-
1
-
-
0018574657
-
Glycophorin A as a cell surface marker of early erythroid differentiation in acute leukemia
-
Andersson, L. C., Gahmberg, C. G., Teerenhovi, L. and Vuopio, P. 1979, Glycophorin A as a cell surface marker of early erythroid differentiation in acute leukemia. International Journal of Cancer, 24, 717-720.
-
(1979)
International Journal of Cancer
, vol.24
, pp. 717-720
-
-
Andersson, L.C.1
Gahmberg, C.G.2
Teerenhovi, L.3
Vuopio, P.4
-
2
-
-
0032400834
-
Functional cell surface expression of band 3, the human red blood cell anion exchange protein (AE1), in K562 erythroleukemia cells: Band 3 enhances the cell surface reactivity of Rh antigens
-
Beckmann, R., Smythe, J. S., Anstee, D. J. and Tanner, M. J. 1998, Functional cell surface expression of band 3, the human red blood cell anion exchange protein (AE1), in K562 erythroleukemia cells: band 3 enhances the cell surface reactivity of Rh antigens. Blood, 92, 4428-4438.
-
(1998)
Blood
, vol.92
, pp. 4428-4438
-
-
Beckmann, R.1
Smythe, J.S.2
Anstee, D.J.3
Tanner, M.J.4
-
3
-
-
0028909047
-
Changes in the blood group Wright antigens are associated with a mutation at amino acid 658 in human erythrocyte band 3: A site of interaction between band 3 and glycophorin A under certain conditions
-
Bruce, L. J., Ring, S. M., Anstee, D. J., Reid, M. E., Wilkinson, S. and Tanner, M. J. 1995, Changes in the blood group Wright antigens are associated with a mutation at amino acid 658 in human erythrocyte band 3: a site of interaction between band 3 and glycophorin A under certain conditions. Blood, 85, 541-547.
-
(1995)
Blood
, vol.85
, pp. 541-547
-
-
Bruce, L.J.1
Ring, S.M.2
Anstee, D.J.3
Reid, M.E.4
Wilkinson, S.5
Tanner, M.J.6
-
4
-
-
0030713102
-
Functional consequences of mutations in the transmembrane domain and the carboxy-terminus of the murine AE1 anion exchanger
-
Chernova, M. N., Humphreys, B. D., Robinson, D. H., Stuart-Tilley, A. K., Garcia, A. M., Brosius, F. C. and Alper, S. L. 1997, Functional consequences of mutations in the transmembrane domain and the carboxy-terminus of the murine AE1 anion exchanger. Biochimica and Biophysics Acta, 1329, 111-123.
-
(1997)
Biochimica and Biophysics Acta
, vol.1329
, pp. 111-123
-
-
Chernova, M.N.1
Humphreys, B.D.2
Robinson, D.H.3
Stuart-Tilley, A.K.4
Garcia, A.M.5
Brosius, F.C.6
Alper, S.L.7
-
5
-
-
0028808517
-
Overexpression of AE1 Prague, but not of AE1 SAO, inhibits wildtype AE1 trafficking in Xenopus oocytes
-
Chernova, M. N., Jarolim, P., Palek, J. and Alper, S. L. 1995, Overexpression of AE1 Prague, but not of AE1 SAO, inhibits wildtype AE1 trafficking in Xenopus oocytes. Journal of Membrane Biology, 148, 203-210.
-
(1995)
Journal of Membrane Biology
, vol.148
, pp. 203-210
-
-
Chernova, M.N.1
Jarolim, P.2
Palek, J.3
Alper, S.L.4
-
6
-
-
0030231133
-
Red cell abnormalities in hereditary spherocytosis: Relevance to diagnosis and understanding of the variable expression of clinical severity
-
Cynober, T., Mohandas, N. and Tchernia, G. 1996, Red cell abnormalities in hereditary spherocytosis: relevance to diagnosis and understanding of the variable expression of clinical severity. Journal of Laboratory and Clinical Medicine, 128, 259-269.
-
(1996)
Journal of Laboratory and Clinical Medicine
, vol.128
, pp. 259-269
-
-
Cynober, T.1
Mohandas, N.2
Tchernia, G.3
-
7
-
-
0027238432
-
Recent data on the molecular pathology of hereditary spherocytosis
-
Dhermy, D. 1993, Recent data on the molecular pathology of hereditary spherocytosis. Nouvelle Revue Française d'Hématologie, 35, 305-306.
