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Volumn 106, Issue 4, 1999, Pages 948-953

Suppression of CDA II expression in a homozygote

Author keywords

CDA II expression; Congenital dyserythropoietic anaemia type II; Erythrocyte membrane proteins

Indexed keywords

ALLELE; ARTICLE; CELL ULTRASTRUCTURE; GENE EXPRESSION REGULATION; GENE MAPPING; GENEALOGY; HEREDITARY HEMOLYTIC ANEMIA; HOMOZYGOTE; HUMAN; HUMAN TISSUE; PHENOTYPE; PRIORITY JOURNAL;

EID: 0032881056     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1999.01626.x     Document Type: Article
Times cited : (7)

References (28)
  • 3
    • 0017336450 scopus 로고
    • Congenital dyserythropoietic anacmia, types I and II: Aberrant pattern of erythrocyte membrane proteins in CDA II. As revealed by two-dimensional polyacrylamide gel electrophoresis
    • Anselstetter, V., Horstmann, H.J. & Heimpel, H. (1977) Congenital dyserythropoietic anacmia, types I and II: aberrant pattern of erythrocyte membrane proteins in CDA II. as revealed by two-dimensional polyacrylamide gel electrophoresis. British Journal of Haematology, 35, 209-215.
    • (1977) British Journal of Haematology , vol.35 , pp. 209-215
    • Anselstetter, V.1    Horstmann, H.J.2    Heimpel, H.3
  • 5
    • 0021986428 scopus 로고
    • Abnormal fatty acid composition of erythrocyte glycosphingolipids in congenital dyserythropoietic anaemia type II
    • Bouhours, J.F., Bouhours, D. & Delaunay. J. (1985) Abnormal fatty acid composition of erythrocyte glycosphingolipids in congenital dyserythropoietic anaemia type II. Journal of Lipid Research, 26, 435-441.
    • (1985) Journal of Lipid Research , vol.26 , pp. 435-441
    • Bouhours, J.F.1    Bouhours, D.2    Delaunay, J.3
  • 7
    • 0027283744 scopus 로고
    • Congenital dyserythropoietic anaemia type II (HEMPAS) and its molecular basis
    • Fukuda, M.N. (1993) Congenital dyserythropoietic anaemia type II (HEMPAS) and its molecular basis. Baillière's Clinical Haematology, 6, 493-511.
    • (1993) Baillière's Clinical Haematology , vol.6 , pp. 493-511
    • Fukuda, M.N.1
  • 8
    • 0023227217 scopus 로고
    • Primary defect of congenital dyserythropoietic anaemia type II: Failure in glycosylation of erythrocyte lactosaminoglycan proteins caused by lowered N-acetylglucosaminyltransferase II
    • Fukuda, M.N., Dell, A. & Scartezzini, P. (1987) Primary defect of congenital dyserythropoietic anaemia type II: failure in glycosylation of erythrocyte lactosaminoglycan proteins caused by lowered N-acetylglucosaminyltransferase II. Journal of Biological Chemistry, 262, 7195-7206.
    • (1987) Journal of Biological Chemistry , vol.262 , pp. 7195-7206
    • Fukuda, M.N.1    Dell, A.2    Scartezzini, P.3
  • 9
    • 0027081573 scopus 로고
    • Incompletely processed N-glycans of serum glycoproteins in congenital dyserythropeitic anaemia type II (HEMPAS)
    • Fukuda, M.N., Gactani, G.F., Izzo, P., Scartezzini, P. & Dell, A. (1992) Incompletely processed N-glycans of serum glycoproteins in congenital dyserythropeitic anaemia type II (HEMPAS). British Journal of Haematology, 82, 745-752.
    • (1992) British Journal of Haematology , vol.82 , pp. 745-752
    • Fukuda, M.N.1    Gactani, G.F.2    Izzo, P.3    Scartezzini, P.4    Dell, A.5
  • 10
    • 0022520245 scopus 로고
