Macey RI. Transport of water and urea in red blood cells. Am J Physiol 1984;246:C195-203.10.1152/ajpcell.1984.246.3.C195Search in Google Scholar
Agre P, Saboori AM, Asimos A, Smith BL. Purification and partial characterization of the Mr 30,000 integral membrane protein associated with the erythrocyte Rh(D) antigen. J Biol Chem 1987;262:17497–503.10.1016/S0021-9258(18)45408-7Search in Google Scholar
Saboori AM, Smith BL, Agre P. Polymorphism in the Mr 32,000 Rh protein purified from Rh(D)-positive and -negative erythrocytes. Proc Natl Acad Sci U S A 1988;85:4042–5.10.1073/pnas.85.11.40422803573131772Search in Google Scholar
Preston GM, Agre P. Isolation of the cDNA for erythrocyte integral membrane protein of 28 kilodaltons: member of an ancient channel family. Proc Natl Acad Sci U S A 1991;88:11110–4.10.1073/pnas.88.24.11110530831722319Search in Google Scholar
Kozono D, Ding X, Iwasaki I, et al. Functional expression and characterization of an archaeal aquaporin. AqpM from Methanothermobacter marburgensis. J Biol Chem 2003;278:10649–56.10.1074/jbc.M21241820012519768Search in Google Scholar
Roudier N, Ripoche P, Gane P, et al. AQP3 deficiency in humans and the molecular basis of a novel blood group system, GIL. J Biol Chem 2002;277:45854–9.10.1074/jbc.M20899920012239222Search in Google Scholar
Vajda Z, Pedersen M, Füchtbauer EM, et al. Delayed onset of brain edema and mislocalization of aquaporin-4 in dystrophin-null transgenic mice. Proc Natl Acad Sci U S A 2002;99:13131–6.10.1073/pnas.19245709913059812232046Search in Google Scholar
Ikeda M, Beitz E, Kozono D, Guggino WB, Agre P, Yasui M. Characterization of aquaporin-6 as a nitrate channel in mammalian cells. Requirement of pore-lining residue threonine 63. J Biol Chem 2002;277:39873–9.10.1074/jbc.M20700820012177001Search in Google Scholar
Carbrey JM, Gorelick-Feldman DA, Kozono D, Praetorius J, Nielsen S, Agre P. Aquaglyceroporin AQP9: solute permeation and metabolic control of expression in liver. Proc Natl Acad Sci U S A 2003;100:2945–50.10.1073/pnas.043799410015144612594337Search in Google Scholar
Endeward V, Musa-Aziz R, Cooper GJ, et al. Evidence that aquaporin 1 is a major pathway for CO2 transport across the human erythrocyte membrane. FASEB J 2006;20:1974–81.10.1096/fj.04-3300com17012249Search in Google Scholar
Smith BL, Preston GM, Spring FA, Anstee DJ, Agre P. Human red cell aquaporin CHIP. I. Molecular characterization of ABH and Colton blood group antigens. J Clin Invest 1994;94:1043–9.10.1172/JCI117418Search in Google Scholar
Heistö H, van der Hart M, Madsen G, et al. Three examples of a new red cell antibody, anti-Coa. Vox Sang 1967;12:18–24.10.1111/j.1423-0410.1967.tb03353.xSearch in Google Scholar
Reid ME, Lomas-Francis C. The blood group antigen factsbook. 2nd ed. San Diego, CA: Academic Press, 2004.10.1016/B978-012586585-2/50007-XSearch in Google Scholar
Wray E, Simpson S. A further example of anti-Coa and two informative families with Co(a-) members. Vox Sang 1968;14:130–2.Search in Google Scholar
Giles CM, Darnborough J, Aspinall P, Fletton MW. Identification of the first example of anti-Cob. Br J Haematol 1970;19:267–9.10.1111/j.1365-2141.1970.tb01623.xSearch in Google Scholar
Race RR, Sanger R. Blood groups in man. 6th ed. Oxford, England: Blackwell Scientific Publications, 1975.Search in Google Scholar
Lewis M, Kaita H, Anderson C, Chown B. Independence of Colton blood group. Transfusion 1971;11:223–4.10.1111/j.1537-2995.1971.tb04406.xSearch in Google Scholar
Rogers MJ, Stiles PA, Wright J. A new minus-minus phenotype: three Co(a-b-) individuals in one family (abstract). Transfusion 1974;14:508.Search in Google Scholar
Moon C, Preston GM, Griffin CA, Jabs EW, Agre P. The human aquaporin-CHIP gene. Structure, organization, and chromosomal localization. J Biol Chem 1993;268:15772–8.10.1016/S0021-9258(18)82322-5Search in Google Scholar
Zelinski T, Kaita H, Gilson T, Coghlan G, Philipps S, Lewis M. Linkage between the Colton blood group locus and ASSP11 on chromosome 7. Genomics 1990;6:623–5.10.1016/0888-7543(90)90496-HSearch in Google Scholar
Agre P, King L, Yasui M, et.al. Topical Review: Aquaporin water channels—from atomic structure to clinical medicine. J Physiol. 2002;542:3–16.10.1113/jphysiol.2002.020818229038212096044Search in Google Scholar
King LS, Agre P. Pathophysiology of the aquaporin water channels. Annu Rev Physiol 1996;58:619–48.10.1146/annurev.ph.58.030196.0031558815812Search in Google Scholar