-
(1993)
Nouvelle Revue Française d'Hématologie
, vol.35
, pp. 305-306
-
-
Dhermy, D.1
-
8
-
-
8544257359
-
Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects
-
published erratum appears in British Journal of Haematology, 99, 474
-
Dhermy, D., Galand, C., Bournier, O., Boulanger, L., Cynober, T., Schismanoff, P. O., Bursaux, E., Tchernia, G., Boivin, P. and Garbarz, M. 1997, Heterogenous band 3 deficiency in hereditary spherocytosis related to different band 3 gene defects. British Journal of Haematology, 98, 32-40 [published erratum appears in British Journal of Haematology, 99, 474].
-
(1997)
British Journal of Haematology
, vol.98
, pp. 32-40
-
-
Dhermy, D.1
Galand, C.2
Bournier, O.3
Boulanger, L.4
Cynober, T.5
Schismanoff, P.O.6
Bursaux, E.7
Tchernia, G.8
Boivin, P.9
Garbarz, M.10
-
9
-
-
9044220232
-
Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis
-
Eber, S. W., Gonzalez, J. M., Lux, M. L., Scarpa, A. L., Tse, W. T., Dornwell, M., Herbers, J., Kugler, W., Ozcan, R., Pekrun, A., Gallagher, P. G., Schroter, W., Forget, B. G. and Lux, S. E. 1996, Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis. Nature Genetics, 13, 214-218.
-
(1996)
Nature Genetics
, vol.13
, pp. 214-218
-
-
Eber, S.W.1
Gonzalez, J.M.2
Lux, M.L.3
Scarpa, A.L.4
Tse, W.T.5
Dornwell, M.6
Herbers, J.7
Kugler, W.8
Ozcan, R.9
Pekrun, A.10
Gallagher, P.G.11
Schroter, W.12
Forget, B.G.13
Lux, S.E.14
-
10
-
-
0033525686
-
Topology of the membrane domain of human erythrocyte anion exchange protein, AE1
-
Fujinaga, J., Tang, X. B. and Casey, J. R. 1999, Topology of the membrane domain of human erythrocyte anion exchange protein, AE1. Journal of Biological Chemistry, 274, 6626-6633.
-
(1999)
Journal of Biological Chemistry
, vol.274
, pp. 6626-6633
-
-
Fujinaga, J.1
Tang, X.B.2
Casey, J.R.3
-
11
-
-
0030937576
-
Topological rules for membrane protein assembly in eukaryotic cells
-
Gafvelin, G., Sakaguchi, M., Andersson, H. and von Heijne, G. 1997, Topological rules for membrane protein assembly in eukaryotic cells. Journal of Biological Chemistry, 272, 6119-6127.
-
(1997)
Journal of Biological Chemistry
, vol.272
, pp. 6119-6127
-
-
Gafvelin, G.1
Sakaguchi, M.2
Andersson, H.3
Von Heijne, G.4
-
12
-
-
0031417692
-
Hematologically important mutations: Band 3 and protein 4.2 variants in hereditary spherocytosis
-
Gallagher, P.G. and Forget, E.G. 1997, Hematologically important mutations: band 3 and protein 4.2 variants in hereditary spherocytosis. Blood Cells Molecular Disease, 23, 417-421.
-
(1997)
Blood Cells Molecular Disease
, vol.23
, pp. 417-421
-
-
Gallagher, P.G.1
Forget, E.G.2
-
13
-
-
0026755895
-
Spectrin beta Tandil, a novel shortened beta-chain variant associated with hereditary elliptocytosis is due to a deletional frameshift mutation in the beta-spectrin gene
-
Garbarz, M., Boulanger, L., Pedroni, S., Lecomte, M. C., Gautero, H., Galand, C., Boivin, P., Feldman, L. and Dhermy, D. 1992, Spectrin beta Tandil, a novel shortened beta-chain variant associated with hereditary elliptocytosis is due to a deletional frameshift mutation in the beta-spectrin gene. Blood, 80, 1066-1073.
