Format
Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 123

1.

Use of cell study models to confirm the weak ABO phenotypes caused by point mutations among Taiwanese.

Chen DP, Tseng CP, Wang WT, Sun CF.

Ann Clin Lab Sci. 2011 Fall;41(4):346-52.

PMID:
22166504
2.

A novel B(weak) hybrid allele lacks three enhancer repeats but generates normal ABO transcript levels.

Thuresson B, Hosseini-Maaf B, Hult AK, Hustinx H, Alan Chester M, Olsson ML.

Vox Sang. 2012 Jan;102(1):55-64. doi: 10.1111/j.1423-0410.2011.01497.x. Epub 2011 May 19.

PMID:
21592135
3.
4.
5.

A unique 502C>T mutation in exon 7 of ABO gene associated with the Bel phenotype in Taiwan.

Lin PH, Li L, Lin-Tsai SJ, Lin KT, Chen JM, Chu DC.

Transfusion. 2003 Sep;43(9):1254-9.

PMID:
12919428
6.

Genomic analysis of clinical samples with serologic ABO blood grouping discrepancies: identification of 15 novel A and B subgroup alleles.

Olsson ML, Irshaid NM, Hosseini-Maaf B, Hellberg A, Moulds MK, Sareneva H, Chester MA.

Blood. 2001 Sep 1;98(5):1585-93.

7.

Molecular genetic analysis of the Bel phenotype.

Sun CF, Chen DP, Lin KT, Wang WT, Wang YC, Yu LC.

Vox Sang. 2003 Oct;85(3):216-20.

PMID:
14516453
8.

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

Seltsam A, Das Gupta C, Bade-Doeding C, Blasczyk R.

Transfusion. 2006 Mar;46(3):434-40.

PMID:
16533287
9.

Identification of a novel A1v-O1v hybrid allele with G829A mutation in a chimeric individual of AelBel phenotype.

Sun CF, Chen DP, Tseng CP, Wang WT, Liu JP.

Transfusion. 2006 May;46(5):780-9.

PMID:
16686846
10.
11.

Structural basis for red cell phenotypic changes in newly identified, naturally occurring subgroup mutants of the human blood group B glycosyltransferase.

Hosseini-Maaf B, Letts JA, Persson M, Smart E, LePennec PY, Hustinx H, Zhao Z, Palcic MM, Evans SV, Chester MA, Olsson ML.

Transfusion. 2007 May;47(5):864-75.

PMID:
17465952
12.

Molecular genetic analysis for the Ae1 and A3 alleles.

Sun CF, Yu LC, Chen IP, Chou DL, Twu YC, Wang WT, Lin M.

Transfusion. 2003 Aug;43(8):1138-44.

PMID:
12869122
13.

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

Hult AK, Yazer MH, Jørgensen R, Hellberg A, Hustinx H, Peyrard T, Palcic MM, Olsson ML.

Transfusion. 2010 Jul;50(7):1471-86. doi: 10.1111/j.1537-2995.2010.02670.x. Epub 2010 May 7.

PMID:
20456702
14.

Molecular genetic analysis for the B subgroup revealing two novel alleles in the ABO gene.

Cai XH, Jin S, Liu X, Shen W, Lu Q, Wang JL, Fan LF, Sun JL, Liu DZ, Xiang D.

Transfusion. 2008 Nov;48(11):2442-7. doi: 10.1111/j.1537-2995.2008.01878.x. Epub 2008 Aug 1.

PMID:
18680548
15.

Mutation of ABO gene in Thai blood donors with A3 phenotype.

Pipatvanichkul A, Permpikul P, Vejbaesya S, Chinswangwatanakul W.

J Med Assoc Thai. 2011 Mar;94(3):379-85.

PMID:
21560847
16.

Aberrant intracellular trafficking of a variant B glycosyltransferase.

Seltsam A, Grüger D, Just B, Figueiredo C, Gupta CD, Deluca DS, Blasczyk R.

Transfusion. 2008 Sep;48(9):1898-905. doi: 10.1111/j.1537-2995.2008.01782.x. Epub 2008 May 29.

PMID:
18513251
17.

A weak blood group A phenotype caused by a new mutation at the ABO locus.

Seltsam A, Hallensleben M, Eiz-Vesper B, Lenhard V, Heymann G, Blasczyk R.

Transfusion. 2002 Mar;42(3):294-301.

PMID:
11961233
18.

Genetic and mechanistic evaluation for the weak A phenotype in Ael blood type with IVS6 + 5G>A ABO gene mutation.

Chen DP, Sun CF, Ning HC, Peng CT, Wang WT, Tseng CP.

Vox Sang. 2015 Jan;108(1):64-71. doi: 10.1111/vox.12196. Epub 2014 Sep 19.

PMID:
25234298
19.

Genetic and mechanistic evaluation for the mixed-field agglutination in B3 blood type with IVS3+5G>A ABO gene mutation.

Chen DP, Tseng CP, Wang WT, Sun CF.

PLoS One. 2012;7(5):e37272. doi: 10.1371/journal.pone.0037272. Epub 2012 May 18.

20.

Two prevalent h alleles in para-Bombay haplotypes among 250,000 Taiwanese.

Chen DP, Tseng CP, Wang WT, Peng CT, Tsao KC, Wu TL, Lin KT, Sun CF.

Ann Clin Lab Sci. 2004 Summer;34(3):314-8.

PMID:
15487706
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk