Transfusion; 2012 Sep; 52(9):2020-9. PubMed ID: 22320258
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel RHD alleles with weak hemagglutination and genetic Exon 9 diversity: weak D Types 45.1, 75, and 76.
    Gassner C; Utz I; Schennach H; Ramoni A; Steiner H; Scholz S; Kreklau U; Körmöczi GF
    Transfusion; 2013 Nov; 53(11 Suppl 2):2954-9. PubMed ID: 23550956
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Comprehensive analysis of RHD alleles in Argentineans with variant D phenotypes.
    Brajovich ME; Boggione CT; Biondi CS; Racca AL; Tarragó M; Nogués N; Muñiz-Díaz E; Cotorruelo CM
    Transfusion; 2012 Feb; 52(2):389-96. PubMed ID: 21883261
    [TBL] [Abstract][Full Text] [Related]  

  • 11. RHD variants in Flanders, Belgium.
    Van Sandt VS; Gassner C; Emonds MP; Legler TJ; Mahieu S; Körmöczi GF
    Transfusion; 2015 Jun; 55(6 Pt 2):1411-7. PubMed ID: 25413499
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Weak D type 1.1 exemplifies another complexity in weak D genotyping.
    Doescher A; Flegel WA; Petershofen EK; Bauerfeind U; Wagner FF
    Transfusion; 2005 Oct; 45(10):1568-73. PubMed ID: 16181206
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Small deletions within the RHD coding sequence: a report of two novel mutational events and a survey of the underlying pathophysiologic mechanisms.
    Chen JM; Fichou Y; Jamet D; Dupont I; Cooper DN; Le Maréchal C; Férec C
    Transfusion; 2013 Jan; 53(1):206-10. PubMed ID: 22612274
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel weak D types 31 and 32: adsorption-elution-supported D antigen analysis and comparison to prevalent weak D types.
    Körmöczi GF; Förstemann E; Gabriel C; Mayr WR; Schönitzer D; Gassner C
    Transfusion; 2005 Oct; 45(10):1574-80. PubMed ID: 16181207
    [TBL] [Abstract][Full Text] [Related]  

  • 15. RHD alleles among pregnant women with serologic discrepant weak D phenotypes from a multiethnic population and risk of alloimmunization.
    Bub CB; Aravechia MG; Costa TH; Kutner JM; Castilho L
    J Clin Lab Anal; 2018 Jan; 32(1):. PubMed ID: 28374955
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Outliers in RhD membrane integration are explained by variant RH haplotypes.
    Yu X; Wagner FF; Witter B; Flegel WA
    Transfusion; 2006 Aug; 46(8):1343-51. PubMed ID: 16934070
    [TBL] [Abstract][Full Text] [Related]  

  • 17. DCS-1, DCS-2, and DFV share amino acid substitutions at the extracellular RhD protein vestibule.
    Flegel WA; von Zabern I; Doescher A; Wagner FF; Vytisková J; Písacka M
    Transfusion; 2008 Jan; 48(1):25-33. PubMed ID: 17900276
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Effective molecular RHD typing strategy for blood donations.
    Polin H; Danzer M; Hofer K; Gassner W; Gabriel C
    Transfusion; 2007 Aug; 47(8):1350-5. PubMed ID: 17655577
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular basis of the RHD gene in blood donors with DEL phenotypes in Shanghai.
    Li Q; Hou L; Guo ZH; Ye LY; Yue DQ; Zhu ZY
    Vox Sang; 2009 Aug; 97(2):139-46. PubMed ID: 19490579
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular and computational analysis of 45 samples with a serologic weak D phenotype detected among 132,479 blood donors in northeast China.
    Zhang X; Li G; Zhou Z; Shao C; Huang X; Li L; Li X; Liu Y; Fan H; Li J
    J Transl Med; 2019 Nov; 17(1):393. PubMed ID: 31775789
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.