-
(1992)
Blood
, vol.80
, pp. 1066-1073
-
-
Garbarz, M.1
Boulanger, L.2
Pedroni, S.3
Lecomte, M.C.4
Gautero, H.5
Galand, C.6
Boivin, P.7
Feldman, L.8
Dhermy, D.9
-
14
-
-
0026499518
-
Glycophorin A facilitates the expression of human band 3-mediated anion transport in Xenopus oocytes
-
Groves, J. D. and Tanner, M. J. 1992, Glycophorin A facilitates the expression of human band 3-mediated anion transport in Xenopus oocytes. Journal of Biological Chemistry, 267, 22163-22170.
-
(1992)
Journal of Biological Chemistry
, vol.267
, pp. 22163-22170
-
-
Groves, J.D.1
Tanner, M.J.2
-
15
-
-
0028918239
-
Co-expressed complementary fragments of the human red cell anion exchanger (band 3, AE1) generate stilbene disulfonate-sensitive anion transport
-
Groves, J. D. and Tanner, M. J. 1995, Co-expressed complementary fragments of the human red cell anion exchanger (band 3, AE1) generate stilbene disulfonate-sensitive anion transport. Journal of Biological Chemistry, 270, 9097-9105.
-
(1995)
Journal of Biological Chemistry
, vol.270
, pp. 9097-9105
-
-
Groves, J.D.1
Tanner, M.J.2
-
16
-
-
0342351613
-
Predicting the orientation of eukaryotic membrane-spanning proteins
-
Hartmann, E., Rapoport, T. A. and Lodish, H. F. 1989, Predicting the orientation of eukaryotic membrane-spanning proteins. Proceedings of the National Academy of Sciences (USA), 86, 5786-5790.
-
(1989)
Proceedings of the National Academy of Sciences (USA)
, vol.86
, pp. 5786-5790
-
-
Hartmann, E.1
Rapoport, T.A.2
Lodish, H.F.3
-
17
-
-
0029825262
-
Hereditary spherocytosis: A review of the clinical and molecular aspects of the disease
-
Hassoun, H. and Palek, J. 1996, Hereditary spherocytosis: a review of the clinical and molecular aspects of the disease. Blood Reviews, 10, 129-147.
-
(1996)
Blood Reviews
, vol.10
, pp. 129-147
-
-
Hassoun, H.1
Palek, J.2
-
18
-
-
15844377239
-
Defective anion transport and marked spherocytosis with membrane instability caused by hereditary total deficiency of red cell band 3 in cattle due to a nonsense mutation
-
Inaba, M., Yawata, A., Koshino, I., Sato, K., Takeuchi, M., Takakuwa, Y., Manno, S., Yawata, Y., Kanzaki, A., Sakai, J., Ban, A., Ono, K. and Maede, Y. 1996, Defective anion transport and marked spherocytosis with membrane instability caused by hereditary total deficiency of red cell band 3 in cattle due to a nonsense mutation. Journal of Clinical Investigation, 97, 1804-1817.
-
(1996)
Journal of Clinical Investigation
, vol.97
, pp. 1804-1817
-
-
Inaba, M.1
Yawata, A.2
Koshino, I.3
Sato, K.4
Takeuchi, M.5
Takakuwa, Y.6
Manno, S.7
Yawata, Y.8
Kanzaki, A.9
Sakai, J.10
Ban, A.11
Ono, K.12
Maede, Y.13
-
19
-
-
0028939295
-
Mutations of conserved arginines in the membrane domain of erythroid band 3 lead to a decrease in membrane-associated band 3 and to the phenotype of hereditary spherocytosis
-
Jarolim, P., Rubin, H. L., Brabec, V., Chrobak, L., Zolotarev, A. S., Alper, S. L., Brugnara, C., Wichterle, H. and Palek, J. 1995, Mutations of conserved arginines in the membrane domain of erythroid band 3 lead to a decrease in membrane-associated band 3 and to the phenotype of hereditary spherocytosis. Blood, 85, 634-640.
-
(1995)
Blood
, vol.85
, pp. 634-640
-
-
Jarolim, P.1
Rubin, H.L.2
Brabec, V.3
Chrobak, L.4
Zolotarev, A.S.5
Alper, S.L.6
Brugnara, C.7
Wichterle, H.8
Palek, J.9
-
20
-
-
0028057275
-
Duplication of 10 nucleotides in the erythroid band 3 (AE1) gene in a kindred with hereditary spherocytosis and band 3 protein deficiency (band 3PRAGUE)
-
Jarolim, P., Rubin, H. L., Liu, S. C., Cho, M. R., Brabec, V., Derick, L. H., Yi, S. J., Saad, S. T., Alper, S. and Brugnara, C. 1994, Duplication of 10 nucleotides in the erythroid band 3 (AE1) gene in a kindred with hereditary spherocytosis and band 3 protein deficiency (band 3PRAGUE). Journal of Clinical Investigation, 93, 121-130.
