-
2
-
-
0025819205
-
Organization of the gene for human erythrocyte membrane protein 4.2: structural similarities with the gene for the a subunit of factor XIII
-
Korsgren C., and Cohen C.M. Organization of the gene for human erythrocyte membrane protein 4.2: structural similarities with the gene for the a subunit of factor XIII. Proc. Natl. Acad. Sci. U. S. A. 88 (1991) 4840-4844
-
(1991)
Proc. Natl. Acad. Sci. U. S. A.
, vol.88
, pp. 4840-4844
-
-
Korsgren, C.1
Cohen, C.M.2
-
3
-
-
0027288548
-
Human erythrocyte membrane protein band 4.2 (pallidin)
-
Cohen C.M., Dotimas E., and Korsgren C. Human erythrocyte membrane protein band 4.2 (pallidin). Semin. Hematol. 30 (1993) 119-137
-
(1993)
Semin. Hematol.
, vol.30
, pp. 119-137
-
-
Cohen, C.M.1
Dotimas, E.2
Korsgren, C.3
-
4
-
-
0025162066
-
Complete amino acid sequence and homologies of human erythrocyte membrane protein band 4.2
-
Korsgren C., Lawler J., Lambert S., Speicher D., and Cohen C.M. Complete amino acid sequence and homologies of human erythrocyte membrane protein band 4.2. Proc. Natl. Acad. Sci. U. S. A. 87 (1990) 613-617
-
(1990)
Proc. Natl. Acad. Sci. U. S. A.
, vol.87
, pp. 613-617
-
-
Korsgren, C.1
Lawler, J.2
Lambert, S.3
Speicher, D.4
Cohen, C.M.5
-
5
-
-
0025117605
-
Molecular cloning of human protein 4.2: a major component of the erythrocyte membrane
-
Sung L.A., Chien S., Chang L.S., Lambert K., Bliss S.A., Bouhassira E.E., Nagel R.L., Schwartz R.S., and Rybicki A.C. Molecular cloning of human protein 4.2: a major component of the erythrocyte membrane. Proc. Natl. Acad. Sci. U. S. A. 87 (1990) 955-959
-
(1990)
Proc. Natl. Acad. Sci. U. S. A.
, vol.87
, pp. 955-959
-
-
Sung, L.A.1
Chien, S.2
Chang, L.S.3
Lambert, K.4
Bliss, S.A.5
Bouhassira, E.E.6
Nagel, R.L.7
Schwartz, R.S.8
Rybicki, A.C.9
-
6
-
-
20844460283
-
Protein-4.2 association with band 3 (AE1, SLCA4) in Xenopus oocytes: effects of three natural protein-4.2 mutations associated with hemolytic anemia
-
Toye A.M., Ghosh S., Young M.T., Jones G.K., Sessions R.B., Ramauge M., Leclerc P., Basu J., Delaunay J., and Tanner M.J. Protein-4.2 association with band 3 (AE1, SLCA4) in Xenopus oocytes: effects of three natural protein-4.2 mutations associated with hemolytic anemia. Blood 105 (2005) 4088-4095
-
(2005)
Blood
, vol.105
, pp. 4088-4095
-
-
Toye, A.M.1
Ghosh, S.2
Young, M.T.3
Jones, G.K.4
Sessions, R.B.5
Ramauge, M.6
Leclerc, P.7
Basu, J.8
Delaunay, J.9
Tanner, M.J.10
-
7
-
-
0026783795
-
Human erythrocyte protein 4.2, a high copy number membrane protein, is N-myristylated
-
Risinger M.A., Dotimas E.M., and Cohen C.M. Human erythrocyte protein 4.2, a high copy number membrane protein, is N-myristylated. J. Biol. Chem. 267 (1992) 5680-5685
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 5680-5685
-
-
Risinger, M.A.1
Dotimas, E.M.2
Cohen, C.M.3
-
8
-
-
0028108225
-
Human erythrocyte membrane protein 4.2 is palmitoylated
-
Das A.K., Bhattacharya R., Kundu M., Chakrabarti P., and Basu J. Human erythrocyte membrane protein 4.2 is palmitoylated. Eur. J. Biochem. 224 (1994) 575-580
-
(1994)
Eur. J. Biochem.
, vol.224
, pp. 575-580
-
-
Das, A.K.1
Bhattacharya, R.2
Kundu, M.3
Chakrabarti, P.4
Basu, J.5
-
9
-
-
0022970081
-
Purification and properties of human erythrocyte band 4.2. Association with the cytoplasmic domain of band 3
-
Korsgren C., and Cohen C.M. Purification and properties of human erythrocyte band 4.2. Association with the cytoplasmic domain of band 3. J. Biol. Chem. 261 (1986) 5536-5543
-
(1986)
J. Biol. Chem.
, vol.261
, pp. 5536-5543
-
-
Korsgren, C.1
Cohen, C.M.2
-
10
-
-
0023766055
-
Associations of human erythrocyte band 4.2. Binding to ankyrin and to the cytoplasmic domain of band 3
-
Korsgren C., and Cohen C.M. Associations of human erythrocyte band 4.2. Binding to ankyrin and to the cytoplasmic domain of band 3. J. Biol. Chem. 263 (1988) 10212-10218
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 10212-10218
-
-
Korsgren, C.1
Cohen, C.M.2
-
11
-
-
0030069982
-
Control of band 3 lateral and rotational mobility by band 4.2 in intact erythrocytes: release of band 3 oligomers from low-affinity binding sites
-
Golan D.E., Corbett J.D., Korsgren C., Thatte H.S., Hayette S., Yawata Y., and Cohen C.M. Control of band 3 lateral and rotational mobility by band 4.2 in intact erythrocytes: release of band 3 oligomers from low-affinity binding sites. Biophys. J. 70 (1996) 1534-1542
-
(1996)
Biophys. J.
, vol.70
, pp. 1534-1542
-
-
Golan, D.E.1
Corbett, J.D.2
Korsgren, C.3
Thatte, H.S.4
Hayette, S.5
Yawata, Y.6
Cohen, C.M.7
-
12
-
-
0037097025
-
Mapping of a spectrin-binding domain of human erythrocyte membrane protein 4.2
-
Mandal D., Moitra P.K., and Basu J. Mapping of a spectrin-binding domain of human erythrocyte membrane protein 4.2. Biochem. J. 364 (2002) 841-847
-
(2002)
Biochem. J.