Mathai JC, Agre P. Hourglass pore-forming domains restrict aquaporin-1 tetramer assembly. Biochemistry 1999;38:923–8.10.1021/bi98236839893987Search in Google Scholar
Jung JS, Preston GM, Smith BL, Guggino WB, Agre P. Molecular structure of the water channel through aquaporin CHIP. The hourglass model. J Biol Chem 1994;269:14648–54.10.1016/S0021-9258(17)36674-7Search in Google Scholar
Preston GM, Smith BL, Zeidel ML, Moulds JJ, Agre P. Mutations in aquaporin-1 in phenotypically normal humans without functional CHIP water channels. Science 1994;265:1585–7.10.1126/science.75215407521540Search in Google Scholar
Chrétien S, Catron JP, de Figueiredo M. A single mutation inside the NPA motif of aquaporin-1 found in a Colton-null phenotype (letter). Blood 1999;93:4021–3.10.1182/blood.V93.11.4021Search in Google Scholar
Joshi SR, Wagner FF, Vasantha K, Panjwani SR, Flegel WA. An AQP1 null allele in an Indian woman with Co(a-b-) phenotype and high-titer anti-Co3 associated with mild HDN. Transfusion 2001;41:1273–8.10.1046/j.1537-2995.2001.41101273.x11606828Search in Google Scholar
Nance S, Kavitsky DL, Meny G, Vege, S, Westhoff CM. An example of anti-Co3 not causing hemolytic disease of the newborn. Transfusion 2002;42(Suppl):105S.Search in Google Scholar
Wagner FF, Flegel WA. A clinically relevant Co(a)-like allele encoded by AQP1 (Q47R) (abstract). Transfusion 2002;42(Suppl):24S–5S.Search in Google Scholar
Arnaud L, Helias V, Menanteau C, Peyrard T, et al. A functional AQP1 allele producing a Co(a-b-) phenotype revises and extends the Colton blood group system. Transfusion 2010. In press.10.1111/j.1537-2995.2010.02687.x20492605Search in Google Scholar
Lacey PA, Robinson J, Collins ML, et al. Studies on the blood of a Co (a-b-) proposita and her family. Transfusion 1987;27:268–71.10.1046/j.1537-2995.1987.27387235637.x3590290Search in Google Scholar
Preston GM, Carroll TP, Guggino WB, Agre P. Appearance of water channels in Xenopus oocytes expressing red cell CHIP28 protein. Science 1992;256:385–7.10.1126/science.256.5055.3851373524Search in Google Scholar
Kozono D, Yasui M, King LS, Agre P. Aquaporin water channels: atomic structure and molecular dynamics meet clinical medicine. J Clin Invest 2002;109:1395–9.10.1172/JCI0215851Search in Google Scholar
Daniels G. Human blood groups. 2nd ed. Malden, MA: Blackwell Science, 2002.10.1002/9780470987018Search in Google Scholar
Issitt PD, Anstee DJ. Applied blood group serology. 4th ed. Durham, NC: Montgomery Scientific Publications, 1998.Search in Google Scholar
Covin RB, Evans KS, Olshock R, Thompson HW. Acute hemolytic transfusion reaction caused by anti-Coa. Immunohematology 2001;17:45–9.10.21307/immunohematology-2019-543Search in Google Scholar
Simpson WKH. Anti-Coa and severe haemolytic disease of the newborn. S Afr Med J 1973;47:1302–4.Search in Google Scholar
Agre P, Smith BL, Baumgarten R, et al. Human red cell aquaporin CHIP. II. Expression during normal fetal development and in a novel form of congenital dyserythropoietic anemia. J Clin Invest 1994;94:1050–8.10.1172/JCI1174192951617521883Search in Google Scholar
Kurtz SR, Kuszaj T, Ouellet R, Valeri CR. Survival of homozygous Coa (Colton) red cells in a patient with anti-Coa. Vox Sang 1982;43:28–30.10.1111/j.1423-0410.1982.tb01113.x7113116Search in Google Scholar
Michalewska B, Wielgos M, Zupanska B, Bartkowiak R. Anti-Coa implicated in severe haemolytic disease of the foetus and newborn. Transfus Med 2008;18:71–3.10.1111/j.1365-3148.2007.00799.x18179649Search in Google Scholar
Dzik WH, Blank J. Accelerated destruction of radiolabeled red cells due to anti-Coltonb. Transfusion 1986;26:246–8.10.1046/j.1537-2995.1986.26386209380.x3705142Search in Google Scholar
Hoffmann JJML, Overbeeke MAM. Characteristics of anti-Cob in vitro and in vivo: a case study. Immunohematology 1996;12:11–13.10.21307/immunohematology-2019-739Search in Google Scholar
Savona-Ventura C, Grech ES, Zieba A. Anti-Co3 and severe hemolytic disease of the newborn. Obstet Gynecol 1989;73:870–2.Search in Google Scholar
Moulds M, Strohm P, McDowell MA, Moulds J. Autoantibody mimicking alloantibody in the Colton blood group system (abstract). Transfusion 1988;28(Suppl):36S.Search in Google Scholar
King LS, Choi M, Fernandez PC, Cartron JP, Agre P. Defective urinary-concentrating ability due to a complete deficiency of aquaporin-1. N Engl J Med 2001;345:175–9.10.1056/NEJM20010719345030411463012Search in Google Scholar
