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 *

323 related articles for article (PubMed ID: 22356480)

  • 21. A simple diagnostic strategy for RhD typing in discrepant cases in the Indian population.
    Kulkarni S; Kasiviswanathan V; Ghosh K
    Blood Transfus; 2013 Jan; 11(1):37-42. PubMed ID: 22871818
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Anti-D reagents should be chosen accordingly to the prevalence of D variants in the obstetric population.
    Lukacevic Krstic J; Dajak S; Bingulac-Popovic J; Dogic V; Mratinovic-Mikulandra J
    J Clin Lab Anal; 2018 Mar; 32(3):. PubMed ID: 28649781
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Anti-D immunization by DEL red blood cells.
    Wagner T; Körmöczi GF; Buchta C; Vadon M; Lanzer G; Mayr WR; Legler TJ
    Transfusion; 2005 Apr; 45(4):520-6. PubMed ID: 15819672
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Diverse and novel RHD variants in Australian blood donors with a weak D phenotype: implication for transfusion management.
    McGowan EC; Lopez GH; Knauth CM; Liew YW; Condon JA; Ramadi L; Parsons K; Turner EM; Flower RL; Hyland CA
    Vox Sang; 2017 Apr; 112(3):279-287. PubMed ID: 28220510
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Serologic and molecular investigations of DAR1 (weak D Type 4.2), DAR1.2, DAR1.3, DAR2 (DARE), and DARA.
    Lejon Crottet S; Haer-Wigman L; Gowland P; Fontana S; Niederhauser C; Hustinx H
    Transfusion; 2013 Nov; 53(11 Suppl 2):3000-8. PubMed ID: 23902153
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Serologic findings of RhD alleles in Egyptians and their clinical implications.
    Hussein E; Teruya J
    Transfus Apher Sci; 2014 Oct; 51(2):184-7. PubMed ID: 25219636
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Serological weak D phenotypes: a review and guidance for interpreting the RhD blood type using the RHD genotype.
    Sandler SG; Chen LN; Flegel WA
    Br J Haematol; 2017 Oct; 179(1):10-19. PubMed ID: 28508413
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. Molecular basis and zygosity determination of D variants including identification of four novel alleles in Chinese individuals.
    He J; Ying Y; Hong X; Xu X; Zhu F; Lv H
    Transfusion; 2015 Jan; 55(1):137-43. PubMed ID: 25070883
    [TBL] [Abstract][Full Text] [Related]  

  • 33. RHD/CE typing by polymerase chain reaction using sequence-specific primers.
    Gassner C; Schmarda A; Kilga-Nogler S; Jenny-Feldkircher B; Rainer E; Müller TH; Wagner FF; Flegel WA; Schönitzer D
    Transfusion; 1997 Oct; 37(10):1020-6. PubMed ID: 9354819
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Detection of weak D antigen by flow cytometry].
    Wu XY; Xu HX; Xiong W; Shao CP
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2013 Apr; 21(2):474-7. PubMed ID: 23628057
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Study on detection of samples of Rh-weak D and Del].
    Wang XZ; Lan JC; Wu XH; Zhou HY; Liu WJ; Liu D; Qi CS; Zeng FQ; Du KQ
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2005 Jun; 13(3):509-11. PubMed ID: 15972154
    [TBL] [Abstract][Full Text] [Related]  

  • 36. RHCE variants inherited with altered RHD alleles in Brazilian blood donors.
    Prisco Arnoni C; Guilhem Muniz J; de Paula Vendrame TA; de Medeiros Person R; Roche Moreira Latini F; Castilho L
    Transfus Med; 2016 Aug; 26(4):285-90. PubMed ID: 27111588
    [TBL] [Abstract][Full Text] [Related]  

  • 37. RHD positive among C/E+ and D-negative blood donors in Tunisia.
    Moussa H; Tsochandaridis M; Kacem N; Chakroun T; Abdelkefi S; Gabert J; Levy A; Jemni Yacoub S
    Transfus Clin Biol; 2014 Dec; 21(6):320-3. PubMed ID: 25458985
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Evaluation of the applicability and effectiveness of a molecular strategy for identifying weak D and DEL phenotype among D- blood donors of mixed origin exhibiting high frequency of RHD*Ψ.
    Dezan MR; Guardalini LGO; Pessoa E; Ribeiro IH; Oliveira VB; Luz F; Novac DR; Gallucci A; Bonifácio S; Gomes F; Levi JE; Pereira AC; Krieger JE; Mendrone-Junior A; Rocha V; Dinardo CL
    Transfusion; 2018 Feb; 58(2):317-322. PubMed ID: 29193119
    [TBL] [Abstract][Full Text] [Related]  

  • 39. RHCE alleles detected after weak and/or discrepant results in automated Rh blood grouping of blood donors in Northern Germany.
    Döscher A; Vogt C; Bittner R; Gerdes I; Petershofen EK; Wagner FF
    Transfusion; 2009 Sep; 49(9):1803-11. PubMed ID: 19453979
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Monoclonal reagents for rhesus-D typing of Irish patients and donors: a review.
    Williams M
    Br J Biomed Sci; 2000; 57(2):142-9. PubMed ID: 10912289
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.