, vol.364
, pp. 841-847
-
-
Mandal, D.1
Moitra, P.K.2
Basu, J.3
-
13
-
-
0036720831
-
Absence of CD47 in protein 4.2-deficient hereditary spherocytosis in man: an interaction between the Rh complex and the band 3 complex
-
Bruce L.J., Ghosh S., King M.J., Layton D.M., Mawby W.J., Stewart G.W., Oldenborg P.A., Delaunay J., and Tanner M.J. Absence of CD47 in protein 4.2-deficient hereditary spherocytosis in man: an interaction between the Rh complex and the band 3 complex. Blood 100 (2002) 1878-1885
-
(2002)
Blood
, vol.100
, pp. 1878-1885
-
-
Bruce, L.J.1
Ghosh, S.2
King, M.J.3
Layton, D.M.4
Mawby, W.J.5
Stewart, G.W.6
Oldenborg, P.A.7
Delaunay, J.8
Tanner, M.J.9
-
14
-
-
0037218067
-
Evidence that the red cell skeleton protein 4.2 interacts with the Rh membrane complex member CD47
-
Mouro-Chanteloup I., Delaunay J., Gane P., Nicolas V., Johansen M., Brown E.J., Peters L.L., Van Kim C.L., Cartron J.P., and Colin Y. Evidence that the red cell skeleton protein 4.2 interacts with the Rh membrane complex member CD47. Blood 101 (2003) 338-344
-
(2003)
Blood
, vol.101
, pp. 338-344
-
-
Mouro-Chanteloup, I.1
Delaunay, J.2
Gane, P.3
Nicolas, V.4
Johansen, M.5
Brown, E.J.6
Peters, L.L.7
Van Kim, C.L.8
Cartron, J.P.9
Colin, Y.10
-
15
-
-
0028344993
-
Band 4.2 abnormalities in human red cells
-
Yawata Y. Band 4.2 abnormalities in human red cells. Am. J. Med. Sci. 307 (1994) 190-203
-
(1994)
Am. J. Med. Sci.
, vol.307
, pp. 190-203
-
-
Yawata, Y.1
-
16
-
-
1642581654
-
Protein 4.2 is critical to CD47-membrane skeleton attachment in human red cells
-
Dahl K.N., Parthasarathy R., Westhoff C.M., Layton D.M., and Discher D.E. Protein 4.2 is critical to CD47-membrane skeleton attachment in human red cells. Blood 103 (2004) 1131-1136
-
(2004)
Blood
, vol.103
, pp. 1131-1136
-
-
Dahl, K.N.1
Parthasarathy, R.2
Westhoff, C.M.3
Layton, D.M.4
Discher, D.E.5
-
17
-
-
1942509531
-
Hereditary spherocytosis-defects in proteins that connect the membrane skeleton to the lipid bilayer
-
Eber S., and Lux S.E. Hereditary spherocytosis-defects in proteins that connect the membrane skeleton to the lipid bilayer. Semin. Hematol. 41 (2004) 118-141
-
(2004)
Semin. Hematol.
, vol.41
, pp. 118-141
-
-
Eber, S.1
Lux, S.E.2
-
18
-
-
42049115740
-
Disorders of red cell membrane
-
An X., and Mohandas N. Disorders of red cell membrane. Br. J. Haematol. 141 (2008) 367-375
-
(2008)
Br. J. Haematol.
, vol.141
, pp. 367-375
-
-
An, X.1
Mohandas, N.2
-
21
-
-
0028937282
-
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., Fattoum S., Cohen C.M., and Delaunay J. A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemia. Br. J. Haematol. 89 (1995) 762-770
-
(1995)
Br. J. Haematol.
, vol.89
, pp. 762-770
-
-
Hayette, S.1
Morle, L.2
Bozon, M.3
Ghanem, A.4
Risinger, M.5
Korsgren, C.6
Tanner, M.J.7
Fattoum, S.8
Cohen, C.M.9
Delaunay, J.10
-
22
-
-
0026504463
-
An alanine-to-threonine substitution in protein 4.2 cDNA is associated with a Japanese form of hereditary hemolytic anemia (protein 4.2NIPPON)
-
Bouhassira E.E., Schwartz R.S., Yawata Y., Ata K., Kanzaki A., Qiu J.J., Nagel R.L., and Rybicki A.C. An alanine-to-threonine substitution in protein 4.2 cDNA is associated with a Japanese form of hereditary hemolytic anemia (protein 4.2NIPPON). Blood 79 (1992) 1846-1854
-
(1992)
Blood
, vol.79
, pp. 1846-1854
-
-
Bouhassira, E.E.1
Schwartz, R.S.2
Yawata, Y.3
Ata, K.4
Kanzaki, A.5
Qiu, J.J.6
Nagel, R.L.7
Rybicki, A.C.8
-
23
-
-
0028810476
-
Band 4.2 Shiga: 317 CGC->TGC in compound heterozygotes with 142 GCT → ACT results in band 4.2 deficiency and microspherocytosis
-
Kanzaki A., Yasunaga M., Okamoto N., Inoue T., Yawata A., Wada H., Andoh A., Hodohara K., Fujiyama Y., Bamba T., et al. Band 4.2 Shiga: 317 CGC->TGC in compound heterozygotes with 142 GCT → ACT results in band 4.2 deficiency and microspherocytosis. Br. J. Haematol. 91 (1995) 333-340
-
(1995)
Br. J. Haematol.
, vol.91
, pp. 333-340
-
-
Kanzaki, A.1
Yasunaga, M.2
Okamoto, N.3
Inoue, T.4
Yawata, A.5
Wada, H.6
Andoh, A.7
Hodohara, K.8
Fujiyama, Y.9
Bamba, T.10
-
24
-
-
0027970175
-
A novel mutation in the erythrocyte protein 4.2 gene of Japanese patients with hereditary spherocytosis (protein 4.2 Fukuoka)
-
Takaoka Y., Ideguchi H., Matsuda M., Sakamoto N., Takeuchi T., and Fukumaki Y. A novel mutation in the erythrocyte protein 4.2 gene of Japanese patients with hereditary spherocytosis (protein 4.2 Fukuoka). Br. J. Haematol. 88 (1994) 527-533
-
(1994)
Br. J. Haematol.
