| 1 | RHAG
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| Human Rhesus-associated glycoprotein mediates facilitated transport of NH(3) into red blood cells.
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| Ripoche P, Bertrand O, Gane P, Birkenmeier C, Colin Y, Cartron JP.
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| Proc Natl Acad Sci U S A 101(49):17222-7. Epub 2004 Dec 7. 2004
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| 2 | RHAG, RHD
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| Cell-surface expression of RhD blood group polypeptide is posttranscriptionally regulated by the RhAG glycoprotein.
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| Mouro-Chanteloup I, D'Ambrosio AM, Gane P, Le Van Kim C, Raynal V, Dhermy D, Cartron JP, Colin Y.
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| Blood 100(3):1038-47. 2002
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| 3 | RHAG
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| Identification of the erythrocyte Rh blood group glycoprotein as a mammalian ammonium transporter.
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| Westhoff CM, Ferreri-Jacobia M, Mak DO, Foskett JK.
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| J Biol Chem 277(15):12499-502. Epub 2002 Feb 22. 2002
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| 4 | RHAG
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| Cloning and characterization of erythroid-specific DNase I-hypersensitive site in human rhesus-associated glycoprotein gene.
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| Iwamoto S, Suganuma H, Kamesaki T, Omi T, Okuda H, Kajii E.
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| J Biol Chem 275(35):27324-31. 2000
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| 5 | RHAG, RHCG
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| The human Rhesus-associated RhAG protein and a kidney homologue promote ammonium transport in yeast.
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| Marini AM, Matassi G, Raynal V, Andre B, Cartron JP, Cherif-Zahar B.
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| Nat Genet 26(3):341-4. 2000
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| 6 | RHAG, RHNR
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| Rhmod syndrome : a family study of the translation-initiator mutation in the Rh50 glycoprotein gene.
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| Huang CH, et al.
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| Am J Hum Genet 64 : 108-117. 1999
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| 7 | RHAG
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| Molecular basis for Rh(null) syndrome: identification of three new missense mutations in the Rh50 glycoprotein gene.
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| Huang CH, Cheng G, Liu Z, Chen Y, Reid ME, Halverson G, Okubo Y.
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| Am J Hematol 62(1):25-32 1999
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| 8 | RHAG, RHCE, RHD
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| Organization of the human RH50A gene (RHAG) and evolution of base composition of the RH gene family.
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| Matassi G, Cherif-Zahar B, Raynal V, Rouger P, Cartron JP.
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| Genomics 47(2):286-93. 1998
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| 9 | RHAG, RHNR
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| A novel single missense mutation identified along the RH50 gene in a composite heterozygous Rhnull blood donor of the regulator type.
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| Hyland CA, Cherif-Zahar B, Cowley N, Raynal V, Parkes J, Saul A, Cartron JP.
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| Blood 91(4):1458-63. 1998
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| 10 | RHAG, RHNR
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| The human Rh50 glycoprotein gene. Structural organization and associated splicing defect resulting in Rh(null) disease.
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| Huang CH.
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| J Biol Chem 273(4):2207-13. 1998
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| 11 | RHAG, RHNR
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| A splicing mutation of the RHAG gene associated with the RHnull phenotype.
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| Kawano M, et al.
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| Ann Hum Genet 62 : 107-113. 1998
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| 12 | RHAG, RHCE, RHNR
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| Rh50 glycoprotein gene and rhnull disease: a silent splice donor is trans to a Gly279-->Glu missense mutation in the conserved transmembrane segment.
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| Huang CH, Liu Z, Cheng G, Chen Y.
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| Blood 92 : 1776-1784. 1998
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| 13 | RHAG, RHNR
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| Rh-deficiency of the regulator type caused by splicing mutations in the human RH50 gene.
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| Cherif-Zahar B, et al.
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| Blood 92 : 2535-2540. 1998
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| 14 | RHAG, RHNR
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| Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency.
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| Cherif-Zahar B, et al.
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| Nat Genet 12 : 168-173. 1996
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| 15 | RHAG, RHCG
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| Isolation of cDNA clones for a 50 kDa glycoprotein of the human erythrocyte membrane associated with Rh (Rhesus) blood-group antigen expression.
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| Ridgwell K, et al.
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| Biochem J 287 : 223-228. 1992
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