2019
DOI: 10.1016/j.jfma.2018.06.014
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Rapid rare ABO blood typing using a single PCR based on a multiplex SNaPshot reaction

Abstract: SNaPshot analysis could be used in reference laboratories for typing known rare subgroups of A and B without DNA cloning and traditional sequencing. Moreover, this method would help to construct databases of genotyped blood donors, and it potentially plays a role in determining fetal-maternal ABO incompatibility.

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Cited by 9 publications
(7 citation statements)
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“…The SNaPshot method used in the present study offers a specific, sensitive, inexpensive and rapid alternative to the simultaneous screening for multiple mutations and subsequent confirmation by sequencing ( Quintans et al., 2004 ; Alina et al., 2005 ; Fondevila et al., 2017 ). This method has been extensively used in the blood group typing ( Palacajornsuk et al., 2009 ; Latini et al., 2014 ; Chen et al., 2019 ) and common mutations in genes related to some cancers ( Filippini et al., 2007 ; Hurst et al., 2009 ; Fariña Sarasqueta et al., 2011 ).…”
Section: Discussionmentioning
confidence: 99%
“…The SNaPshot method used in the present study offers a specific, sensitive, inexpensive and rapid alternative to the simultaneous screening for multiple mutations and subsequent confirmation by sequencing ( Quintans et al., 2004 ; Alina et al., 2005 ; Fondevila et al., 2017 ). This method has been extensively used in the blood group typing ( Palacajornsuk et al., 2009 ; Latini et al., 2014 ; Chen et al., 2019 ) and common mutations in genes related to some cancers ( Filippini et al., 2007 ; Hurst et al., 2009 ; Fariña Sarasqueta et al., 2011 ).…”
Section: Discussionmentioning
confidence: 99%
“…The genomic DNA of leukocytes was extracted following the method of DNA isolation kit (TIANGEN BIOTECH [Beijing] CO., LTD). Then, the preliminary genotype was detected with PCR‐SSP, and the specific primers were designed according to single nucleotide polymorphism 4 . The exons 6 and 7 of the ABO gene were amplified using PCR and their sequences were determined by direct sequencing, and the results were analyzed by comparing with reference sequence A101 (NG‐006669).…”
Section: Brief Methodsmentioning
confidence: 99%
“…Scholars have recently advocated using RhD genetic testing for patients with a weak D phenotype to obtain accurate and actionable results for RhD blood typing and Rh Ig administration. [63][64][65] There is still a vast capacity for improving HDN's understanding and management in both developed and developing countries. Universal research-backed guidelines regarding RBC antigen matching transfusion techniques for women before pregnancy or during intrauterine transfusion would be a good place to start.…”
Section: Trends and Future Prospectsmentioning
confidence: 99%