    • Anomalous clustering of underglycosylated band 3 in erythrocytes and their precursor cells in congenital dyserythropoietic anemia type II
    • Fukuda, M.N., Klier, G., Yu, J. & Scartezzini, P. (1986) Anomalous clustering of underglycosylated band 3 in erythrocytes and their precursor cells in congenital dyserythropoietic anemia type II. Blood, 68, 521-529.
    • (1986) Blood , vol.68 , pp. 521-529
    • Fukuda, M.N.1    Klier, G.2    Yu, J.3    Scartezzini, P.4
  • 12
    • 0024506085 scopus 로고
    • Defective glycosylation of erythrocyte membrane glycoconjugates in a variant of congenital dyserythropoietic anemia type II: Association of low level of membrane-bound form of galactosyltransferase
    • Fukuda, M.N., Masri, K.A., Dell, A., Thonar, E.J.M., Klier, G. & Lowenthal, R.M. (1989) Defective glycosylation of erythrocyte membrane glycoconjugates in a variant of congenital dyserythropoietic anemia type II: association of low level of membrane-bound form of galactosyltransferase. Blood, 73, 1331-1339.
    • (1989) Blood , vol.73 , pp. 1331-1339
    • Fukuda, M.N.1    Masri, K.A.2    Dell, A.3    Thonar, E.J.M.4    Klier, G.5    Lowenthal, R.M.6
  • 13
    • 0021320047 scopus 로고
    • Defect in glycosylation of erythrocyte membrane proteins in congenital dyserythropoietic anaemia type II (HEMPAS)
    • Fukuda, M.N., Papayannopoulou, T., Gordon-Smith, F.C., Rochant, H. & Testa, U. (1984) Defect in glycosylation of erythrocyte membrane proteins in congenital dyserythropoietic anaemia type II (HEMPAS). British Journal of Haematology, 56, 55-68.
    • (1984) British Journal of Haematology , vol.56 , pp. 55-68
    • Fukuda, M.N.1    Papayannopoulou, T.2    Gordon-Smith, F.C.3    Rochant, H.4    Testa, U.5
  • 15
    • 0020067631 scopus 로고
    • Erythrocyte membrane proteins in an unusual case of congenital dyserythropoietic anaemia type II (CDA II)
    • Harlow, R.W.H. & Lowenthal, R.M. (1982) Erythrocyte membrane proteins in an unusual case of congenital dyserythropoietic anaemia type II (CDA II). British Journal of Haematology, 50, 35-41.
    • (1982) British Journal of Haematology , vol.50 , pp. 35-41
    • Harlow, R.W.H.1    Lowenthal, R.M.2
  • 16
    • 0014264724 scopus 로고
    • Congenital dyserythropoietic anemia with karyorrhexis and multinuclearity of erythroblasts
    • Heimpel, H. & Wendt, F. (1968) Congenital dyserythropoietic anemia with karyorrhexis and multinuclearity of erythroblasts. Helvetica Medica Acta, 34, 103-115.
    • (1968) Helvetica Medica Acta , vol.34 , pp. 103-115
    • Heimpel, H.1    Wendt, F.2
  • 18
    • 0032189079 scopus 로고    scopus 로고
    • Genetic heterogeneity of congenital dyserythropoiesis anemia II (CDA II)
    • Iolascon, A., De Mattia, D., Perrotta, S., Carella, M. & Gasparini, P. (1998) Genetic heterogeneity of congenital dyserythropoiesis anemia II (CDA II). (Letter). Blood, 92, 2593-2594.
    • (1998) Blood , vol.92 , pp. 2593-2594
    • Iolascon, A.1    De Mattia, D.2    Perrotta, S.3    Carella, M.4    Gasparini, P.5
  • 19
    • 0030775892 scopus 로고    scopus 로고
    • Exclusion of three candidate genes as determinants of congenital dyserythropoietic anemia type II (CDA II)
    • Iolascon, A., Miraglia del Giudice, E., Perrotta, S., Granatiero, M., Zelante, L. & Gasparini, P. (1997) Exclusion of three candidate genes as determinants of congenital dyserythropoietic anemia type II (CDA II). Blood, 90, 4197-4200.
