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Results: 1 to 20 of 142

Similar articles for PubMed (Select 8175676)

1.

Molecular basis for plasma alpha(1,3)-fucosyltransferase gene deficiency (FUT6).

Mollicone R, Reguigne I, Fletcher A, Aziz A, Rustam M, Weston BW, Kelly RJ, Lowe JB, Oriol R.

J Biol Chem. 1994 Apr 29;269(17):12662-71.

2.

Two Novel α 1,2-Fucosyltransferase Alleles in an H-Deficient Phenotype Individual.

He Z, Liu F.

Transfus Med Hemother. 2014 Oct;41(5):375-9. doi: 10.1159/000366235. Epub 2014 Aug 17.

3.

[Effect of α -1,2 fucosyltransferase gene 682A> G and 547_552delAG mutations on the activity of fucosyltransferase].

Tao S, He Y, Xu X, Hong X, He J, Zhu F, Lyu H.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Oct;31(5):591-4. doi: 10.3760/cma.j.issn.1003-9406.2014.01.011. Chinese.

PMID:
25297588
4.

[Distribution specificity of human fucosyltransferase 5 and its expression and localization in spermatids].

Li FR, Zhou YS, Zhu LH, Cui HG, Wang BJ, Ding M, Pang H.

Fa Yi Xue Za Zhi. 2012 Apr;28(2):112-4, 119. Chinese.

PMID:
22619806
5.

C35T mutation could slightly decrease the activity of human α-(1,2)-fucosyltransferase.

Tao S, He Y, Ying Y, Hong X, Xu X, Zhu F, Lv H, Yan L.

Transfus Clin Biol. 2012 Feb;19(1):5-10. doi: 10.1016/j.tracli.2011.06.003. Epub 2012 Jan 21. Erratum in: Transfus Clin Biol. 2012 Apr;19(2):78.

PMID:
22266267
6.

A novel FUT1 allele was identified in a Chinese individual with para-Bombay phenotype.

Xu X, Tao S, Ying Y, Hong X, He Y, Zhu F, Lv H, Yan L.

Transfus Med. 2011 Dec;21(6):385-93. doi: 10.1111/j.1365-3148.2011.01111.x. Epub 2011 Oct 12.

PMID:
21988368
7.

[Para-Bombay phenotype caused by combined heterozygote of two bases deletion on fut1 alleles].

Ma KR, Tao SD, Lan XF, Hong XZ, Xu XG, Zhu FM, Lü HJ, Yan LX.

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2011 Feb;19(1):223-6. Chinese.

PMID:
21362257
8.

[Fut1 gene mutation for para-bombay blood type individual in Fujian Province of China].

Huang HB, Fan LP, Wai SJ, Zeng F, Lin HY, Zhang R.

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2010 Oct;18(5):1338-40. Chinese.

PMID:
21129289
9.

[The genetic diversity in the full coding region of human FUT5 gene in a Chinese Han population].

Li FR, Tian XF, Zhou YS, Wang BJ, Ding M, Pang H.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Aug;27(4):473-6. doi: 10.3760/cma.j.issn.1003-9406.2010.04.026. Chinese.

PMID:
20677162
10.

[Analysis of alpha-1,2-fucosyltransferase gene mutations in a Chinese family with para-Bombay phenotype].

Xu XG, Hong XZ, Liu Y, Ying YL, Tao SD, He YM, Zhu FM, Lv HJ, Yan LX.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Jun;27(3):250-4. doi: 10.3760/cma.j.issn.1003-9406.2010.0.003. Chinese.

PMID:
20533259
11.

Infection-associated FUT2 (Fucosyltransferase 2) genetic variation and impact on functionality assessed by in vivo studies.

Silva LM, Carvalho AS, Guillon P, Seixas S, Azevedo M, Almeida R, Ruvoën-Clouet N, Reis CA, Le Pendu J, Rocha J, David L.

Glycoconj J. 2010 Jan;27(1):61-8. doi: 10.1007/s10719-009-9255-8. Epub 2009 Sep 16.

PMID:
19757028
12.

Alport syndrome. Molecular genetic aspects.

Hertz JM.

Dan Med Bull. 2009 Aug;56(3):105-52.

PMID:
19728970
13.

Missense and nonsense mutations in melanocortin 1 receptor (MC1R) gene of different goat breeds: association with red and black coat colour phenotypes but with unexpected evidences.

Fontanesi L, Beretti F, Riggio V, Dall'Olio S, González EG, Finocchiaro R, Davoli R, Russo V, Portolano B.

BMC Genet. 2009 Aug 25;10:47. doi: 10.1186/1471-2156-10-47.

14.

Identification of 14 new alleles at the fucosyltransferase 1, 2, and 3 loci in Styrian blood donors, Austria.

Matzhold EM, Helmberg W, Wagner T, Drexler C, Ulrich S, Winkler A, Lanzer G.

Transfusion. 2009 Oct;49(10):2097-108. doi: 10.1111/j.1537-2995.2009.02293.x. Epub 2009 Jun 30.

PMID:
19572973
15.

Induction of sialyl-Lex expression by herpes simplex virus type 1 is dependent on viral immediate early RNA-activated transcription of host fucosyltransferase genes.

Nyström K, Nordén R, Muylaert I, Elias P, Larson G, Olofsson S.

Glycobiology. 2009 Aug;19(8):847-59. doi: 10.1093/glycob/cwp057. Epub 2009 Apr 15.

17.

[Molecular genetic analysis of FUT1 and FUT2 gene in para-Bombay Chinese: a novel FUT1 allele is identified].

Su Yq, Wei TL, Yu Q, Liang YL, Li DC.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2007 Oct;24(5):520-3. Chinese.

PMID:
17922418
18.

[Molecular genetic basis for para-Bombay phenotypes in two cases].

He YM, Xu XG, Zhu FM, Yan LX.

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2007 Jun;15(3):626-9. Chinese.

PMID:
17605880
19.

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
20.

En bloc duplications, mutation rates, and densities of amino acid changes clarify the evolution of vertebrate alpha-1,3/4-fucosyltransferases.

Petit D, Maftah A, Julien R, Petit JM.

J Mol Evol. 2006 Sep;63(3):353-64. Epub 2006 Aug 21.

PMID:
16927008
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