1例ABO正反定不符的血型分子生物学鉴定

康丹, 郝一文. 1例ABO正反定不符的血型分子生物学鉴定[J]. 临床血液学杂志, 2019, 32(10): 810-812. doi: 10.13201/j.issn.1004-2806-b.2019.10.023
引用本文: 康丹, 郝一文. 1例ABO正反定不符的血型分子生物学鉴定[J]. 临床血液学杂志, 2019, 32(10): 810-812. doi: 10.13201/j.issn.1004-2806-b.2019.10.023
KANG Dan, HAO Yiwen. A case report of ABO positive-negative inconsistency in blood group molecular biology identification[J]. J Clin Hematol, 2019, 32(10): 810-812. doi: 10.13201/j.issn.1004-2806-b.2019.10.023
Citation: KANG Dan, HAO Yiwen. A case report of ABO positive-negative inconsistency in blood group molecular biology identification[J]. J Clin Hematol, 2019, 32(10): 810-812. doi: 10.13201/j.issn.1004-2806-b.2019.10.023

1例ABO正反定不符的血型分子生物学鉴定

详细信息
    通讯作者: 郝一文,E-mail:hyw82666@163.com
  • 中图分类号: R457.1

A case report of ABO positive-negative inconsistency in blood group molecular biology identification

More Information
  • 加载中
  • [1]

    Ricci Hagman J,Hult AK,Westman JS,et al.Multiple miscarriages in two sisters of Thai origin with the rare Pk phenotype caused by a novel nonsense mutation at the B3GALNT1 locus[J].Transfus Med,2019,29:202-208.

    [2]

    Qin WY,Gan LN,Xia RW,et al.Promoter identification and analysis of key glycosphingolipid biosynthesis-globo series pathway genes in piglets[J].Genet Mol Res,2017,16.

    [3]

    Westman JS,Benktander J,Storry JR,et al.Identification of the Molecular and Genetic Basis of PX2,a Glycosphingolipid Blood Group Antigen Lacking on Globoside-deficient Erythrocytes[J].J Biol Chem,2015,290:18505-18518.

    [4]

    Cooling L,Dake LR,Haverty D,et al.A hemolytic anti-LKE associated with a rare LKE-negative, "weak P" red blood cell phenotype:alloanti-LKE and alloanti-P recognize galactosylgloboside and monosialogalactosylgloboside (LKE) antigens[J].Transfusion,2015,55:115-28.

    [5]

    Moghaddam M,Naghi AA.Clinical significance of antibodies to antigens in the Raph,John Milton Hagen,I,Globoside,Gill,Rh-associated glycoprotein,FORS,JR,LAN,Vel,CD59,and Augustine blood group systems[J].Immunohematology,2018,34:85-90.

    [6]

    Kaczmarek R,Szymczak-Kulus K,Berez 'nicka A,et al.Single nucleotide polymorphisms in A4GALT spur extra products of the human Gb3/CD77 synthase and underlie the P1PK blood group system[J].PLoS One,2018,13:e0196627.

    [7]

    Cooling L,Dake LR,Haverty D,et al.A hemolytic anti-LKE associated with a rare LKE-negative, "weak P" red blood cell phenotype:alloanti-LKE and alloanti-P recognize galactosylgloboside and monosialogalactosylgloboside (LKE) antigens[J].Transfusion,2015,55:115-128.

    [8]

    Ricci Hagman J,Hult AK,Westman JS,et al.Multiple miscarriages in two sisters of Thai origin with the rare Pk phenotype caused by a novel nonsense mutation at the B3GALNT1 locus[J].Transfus Med,2019,29:202-208.

    [9]

    Yamamoto M,Cid E,Yamamoto F.ABO blood group A transferases catalyze the biosynthesis of FORS blood group FORS1 antigen upon deletion of exon 3 or 4[J].Blood Adv,2017,1:2756-2766.

    [10]

    Sorbolini S,Gaspa G,Steri R,et al.Use of canonical discriminant analysis to study signatures of selection in cattle[J].Genet Sel Evol,2016,48:58.

    [11]

    Dong WH,Dai CH,Sun L,et al.Expression of key glycosphingolipid biosynthesis-globo series pathway genes in Escherichia coli F18-resistant and Escherichia coli F18-sensitive piglets[J].Anim Genet,2016,47:428-435.

    [12]

    Lan X,Hong X,Xu X,et al[A rare Pk phenotype caused by a 433 C>T mutation of the β-1,3-N-acetylgalactosyltransferase gene] [J].Zhonghua Yi Xue Yi Chuan Xue Za Zhi,2015,32:381-384.

    [13]

    Ducro BJ,Schurink A,Bastiaansen JW,et al.A nonsense mutation in B3GALNT2 is concordant with hydrocephalus in Friesian horses[J].BMC Genomics,2015,16:761.

    [14]

    Volynsky P,Efremov R,Mikhalev I,et al.Why human anti-Galα1-4Galβ1-4Glc natural antibodies do not recognize the trisaccharide on erythrocyte membrane?Molecular dynamics and immunochemical investigation[J].Mol Immunology,2017,90:87-97.

    [16]

    Patnaik SK,Helmberg W,Blumenfeld OO.BGMUT:NCBI dbRBC database of allelic variations of genes encoding antigens of blood group systems[J].Nucleic Acids Res,2012,40,:D1023-9.

    [17]

    Marion E.Reid.The Blood Group Antigen[M].FactsBook,2012:609-613.

    [18]

    Geoff Daniels.Human Blood Groups[M].3rd edition,2012:162-174.

    [19]

    Kaczmarek R,Mikolajewicz K,Szymczak K,et al.Evaluation of an amino acid residue critical for the specificity and activity of human Gb3/CD77 synthase[J].Glycoconj J,2016,33:963-973.

    [20]

    Cooling L,Dake LR,Haverty D,et al.A hemolytic anti-LKE associated with a rare LKE-negative, "weak P" red blood cell phenotype:alloanti-LKE and alloanti-P recognize galactosylgloboside and monosialogalactosylgloboside (LKE) antigens[J].Transfusion,2015,55:115-128.

    [21]

    卞洁,李树中,李凌波,等.一个新的血型抗原——Langereis血型系统[J].临床血液学杂志,2015,28(12):1096-1100.

    [22]

    徐姿,李树中,卞洁,等.红细胞血型抗原的研究进展[J].临床血液学杂志,2016,29(4):345-350.

    [23]

    刘芸,陆敏,徐姿,等.多凝集红细胞的研究进展[J].临床血液学杂志,2016,29(6):215-217.

    [24]

    方莹,李树中,李中华,等.forssman血型系统[J].临床血液学杂志,2016,29(2):171-174.

    [25]

    张志琴,张黎雯,谢怡萍,等.Duffy血型系统抗原研究进展[J].临床血液学杂志,2017,30(4):327-330.

    [26]

    倪强,李树中,雒晶,等.GIL抗原研究进展[J].临床血液学杂志,2017,30(10):812-814.

    [27]

    俞黎娅,李树中,雒晶晶,等.VEL血型抗原研究进展[J].临床血液学杂志,2018,31(2):161-163.

    [28]

    刘芸,李树中,李中华,等.AUG血型抗原研究进展[J].临床血液学杂志,2018,31(6):485-490.

    [29]

    范春丽,李树中,李中华,等.P1PK血型抗原研究进展[J].临床血液学杂志,2018,31(8):643-648.

  • 加载中
计量
  • 文章访问数:  193
  • PDF下载数:  931
  • 施引文献:  0
出版历程
收稿日期:  2019-02-25

目录