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Journal Abstract Search

325 related items for PubMed ID: 18931342

  • 21. Extensive clinical, serologic and molecular studies lead to the first reported Rhmod phenotype in Argentina.
    Mufarrege N, Franco N, Trucco Boggione C, Arnoni C, de Paula Vendrame T, Bartoli S, Ensinck A, Principi C, Lujan Brajovich M, Mattaloni S, Riquelme B, Biondi C, Castilho L, Cotorruelo C.
    Transfusion; 2020 Jul; 60(7):1373-1377. PubMed ID: 32378229
    [Abstract] [Full Text] [Related]

  • 22. The human Rhesus-associated RhAG protein and a kidney homologue promote ammonium transport in yeast.
    Marini AM, Matassi G, Raynal V, André B, Cartron JP, Chérif-Zahar B.
    Nat Genet; 2000 Nov; 26(3):341-4. PubMed ID: 11062476
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  • 23. A family study of the Chinese Rhnull individual of the regulator type: a novel single missense mutation identified in RHAG gene.
    Tian L, Song N, Yao ZQ, Huang M, Hou L.
    Transfusion; 2011 Dec; 51(12):2686-9. PubMed ID: 21682734
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  • 24. Sequence, organization, and evolution of Rh50 glycoprotein genes in nonhuman primates.
    Huang CH, Liu Z, Apoil PA, Blancher A.
    J Mol Evol; 2000 Jul; 51(1):76-87. PubMed ID: 10903374
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  • 25. Evolutionary history of the Rh blood group-related genes in vertebrates.
    Kitano T, Saitou N.
    Immunogenetics; 2000 Aug; 51(10):856-62. PubMed ID: 10970100
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  • 26. Structure, function and significance of Rh proteins in red cells.
    Burton NM, Anstee DJ.
    Curr Opin Hematol; 2008 Nov; 15(6):625-30. PubMed ID: 18832935
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  • 27. Rhmod syndrome: a family study of the translation-initiator mutation in the Rh50 glycoprotein gene.
    Huang C, Cheng GJ, Reid ME, Chen Y.
    Am J Hum Genet; 1999 Jan; 64(1):108-17. PubMed ID: 9915949
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  • 34. In vitro generated Rh(null) red cells recapitulate the in vivo deficiency: a model for rare blood group phenotypes and erythroid membrane disorders.
    Cambot M, Mazurier C, Canoui-Poitrine F, Hebert N, Picot J, Clay D, Picard V, Ripoche P, Douay L, Dubart-Kupperschmitt A, Cartron JP.
    Am J Hematol; 2013 May; 88(5):343-9. PubMed ID: 23417980
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  • 36. Role of RhAG and AQP1 in NH3 and CO2 gas transport in red cell ghosts: a stopped-flow analysis.
    Ripoche P, Goossens D, Devuyst O, Gane P, Colin Y, Verkman AS, Cartron JP.
    Transfus Clin Biol; 2006 May; 13(1-2):117-22. PubMed ID: 16574458
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  • 37. The "stomatin" gene and protein in overhydrated hereditary stomatocytosis.
    Fricke B, Argent AC, Chetty MC, Pizzey AR, Turner EJ, Ho MM, Iolascon A, von Düring M, Stewart GW.
    Blood; 2003 Sep 15; 102(6):2268-77. PubMed ID: 12750157
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  • 38. Relative CO₂/NH₃ permeabilities of human RhAG, RhBG and RhCG.
    Geyer RR, Parker MD, Toye AM, Boron WF, Musa-Aziz R.
    J Membr Biol; 2013 Dec 15; 246(12):915-26. PubMed ID: 24077989
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  • 39. Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis.
    Stewart AK, Kedar PS, Shmukler BE, Vandorpe DH, Hsu A, Glader B, Rivera A, Brugnara C, Alper SL.
    Am J Physiol Cell Physiol; 2011 May 15; 300(5):C1034-46. PubMed ID: 21209359
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