Ji Y - Search Results

1

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. Among authors: ji y. Transfusion. 2019 Jan;59(1):405-411. doi: 10.1111/trf.14969. Epub 2018 Oct 4. Transfusion. 2019. PMID: 30284303

2

[High-throughput genotyping multiplex ligation-dependent probe amplification for assisting diagnosis in a case of anti-Di(a)-induced severe hemolytic disease of the newborn].

Ji Y, Mo C, Wei L, Zhou X, Zhang R, Zhao Y, Luo H, Wang Z, Luo G. Ji Y, et al. Nan Fang Yi Ke Da Xue Xue Bao. 2012 Feb;32(2):234-8. Nan Fang Yi Ke Da Xue Xue Bao. 2012. PMID: 22381766 Chinese.

3

[Serological and genetic study of a pedigree featuring a rare p phenotype].

Wei L, Ji YL, Luo H, Mo CY, Zhang RQ, Zhao Y, Wang Z, Luo GP. Wei L, et al. Among authors: ji yl. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012 Dec;29(6):701-4. doi: 10.3760/cma.j.issn.1003-9406.2012.06.017. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2012. PMID: 23225054 Chinese.

4

[Anti-Mur screening and Mur antigen genotyping of voluntary blood donors in Guangzhou].

Wei L, Ji Y, Mo C, Zhang R, Zhao Y, Luo H, Wang Z, Luo G. Wei L, et al. Among authors: ji y. Nan Fang Yi Ke Da Xue Xue Bao. 2012 Dec;32(12):1833-5. Nan Fang Yi Ke Da Xue Xue Bao. 2012. PMID: 23268422 Chinese.

5

The summary of FUT1 and FUT2 genotyping analysis in Chinese para-Bombay individuals including additional nine probands from Guangzhou in China.

Luo G, Wei L, Wang Z, Luo H, Zhao Y, Zhang R, Mo C, Ji Y. Luo G, et al. Among authors: ji y. Transfusion. 2013 Dec;53(12):3224-9. doi: 10.1111/trf.12183. Epub 2013 Apr 8. Transfusion. 2013. PMID: 23560544

6

H435-containing immunoglobulin G3 allotypes are transported efficiently across the human placenta: implications for alloantibody-mediated diseases of the newborn.

Einarsdottir H, Ji Y, Visser R, Mo C, Luo G, Scherjon S, van der Schoot CE, Vidarsson G. Einarsdottir H, et al. Among authors: ji y. Transfusion. 2014 Mar;54(3):665-71. doi: 10.1111/trf.12334. Epub 2013 Jul 7. Transfusion. 2014. PMID: 23829325

7

A novel 519_525dup mutation of KLF1 gene identified in a Chinese blood donor with Lu(a-b-) phenotype.

Wang Z, Luo G, Ji Y. Wang Z, et al. Among authors: ji y. Transfusion. 2013 Jul;53(7):1619-20. doi: 10.1111/trf.12212. Transfusion. 2013. PMID: 23844643 No abstract available.

8

Comprehensive genotyping for 18 blood group systems using a multiplex ligation-dependent probe amplification assay shows a high degree of accuracy.

Haer-Wigman L, Ji Y, Lodén M, de Haas M, van der Schoot CE, Veldhuisen B. Haer-Wigman L, et al. Among authors: ji y. Transfusion. 2013 Nov;53(11 Suppl 2):2899-909. doi: 10.1111/trf.12410. Epub 2013 Aug 29. Transfusion. 2013. PMID: 23992446

9

Novel alleles at the Kell blood group locus that lead to Kell variant phenotype in the Dutch population.

Ji Y, Veldhuisen B, Ligthart P, Haer-Wigman L, Jongerius J, Boujnan M, Ait Soussan A, Luo G, Fu Y, van der Schoot CE, de Haas M. Ji Y, et al. Transfusion. 2015 Feb;55(2):413-21. doi: 10.1111/trf.12838. Epub 2014 Aug 25. Transfusion. 2015. PMID: 25156717 Clinical Trial.

10

GYP*Kip, a novel GYP(B-A-B) hybrid allele, encoding the MNS48 (KIPP) antigen.

Lopez GH, Wei L, Ji Y, Condon JA, Luo G, Hyland CA, Flower RL. Lopez GH, et al. Among authors: ji y. Transfusion. 2016 Feb;56(2):539-41. doi: 10.1111/trf.13450. Epub 2015 Dec 31. Transfusion. 2016. PMID: 26718482 No abstract available.

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