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