Yousuf F, Azam I, Tareen A, Kazmi K, Muhammad J, Iqbal M
Pak J Med Sci. 2023; 39(1):133-138.
PMID: 36694759
PMC: 9843019.
DOI: 10.12669/pjms.39.1.5905.
Hult A, Hellberg A, Storry J, Pisacka M, Olsson M
Transfusion. 2022; 62(10):E55-E58.
PMID: 36125051
PMC: 9826363.
DOI: 10.1111/trf.17109.
Pujol-Moix N, Martinez-Perez A, Sabater-Lleal M, Llobet D, Vilalta N, Hamsten A
Int J Mol Sci. 2019; 20(13).
PMID: 31262040
PMC: 6651679.
DOI: 10.3390/ijms20133221.
Fidalgo T, Martinho P, Pinto C, Oliveira A, Salvado R, Borras N
Res Pract Thromb Haemost. 2018; 1(1):69-80.
PMID: 30046676
PMC: 6058207.
DOI: 10.1002/rth2.12016.
Gorakshakar A, Gogri H, Ghosh K
Indian J Med Res. 2018; 146(3):305-315.
PMID: 29355136
PMC: 5793464.
DOI: 10.4103/ijmr.IJMR_914_16.
FUT1 mutations responsible for the H-deficient phenotype in the Polish population, including the first example of an abolished start codon.
Michalewska B, Olsson M, Naremska G, Walenciak J, Hult A, Ozog A
Blood Transfus. 2016; 16(1):101-104.
PMID: 27893357
PMC: 5770320.
DOI: 10.2450/2016.0135-16.
Mixed field reactions in ABO and Rh typing chimerism likely resulting from twin haematopoiesis.
Sharpe C, Lane D, Cote J, Hosseini-Maaf B, Goldman M, Olsson M
Blood Transfus. 2014; 12(4):608-10.
PMID: 24887220
PMC: 4212043.
DOI: 10.2450/2014.0261-13.
Do ABO blood group antigens hamper the therapeutic efficacy of mesenchymal stromal cells?.
Moll G, Hult A, Von Bahr L, Alm J, Heldring N, Hamad O
PLoS One. 2014; 9(1):e85040.
PMID: 24454787
PMC: 3890285.
DOI: 10.1371/journal.pone.0085040.
ABO blood group polymorphisms and risk for ischemic stroke and peripheral arterial disease.
Sabino A, Ribeiro D, Domingheti C, Rios D, Dusse L, Carvalho M
Mol Biol Rep. 2014; 41(3):1771-7.
PMID: 24449362
DOI: 10.1007/s11033-014-3026-8.
Evidence of Endothelial Activation in Asymptomatic Plasmodium falciparum Parasitemia and Effect of Blood Group on Levels of von Willebrand Factor in Malaria.
Park G, Ireland K, Opoka R, John C
J Pediatric Infect Dis Soc. 2013; 1(1):16-25.
PMID: 23687570
PMC: 3656549.
DOI: 10.1093/jpids/pis010.
Allelic Prevalence of ABO Blood Group Genes in Iranian Azari Population.
Nojavan M, Shamsasenjan K, Movassaghpour A, Akbarzadehlaleh P, Torabi S, Ghojazadeh M
Bioimpacts. 2013; 2(4):207-12.
PMID: 23678461
PMC: 3648936.
DOI: 10.5681/bi.2012.016.
ABO genotyping: the quest for clinical applications.
Flegel W
Blood Transfus. 2012; 11(1):6-9.
PMID: 23245718
PMC: 3557469.
DOI: 10.2450/2012.0250-12.
The development of severe neonatal alloimmune thrombocytopenia due to anti-HPA-1a antibodies is correlated to maternal ABO genotypes.
Ahlen M, Husebekk A, Killie M, Kjeldsen-Kragh J, Olsson M, Skogen B
Clin Dev Immunol. 2011; 2012:156867.
PMID: 22110529
PMC: 3216343.
DOI: 10.1155/2012/156867.
Prevalence, serologic and genetic studies of high expressers of the blood group A antigen on platelets*.
SantAnna Gomes B, Estalote A, Palatnik M, Pimenta G, Pereira B, Do Nascimento E
Transfus Med. 2010; 20(5):303-14.
PMID: 20553427
PMC: 2988417.
DOI: 10.1111/j.1365-3148.2010.01017.x.
Genotype-phenotype correlation in combined deficiency of factor V and factor VIII.
Zhang B, Spreafico M, Zheng C, Yang A, Platzer P, Callaghan M
Blood. 2008; 111(12):5592-600.
PMID: 18391077
PMC: 2424156.
DOI: 10.1182/blood-2007-10-113951.
Molecular genotyping and frequencies of A1, A2, B, O1 and O2 alleles of the ABO blood group system in a Kuwaiti population.
El-Zawahri M, Luqmani Y
Int J Hematol. 2008; 87(3):303-9.
PMID: 18247104
DOI: 10.1007/s12185-008-0036-0.
Haemostatic genetic variants, ABO blood group and bleeding risk during oral anticoagulant treatment after cerebral ischaemia of arterial origin.
Pruissen D, Rosendaal F, Gorter J, Garcia A, Kappelle L, Algra A
J Neurol. 2007; 254(12):1660-5.
PMID: 17994314
DOI: 10.1007/s00415-007-0609-5.
ABO exon and intron analysis in individuals with the AweakB phenotype reveals a novel O1v-A2 hybrid allele that causes four missense mutations in the A transferase.
Hosseini-Maaf B, Hellberg A, Rodrigues M, Alan Chester M, Olsson M
BMC Genet. 2003; 4:17.
PMID: 14617382
PMC: 305365.
DOI: 10.1186/1471-2156-4-17.