Characterization of Jk(a+weak): a new blood group phenotype associated with an altered JK*01 allele
作者： Elisabet S. Wester , Jill R. Storry , Martin L. Olsson
DOI: 10.1111/J.1537-2995.2010.02795.X
关键词:
摘要: The clinically important Kidd (JK) blood group system is considered to be relatively uncomplicated, both serologically and genetically. JK*01 JK*02 alleles give rise Jk(a) Jk(b) antigens, respectively, silenced result in Jk(a-b-). Other inherited variants analogous Fy(x) weak D phenotypes have not been characterized for JK, although recent abstracts indicate their presence.
sci-hub.se 参考文章(27)
Niva Parasol, Marion Reid, Maria Rios, Lilian Castilho, Ilana Harari, Nechama S. Kosower, A novel mutation in the coding sequence of the FY*B allele of the Duffy chemokine receptor gene is associated with an altered erythrocyte phenotype Blood. ,vol. 92, pp. 2237- 2243 ,(1998) , 10.1182/BLOOD.V92.7.2237
S. Martial, B. Olives, L. Abrami, C. Couriaud, P. Bailly, G. You, M. A. Hediger, J. P. Cartron, P. Ripoche, G. Rousselet, Functional differentiation of the human red blood cell and kidney urea transporters. American Journal of Physiology-renal Physiology. ,vol. 271, ,(1996) , 10.1152/AJPRENAL.1996.271.6.F1264
Christophe Tournamille, Caroline Le Van Kim, Pierre Gane, Pierre Yves Le Pennec, Francis Roubinet, Jérôme Babinet, Jean Pierre Cartron, Yves Colin, Arg89Cys Substitution Results in Very Low Membrane Expression of the Duffy Antigen/Receptor for Chemokines in Fyx Individuals Blood. ,vol. 92, pp. 2147- 2156 ,(1998) , 10.1182/BLOOD.V92.6.2147
Franz F. Wagner, Alexander Frohmajer, Birgit Ladewig, Nicole I. Eicher, Cornelie B. Lonicer, Thomas H. Müller, Manfred H. Siegel, Willy A. Flegel, Weak D alleles express distinct phenotypes Blood. ,vol. 95, pp. 2699- 2708 ,(2000) , 10.1182/BLOOD.V95.8.2699
B Olives, P Neau, P Bailly, M A Hediger, G Rousselet, J P Cartron, P Ripoche, Cloning and functional expression of a urea transporter from human bone marrow cells. Journal of Biological Chemistry. ,vol. 269, pp. 31649- 31652 ,(1994) , 10.1016/S0021-9258(18)31744-7
A. A. Komar, SNPs, Silent But Not Invisible Science. ,vol. 315, pp. 466- 467 ,(2007) , 10.1126/SCIENCE.1138239
Franz F. Wagner, Christoph Gassner, Thomas H. Müller, Diether Schönitzer, Friedrich Schunter, Willy A. Flegel, Molecular Basis of Weak D Phenotypes Blood. ,vol. 93, pp. 385- 393 ,(1999) , 10.1182/BLOOD.V93.1.385.401K19_385_393
Elena J. Levin, Matthias Quick, Ming Zhou, Crystal structure of a bacterial homologue of the kidney urea transporter Nature. ,vol. 462, pp. 757- 761 ,(2009) , 10.1038/NATURE08558
G. A. Geitvik, B. Høyheim, T. Gedde-Dahl, K. H. Grzeschik, R. Lothe, H. Tomter, B. Olaisen, The Kidd (JK) blood group locus assigned to chromosome 18 by close linkage to a DNA-RFLP. Human Genetics. ,vol. 77, pp. 205- 209 ,(1987) , 10.1007/BF00284470
Bernadette Olivès, Sonia Martial, Marie-Geneviève Mattei, Giorgio Matassi, Germain Rousselet, Pierre Ripoche, Jean-Pierre Cartron, Pascal Bailly, Molecular characterization of a new urea transporter in the human kidney FEBS Letters. ,vol. 386, pp. 156- 160 ,(1996) , 10.1016/0014-5793(96)00425-5