, vol.88
, pp. 527-533
-
-
Takaoka, Y.1
Ideguchi, H.2
Matsuda, M.3
Sakamoto, N.4
Takeuchi, T.5
Fukumaki, Y.6
-
25
-
-
0029070964
-
A novel mutation causing an aberrant splicing in the protein 4.2 gene associated with hereditary spherocytosis (protein 4.2Notame)
-
Matsuda M., Hatano N., Ideguchi H., Takahira H., and Fukumaki Y. A novel mutation causing an aberrant splicing in the protein 4.2 gene associated with hereditary spherocytosis (protein 4.2Notame). Hum. Mol. Genet. 4 (1995) 1187-1191
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1187-1191
-
-
Matsuda, M.1
Hatano, N.2
Ideguchi, H.3
Takahira, H.4
Fukumaki, Y.5
-
26
-
-
0033968683
-
Heavy transfusions and presence of an anti-protein 4.2 antibody in 4. 2(-) hereditary spherocytosis (949delG)
-
Beauchamp-Nicoud A., Morle L., Lutz H.U., Stammler P., Agulles O., Petermann-Khder R., Iolascon A., Perrotta S., Cynober T., Tchernia G., Delaunay J., and Baudin-Creuza V. Heavy transfusions and presence of an anti-protein 4.2 antibody in 4. 2(-) hereditary spherocytosis (949delG). Haematologica 85 (2000) 19-24
-
(2000)
Haematologica
, vol.85
, pp. 19-24
-
-
Beauchamp-Nicoud, A.1
Morle, L.2
Lutz, H.U.3
Stammler, P.4
Agulles, O.5
Petermann-Khder, R.6
Iolascon, A.7
Perrotta, S.8
Cynober, T.9
Tchernia, G.10
Delaunay, J.11
Baudin-Creuza, V.12
-
27
-
-
64649089138
-
Alterations in the band3/Rh Protein Complex in Erythrocyte Membranes of Protein 4.2 (Chartres) deficient Cells Occur Late during Erythropoiesis
-
[Abstract 3460]
-
Akker E.v.d., Satchwell T.J., Flatt J.F., Pellegrin S., Maigre M., Sessions R.B., Daniels G., Delaunay J., Bruce L.J., and Toye A.M. Alterations in the band3/Rh Protein Complex in Erythrocyte Membranes of Protein 4.2 (Chartres) deficient Cells Occur Late during Erythropoiesis. Blood 112 (2008) 1187 [Abstract 3460]
-
(2008)
Blood
, vol.112
, pp. 1187
-
-
Akker, E.v.d.1
Satchwell, T.J.2
Flatt, J.F.3
Pellegrin, S.4
Maigre, M.5
Sessions, R.B.6
Daniels, G.7
Delaunay, J.8
Bruce, L.J.9
Toye, A.M.10
-
28
-
-
45949090713
-
Band 3 Courcouronnes (Ser667Phe): a trafficking mutant differentially rescued by wild-type band 3 and glycophorin A
-
Toye A.M., Williamson R.C., Khanfar M., Bader-Meunier B., Cynober T., Thibault M., Tchernia G., Dechaux M., Delaunay J., and Bruce L.J. Band 3 Courcouronnes (Ser667Phe): a trafficking mutant differentially rescued by wild-type band 3 and glycophorin A. Blood 111 (2008) 5380-5389
-
(2008)
Blood
, vol.111
, pp. 5380-5389
-
-
Toye, A.M.1
Williamson, R.C.2
Khanfar, M.3
Bader-Meunier, B.4
Cynober, T.5
Thibault, M.6
Tchernia, G.7
Dechaux, M.8
Delaunay, J.9
Bruce, L.J.10
-
29
-
-
0032781763
-
4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosis
-
Perrotta S., Iolascon A., Polito R., d'Urzo G., Conte M.L., and Miraglia del Giudice E. 4.2 Nippon mutation in a non-Japanese patient with hereditary spherocytosis. Haematologica 84 (1999) 660-662
-
(1999)
Haematologica
, vol.84
, pp. 660-662
-
-
Perrotta, S.1
Iolascon, A.2
Polito, R.3
d'Urzo, G.4
Conte, M.L.5
Miraglia del Giudice, E.6
-
30
-
-
0029026258
-
Band 4.2 Komatsu: 523 GAT → TAT (175 Asp → Tyr) in exon 4 of the band 4.2 gene associated with total deficiency of band 4.2, hemolytic anemia with ovalostomatocytosis and marked disruption of the cytoskeletal network
-
Kanzaki A., Yawata Y., Yawata A., Inoue T., Okamoto N., Wada H., Harano T., Harano K., Wilmotte R., Hayette S., et al. Band 4.2 Komatsu: 523 GAT → TAT (175 Asp → Tyr) in exon 4 of the band 4.2 gene associated with total deficiency of band 4.2, hemolytic anemia with ovalostomatocytosis and marked disruption of the cytoskeletal network. Int. J. Hematol. 61 (1995) 165-178
-
(1995)
Int. J. Hematol.
, vol.61
, pp. 165-178
-
-
Kanzaki, A.1
Yawata, Y.2
Yawata, A.3
Inoue, T.4
Okamoto, N.5
Wada, H.6
Harano, T.7
Harano, K.8
Wilmotte, R.9
Hayette, S.10
-
31
-
-
34047147516
-
Protein 4.2 Komatsu (D175Y) associated with the lack of interaction with ankyrin in human red blood cells
-
Su Y., Ding Y., Jiang M., Hu X., and Zhang Z. Protein 4.2 Komatsu (D175Y) associated with the lack of interaction with ankyrin in human red blood cells. Blood Cells Mol. Dis. 38 (2007) 221-228
-
(2007)
Blood Cells Mol. Dis.
, vol.38
, pp. 221-228
-
-
Su, Y.1
Ding, Y.2
Jiang, M.3
Hu, X.4
Zhang, Z.5
-
32
-
-
0030946079
-
Modulation of clinical expression and band 3 deficiency in hereditary spherocytosis
-
Alloisio N., Texier P., Vallier A., Ribeiro M.L., Morle L., Bozon M., Bursaux E., Maillet P., Goncalves P., Tanner M.J., Tamagnini G., and Delaunay J. Modulation of clinical expression and band 3 deficiency in hereditary spherocytosis. Blood 90 (1997) 414-420
-
(1997)
Blood
, vol.90
, pp. 414-420
-
-
Alloisio, N.1
Texier, P.2
Vallier, A.3
Ribeiro, M.L.4
Morle, L.5
Bozon, M.6
Bursaux, E.7
Maillet, P.8
Goncalves, P.9
Tanner, M.J.10
Tamagnini, G.11
Delaunay, J.12
-
33
-
-
9844241062
-
Total absence of protein 4.2 and partial deficiency of band 3 in hereditary spherocytosis
-
Kanzaki A., Hayette S., Morle L., Inoue F., Matsuyama R., Inoue T., Yawata A., Wada H., Vallier A., Alloisio N., Yawata Y., and Delaunay J. Total absence of protein 4.2 and partial deficiency of band 3 in hereditary spherocytosis. Br. J. Haematol. 99 (1997) 522-530
-
(1997)
Br. J. Haematol.
, vol.99
, pp. 522-530
-
-
Kanzaki, A.1
Hayette, S.2
Morle, L.3
Inoue, F.4
Matsuyama, R.5
Inoue, T.6
Yawata, A.7
Wada, H.8
Vallier, A.9
Alloisio, N.10
Yawata, Y.11
Delaunay, J.12
-
35
-
-
41949136941
-
Red cell membrane transport abnormalities
-
Bruce L.J. Red cell membrane transport abnormalities. Curr. Opin. Hematol. 15 (2008) 184-190
-
(2008)
Curr. Opin. Hematol.
