Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Francisco C. A. Gomes"'
2
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 ofRHD*Ψ
Autor: Vanderson Rocha, Ingrid Helena Ribeiro, Marcia Regina Dezan, Denise Rossite Novac, V.B. Oliveira, José Eduardo Levi, Carla Luana Dinardo, Alexandre C. Pereira, Alfredo Mendrone-Junior, Fabio Luz, Francisco C. A. Gomes, Antonio Gallucci, Elaine Pessoa, Luis Giovani O. Guardalini, José Eduardo Krieger, SL Bonifácio
Publikováno v: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
BACKGROUND Molecular tests designed to detect the presence of active RHD gene among D- donors have been successfully applied in people of European ancestry, but not in admixed populations with a considerable frequency of RHD*Ψ. Our goal was to evalu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5748d0875dd22cbc1b24ff8d8fe4788
https://doi.org/10.1111/trf.14425
Zobrazit plný text záznamu
3
318C/T polymorphism of theCTLA-4gene is an independent risk factor for RBC alloimmunization among sickle cell disease patients
Autor: Julia Daher Carneiro Marsiglia, Marcia Regina Dezan, Ester Cerdeira Sabino, A. C. Pereira, Francisco C. A. Gomes, José Eduardo Levi, Carla Luana Dinardo, S. F. Menosi Gualandro, José Eduardo Krieger, V.B. Oliveira, Vanderson Rocha, Alfredo Mendrone-Junior
Publikováno v: International Journal of Immunogenetics. 44:219-224
Summary Cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) molecule is expressed on T-lymphocyte membrane and negatively influences the antigen-presenting process. Reduced expression of CTLA-4 due to gene polymorphisms is associated with increased
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec5dab2361e50b9f5866cd6b6dd577ea
https://doi.org/10.1111/iji.12334
Zobrazit plný text záznamu
4
Implementing a fully automated high-throughput strategy for blood donor genotyping
Autor: Hadassa Campos Santos, José Eduardo Krieger, José Eduardo Levi, Carla Luana Dinardo, A. J. O. Gallucci, Ester Cerdeira Sabino, Marcia Regina Dezan, V. G. Rocha, Helves Domingues, V.B. Oliveira, Alfredo Mendrone-Junior, Juliana Vieira dos Santos Bianchi, A. C. Pereira, Francisco C. A. Gomes
Publikováno v: ISBT Science Series. 12:357-364
Background High-throughput molecular assays are essential tools for the search of rare blood donors. Aims and methods To evaluate a fully automated workflow designed for genotyping blood donors’ red blood cell (RBC) and platelets (PTL) antigens usi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a1c0c24bf257bd3b6311c7ca81d1f277
https://doi.org/10.1111/voxs.12354
Zobrazit plný text záznamu
5
Effectiveness of a red cell antigen-matching transfusion protocol in sickle cell disease patients
Autor: J. H. Solano, Marcia Regina Dezan, José Eduardo Krieger, Juliana Vieira dos Santos Bianchi, V. Rodrigues, Alfredo Mendrone-Junior, Ester Cerdeira Sabino, S. F. M. Guallandro, José Eduardo Levi, Francisco C. A. Gomes, V.B. Oliveira, Carla Luana Dinardo, Alexandre C. Pereira, S. L. Bonifácio
Publikováno v: ISBT Science Series. 11:132-139
Background and objectives To date, it is unclear whether antigen matching is effective in reducing antibody development and whether transfusing blood from non-Caucasian donors reduces alloimmunization in sickle cell disease patients (SCP). This study
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::cb7023738ef1f717c8e08ada62f83f46
https://doi.org/10.1111/voxs.12281
Zobrazit plný text záznamu
6
Defining the clinical relevance of red blood cell autoantibodies by Monocyte Monolayer Assay
Autor: Luciana Tucunduva, Marina C. A. V. Conrado, Francisco C. A. Gomes, Ingrid Helena Ribeiro, V.B. Oliveira, Juliana B. Vieira, Amanda N. D'Avila, Alfredo Mendrone-Junior, Vanderson Rocha, Carla Luana Dinardo, SL Bonifácio, Marcia Regina Dezan
Publikováno v: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Background The Monocyte Monolayer Assay (MMA) is an in vitro simulation of red blood cell (RBC) alloantibody behavior. It has been classically applied to predict the risks of post-transfusion hemolytic reactions when transfusing incompatible RBC unit
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a82dd2447dd3466dbe42d0388fc48473
Zobrazit plný text záznamu
7
Prophylactic strategies for acute hemolysis secondary to plasma-incompatible platelet transfusions: correlation between qualitative hemolysin test and isohemagglutinin titration
Autor: Cinthia Silvestre Landim, Francisco C. A. Gomes, Carla Luana Dinardo, Alfredo Mendrone-Junior, Bernardete Martin Zeza
Publikováno v: Revista Brasileira de Hematologia e Hemoterapia
Revista Brasileira de Hematologia e Hemoterapia, Vol 37, Iss 4, Pp 217-222 (2015)
Revista Brasileira de Hematologia e Hemoterapia v.37 n.4 2015
Revista brasileira de hematologia e hemoterapia
Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)
instacron:ABHHTC
Revista Brasileira de Hematologia e Hemoterapia, Volume: 37, Issue: 4, Pages: 217-222, Published: AUG 2015
OBJECTIVE: Brazilian legislation has recently suggested the use of the qualitative hemolysin test instead of isohemagglutinin titers as prophylaxis for acute hemolysis related to plasma-incompatible platelet transfusions. The efficacy of this test in
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aefbcfde4ff2a80e177d7e6cbb38d315
Zobrazit plný text záznamu
9
RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients
Autor: Francisco C. A. Gomes, Lucas A M Franco, José Eduardo Krieger, Sandra Fátima Menosi Gualandro, Karen Z. Chinoca, Ingrid Helena Ribeiro, Leonardo Varuzza, Ester Cerdeira Sabino, Marcia Regina Dezan, José Eduardo Levi, Carla Luana Dinardo, Alexandre C. Pereira, V.B. Oliveira, Alfredo Mendrone-Junior, Vanderson Rocha, Roberto Ribeiro, Juliana B. Vieira
Publikováno v: Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Background The complexity of Rh genetic variation among sickle cell disease (SCD) patients is high. Conventional molecular assays cannot identify all genetic variants already described for the RH locus as well as foresee novel alleles. Sequencing RHD
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27da8821b45efa886675e0f7f1353e99
https://pubmed.ncbi.nlm.nih.gov/28388467
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje