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 *

101 related articles for article (PubMed ID: 32871036)

  • 1. RH genotyping by nonspecific quantitative next-generation sequencing.
    Stef M; Fennell K; Apraiz I; Arteta D; González C; Nogués N; Ochoa-Garay G
    Transfusion; 2020 Nov; 60(11):2691-2701. PubMed ID: 32871036
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Overcoming the challenges of interpreting complex and uncommon RH alleles from whole genomes.
    Halls JBL; Vege S; Simmons DP; Aeschlimann J; Bujiriri B; Mah HH; Lebo MS; Vijay Kumar PK; Westhoff CM; Lane WJ
    Vox Sang; 2020 Nov; 115(8):790-801. PubMed ID: 32567058
    [TBL] [Abstract][Full Text] [Related]  

  • 3. RHD and RHCE variant and zygosity genotyping via multiplex ligation-dependent probe amplification.
    Haer-Wigman L; Veldhuisen B; Jonkers R; Lodén M; Madgett TE; Avent ND; de Haas M; van der Schoot CE
    Transfusion; 2013 Jul; 53(7):1559-74. PubMed ID: 23043317
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Evaluation of targeted exome sequencing for 28 protein-based blood group systems, including the homologous gene systems, for blood group genotyping.
    Schoeman EM; Lopez GH; McGowan EC; Millard GM; O'Brien H; Roulis EV; Liew YW; Martin JR; McGrath KA; Powley T; Flower RL; Hyland CA
    Transfusion; 2017 Apr; 57(4):1078-1088. PubMed ID: 28338218
    [TBL] [Abstract][Full Text] [Related]  

  • 5. RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients.
    Dezan MR; Ribeiro IH; Oliveira VB; Vieira JB; Gomes FC; Franco LAM; Varuzza L; Ribeiro R; Chinoca KZ; Levi JE; Krieger JE; Pereira AC; Gualandro SFM; Rocha VG; Mendrone-Junior A; Sabino EC; Dinardo CL
    Blood Cells Mol Dis; 2017 Jun; 65():8-15. PubMed ID: 28388467
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Machine learning to optimize automated RH genotyping using whole-exome sequencing data.
    Chang TC; Yu J; Wang Z; Hankins JS; Weiss MJ; Wu G; Westhoff CM; Chou ST; Zheng Y
    Blood Adv; 2024 Jun; 8(11):2651-2659. PubMed ID: 38522094
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Accurate long-read sequencing allows assembly of the duplicated RHD and RHCE genes harboring variants relevant to blood transfusion.
    Zhang Z; An HH; Vege S; Hu T; Zhang S; Mosbruger T; Jayaraman P; Monos D; Westhoff CM; Chou ST
    Am J Hum Genet; 2022 Jan; 109(1):180-191. PubMed ID: 34968422
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. A novel algorithm comprehensively characterizes human RH genes using whole-genome sequencing data.
    Chang TC; Haupfear KM; Yu J; Rampersaud E; Sheehan VA; Flanagan JM; Hankins JS; Weiss MJ; Wu G; Vege S; Westhoff CM; Chou ST; Zheng Y
    Blood Adv; 2020 Sep; 4(18):4347-4357. PubMed ID: 32915977
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Complete
    Tounsi WA; Madgett TE; Avent ND
    Blood Adv; 2018 Oct; 2(20):2713-2723. PubMed ID: 30337299
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Integrated analyses reveal unexpected complex inversion and recombination in RH genes.
    Li M; Wang L; Li A; Wang B; Yang X; Zhang Y; Chen C; Sun F; Zhu Z; Ye L
    Blood Adv; 2024 Jun; 8(12):3154-3165. PubMed ID: 38551808
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular matching for patients with haematological diseases expressing altered RHD-RHCE genotypes.
    Cruz BR; de Souza Silva TC; de Souza Castro B; Chiba AK; Moritz E; Braga JP; Figueiredo MS; Bordin JO
    Vox Sang; 2019 Aug; 114(6):605-615. PubMed ID: 31087345
    [TBL] [Abstract][Full Text] [Related]  

  • 13. DNA Reference Reagents for Genotyping RH Variants.
    Sippert E; Volkova E; Rippee-Brooks M; Denomme GA; Flegel WA; Lee C; Araojo R; Illoh O; Liu Z; Rios M;
    J Mol Diagn; 2024 Jun; 26(6):456-466. PubMed ID: 38494079
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A convenient qualitative and quantitative method to investigate RHD-RHCE hybrid genes.
    Fichou Y; Le Maréchal C; Bryckaert L; Dupont I; Jamet D; Chen JM; Férec C
    Transfusion; 2013 Nov; 53(11 Suppl 2):2974-82. PubMed ID: 23550903
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comprehensive phenotypic and molecular investigation of RhD and RhCE variants in Moroccan blood donors.
    El Housse H; El Wafi M; Ouabdelmoumene Z; Zarati F; Alid R; Nourichafi N; Bouisk K; Benajiba M; Férec C; Fichou Y; Habti N
    Blood Transfus; 2019 Mar; 17(2):151-156. PubMed ID: 30418133
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Study on RHCE genotyping of Rh blood group in Uygur nationality of Xinjiang in China].
    Bai XH; Lan JC; Gong XY; Cui L; Zhou HY
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2010 Oct; 18(5):1335-7. PubMed ID: 21129288
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The analysis of nucleotide substitutions, gaps, and recombination events between RHD and RHCE genes through complete sequencing.
    Okuda H; Suganuma H; Kamesaki T; Kumada M; Tsudo N; Omi T; Iwamoto S; Kajii E
    Biochem Biophys Res Commun; 2000 Aug; 274(3):670-83. PubMed ID: 10924335
    [TBL] [Abstract][Full Text] [Related]  

  • 18. RHD and RHCE molecular analysis in weak D blood donors and in patients with Rh antibodies against their own corresponding Rh antigen.
    Souza Silva TC; Cruz BR; Costa SS; Chiba AK; Barros MMO; Langhi DM; Bordin JO
    Blood Transfus; 2020 Jul; 18(4):295-303. PubMed ID: 32697929
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genotyping of RHD by multiplex polymerase chain reaction analysis of six RHD-specific exons.
    Maaskant-van Wijk PA; Faas BH; de Ruijter JA; Overbeeke MA; von dem Borne AE; van Rhenen DJ; van der Schoot CE
    Transfusion; 1998; 38(11-12):1015-21. PubMed ID: 9838930
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Diversity of RH and transfusion support in Brazilian sickle cell disease patients with unexplained Rh antibodies.
    Dinardo CL; Kelly S; Dezan MR; Ribeiro IH; Castilho SL; Schimidt LC; Valgueiro MDC; Preiss LR; Custer B; Sabino EC; Westhoff CM;
    Transfusion; 2019 Oct; 59(10):3228-3235. PubMed ID: 31408202
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.