-
(1994)
Journal of Clinical Investigation
, vol.93
, pp. 121-130
-
-
Jarolim, P.1
Rubin, H.L.2
Liu, S.C.3
Cho, M.R.4
Brabec, V.5
Derick, L.H.6
Yi, S.J.7
Saad, S.T.8
Alper, S.9
Brugnara, C.10
-
21
-
-
13344262715
-
A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis
-
Jenkins, P. B., Abou-Alfa, G. K., Dhermy, D., Bursaux, E., Feo, C., Scarpa, A. L., Lux, S. E., Garbarz, M., Forget, B. G. and Gallagher, P. G. 1996, A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosis. Journal of Clinical Investigation, 97, 373-380.
-
(1996)
Journal of Clinical Investigation
, vol.97
, pp. 373-380
-
-
Jenkins, P.B.1
Abou-Alfa, G.K.2
Dhermy, D.3
Bursaux, E.4
Feo, C.5
Scarpa, A.L.6
Lux, S.E.7
Garbarz, M.8
Forget, B.G.9
Gallagher, P.G.10
-
22
-
-
0014949207
-
Cleavage of structural proteins during the assembly of the head of bacteriophage T4
-
Laemmli, U. K. 1970, Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature, 227, 680-685.
-
(1970)
Nature
, vol.227
, pp. 680-685
-
-
Laemmli, U.K.1
-
24
-
-
0025078761
-
Functional expression and subcellular localization of an anion exchanger cloned from choroid plexus
-
Lindsey, A. E., Schneider, K., Simmons, D. M., Baron, R., Lee, B S. and Kopito, R. R. 1990, Functional expression and subcellular localization of an anion exchanger cloned from choroid plexus. Proceedings of the National Academy of Sciences (USA), 87, 5278-5282.
-
(1990)
Proceedings of the National Academy of Sciences (USA)
, vol.87
, pp. 5278-5282
-
-
Lindsey, A.E.1
Schneider, K.2
Simmons, D.M.3
Baron, R.4
Lee, B.S.5
Kopito, R.R.6
-
25
-
-
0003147477
-
Disorders of the red cell membrane
-
R. I. Handin, S. E. Lux and T. P. Stossel, eds (Philadelphia: Lippincott, S.B. company)
-
Lux, S. E. and Palek, J. 1995, Disorders of the red cell membrane. In Blood: Principles and practice of hematology, R. I. Handin, S. E. Lux and T. P. Stossel, eds (Philadelphia: Lippincott, S.B. company), p. 1701.
-
(1995)
Blood: Principles and Practice of Hematology
, pp. 1701
-
-
Lux, S.E.1
Palek, J.2
-
26
-
-
0024316871
-
Cloning and characterization of band 3, the human erythrocyte anion-exchange protein (AE1)
-
Lux, S. E., John, K. M., Kopito, R. R. and Lodish, H. F. 1989, Cloning and characterization of band 3, the human erythrocyte anion-exchange protein (AE1). Proceedings of the National Academy of Sciences (USA), 86, 9089-9093.
-
(1989)
Proceedings of the National Academy of Sciences (USA)
, vol.86
, pp. 9089-9093
-
-
Lux, S.E.1
John, K.M.2
Kopito, R.R.3
Lodish, H.F.4
-
27
-
-
0023664635
-
Sequence from picomole quantities of proteins electroblotted onto polyvinylidene difluoride membranes
-
Matsudaira, P. 1987, Sequence from picomole quantities of proteins electroblotted onto polyvinylidene difluoride membranes. Journal of Biological Chemistry, 262, 10035-10038.