, vol.15
, pp. 184-190
-
-
Bruce, L.J.1
-
36
-
-
0034329189
-
Crystallographic structure and functional interpretation of the cytoplasmic domain of erythrocyte membrane band 3
-
Zhang D., Kiyatkin A., Bolin J.T., and Low P.S. Crystallographic structure and functional interpretation of the cytoplasmic domain of erythrocyte membrane band 3. Blood 96 (2000) 2925-2933
-
(2000)
Blood
, vol.96
, pp. 2925-2933
-
-
Zhang, D.1
Kiyatkin, A.2
Bolin, J.T.3
Low, P.S.4
-
37
-
-
0038157322
-
A band 3-based macrocomplex of integral and peripheral proteins in the RBC membrane
-
Bruce L.J., Beckmann R., Ribeiro M.L., Peters L.L., Chasis J.A., Delaunay J., Mohandas N., Anstee D.J., and Tanner M.J. A band 3-based macrocomplex of integral and peripheral proteins in the RBC membrane. Blood 101 (2003) 4180-4188
-
(2003)
Blood
, vol.101
, pp. 4180-4188
-
-
Bruce, L.J.1
Beckmann, R.2
Ribeiro, M.L.3
Peters, L.L.4
Chasis, J.A.5
Delaunay, J.6
Mohandas, N.7
Anstee, D.J.8
Tanner, M.J.9
-
38
-
-
0019321291
-
Association between ankyrin and the cytoplasmic domain of band 3 isolated from the human erythrocyte membrane
-
Bennett V., and Stenbuck P.J. Association between ankyrin and the cytoplasmic domain of band 3 isolated from the human erythrocyte membrane. J. Biol. Chem. 255 (1980) 6424-6432
-
(1980)
J. Biol. Chem.
, vol.255
, pp. 6424-6432
-
-
Bennett, V.1
Stenbuck, P.J.2
-
39
-
-
0034663120
-
Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3
-
Ribeiro M.L., Alloisio N., Almeida H., Gomes C., Texier P., Lemos C., Mimoso G., Morle L., Bey-Cabet F., Rudigoz R.C., Delaunay J., and Tamagnini G. Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3. Blood 96 (2000) 1602-1604
-
(2000)
Blood
, vol.96
, pp. 1602-1604
-
-
Ribeiro, M.L.1
Alloisio, N.2
Almeida, H.3
Gomes, C.4
Texier, P.5
Lemos, C.6
Mimoso, G.7
Morle, L.8
Bey-Cabet, F.9
Rudigoz, R.C.10
Delaunay, J.11
Tamagnini, G.12
-
40
-
-
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. Anion exchanger 1 (band 3) is required to prevent erythrocyte membrane surface loss but not to form the membrane skeleton. Cell 86 (1996) 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
-
41
-
-
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. 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. J. Clin. Invest. 97 (1996) 1804-1817
-
(1996)
J. Clin. Invest.
, 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
-
42
-
-
0029822180
-
Increased rotational mobility and extractability of band 3 from protein 4.2-deficient erythrocyte membranes: evidence of a role for protein 4.2 in strengthening the band 3-cytoskeleton linkage
-
Rybicki A.C., Schwartz R.S., Hustedt E.J., and Cobb C.E. Increased rotational mobility and extractability of band 3 from protein 4.2-deficient erythrocyte membranes: evidence of a role for protein 4.2 in strengthening the band 3-cytoskeleton linkage. Blood 88 (1996) 2745-2753
-
(1996)
Blood
, vol.88
, pp. 2745-2753
-
-
Rybicki, A.C.1
Schwartz, R.S.2
Hustedt, E.J.3
Cobb, C.E.4
-
43
-
-
0028177789
-
Electron microscopic and physicobiochemical studies on disorganization of the cytoskeletal network and integral protein (band 3) in red cells of band 4.2 deficiency with a mutation (codon 142: GCT → ACT)
-
Inoue T., Kanzaki A., Yawata A., Tsuji A., Ata K., Okamoto N., Wada H., Higo I., Sugihara T., Yamada O., et al. Electron microscopic and physicobiochemical studies on disorganization of the cytoskeletal network and integral protein (band 3) in red cells of band 4.2 deficiency with a mutation (codon 142: GCT → ACT). Int. J. Hematol. 59 (1994) 157-175
-
(1994)
Int. J. Hematol.
, vol.59
, pp. 157-175
-
-
Inoue, T.1
Kanzaki, A.2
Yawata, A.3
Tsuji, A.4
Ata, K.5
Okamoto, N.6
Wada, H.7
Higo, I.8
Sugihara, T.9
Yamada, O.10
-
44
-
-
0030043891
-
Electron microscopic evidence of impaired intramembrane particles and instability of the cytoskeletal network in band 4.2 deficiency in human red cells
-
Yawata Y., Yawata A., Kanzaki A., Inoue T., Okamoto N., Uehira K., Yasunaga M., and Nakamura Y. Electron microscopic evidence of impaired intramembrane particles and instability of the cytoskeletal network in band 4.2 deficiency in human red cells. Cell Motil. Cytoskelet. 33 (1996) 95-105
-
(1996)
Cell Motil. Cytoskelet.
, vol.33
, pp. 95-105
-
-
Yawata, Y.1
Yawata, A.2
Kanzaki, A.3
Inoue, T.4
Okamoto, N.5
Uehira, K.6
Yasunaga, M.7
Nakamura, Y.8
-
45
-
-
0027532063
-
Human erythrocyte protein 4.2 deficiency associated with hemolytic anemia and a homozygous 40glutamic acid → lysine substitution in the cytoplasmic domain of band 3 (band 3Montefiore)
-
Rybicki A.C., Qiu J.J., Musto S., Rosen N.L., Nagel R.L., and Schwartz R.S. Human erythrocyte protein 4.2 deficiency associated with hemolytic anemia and a homozygous 40glutamic acid → lysine substitution in the cytoplasmic domain of band 3 (band 3Montefiore). Blood 81 (1993) 2155-2165
-
(1993)
Blood
, vol.81
, pp. 2155-2165
-
-
Rybicki, A.C.1
Qiu, J.J.2
Musto, S.3
Rosen, N.L.4
Nagel, R.L.5
Schwartz, R.S.6
-
46
-
-
7344233086
-
Homozygous missense mutation (band 3 Fukuoka: G130R): a mild form of hereditary spherocytosis with near-normal band 3 content and minimal changes of membrane ultrastructure despite moderate protein 4.2 deficiency
-
Inoue T., Kanzaki A., Kaku M., Yawata A., Takezono M., Okamoto N., Wada H., Sugihara T., Yamada O., Katayama Y., Nagata N., and Yawata Y. Homozygous missense mutation (band 3 Fukuoka: G130R): a mild form of hereditary spherocytosis with near-normal band 3 content and minimal changes of membrane ultrastructure despite moderate protein 4.2 deficiency. Br. J. Haematol. 102 (1998) 932-939
-
(1998)
Br. J. Haematol.
