Literature DB >> 27893357

FUT1 mutations responsible for the H-deficient phenotype in the Polish population, including the first example of an abolished start codon.

Bogumila Michalewska1, Martin L Olsson2,3, Grazyna Naremska4, Jolanta Walenciak5, Annika K Hult2,3, Agnieszka Ozog1, Katarzyna Guz1, Ewa Brojer1, Jill R Storry2,3.   

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Year:  2016        PMID： 27893357      PMCID： PMC5770320          DOI： 10.2450/2016.0135-16

Source DB:  PubMed          Journal:  Blood Transfus        ISSN： 1723-2007            Impact factor:   3.443


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  16 in total

Review 1.  Polymorphism and recombination events at the ABO locus: a major challenge for genomic ABO blood grouping strategies.

Authors:  M L Olsson; M A Chester
Journal:  Transfus Med       Date:  2001-08       Impact factor: 2.019

2.  Allelic genes of blood group antigens: a source of human mutations and cSNPs documented in the Blood Group Antigen Gene Mutation Database.

Authors:  Olga O Blumenfeld; Santosh K Patnaik
Journal:  Hum Mutat       Date:  2004-01       Impact factor: 4.878

3.  Edinburgh and early transfusion in the New World.

Authors:  P J Schmidt
Journal:  Vox Sang       Date:  2004-07       Impact factor: 2.144

4.  Weak A phenotypes associated with novel ABO alleles carrying the A2-related 1061C deletion and various missense substitutions.

Authors:  Annika K Hult; Mark H Yazer; René Jørgensen; Asa Hellberg; Hein Hustinx; Thierry Peyrard; Monica M Palcic; Martin L Olsson
Journal:  Transfusion       Date:  2010-05-07       Impact factor: 3.157

5.  Many genetically defined ABO subgroups exhibit characteristic flow cytometric patterns.

Authors:  Annika K Hult; Martin L Olsson
Journal:  Transfusion       Date:  2009-10-05       Impact factor: 3.157

6.  Missense mutation of FUT1 and deletion of FUT2 are responsible for Indian Bombay phenotype of ABO blood group system.

Authors:  Y Koda; M Soejima; P H Johnson; E Smart; H Kimura
Journal:  Biochem Biophys Res Commun       Date:  1997-09-08       Impact factor: 3.575

7.  A rapid and simple ABO genotype screening method using a novel B/O2 versus A/O2 discriminating nucleotide substitution at the ABO locus.

Authors:  M L Olsson; M A Chester
Journal:  Vox Sang       Date:  1995       Impact factor: 2.144

8.  Sequence and expression of a candidate for the human Secretor blood group alpha(1,2)fucosyltransferase gene (FUT2). Homozygosity for an enzyme-inactivating nonsense mutation commonly correlates with the non-secretor phenotype.

Authors:  R J Kelly; S Rouquier; D Giorgi; G G Lennon; J B Lowe
Journal:  J Biol Chem       Date:  1995-03-03       Impact factor: 5.157

9.  A weak blood group A phenotype caused by a translation-initiator mutation in the ABO gene.

Authors:  Axel Seltsam; Christa Das Gupta; Christina Bade-Doeding; Rainer Blasczyk
Journal:  Transfusion       Date:  2006-03       Impact factor: 3.157

10.  Molecular basis for H blood group deficiency in Bombay (Oh) and para-Bombay individuals.

Authors:  R J Kelly; L K Ernst; R D Larsen; J G Bryant; J S Robinson; J B Lowe
Journal:  Proc Natl Acad Sci U S A       Date:  1994-06-21       Impact factor: 11.205
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