Detalhe da pesquisa
1.
Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation.
Blood
; 137(17): 2394-2402, 2021 04 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-33512453
2.
Frequency and characterization of RHD and RHCE variants in the Noir Marron population from French Guiana.
Transfusion
; 62(12): 2631-2638, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36286083
3.
The Comoros Show the Earliest Austronesian Gene Flow into the Swahili Corridor.
Am J Hum Genet
; 102(1): 58-68, 2018 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29304377
4.
DO/ART4 gene sequencing in sub-Saharan cohorts and African migrants: useful data describing the diversity and spreading of rare variants.
Transfusion
; 59(12): 3755-3766, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31750977
5.
Multiplex Lateral Flow Assay for Rapid Visual Blood Group Genotyping.
Anal Chem
; 90(12): 7502-7509, 2018 06 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-29842785
6.
First description of a D-CE-D hybrid gene on a weak D Type 2 molecular background.
Transfusion
; 57(5): 1248-1253, 2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-28164316
7.
RHCE*01 (c.499A>G, p.Met167Val) allele: Weak RhE expression which does not require the E-specific proline 226.
Transfusion
; 61(2): E18-E20, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33399221
8.
New KEL*01M and KEL*02M alleles: structural modeling to assess the impact of amino acid changes.
Transfusion
; 56(5): 1223-9, 2016 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-26996808
9.
Sub-Saharan red cell antigen phenotypes and glucose-6-phosphate dehydrogenase deficiency variants in French Guiana.
Malar J
; 15: 310, 2016 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27267757
10.
RH diversity in Mali: characterization of a new haplotype RHD*DIVa/RHCE*ceTI(D2).
Transfusion
; 55(6 Pt 2): 1423-31, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25857637
11.
Sequencing of the ART4 gene in sub-Saharan cohorts reveals ethnic differences and two new DO alleles: DO*B-Ile5Thr and DO*B-Trp266Arg.
Transfusion
; 55(10): 2376-83, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25988428
12.
Short duplication within the RHCE gene associated with an in cis deleted RHD causing a Rhnull amorph phenotype in an immunized pregnant woman with anti-Rh29.
Transfusion
; 55(6 Pt 2): 1407-10, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25413218
13.
Synonymous nucleotide polymorphisms influence Dombrock blood group protein expression in K562 cells.
Br J Haematol
; 164(1): 131-41, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24125118
14.
The c.939G>A synonymous polymorphism in RHCE can be encountered on different molecular backgrounds.
Transfusion
; 59(6): 2160-2161, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30919985
15.
Identification and characterization of three novel RHCE*ce variant alleles affecting Rhc (RH4) reactivity.
Transfusion
; 59(8): 2754-2755, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31250454
16.
Heterogeneity of alleles encoding high- and low-prevalence red blood cell antigens across Africa: useful data to facilitate transfusion in African patients.
Br J Haematol
; 163(4): 528-36, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24032660
17.
A comprehensive survey of both RHD and RHCE allele frequencies in sub-Saharan Africa.
Transfusion
; 53(11 Suppl 2): 3009-17, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24033223
18.
RHCE*cE734C allele encodes an altered c antigen and a suppressed E antigen not detected with standard reagents.
Transfusion
; 53(5): 955-61, 2013 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22958092
19.
Weak D caused by a founder deletion in the RHD gene.
Transfusion
; 52(11): 2348-55, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22420867
20.
Characterization of novel RHD alleles: relationship between phenotype, genotype, and trimeric architecture.
Transfusion
; 52(9): 2020-9, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22320258