    • (1997) Blood , vol.90 , pp. 4197-4200
    • Iolascon, A.1    Miraglia del Giudice, E.2    Perrotta, S.3    Granatiero, M.4    Zelante, L.5    Gasparini, P.6
  • 21
    • 0004038637 scopus 로고
    • Oxford University Press
    • Lewin, B. (1995) In Genes V. p. 102. Oxford University Press.
    • (1995) Genes V , pp. 102
    • Lewin, B.1
  • 22
    • 0020571298 scopus 로고
    • Incomplete glycosylation of erythrocyte membrane proteins in congenital dyserythropoietic anaemia type II (CDAII)
    • Mawby, W.J., Tanner, M.J.A., Anstee, D.J. & Clamp, J.R. (1983) Incomplete glycosylation of erythrocyte membrane proteins in congenital dyserythropoietic anaemia type II (CDAII). British Journal of Haematology, 55, 357-368.
    • (1983) British Journal of Haematology , vol.55 , pp. 357-368
    • Mawby, W.J.1    Tanner, M.J.A.2    Anstee, D.J.3    Clamp, J.R.4
  • 24
    • 0019977542 scopus 로고
    • Decreased glycosylation of band 3 and band 4.5 glycoproteins of erythrocyte membrane in congenital dyserythropoietic anaemia type II
    • Scartezzini, P., Forni, G.L., Baldi, M., Izzo, C. & Sansone, G. (1982) Decreased glycosylation of band 3 and band 4.5 glycoproteins of erythrocyte membrane in congenital dyserythropoietic anaemia type II. British Journal of Haematology, 51, 569-576.
    • (1982) British Journal of Haematology , vol.51 , pp. 569-576
    • Scartezzini, P.1    Forni, G.L.2    Baldi, M.3    Izzo, C.4    Sansone, G.5
  • 25
    • 0028012360 scopus 로고
    • Aberrant regulation of complement by the erythrocytes of hereditary erythroblastic multinuclearity with a positive acidified serum lysis test (HEMPAS)
    • Tomita, A. & Porter, C.J. (1994) Aberrant regulation of complement by the erythrocytes of hereditary erythroblastic multinuclearity with a positive acidified serum lysis test (HEMPAS). Blood, 83, 250-259.
    • (1994) Blood , vol.83 , pp. 250-259
    • Tomita, A.1    Porter, C.J.2
  • 26
    • 0022512321 scopus 로고
    • A variant of the congenital dyserythropoietic anaemia type II with structural abnormalities in the granulocytic series
    • Vermylen, C., Scheiff, J.M., Rodhain, J., Ninane, J. & Cornu, G. (1986) A variant of the congenital dyserythropoietic anaemia type II with structural abnormalities in the granulocytic series. European Journal of Pediatrics, 145, 232-235.
    • (1986) European Journal of Pediatrics , vol.145 , pp. 232-235
    • Vermylen, C.1    Scheiff, J.M.2    Rodhain, J.3    Ninane, J.4    Cornu, G.5
  • 27
    • 0014191358 scopus 로고
    • Kongenitale dyserythropoietische anämie bei einem zweieiigen zwillingspaar
    • Wendt, F. & Heimpel, H. (1967) Kongenitale dyserythropoietische Anämie bei einem zweieiigen Zwillingspaar. Medizinische Klinik, 62, 172-177.
    • (1967) Medizinische Klinik , vol.62 , pp. 172-177
    • Wendt, F.1    Heimpel, H.2
  • 28
    • 0031685438 scopus 로고    scopus 로고
    • Congenital dyserythropoietic anaemias: Clinical features, haematological morphology and new biochemical data
    • Wickramasinghe, S.N. (1998) Congenital dyserythropoietic anaemias: clinical features, haematological morphology and new biochemical data. Blood Reviews, 12, 178-200.
    • (1998) Blood Reviews , vol.12 , pp. 178-200
    • Wickramasinghe, S.N.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.