, vol.102
, pp. 932-939
-
-
Inoue, T.1
Kanzaki, A.2
Kaku, M.3
Yawata, A.4
Takezono, M.5
Okamoto, N.6
Wada, H.7
Sugihara, T.8
Yamada, O.9
Katayama, Y.10
Nagata, N.11
Yawata, Y.12
-
47
-
-
0026696751
-
Band 3 Tuscaloosa: Pro327-Arg327 substitution in the cytoplasmic domain of erythrocyte band 3 protein associated with spherocytic hemolytic anemia and partial deficiency of protein 4.2
-
Jarolim P., Palek J., Rubin H.L., Prchal J.T., Korsgren C., and Cohen C.M. Band 3 Tuscaloosa: Pro327-Arg327 substitution in the cytoplasmic domain of erythrocyte band 3 protein associated with spherocytic hemolytic anemia and partial deficiency of protein 4.2. Blood 80 (1992) 523-529
-
(1992)
Blood
, vol.80
, pp. 523-529
-
-
Jarolim, P.1
Palek, J.2
Rubin, H.L.3
Prchal, J.T.4
Korsgren, C.5
Cohen, C.M.6
-
48
-
-
31044456156
-
Structure and stability of hereditary spherocytosis mutants of the cytosolic domain of the erythrocyte anion exchanger 1 protein
-
Bustos S.P., and Reithmeier R.A. Structure and stability of hereditary spherocytosis mutants of the cytosolic domain of the erythrocyte anion exchanger 1 protein. Biochemistry 45 (2006) 1026-1034
-
(2006)
Biochemistry
, vol.45
, pp. 1026-1034
-
-
Bustos, S.P.1
Reithmeier, R.A.2
-
49
-
-
35148883146
-
Structure of the cytoplasmic domain of erythrocyte band 3 hereditary spherocytosis variant P327R: band 3 Tuscaloosa
-
Zhou Z., DeSensi S.C., Stein R.A., Brandon S., Song L., Cobb C.E., Hustedt E.J., and Beth A.H. Structure of the cytoplasmic domain of erythrocyte band 3 hereditary spherocytosis variant P327R: band 3 Tuscaloosa. Biochemistry 46 (2007) 10248-10257
-
(2007)
Biochemistry
, vol.46
, pp. 10248-10257
-
-
Zhou, Z.1
DeSensi, S.C.2
Stein, R.A.3
Brandon, S.4
Song, L.5
Cobb, C.E.6
Hustedt, E.J.7
Beth, A.H.8
-
50
-
-
0029007269
-
Identification of a band-3 binding site near the N-terminus of erythrocyte membrane protein 4.2
-
Rybicki A.C., Musto S., and Schwartz R.S. Identification of a band-3 binding site near the N-terminus of erythrocyte membrane protein 4.2. Biochem. J. 309 Pt 2 (1995) 677-681
-
(1995)
Biochem. J.
, vol.309
, Issue.PART 2
, pp. 677-681
-
-
Rybicki, A.C.1
Musto, S.2
Schwartz, R.S.3
-
51
-
-
0033152772
-
Mapping of a palmitoylatable band 3-binding domain of human erythrocyte membrane protein 4.2
-
Bhattacharyya R., Das A.K., Moitra P.K., Pal B., Mandal I., and Basu J. Mapping of a palmitoylatable band 3-binding domain of human erythrocyte membrane protein 4.2. Biochem. J. 340 Pt 2 (1999) 505-512
-
(1999)
Biochem. J.
, vol.340
, Issue.PART 2
, pp. 505-512
-
-
Bhattacharyya, R.1
Das, A.K.2
Moitra, P.K.3
Pal, B.4
Mandal, I.5
Basu, J.6
-
52
-
-
33748304116
-
Associations of protein 4.2 with band 3 and ankyrin
-
Su Y., Ding Y., Jiang M., Jiang W., Hu X., and Zhang Z. Associations of protein 4.2 with band 3 and ankyrin. Mol. Cell. Biochem. 289 (2006) 159-166
-
(2006)
Mol. Cell. Biochem.
, vol.289
, pp. 159-166
-
-
Su, Y.1
Ding, Y.2
Jiang, M.3
Jiang, W.4
Hu, X.5
Zhang, Z.6
-
53
-
-
0032701977
-
Mild spherocytosis and altered red cell ion transport in protein 4. 2-null mice
-
Peters L.L., Jindel H.K., Gwynn B., Korsgren C., John K.M., Lux S.E., Mohandas N., Cohen C.M., Cho M.R., Golan D.E., and Brugnara C. Mild spherocytosis and altered red cell ion transport in protein 4. 2-null mice. J. Clin. Invest. 103 (1999) 1527-1537
-
(1999)
J. Clin. Invest.
, vol.103
, pp. 1527-1537
-
-
Peters, L.L.1
Jindel, H.K.2
Gwynn, B.3
Korsgren, C.4
John, K.M.5
Lux, S.E.6
Mohandas, N.7
Cohen, C.M.8
Cho, M.R.9
Golan, D.E.10
Brugnara, C.11
-
54
-
-
0030879136
-
Membrane cation and anion transport activities in erythrocytes of hereditary spherocytosis: effects of different membrane protein defects
-
De Franceschi L., Olivieri O., Miraglia del Giudice E., Perrotta S., Sabato V., Corrocher R., and Iolascon A. Membrane cation and anion transport activities in erythrocytes of hereditary spherocytosis: effects of different membrane protein defects. Am. J. Hematol. 55 (1997) 121-128
-
(1997)
Am. J. Hematol.
, vol.55
, pp. 121-128
-
-
De Franceschi, L.1
Olivieri, O.2
Miraglia del Giudice, E.3
Perrotta, S.4
Sabato, V.5
Corrocher, R.6
Iolascon, A.7
-
55
-
-
0027383828
-
A role for band 4.2 in human erythrocyte band 3 mediated anion transport
-
Malik S., Sami M., and Watts A. A role for band 4.2 in human erythrocyte band 3 mediated anion transport. Biochemistry 32 (1993) 10078-10084
-
(1993)
Biochemistry
, vol.32
, pp. 10078-10084
-
-
Malik, S.1
Sami, M.2
Watts, A.3
-
56
-
-
0028670772
-
The major kidney AE1 isoform does not bind ankyrin (Ank1) in vitro. An essential role for the 79 NH2-terminal amino acid residues of band 3
-
Ding Y., Casey J.R., and Kopito R.R. The major kidney AE1 isoform does not bind ankyrin (Ank1) in vitro. An essential role for the 79 NH2-terminal amino acid residues of band 3. J. Biol. Chem. 269 (1994) 32201-32208
-
(1994)
