-
1
-
-
1842393681
-
Band 3 Coimbra: A variant associated with dominant hereditary spherocytosis and band 3 deficiency
-
Alloisio, N., Texier, P., Forrissier, A., Ribeiro, M.L., Morlé, L., Bozon, M., Bursaux, E., Maillet, P., Tanner, M.J.A., Tamagnini, G. & Delaunay, J. (1993) Band 3 Coimbra: a variant associated with dominant hereditary spherocytosis and band 3 deficiency. Blood, 82, (Suppl. 1), 4a.
-
(1993)
Blood
, vol.82
, Issue.1 SUPPL.
-
-
Alloisio, N.1
Texier, P.2
Forrissier, A.3
Ribeiro, M.L.4
Morlé, L.5
Bozon, M.6
Bursaux, E.7
Maillet, P.8
Tanner, M.J.A.9
Tamagnini, G.10
Delaunay, J.11
-
2
-
-
0017347447
-
International Committee for Standardization in Haematology: Recommended methods for red-cell enzyme analysis
-
Beutler, E., Blume, K.G., Kaplan, J.C., Lohr, G.W., Ramot, B. & Valentine, W.N. (1977) International Committee for Standardization in Haematology: recommended methods for red-cell enzyme analysis. British Journal of Haematology, 35, 331-341.
-
(1977)
British Journal of Haematology
, vol.35
, pp. 331-341
-
-
Beutler, E.1
Blume, K.G.2
Kaplan, J.C.3
Lohr, G.W.4
Ramot, B.5
Valentine, W.N.6
-
3
-
-
0015605437
-
The role of the sinus wall in the passage of erythrocytes through the spleen
-
Chen, L.T. & Weiss, L. (1973) The role of the sinus wall in the passage of erythrocytes through the spleen. Blood, 41, 529-537.
-
(1973)
Blood
, vol.41
, pp. 529-537
-
-
Chen, L.T.1
Weiss, L.2
-
4
-
-
0026050782
-
Role of spleen in hereditary spherocytosis: Evidence for increased in vitro proteolysis of red cell membrane
-
De Matteis, M.C., De Angelis, V., Sorrentino, F., Bonollo, E. & Vettore, L. (1991) Role of spleen in hereditary spherocytosis: evidence for increased in vitro proteolysis of red cell membrane. British Journal of Haematology, 79, 108-112.
-
(1991)
British Journal of Haematology
, vol.79
, pp. 108-112
-
-
De Matteis, M.C.1
De Angelis, V.2
Sorrentino, F.3
Bonollo, E.4
Vettore, L.5
-
5
-
-
0024356616
-
Morphologic and morphometric light and electron microscopic studies of the spleen in patients with hereditary spherocytosis and autoimmune haemolytic anaemia
-
Ferreira, J.A., Feliu, E., Rozman, C., Berga, L., Bombi, A., Marti, M., Vives-Corrons, L., Climent, C. & Ferràn, M.J. (1989) Morphologic and morphometric light and electron microscopic studies of the spleen in patients with hereditary spherocytosis and autoimmune haemolytic anaemia. British Journal of Haematology, 72, 246-253.
-
(1989)
British Journal of Haematology
, vol.72
, pp. 246-253
-
-
Ferreira, J.A.1
Feliu, E.2
Rozman, C.3
Berga, L.4
Bombi, A.5
Marti, M.6
Vives-Corrons, L.7
Climent, C.8
Ferràn, M.J.9
-
6
-
-
1842382295
-
Band 3 Noirterre: A nonsense mutation of the erythrocyte band 3 gene causing dominant hereditary spherocytosis
-
Gallagher, P.G., Abou-Alfa, G.K., Floyd, P., Dhermy, D., Bursaux, E., Scarpa, A., Garbarz, M. & Forget, B.G. (1994) Band 3 Noirterre: a nonsense mutation of the erythrocyte band 3 gene causing dominant hereditary spherocytosis. Blood, 84, (Suppl. 1), 6a.
-
(1994)
Blood
, vol.84
, Issue.1 SUPPL.
-
-
Gallagher, P.G.1
Abou-Alfa, G.K.2
Floyd, P.3
Dhermy, D.4
Bursaux, E.5
Scarpa, A.6
Garbarz, M.7
Forget, B.G.8
-
7
-
-
0028927865
-
Protein damage and methylation-mediated repair in the erythrocyte
-
Galletti, P., Ingrosso, D., Manna, C., Clemente, G. & Zappia, V. (1995) Protein damage and methylation-mediated repair in the erythrocyte. Biochemical Journal, 306, 313-325.
-
(1995)
Biochemical Journal
, vol.306
, pp. 313-325
-
-
Galletti, P.1
Ingrosso, D.2
Manna, C.3
Clemente, G.4
Zappia, V.5
-
8
-
-
0020961480
-
Increased methyl esterification of membrane proteins in aged red blood cells: Preferential esterification of ankyrin and band 4.1 cytoskeletal proteins
-
Galletti, P., Ingrosso, D., Nappi, A., Gragnaniello, V., Iolascon, A. & Pinto, L. (1983) Increased methyl esterification of membrane proteins in aged red blood cells: preferential esterification of ankyrin and band 4.1 cytoskeletal proteins. European Journal of Biochemistry, 135, 25-31.
