RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients (2017)
- Autores:
- Dezana, Marcia R.
- Ribeiro, Ingrid Helena
- Oliveira, Valéria B.
- Vieira, Juliana B.
- Gomes, Francisco C.
- Franco, Lucas A. M.
- Varuzza, Leonardo
- Ribeiro, Roberto
- Chinoca, Karen Ziza
- Levi, José Eduardo
- Krieger, José Eduardo
- Pereira, Alexandre Costa
- Gualandro, Sandra F.M.
- Rocha, Vanderson G.
- Mendrone-Junior,Alfredo
- Sabino, Ester Cerdeira
- Dinardo, Carla Luana
- Autores USP: KRIEGER, JOSE EDUARDO - FM ; GUALANDRO, SANDRA FATIMA MENOSI - FM ; ROCHA, VANDERSON GERALDO - FM ; SABINO, ESTER CERDEIRA - FM
- Unidade: FM
- DOI: 10.1016/j.bcmd.2017.03.014
- Assuntos: GENÓTIPOS; TÉCNICAS CITOLÓGICAS; REAÇÃO EM CADEIA POR POLIMERASE; TRANSFUSÃO DE SANGUE; SEQUENCIAMENTO GENÉTICO
- Idioma: Inglês
- Imprenta:
- Local: California
- Data de publicação: 2017
- Fonte:
- Título do periódico: Blood Cells, Molecules, and Diseases
- ISSN: 1079-9796
- Volume/Número/Paginação/Ano: v. 65, n. 1, p. 8-15, 2017
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
DEZANA, Marcia R. et al. RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients. Blood Cells, Molecules, and Diseases, v. 65, n. 1, p. 8-15, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.bcmd.2017.03.014. Acesso em: 25 abr. 2024. -
APA
Dezana, M. R., Ribeiro, I. H., Oliveira, V. B., Vieira, J. B., Gomes, F. C., Franco, L. A. M., et al. (2017). RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients. Blood Cells, Molecules, and Diseases, 65( 1), 8-15. doi:10.1016/j.bcmd.2017.03.014 -
NLM
Dezana 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. RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients [Internet]. Blood Cells, Molecules, and Diseases. 2017 ; 65( 1): 8-15.[citado 2024 abr. 25 ] Available from: https://doi.org/10.1016/j.bcmd.2017.03.014 -
Vancouver
Dezana 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. RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients [Internet]. Blood Cells, Molecules, and Diseases. 2017 ; 65( 1): 8-15.[citado 2024 abr. 25 ] Available from: https://doi.org/10.1016/j.bcmd.2017.03.014 - -318C/T polymorphism of the CTLA-4 gene is an independent risk factor for RBC alloimmunization among sickle cell disease patients
- High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotype
- Effectiveness of strategies to screen for blood donors with RH variants in a mixed population
- Prevalence and laboratorial determinants of the clinical relevance of antibodies of undetermined specificity
- SMIM1 intron 2 gene variations leading to variability in Vel antigen expression among Brazilian blood donors
- Impact of HLA-G+3142C>G on the development of antibodies to blood group systems other than the Rh and Kell among sensitized patients with sickle cell disease
- Massive autoimmune hemolysis documented by monocyte monolayer assay in a multiply transfused patient using reticulocytes isolated by simple centrifugation in microhematocrit tubes
- Risk factors for deferral due to low hematocrit and iron depletion among prospective blood donors in a Brazilian center
- Identification and Characterization of Hematopoietic Stem Cell Transplant Candidates in a Sickle Cell Disease Cohort
- Short form health survey (SF-36) differs between genotypic groups of patients with suspected hereditary hemochromatosis
Informações sobre o DOI: 10.1016/j.bcmd.2017.03.014 (Fonte: oaDOI API)
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