| Human BTR1, a new bicarbonate transporter superfamily member and human AE4 from kidney. Parker M.D., Ourmozdi E.P., Tanner M.J.A.
Biochem. Biophys. Res. Commun. 282:1103-1109(2001) · UniProtKB (2) |
| Band 3 mutations, renal tubular acidosis and South-East Asian ovalocytosis in Malaysia and Papua New Guinea: loss of up to 95% band 3 transport in red cells. Bruce L.J., Wrong O., Toye A.M., Young M.T., Ogle G., Ismail Z., Sinha A.K., McMaster P., Hwaihwanje I., Nash G.B. et al.
Biochem. J. 350:41-51(2000) · UniProtKB (1) |
| Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis. Karet F.E., Gainza F.J., Gyory A.Z., Unwin R.J., Wrong O., Tanner M.J.A., Nayir A., Alpay H., Santos F., Hulton S.A. et al.
Proc. Natl. Acad. Sci. U.S.A. 95:6337-6342(1998) · UniProtKB (1) |
| Band 3 Chur: a variant associated with band 3-deficient hereditary spherocytosis and substitution in a highly conserved position of transmembrane segment 11. Maillet P., Vallier A., Reinhart W.H., Wyss E.J., Ott P., Texier P., Baklouti F., Tanner M.J.A., Delaunay J., Alloisio N.
Br. J. Haematol. 91:804-810(1995) · UniProtKB (1) |
| Identification of functioning regulatory sites and a new myosin binding site in the C-terminal 288 amino acids of caldesmon expressed from a human clone. Huber P.A.J., Redwood C.S., Avent N.D., Tanner M.J.A., Marston S.B.
J. Muscle Res. Cell Motil. 14:385-391(1993) · UniProtKB (1) |
| The solution structures of the first and second transmembrane-spanning segments of band 3. Gargaro A.R., Bloomberg G.B., Dempsey C.E., Murray M., Tanner M.J.A.
Eur. J. Biochem. 221:445-454(1994) · UniProtKB (1) |
| Isolation and characterization of CD47 glycoprotein: a multispanning membrane protein which is the same as integrin-associated protein (IAP) and the ovarian tumour marker OA3. Mawby W.J., Holmes C.H., Anstee D.J., Spring F.A., Tanner M.J.A.
Biochem. J. 304:525-530(1994) · UniProtKB (1) |
| A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemia. Hayette S., Morle L., Bozon M., Ghanem A., Risinger M., Korsgren C., Tanner M.J.A., Fattoum S., Cohen C.M., Delaunay J.
Br. J. Haematol. 89:762-770(1995) · UniProtKB (1) · Mapped (4) |
| Molecular basis of reduced or absent expression of decay-accelerating factor in Cromer blood group phenotypes. Lublin D.M., Mallinson G., Poole J., Reid M.E., Thompson E.S., Ferdman B.R., Telen M.J., Anstee D.J., Tanner M.J.A.
Blood 84:1276-1282(1994) · UniProtKB (1) |
| The human erythrocyte anion-transport protein. Partial amino acid sequence, conformation and a possible molecular mechanism for anion exchange. Brock C.J., Tanner M.J.A., Kempf C.
Biochem. J. 213:577-586(1983) · UniProtKB (1) |
| Human erythrocyte membrane sialoglycoprotein beta. The cDNA sequence suggests the absence of a cleaved N-terminal signal sequence. High S., Tanner M.J.A.
Biochem. J. 243:277-280(1987) · UniProtKB (1) |
| The complete amino acid sequence of the human erythrocyte membrane anion-transport protein deduced from the cDNA sequence. Tanner M.J.A., Martin P.G., High S.
Biochem. J. 256:703-712(1988) · UniProtKB (1) |
| Isolation of cDNA clones for human erythrocyte membrane sialoglycoproteins alpha and delta. Tate C.G., Tanner M.J.A.
Biochem. J. 254:743-750(1988) · UniProtKB (2) |
| Protein-sequence studies on Rh-related polypeptides suggest the presence of at least two groups of proteins which associate in the human red-cell membrane. Avent N.D., Ridgwell K., Mawby W.J., Tanner M.J.A., Anstee D.J., Kumpel B.
Biochem. J. 256:1043-1046(1988) · UniProtKB (3) |
| Rearrangements of the red-cell membrane glycophorin C (sialoglycoprotein beta) gene. A further study of alterations in the glycophorin C gene. High S., Tanner M.J.A., Macdonald E.N., Anstee D.J.
Biochem. J. 262:47-54(1989) · UniProtKB (1) |
| Complete cDNA sequence of human foetal liver peroxisomal 3-oxoacyl-CoA thiolase. Fairbairn L.J., Tanner M.J.A.
Nucleic Acids Res. 17:3588-3588(1989) · UniProtKB (1) |
| cDNA cloning of a 30 kDa erythrocyte membrane protein associated with Rh (Rhesus)-blood-group-antigen expression. Avent N.D., Ridgwell K., Tanner M.J.A., Anstee D.J.
Biochem. J. 271:821-825(1990) · UniProtKB (1) |
| Biochemical studies on red blood cells from a patient with the Inab phenotype (decay-accelerating factor deficiency). Reid M.E., Mallinson G., Sim R.B., Poole J., Pausch V., Merry A.H., Liew Y.W., Tanner M.J.A.
Blood 78:3291-3297(1991) · UniProtKB (1) |
| Basis of unique red cell membrane properties in hereditary ovalocytosis. Schofield A.E., Tanner M.J.A., Pinder J.C., Clough B., Bayley P.M., Nash G.B., Dluzewski A.R., Reardon D.M., Cox T.M., Wilson R.J.M. et al.
J. Mol. Biol. 223:949-958(1992) · UniProtKB (1) |
| Isolation of cDNA clones for a 50 kDa glycoprotein of the human erythrocyte membrane associated with Rh (rhesus) blood-group antigen expression. Ridgwell K., Spurr N.K., Laguda B., Macgeoch C., Avent N.D., Tanner M.J.A.
Biochem. J. 287:223-228(1992) · UniProtKB (1) |