-
(1983)
European Journal of Biochemistry
, vol.135
, pp. 25-31
-
-
Galletti, P.1
Ingrosso, D.2
Nappi, A.3
Gragnaniello, V.4
Iolascon, A.5
Pinto, L.6
-
9
-
-
0023205819
-
Microcirculation of the spleen: New concepts, new challenges
-
Groom, A.C. (1987) Microcirculation of the spleen: new concepts, new challenges. Microvascular Research, 34, 269-283
-
(1987)
Microvascular Research
, vol.34
, pp. 269-283
-
-
Groom, A.C.1
-
10
-
-
0025949363
-
The mechanism of decline of age-dependent enzymes in the red blood cell
-
Haram, S., Carriero, D., Seaman, C. & Piomelli, S. (1991) The mechanism of decline of age-dependent enzymes in the red blood cell. Enzyme (Basel), 45, 47-53.
-
(1991)
Enzyme (Basel)
, vol.45
, pp. 47-53
-
-
Haram, S.1
Carriero, D.2
Seaman, C.3
Piomelli, S.4
-
11
-
-
0028957062
-
Increased membrane-protein methylation in hereditary spherocytosis: A marker of cytoskeletal disarray
-
Ingrosso, D., D'Angelo, S., Perna, A.F., Iolascon, A., Miraglia del Giudice, E., Perrotta, S., Zappia, V. & Galletti, P. (1995) Increased membrane-protein methylation in hereditary spherocytosis: a marker of cytoskeletal disarray. European Journal of Biochemistry, 228, 894-898.
-
(1995)
European Journal of Biochemistry
, vol.228
, pp. 894-898
-
-
Ingrosso, D.1
D'Angelo, S.2
Perna, A.F.3
Iolascon, A.4
Miraglia Del Giudice, E.5
Perrotta, S.6
Zappia, V.7
Galletti, P.8
-
12
-
-
3042972346
-
Molecular characterization of hereditary spherocytosis with band 3 deficiency
-
Jarolim, P., Murray, J., Rubin, H.L., Palek, J., and the Hemolytic Anemia Study Group (1994a) Molecular characterization of hereditary spherocytosis with band 3 deficiency. Blood, 84, (Suppl. 1), 362a.
-
(1994)
Blood
, vol.84
, Issue.1 SUPPL.
-
-
Jarolim, P.1
Murray, J.2
Rubin, H.L.3
Palek, J.4
-
13
-
-
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. & 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
-
14
-
-
0028057275
-
PRAGUE)
-
PRAGUE). 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
Derich, L.H.6
Yi, S.J.7
Saad, S.T.O.8
Alper, S.9
Brugnara, C.10
Golan, D.E.11
Palek, J.12
-
15
-
-
0028064834
-
Erythrocyte membrane protein alterations underlying clinical heterogeneity in hereditary spherocytosis
-
Miraglia del Giudice, E., Iolascon, A., Pinto, L., Nobili, B. & 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 Del Giudice, E.1
Iolascon, A.2
Pinto, L.3
Nobili, B.4
Perrotta, S.5
-
16
-
-
0001872040
-
The function and enzymology of protein D-aspartyl/L-isoaspartyl methyltransferases in eukaryotic and prokaryotic cells
-
(ed. by W. K. Paik and S. Kim), CRC Press, Boca Raton
-
Ota, I.M. & Clarke, S. (1990) The function and enzymology of protein D-aspartyl/L-isoaspartyl methyltransferases in eukaryotic and prokaryotic cells. Protein Methylation (ed. by W. K. Paik and S. Kim), pp. 179-194. CRC Press, Boca Raton.
-
(1990)
Protein Methylation
, pp. 179-194
-
-
Ota, I.M.1
Clarke, S.2
-
17
-
-
0023485004
-
Hereditary elliptocytosis, spherocytosis and related disorders: Consequences of a deficiency or a mutation of membrane skeletal proteins
-
Palek, J. (1987) Hereditary elliptocytosis, spherocytosis and related disorders: consequences of a deficiency or a mutation of membrane skeletal proteins. Blood Reviews, 1, 147-168.
-
(1987)
Blood Reviews
, vol.1
, pp. 147-168
-
-
Palek, J.1
-
18
-
-
0027429066
-
Clinical expression and laboratory detection of red blood cell membrane protein mutations
-
Palek, J. & 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
-
19
-
-
0026628758
-
Mutations of the red blood cell membrane proteins: From clinical evaluation to detection of the underlying genetic defect
-
Palek, J. & Sahr, K.E. (1992) Mutations of the red blood cell membrane proteins: from clinical evaluation to detection of the underlying genetic defect. Blood, 80, 308-330.
-
(1992)
Blood
, vol.80
, pp. 308-330
-
-
Palek, J.1
Sahr, K.E.2
-
20
-
-
0027302413
-
Enzymatic methyl esterification of erythrocyte membrane proteins is impaired in chronic renal failure: Evidence for high levels of the natural inhibitor S-adenosylhomocysteine
-
Perna, A.F., Ingrosso, D., Zappia, V., Galletti, P., Capasso, G. & De Santo, N.G. (1993) Enzymatic methyl esterification of erythrocyte membrane proteins is impaired in chronic renal failure: evidence for high levels of the natural inhibitor S-adenosylhomocysteine. Journal of Clinical Investigation, 91, 2497-2503.
-
(1993)
Journal of Clinical Investigation
, vol.91
, pp. 2497-2503
-
-
Perna, A.F.1
Ingrosso, D.2
Zappia, V.3
Galletti, P.4
Capasso, G.5
De Santo, N.G.6
-
21
-
-
0028235242
-
Hereditary spherocytosis associated with protein band 3 defect in a Swiss kindred
-
Reinhart, W.H., Wyss, E.J., Arnold, D. & Ott, P. (1994) Hereditary spherocytosis associated with protein band 3 defect in a Swiss kindred. British Journal of Haematology, 86, 147-155.
-
(1994)
British Journal of Haematology
, vol.86
, pp. 147-155
-
-
Reinhart, W.H.1
Wyss, E.J.2
Arnold, D.3
Ott, P.4
|