J. Biol. Chem.
, vol.269
, pp. 32201-32208
-
-
Ding, Y.1
Casey, J.R.2
Kopito, R.R.3
-
57
-
-
0025338725
-
Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8
-
Lux S.E., Tse W.T., Menninger J.C., John K.M., Harris P., Shalev O., Chilcote R.R., Marchesi S.L., Watkins P.C., Bennett V., et al. Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8. Nature 345 (1990) 736-739
-
(1990)
Nature
, vol.345
, pp. 736-739
-
-
Lux, S.E.1
Tse, W.T.2
Menninger, J.C.3
John, K.M.4
Harris, P.5
Shalev, O.6
Chilcote, R.R.7
Marchesi, S.L.8
Watkins, P.C.9
Bennett, V.10
-
58
-
-
0028856351
-
Decreased content of protein 4.2 in ankyrin-deficient normoblastosis (nb/nb) mouse red blood cells: evidence for ankyrin enhancement of protein 4.2 membrane binding
-
Rybicki A.C., Musto S., and Schwartz R.S. Decreased content of protein 4.2 in ankyrin-deficient normoblastosis (nb/nb) mouse red blood cells: evidence for ankyrin enhancement of protein 4.2 membrane binding. Blood 86 (1995) 3583-3589
-
(1995)
Blood
, vol.86
, pp. 3583-3589
-
-
Rybicki, A.C.1
Musto, S.2
Schwartz, R.S.3
-
59
-
-
35348908351
-
An 11-amino acid beta-hairpin loop in the cytoplasmic domain of band 3 is responsible for ankyrin binding in mouse erythrocytes
-
Stefanovic M., Markham N.O., Parry E.M., Garrett-Beal L.J., Cline A.P., Gallagher P.G., Low P.S., and Bodine D.M. An 11-amino acid beta-hairpin loop in the cytoplasmic domain of band 3 is responsible for ankyrin binding in mouse erythrocytes. Proc. Natl. Acad. Sci. U. S. A. 104 (2007) 13972-13977
-
(2007)
Proc. Natl. Acad. Sci. U. S. A.
, vol.104
, pp. 13972-13977
-
-
Stefanovic, M.1
Markham, N.O.2
Parry, E.M.3
Garrett-Beal, L.J.4
Cline, A.P.5
Gallagher, P.G.6
Low, P.S.7
Bodine, D.M.8
-
60
-
-
0028063239
-
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., and Tanner M.J. 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. Biochem. J. 304 Pt 2 (1994) 525-530
-
(1994)
Biochem. J.
, vol.304
, Issue.PART 2
, pp. 525-530
-
-
Mawby, W.J.1
Holmes, C.H.2
Anstee, D.J.3
Spring, F.A.4
Tanner, M.J.5
-
61
-
-
0034674421
-
Role of CD47 as a marker of self on red blood cells
-
Oldenborg P.A., Zheleznyak A., Fang Y.F., Lagenaur C.F., Gresham H.D., and Lindberg F.P. Role of CD47 as a marker of self on red blood cells. Science 288 (2000) 2051-2054
-
(2000)
Science
, vol.288
, pp. 2051-2054
-
-
Oldenborg, P.A.1
Zheleznyak, A.2
Fang, Y.F.3
Lagenaur, C.F.4
Gresham, H.D.5
Lindberg, F.P.6
-
62
-
-
0033506288
-
RH blood group system and molecular basis of Rh-deficiency
-
Cartron J.P. RH blood group system and molecular basis of Rh-deficiency. Baillieres Best Pract. Res. Clin. Haematol. 12 (1999) 655-689
-
(1999)
Baillieres Best Pract. Res. Clin. Haematol.
, vol.12
, pp. 655-689
-
-
Cartron, J.P.1
-
63
-
-
0037309110
-
Fractional attachment of CD47 (IAP) to the erythrocyte cytoskeleton and visual colocalization with Rh protein complexes
-
Dahl K.N., Westhoff C.M., and Discher D.E. Fractional attachment of CD47 (IAP) to the erythrocyte cytoskeleton and visual colocalization with Rh protein complexes. Blood 101 (2003) 1194-1199
-
(2003)
Blood
, vol.101
, pp. 1194-1199
-
-
Dahl, K.N.1
Westhoff, C.M.2
Discher, D.E.3
-
64
-
-
0027443140
-
Molecular cloning of integrin-associated protein: an immunoglobulin family member with multiple membrane-spanning domains implicated in alpha v beta 3-dependent ligand binding
-
Lindberg F.P., Gresham H.D., Schwarz E., and Brown E.J. Molecular cloning of integrin-associated protein: an immunoglobulin family member with multiple membrane-spanning domains implicated in alpha v beta 3-dependent ligand binding. J. Cell Biol. 123 (1993) 485-496
-
(1993)
J. Cell Biol.
, vol.123
, pp. 485-496
-
-
Lindberg, F.P.1
Gresham, H.D.2
Schwarz, E.3
Brown, E.J.4
-
65
-
-
0346422852
-
The red cell storage lesion and its implication for transfusion
-
Chin-Yee I., Arya N., and d'Almeida M.S. The red cell storage lesion and its implication for transfusion. Transfus. Sci. 18 (1997) 447-458
-
(1997)
Transfus. Sci.
, vol.18
, pp. 447-458
-
-
Chin-Yee, I.1
Arya, N.2
d'Almeida, M.S.3
-
66
-
-
15244346663
-
Red cell storage lesion: the potential impact of storage-induced CD47 decline on immunomodulation and the survival of leucofiltered red cells
-
Bessos H., and Seghatchian J. Red cell storage lesion: the potential impact of storage-induced CD47 decline on immunomodulation and the survival of leucofiltered red cells. Transfus. Apher. Sci. 32 (2005) 227-232
-
(2005)
Transfus. Apher. Sci.
, vol.32
, pp. 227-232
-
-
Bessos, H.1
Seghatchian, J.2
-
67
-
-
34548181867
-
Proteomic analysis of RBC membrane protein degradation during blood storage
-
D'Amici G.M., Rinalducci S., and Zolla L. Proteomic analysis of RBC membrane protein degradation during blood storage. J. Proteome Res. 6 (2007) 3242-3255
-
(2007)
J. Proteome Res.
, vol.6
, pp. 3242-3255
-
-
D'Amici, G.M.1
Rinalducci, S.2
Zolla, L.3
-
68
-
-
0033790239
-
Protein 4.1R core domain structure and insights into regulation of cytoskeletal organization
-
Han B.G., Nunomura W., Takakuwa Y., Mohandas N., and Jap B.K. Protein 4.1R core domain structure and insights into regulation of cytoskeletal organization. Nat. Struct. Biol. 7 (2000) 871-875
-
(2000)
Nat. Struct. Biol.
