Wen J - Search Results

1

Identification of a novel frequent RHCE*ce308T variant allele in Chinese D- individuals, resulting in a C+c- phenotype.

Stegmann TC, Ji Y, Bijman R, Wang Z, Wen J, Wei L, Veldhuisen B, Haer-Wigman L, Lighthart P, Lodén-van Straaten M, Luo G, van der Schoot CE. Stegmann TC, et al. Among authors: wen j. Transfusion. 2016 Sep;56(9):2314-21. doi: 10.1111/trf.13709. Epub 2016 Jun 24. Transfusion. 2016. PMID: 27338008

2

The distribution of MNS hybrid glycophorins with Mur antigen expression in Chinese donors including identification of a novel GYP.Bun allele.

Wei L, Shan ZG, Flower RL, Wang Z, Wen JZ, Luo GP, Ji YL. Wei L, et al. Among authors: wen jz. Vox Sang. 2016 Oct;111(3):308-314. doi: 10.1111/vox.12421. Epub 2016 May 27. Vox Sang. 2016. PMID: 27232276

3

Validation of the multiplex ligation-dependent probe amplification assay and its application on the distribution study of the major alleles of 17 blood group systems in Chinese donors from Guangzhou.

Ji Y, Wen J, Veldhuisen B, Haer-Wigman L, Wang Z, Lodén-van Straaten M, Wei L, Luo G, Fu Y, van der Schoot CE. Ji Y, et al. Among authors: wen j. Transfusion. 2017 Feb;57(2):423-432. doi: 10.1111/trf.13940. Epub 2016 Nov 27. Transfusion. 2017. PMID: 27891625

4

RHD genotype and zygosity analysis in the Chinese Southern Han D+, D- and D variant donors using the multiplex ligation-dependent probe amplification assay.

Ji YL, Luo H, Wen JZ, Haer-Wigman L, Veldhuisen B, Wei L, Wang Z, Ligthart P, Lodén-van Straaten M, Fu YS, van der Schoot CE, Luo GP. Ji YL, et al. Among authors: wen jz. Vox Sang. 2017 Oct;112(7):660-670. doi: 10.1111/vox.12554. Epub 2017 Aug 18. Vox Sang. 2017. PMID: 28833187

5

[Phenotype Types and Genetic Mutation Mechanism of Rhesus D Variant Individuals].

Luo H, Wen JZ, Zhang RQ, Ji YL, Mo CY, Wei L, Wang Z, Liao ZJ, Luo GP. Luo H, et al. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2017 Dec;25(6):1804-1809. doi: 10.7534/j.issn.1009-2137.2017.06.041. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2017. PMID: 29262920 Chinese.

6

Genotyping analysis of MNS blood group GP(B-A-B) hybrid glycophorins in the Chinese Southern Han population using a high-resolution melting assay.

Wei L, Lopez GH, Zhang Y, Wen J, Wang Z, Fu Y, Hyland CA, Flower RL, Luo G, Ji Y. Wei L, et al. Among authors: wen j. Transfusion. 2018 Jul;58(7):1763-1771. doi: 10.1111/trf.14641. Epub 2018 Jun 13. Transfusion. 2018. PMID: 29897102

7

A variant RhAG protein encoded by the RHAG*572A allele causes serological weak D expression while maintaining normal RhCE phenotypes.

Wen J, Verhagen OJHM, Jia S, Liang Q, Wang Z, Wei L, Luo H, Luo G, Vidarsson G, van den Akker E, Ji Y, van der Schoot CE. Wen J, et al. Transfusion. 2019 Jan;59(1):405-411. doi: 10.1111/trf.14969. Epub 2018 Oct 4. Transfusion. 2019. PMID: 30284303

8

Identification of a novel DI*02(2558T) allele associated with weakened expression of DI2 antigen.

Wen J, van den Akker E, Luo G, Jia S, Wei L, Wang Z, van der Schoot CE, Ji Y. Wen J, et al. Transfusion. 2020 Nov;60(11):2675-2683. doi: 10.1111/trf.16013. Epub 2020 Aug 13. Transfusion. 2020. PMID: 32789883 Clinical Trial.

9

Serological screening and genetic analysis of RhCE variants in the Chinese Southern Han donors.

Jia S, Chen J, Wen J, Wang Z, Wei L, Fu Y, Luo G, Ji Y. Jia S, et al. Among authors: wen j. Transfus Med. 2021 Aug;31(4):271-276. doi: 10.1111/tme.12788. Epub 2021 May 16. Transfus Med. 2021. PMID: 33998062

10

Molecular genetic analysis of Mi^a -positive hybrid glycophorins revealed two novel alleles of GP.Vw and multiple variant transcripts of GYPB existing in both the homozygous GP.Mur and wild-type GPB individuals.

Wei L, Sun A, Wen J, Wang Z, Li Q, Liao Y, Luo G, Ji Y. Wei L, et al. Among authors: wen j. Transfusion. 2021 Aug;61(8):2477-2486. doi: 10.1111/trf.16450. Epub 2021 Jun 12. Transfusion. 2021. PMID: 34117642

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