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Journal Abstract Search


325 related items for PubMed ID: 18931342

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  • 2. Human RhAG ammonia channel is impaired by the Phe65Ser mutation in overhydrated stomatocytic red cells.
    Genetet S, Ripoche P, Picot J, Bigot S, Delaunay J, Armari-Alla C, Colin Y, Mouro-Chanteloup I.
    Am J Physiol Cell Physiol; 2012 Jan 15; 302(2):C419-28. PubMed ID: 22012326
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  • 3. Hereditary stomatocytosis and cation-leaky red cells--recent developments.
    Bruce LJ.
    Blood Cells Mol Dis; 2009 Jan 15; 42(3):216-22. PubMed ID: 19261491
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  • 8. A new blood group system, RHAG: three antigens resulting from amino acid substitutions in the Rh-associated glycoprotein.
    Tilley L, Green C, Poole J, Gaskell A, Ridgwell K, Burton NM, Uchikawa M, Tsuneyama H, Ogasawara K, Akkøk CA, Daniels G.
    Vox Sang; 2010 Feb 15; 98(2):151-9. PubMed ID: 19744193
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  • 9. Mice expressing RHAG and RHD human blood group genes.
    Goossens D, da Silva N, Metral S, Cortes U, Callebaut I, Picot J, Mouro-Chanteloup I, Cartron JP.
    PLoS One; 2013 Feb 15; 8(11):e80460. PubMed ID: 24260394
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  • 10. Mechanism of genetic complementation of ammonium transport in yeast by human erythrocyte Rh-associated glycoprotein.
    Westhoff CM, Siegel DL, Burd CG, Foskett JK.
    J Biol Chem; 2004 Apr 23; 279(17):17443-8. PubMed ID: 14966114
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  • 11. Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1.
    Bruce LJ, Robinson HC, Guizouarn H, Borgese F, Harrison P, King MJ, Goede JS, Coles SE, Gore DM, Lutz HU, Ficarella R, Layton DM, Iolascon A, Ellory JC, Stewart GW.
    Nat Genet; 2005 Nov 23; 37(11):1258-63. PubMed ID: 16227998
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  • 12. Generation and characterisation of Rhd and Rhag null mice.
    Goossens D, Trinh-Trang-Tan MM, Debbia M, Ripoche P, Vilela-Lamego C, Louache F, Vainchenker W, Colin Y, Cartron JP.
    Br J Haematol; 2010 Jan 23; 148(1):161-72. PubMed ID: 19807729
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  • 13. Molecular basis for Rh(null) syndrome: identification of three new missense mutations in the Rh50 glycoprotein gene.
    Huang CH, Cheng G, Liu Z, Chen Y, Reid ME, Halverson G, Okubo Y.
    Am J Hematol; 1999 Sep 23; 62(1):25-32. PubMed ID: 10467273
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  • 14. SNPs altering ammonium transport activity of human Rhesus factors characterized by a yeast-based functional assay.
    Deschuyteneer A, Boeckstaens M, De Mees C, Van Vooren P, Wintjens R, Marini AM.
    PLoS One; 2013 Sep 23; 8(8):e71092. PubMed ID: 23967154
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  • 15. A RHAG point mutation selectively disrupts Rh antigen expression.
    Mu S, Cui Y, Wang W, Wang L, Xu H, Zhu O, Zhu D.
    Transfus Med; 2019 Apr 23; 29(2):121-127. PubMed ID: 29508504
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  • 16. Overhydrated stomatocytosis associated with a complex RHAG genotype including a novel de novo mutation.
    Jamwal M, Aggarwal A, Sachdeva MUS, Sharma P, Malhotra P, Maitra A, Das R.
    J Clin Pathol; 2018 Jul 23; 71(7):648-652. PubMed ID: 29559519
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  • 17. Alterations of red blood cell metabolome in overhydrated hereditary stomatocytosis.
    Darghouth D, Koehl B, Heilier JF, Madalinski G, Bovee P, Bosman G, Delaunay J, Junot C, Roméo PH.
    Haematologica; 2011 Dec 23; 96(12):1861-5. PubMed ID: 21859730
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  • 18. Cation-leak stomatocytosis in standard schnauzers does not cosegregate with coding mutations in the RhAG, SLC4A1, or GLUT1 genes associated with human disease.
    Shmukler BE, Rivera A, Vandorpe DH, Alves J, Bonfanti U, Paltrinieri S, Alper SL.
    Blood Cells Mol Dis; 2012 Apr 15; 48(4):219-25. PubMed ID: 22406315
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  • 19. The challenge of understanding ammonium homeostasis and the role of the Rh glycoproteins.
    Bakouh N, Benjelloun F, Cherif-Zahar B, Planelles G.
    Transfus Clin Biol; 2006 Apr 15; 13(1-2):139-46. PubMed ID: 16564724
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  • 20. Stomatin-deficient cryohydrocytosis results from mutations in SLC2A1: a novel form of GLUT1 deficiency syndrome.
    Flatt JF, Guizouarn H, Burton NM, Borgese F, Tomlinson RJ, Forsyth RJ, Baldwin SA, Levinson BE, Quittet P, Aguilar-Martinez P, Delaunay J, Stewart GW, Bruce LJ.
    Blood; 2011 Nov 10; 118(19):5267-77. PubMed ID: 21791420
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