, vol.7
, pp. 871-875
-
-
Han, B.G.1
Nunomura, W.2
Takakuwa, Y.3
Mohandas, N.4
Jap, B.K.5
-
69
-
-
0034637458
-
Regulation of protein 4.1R, p55, and glycophorin C ternary complex in human erythrocyte membrane
-
Nunomura W., Takakuwa Y., Parra M., Conboy J., and Mohandas N. Regulation of protein 4.1R, p55, and glycophorin C ternary complex in human erythrocyte membrane. J. Biol. Chem. 275 (2000) 24540-24546
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 24540-24546
-
-
Nunomura, W.1
Takakuwa, Y.2
Parra, M.3
Conboy, J.4
Mohandas, N.5
-
70
-
-
0026772154
-
Identification of the binding interface involved in linkage of cytoskeletal protein 4.1 to the erythrocyte anion exchanger
-
Jons T., and Drenckhahn D. Identification of the binding interface involved in linkage of cytoskeletal protein 4.1 to the erythrocyte anion exchanger. EMBO J. 11 (1992) 2863-2867
-
(1992)
EMBO J.
, vol.11
, pp. 2863-2867
-
-
Jons, T.1
Drenckhahn, D.2
-
71
-
-
33750727697
-
Protein 4.1, a component of the erythrocyte membrane skeleton and its related homologue proteins forming the protein 4.1/FERM superfamily
-
Diakowski W., Grzybek M., and Sikorski A.F. Protein 4.1, a component of the erythrocyte membrane skeleton and its related homologue proteins forming the protein 4.1/FERM superfamily. Folia Histochem. Cytobiol. 44 (2006) 231-248
-
(2006)
Folia Histochem. Cytobiol.
, vol.44
, pp. 231-248
-
-
Diakowski, W.1
Grzybek, M.2
Sikorski, A.F.3
-
72
-
-
0026774620
-
Localization of the protein 4.1-binding site on the cytoplasmic domain of erythrocyte membrane band 3
-
Lombardo C.R., Willardson B.M., and Low P.S. Localization of the protein 4.1-binding site on the cytoplasmic domain of erythrocyte membrane band 3. J. Biol. Chem. 267 (1992) 9540-9546
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 9540-9546
-
-
Lombardo, C.R.1
Willardson, B.M.2
Low, P.S.3
-
73
-
-
0030817220
-
A markedly disrupted skeletal network with abnormally distributed intramembrane particles in complete protein 4.1-deficient red blood cells (allele 4.1 Madrid): implications regarding a critical role of protein 4.1 in maintenance of the integrity of the red blood cell membrane
-
Yawata A., Kanzaki A., Gilsanz F., Delaunay J., and Yawata Y. A markedly disrupted skeletal network with abnormally distributed intramembrane particles in complete protein 4.1-deficient red blood cells (allele 4.1 Madrid): implications regarding a critical role of protein 4.1 in maintenance of the integrity of the red blood cell membrane. Blood 90 (1997) 2471-2481
-
(1997)
Blood
, vol.90
, pp. 2471-2481
-
-
Yawata, A.1
Kanzaki, A.2
Gilsanz, F.3
Delaunay, J.4
Yawata, Y.5
-
74
-
-
45849147331
-
Protein 4.1R-dependent multiprotein complex: new insights into the structural organization of the red blood cell membrane
-
Salomao M., Zhang X., Yang Y., Lee S., Hartwig J.H., Chasis J.A., Mohandas N., and An X. Protein 4.1R-dependent multiprotein complex: new insights into the structural organization of the red blood cell membrane. Proc. Natl. Acad. Sci. U. S. A. 105 (2008) 8026-8031
-
(2008)
Proc. Natl. Acad. Sci. U. S. A.
, vol.105
, pp. 8026-8031
-
-
Salomao, M.1
Zhang, X.2
Yang, Y.3
Lee, S.4
Hartwig, J.H.5
Chasis, J.A.6
Mohandas, N.7
An, X.8
-
75
-
-
0026664112
-
Zinc ions and alkaline pH alter the phosphorylated state of proteins 3 and 4.2 in human erythrocyte membranes
-
Fennell Jr. R.L., and Soslau G. Zinc ions and alkaline pH alter the phosphorylated state of proteins 3 and 4.2 in human erythrocyte membranes. Thromb. Res. 66 (1992) 637-647
-
(1992)
Thromb. Res.
, vol.66
, pp. 637-647
-
-
Fennell Jr., R.L.1
Soslau, G.2
-
76
-
-
0026636507
-
Characterization of the phosphorylated state of protein 4.2 from a patient partially deficient in protein 4.2
-
Fennell Jr. R.L., Rybicki A.C., Schwartz R.S., and Soslau G. Characterization of the phosphorylated state of protein 4.2 from a patient partially deficient in protein 4.2. Thromb. Res. 66 (1992) 629-636
-
(1992)
Thromb. Res.
, vol.66
, pp. 629-636
-
-
Fennell Jr., R.L.1
Rybicki, A.C.2
Schwartz, R.S.3
Soslau, G.4
-
77
-
-
0021916721
-
Mercuric and cadmium ions stimulate phosphorylation of band 4.2 protein on human erythrocyte membranes
-
Suzuki K., Ikebuchi H., and Terao T. Mercuric and cadmium ions stimulate phosphorylation of band 4.2 protein on human erythrocyte membranes. J. Biol. Chem. 260 (1985) 4526-4530
-
(1985)
J. Biol. Chem.
, vol.260
, pp. 4526-4530
-
-
Suzuki, K.1
Ikebuchi, H.2
Terao, T.3
-
79
-
-
0033564954
-
The expression of human blood group antigens during erythropoiesis in a cell culture system
-
Southcott M.J., Tanner M.J., and Anstee D.J. The expression of human blood group antigens during erythropoiesis in a cell culture system. Blood 93 (1999) 4425-4435
-
(1999)
Blood
, vol.93
, pp. 4425-4435
-
-
Southcott, M.J.1
Tanner, M.J.2
Anstee, D.J.3
-
80
-
-
0032750479
-
Time-course expression of polypeptides carrying blood group antigens during human erythroid differentiation
-
Bony V., Gane P., Bailly P., and Cartron J.P. Time-course expression of polypeptides carrying blood group antigens during human erythroid differentiation. Br. J. Haematol. 107 (1999) 263-274
-
(1999)
Br. J. Haematol.
, vol.107
, pp. 263-274
-
-
Bony, V.1
Gane, P.2
Bailly, P.3
Cartron, J.P.4
-
81
-
-
0034983757
-
Flow cytometric analysis of the association between blood group-related proteins and the detergent-insoluble material of K562 cells and erythroid precursors
-
Gane P., Le Van Kim C., Bony V., El Nemer W., Mouro I., Nicolas V., Colin Y., and Cartron J.P. Flow cytometric analysis of the association between blood group-related proteins and the detergent-insoluble material of K562 cells and erythroid precursors. Br. J. Haematol. 113 (2001) 680-688
-
(2001)
Br. J. Haematol.