-
(1987)
Journal of Biological Chemistry
, vol.262
, pp. 10035-10038
-
-
Matsudaira, P.1
-
28
-
-
0029150191
-
The ANK repeats of erythrocyte ankyrin form two distinct but cooperative binding sites for the erythrocyte anion exchanger
-
Michaely, P. and Bennett, V. 1995, The ANK repeats of erythrocyte ankyrin form two distinct but cooperative binding sites for the erythrocyte anion exchanger. Journal of Biological Chemistry, 270, 22050-22057.
-
(1995)
Journal of Biological Chemistry
, vol.270
, pp. 22050-22057
-
-
Michaely, P.1
Bennett, V.2
-
29
-
-
0028064834
-
Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis
-
Miraglia, D. G., Iolascon, A., Pinto, L., Nobili, B. and Perrotta, S. 1994, Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis. British Journal of Haematology, 88, 52-55.
-
(1994)
British Journal of Haematology
, vol.88
, pp. 52-55
-
-
Miraglia, D.G.1
Iolascon, A.2
Pinto, L.3
Nobili, B.4
Perrotta, S.5
-
30
-
-
0032561457
-
Assessment of topogenic functions of anticipated transmembrane segments of human band 3
-
Ota, K., Sakaguchi, M., Hamasaki, N. and Mihara, K. 1998, Assessment of topogenic functions of anticipated transmembrane segments of human band 3. Journal of Biological Chemistry, 273, 28286-28291.
-
(1998)
Journal of Biological Chemistry
, vol.273
, pp. 28286-28291
-
-
Ota, K.1
Sakaguchi, M.2
Hamasaki, N.3
Mihara, K.4
-
31
-
-
0027429066
-
Clinical expression and laboratory detection of red blood cell membrane protein mutations
-
Palek, J. and Jarolim, P. 1993, Clinical expression and laboratory detection of red blood cell membrane protein mutations. Seminars in Hematology, 30, 249-283.
-
(1993)
Seminars in Hematology
, vol.30
, pp. 249-283
-
-
Palek, J.1
Jarolim, P.2
-
32
-
-
16044367177
-
Anion exchanger 1 (band 3) is required to prevent erythrocyte membrane surface loss but not to form the membrane skeleton
-
Peters, L. L., Shivdasani, R. A., Liu, S. C., Hanspal, M., John, K. M., Gonzalez, J. M., Brugnara, C., Gwynn, B., Mohandas, N., Alper, S. L., Orkin, S. H. and Lux, S. E., 1996, Anion exchanger 1 (band 3) is required to prevent erythrocyte membrane surface loss but not to form the membrane skeleton. Cell, 86, 917-927.
-
(1996)
Cell
, vol.86
, pp. 917-927
-
-
Peters, L.L.1
Shivdasani, R.A.2
Liu, S.C.3
Hanspal, M.4
John, K.M.5
Gonzalez, J.M.6
Brugnara, C.7
Gwynn, B.8
Mohandas, N.9
Alper, S.L.10
Orkin, S.H.11
Lux, S.E.12
-
33
-
-
0030745799
-
Mapping the ends of transmembrane segments in a polytopic membrane protein. Scanning N-glycosylation mutagenesis of extracytosolic loops in the anion exchanger, band 3
-
Popov, M., Tam, L. Y., Li, J. and Reithmeier, R. A., 1997, Mapping the ends of transmembrane segments in a polytopic membrane protein. Scanning N-glycosylation mutagenesis of extracytosolic loops in the anion exchanger, band 3. Journal of Biological Chemistry, 272, 18325-18332.
-
(1997)
Journal of Biological Chemistry
, vol.272
, pp. 18325-18332
-
-
Popov, M.1
Tam, L.Y.2
Li, J.3
Reithmeier, R.A.4
-
34
-
-
0033526097
-
Early assembly step of a retroviral envelope glycoprotein: Analysis using a dominant negative assay
-
Rosenberg, A. R., Delamarre, L., Pique, C., Le, B. I, Griffith, G. and Dokhelar M.C., 1999, Early assembly step of a retroviral envelope glycoprotein: analysis using a dominant negative assay. Journal of Cell Biology, 145, 57-68.
-
(1999)
Journal of Cell Biology
, vol.145
, pp. 57-68
-
-
Rosenberg, A.R.1
Delamarre, L.2
Pique, C.3
Le B. I4
Griffith, G.5
Dokhelar, M.C.6
-
35
-
-
0028091593
-
Red cell membrane protein abnormalities in hereditary spherocytosis in Brazil
-
Saad, S. T., Costa, F. F., Vicentim, D. L., Salles, T. S. and Pranke, P. H. 1994, Red cell membrane protein abnormalities in hereditary spherocytosis in Brazil. British Journal of Haematology, 88, 295-299.