, vol.113
, pp. 680-688
-
-
Gane, P.1
Le Van Kim, C.2
Bony, V.3
El Nemer, W.4
Mouro, I.5
Nicolas, V.6
Colin, Y.7
Cartron, J.P.8
-
83
-
-
0023021576
-
Control of erythroid differentiation: asynchronous expression of the anion transporter and the peripheral components of the membrane skeleton in AEV-and S13-transformed cells
-
Woods C.M., Boyer B., Vogt P.K., and Lazarides E. Control of erythroid differentiation: asynchronous expression of the anion transporter and the peripheral components of the membrane skeleton in AEV-and S13-transformed cells. J. Cell Biol. 103 (1986) 1789-1798
-
(1986)
J. Cell Biol.
, vol.103
, pp. 1789-1798
-
-
Woods, C.M.1
Boyer, B.2
Vogt, P.K.3
Lazarides, E.4
-
84
-
-
0024273235
-
The erythroid membrane skeleton: expression and assembly during erythropoiesis
-
Woods C.M., and Lazarides E. The erythroid membrane skeleton: expression and assembly during erythropoiesis. Annu. Rev. Med. 39 (1988) 107-122
-
(1988)
Annu. Rev. Med.
, vol.39
, pp. 107-122
-
-
Woods, C.M.1
Lazarides, E.2
-
85
-
-
0023808927
-
Unequal synthesis and differential degradation of alpha and beta spectrin during murine erythroid differentiation
-
Lehnert M.E., and Lodish H.F. Unequal synthesis and differential degradation of alpha and beta spectrin during murine erythroid differentiation. J. Cell Biol. 107 (1988) 413-426
-
(1988)
J. Cell Biol.
, vol.107
, pp. 413-426
-
-
Lehnert, M.E.1
Lodish, H.F.2
-
86
-
-
0032976231
-
Late expression of red cell membrane protein 4.2 in normal human erythroid maturation with seven isoforms of the protein 4.2 gene
-
Wada H., Kanzaki A., Yawata A., Inoue T., Kaku M., Takezono M., Sugihara T., Yamada O., and Yawata Y. Late expression of red cell membrane protein 4.2 in normal human erythroid maturation with seven isoforms of the protein 4.2 gene. Exp. Hematol. 27 (1999) 54-62
-
(1999)
Exp. Hematol.
, vol.27
, pp. 54-62
-
-
Wada, H.1
Kanzaki, A.2
Yawata, A.3
Inoue, T.4
Kaku, M.5
Takezono, M.6
Sugihara, T.7
Yamada, O.8
Yawata, Y.9
-
87
-
-
11144224801
-
Different steroids co-regulate long-term expansion versus terminal differentiation in primary human erythroid progenitors
-
Leberbauer C., Boulme F., Unfried G., Huber J., Beug H., and Mullner E.W. Different steroids co-regulate long-term expansion versus terminal differentiation in primary human erythroid progenitors. Blood 105 (2005) 85-94
-
(2005)
Blood
, vol.105
, pp. 85-94
-
-
Leberbauer, C.1
Boulme, F.2
Unfried, G.3
Huber, J.4
Beug, H.5
Mullner, E.W.6
-
88
-
-
0036901574
-
Transglutaminases: nature's biological glues
-
Griffin M., Casadio R., and Bergamini C.M. Transglutaminases: nature's biological glues. Biochem. J. 368 (2002) 377-396
-
(2002)
Biochem. J.
, vol.368
, pp. 377-396
-
-
Griffin, M.1
Casadio, R.2
Bergamini, C.M.3
-
89
-
-
0035980007
-
Evolution of transglutaminase genes: identification of a transglutaminase gene cluster on human chromosome 15q15. Structure of the gene encoding transglutaminase X and a novel gene family member, transglutaminase Z
-
Grenard P., Bates M.K., and Aeschlimann D. Evolution of transglutaminase genes: identification of a transglutaminase gene cluster on human chromosome 15q15. Structure of the gene encoding transglutaminase X and a novel gene family member, transglutaminase Z. J. Biol. Chem. 276 (2001) 33066-33078
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 33066-33078
-
-
Grenard, P.1
Bates, M.K.2
Aeschlimann, D.3
-
90
-
-
0034695929
-
Tissue transglutaminase is an integrin-binding adhesion coreceptor for fibronectin
-
Akimov S.S., Krylov D., Fleischman L.F., and Belkin A.M. Tissue transglutaminase is an integrin-binding adhesion coreceptor for fibronectin. J. Cell Biol. 148 (2000) 825-838
-
(2000)
J. Cell Biol.
, vol.148
, pp. 825-838
-
-
Akimov, S.S.1
Krylov, D.2
Fleischman, L.F.3
Belkin, A.M.4
-
91
-
-
0028818837
-
Interaction site of GTP binding Gh (transglutaminase II) with phospholipase C
-
Hwang K.C., Gray C.D., Sivasubramanian N., and Im M.J. Interaction site of GTP binding Gh (transglutaminase II) with phospholipase C. J. Biol. Chem. 270 (1995) 27058-27062
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 27058-27062
-
-
Hwang, K.C.1
Gray, C.D.2
Sivasubramanian, N.3
Im, M.J.4
-
92
-
-
0001050957
-
The structural basis for the regulation of tissue transglutaminase by calcium ions
-
Casadio R., Polverini E., Mariani P., Spinozzi F., Carsughi F., Fontana A., Polverino de Laureto P., Matteucci G., and Bergamini C.M. The structural basis for the regulation of tissue transglutaminase by calcium ions. Eur. J. Biochem. 262 (1999) 672-679
-
(1999)
Eur. J. Biochem.
, vol.262
, pp. 672-679
-
-
Casadio, R.1
Polverini, E.2
Mariani, P.3
Spinozzi, F.4
Carsughi, F.5
Fontana, A.6
Polverino de Laureto, P.7
Matteucci, G.8
Bergamini, C.M.9
-
93
-
-
0029873722
-
Human erythrocyte dematin and protein 4.2 (pallidin) are ATP binding proteins
-
Azim A.C., Marfatia S.M., Korsgren C., Dotimas E., Cohen C.M., and Chishti A.H. Human erythrocyte dematin and protein 4.2 (pallidin) are ATP binding proteins. Biochemistry 35 (1996) 3001-3006
-
(1996)
Biochemistry
, vol.35
, pp. 3001-3006
-
-
Azim, A.C.1
Marfatia, S.M.2
Korsgren, C.3
Dotimas, E.4
Cohen, C.M.5
Chishti, A.H.6
-
94
-
-
38549156658
-
Transglutaminase 2 undergoes a large conformational change upon activation
-
Pinkas D.M., Strop P., Brunger A.T., and Khosla C. Transglutaminase 2 undergoes a large conformational change upon activation. PLoS Biol. 5 (2007) e327
-
(2007)
PLoS Biol.
, vol.5
-
-
Pinkas, D.M.1
Strop, P.2
Brunger, A.T.3
Khosla, C.4
|