-
(1994)
British Journal of Haematology
, vol.88
, pp. 295-299
-
-
Saad, S.T.1
Costa, F.F.2
Vicentim, D.L.3
Salles, T.S.4
Pranke, P.H.5
-
36
-
-
0032566739
-
Testing the charge difference hypothesis for the assembly of a eucaryotic multi-spanning membrane protein
-
Sato, M., Hresko, R. and Mueckler, M. 1998, Testing the charge difference hypothesis for the assembly of a eucaryotic multi-spanning membrane protein. Journal of Biological Chemistry, 273, 25203-25208.
-
(1998)
Journal of Biological Chemistry
, vol.273
, pp. 25203-25208
-
-
Sato, M.1
Hresko, R.2
Mueckler, M.3
-
37
-
-
0029821217
-
Targeted disruption of the murine erythroid band 3 gene results in spherocytosis and severe haemolytic anaemia despite a normal membrane skeleton
-
Southgate, C. D., Chishti, A. H., Mitchell, B., Yi, S. J. and Palek, J. 1996, Targeted disruption of the murine erythroid band 3 gene results in spherocytosis and severe haemolytic anaemia despite a normal membrane skeleton. Nature Genetics, 14, 227-230.
-
(1996)
Nature Genetics
, vol.14
, pp. 227-230
-
-
Southgate, C.D.1
Chishti, A.H.2
Mitchell, B.3
Yi, S.J.4
Palek, J.5
-
38
-
-
0017863277
-
Preparation and analysis of seven major, topographically defined fragments of band 3, the predominant transmembrane polypeptide of human erythrocyte membranes
-
Steck, T. L., Koziarz, J. J., Singh, M. K., Reddy, G. and Kohler, H. 1978, Preparation and analysis of seven major, topographically defined fragments of band 3, the predominant transmembrane polypeptide of human erythrocyte membranes. Biochemistry, 17, 1216-1222.
-
(1978)
Biochemistry
, vol.17
, pp. 1216-1222
-
-
Steck, T.L.1
Koziarz, J.J.2
Singh, M.K.3
Reddy, G.4
Kohler, H.5
-
39
-
-
0031466796
-
The structure and function of band 3 (AE1): Recent developments
-
Tanner, M. J. 1997, The structure and function of band 3 (AE1): recent developments. Molecular Membrane Biology, 14, 155-165.
-
(1997)
Molecular Membrane Biology
, vol.14
, pp. 155-165
-
-
Tanner, M.J.1
-
40
-
-
0029889279
-
Vectors for expression of protein-A-tagged proteins in vertebrate cells
-
Uetz, P. and Zeller, R. 1996, Vectors for expression of protein-A-tagged proteins in vertebrate cells. Analytical Biochemistry, 237, 161-163.
-
(1996)
Analytical Biochemistry
, vol.237
, pp. 161-163
-
-
Uetz, P.1
Zeller, R.2
-
41
-
-
0030968672
-
Getting greasy: How transmembrane polypeptide segments integrate into the lipid bilayer
-
von Heijne, G. 1997, Getting greasy: how transmembrane polypeptide segments integrate into the lipid bilayer. Molecular Microbiology, 24, 249-253.
-
(1997)
Molecular Microbiology
, vol.24
, pp. 249-253
-
-
Von Heijne, G.1
-
42
-
-
0024286463
-
v-erbA specifically suppresses transcription of the avian erythrocyte anion transporter (band 3) gene
-
Zenke, M., Kahn, P., Disela, C., Vennstrom, B., Leutz, A., Keegan, K., Hayman, M. J., Choi, H. R., Yew, N. and Engel, J. D. 1988, v-erbA specifically suppresses transcription of the avian erythrocyte anion transporter (band 3) gene. Cell, 52, 107-119.
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(1988)
Cell
, vol.52
, pp. 107-119
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Zenke, M.1
Kahn, P.2
Disela, C.3
Vennstrom, B.4
Leutz, A.5
Keegan, K.6
Hayman, M.J.7
Choi, H.R.8
Yew, N.9
Engel, J.D.10
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