Perbandingan Mutasi Band 3 dan Fragilitas Eritrosit pada Thalassemia β Minor dan Non Thalassemia β Minor yang Diseleksi dari 1800 Mahasiswa USU Berdasarkan Nilai Mentzer Index
DAFTAR PUSTAKA
[FK UI] Fakultas Kedokteran Universitas Indonesia, Bagian Ilmu Kesehatan
Anak. 1985. Buku Kuliah Ilmu Kesehatan Anak 1. Percetakan Infomedika,
Jakarta.A
Suryohudoyo, P. 2000. Kapita Selekta : Ilmu Kedokteran Molekuler.
Shinar, E, Shalev, O, Rachmilewitz, E.A. and Schrier, S.L. Erythrocyte membrane
skeleton abnormalities in severe β thalassemia. Blood 1987 70: 158-64.
Rachmilewitz, E.A. Pathologic changes of red blood cell membranes in
Thalassemia. Birth Defects : Original Article Series 1987 18: 219-22.
Rachmilewitz, E.A, Shinar, R, Shalev, O,. and Schrier, S.L. Erythrocyte
membrane alteration in β-thalassemia. Clinical Haematology 1985 14: 163182.
Chasis, J.A., Mohandas, N. Erythrocyte membrane deformability and stability :
two distinct membrane properties that are independently regulated by
skeletal protein associations. J Cell Biology 1986 103: 343-350.
Passow, H. The band 3 proteins. An introduction. Progress in Cell Research 1992
2: 1-6.
Tanner, M.J.A. Molecular and cellular biology of the erythrocyte anion exchanger
(AE1). Semin Hematology 1993 30(1): 34-57.
Yuan, J, Bunyaratvej, A, Fucharoen, S, Fung, C, Shinar, E and Schrier, S.L. The
instability of the membrane skeleton in thalassemic red blood cells. Blood
1995 86: 3945-3950
68
Universitas Sumatera Utara
Voet, D, Voet, J.G. 1995. Biochemistry. Ed2. John Wiley & Sons, Inc., New
York.
Hamasaki, N. The role of band 3 protein in oxygen delivery by red blood cells.
Indian Journal of Clinical Biochemistry 1999 14(1): 49-58.
Wang, D.N. Band 3 protein : structure, flexibility and function. FEBS Letters
346(1994) : 26-31.
Dhermy, D, Bournier, O, Bourgeois, M and Grandchamp, B. The red blood cell
band 3 variant associated with dominant hereditary spherocytosis causes
defective membrane targeting of the molecule and a dominant negative
effect. Molecular Membrane Biology 1999, 16: 305-312.
Mohandas, N, Winardi, R, Knowles, D, Leung, A, Parra, M, George, E, Conboy,
J, and Chasis, J. Molecular basis for membrane rigidity of hereditary
ovalocytosis, a novel mechanism involving the cytoplasmic domain of band
3. J Clin Invest 1992, 89: 686-692.
Jarolim, P, Palek, J, Amato, D, Hassan, K, Sapak, P, Nurse, G.T., Rubin, H.L.,
Sen Zhai, Shar, K.E., Chun Liu, S. Deletion in erythrocyte band 3 gene in
malaria-resistant southeast asian ovalositosis. Proc Nati Acad Sci 1991, 88:
11022-11026.
Kuma, H, Inoue, K, Fu, G, Ando, S, Lee, S, Sugihara, G and Hamasaki, N.
Secondary structures of synthetic peptides corresponding to the first
membrane-contact portion of normal band 3 and its deletion mutant
(southeast asian ovalocytosis). J. Biochem 1998, 124: 509-518.
Kurniati. 2000. Analisis pola protein membran sel darah merah normal dan
talasemia secara elektroforesis. Tesis Magister Program Studi Ilmu
Biomedik, FK UI.
69
Universitas Sumatera Utara
Cappellini, M.D., Tavazzi, D, Duca, L, Graziadei, G, Mannu, F, Turrini, F, Arese,
P and Fiorelli, G. Metabolic indicators of oxidative stress correlate with
haemichrome attachment
to
membrane, band
3
aggregation and
erythrophagocytosis in β-thalassemia intermedia. British Journal of
Haematology 1999, 104: 504-512.
Olivieri, N.F. The β-thalassemias. The New England Journal of Medicine,
vol.341, number 2: 99-109.
Rund, D, Rachmilewitz, E. β thalassemia. The New England Journal of Medicine
2005, 353: 1135-1146.
Weatherall, D.J. The thalassemias. British Medical Journal 1997, 314: 1675-1678.
Shinar, E, Rachmilewitz, E.A. Oxidative denaturation of red blood cells in
thalassemia. Semin Hematology 1990, 27: 70-82.
Weatherall, D.J. and Clegg, J.B.,contribution by Gibbons, R, Higgs, D.R., Old,
J.M., Olivieri, N.F., Thein, S.L., Wood, W.G. 2001. The thalassemia
syndromes. 4th ed.
Popov, M, Li, J and Reithmeier, A.F. Transmembrane folding of the human
erythrocyte anion exchanger (AE1, Band3) determined by scanning and
insertional N-glycosylation mutagenesis. Biochem. J. 1999, 339: 269-279.
Ntaois, G., Chatzinikolaou, A, Saouli, Z, Girtovitis, F, Tsapanidou, M, Kaiafa, G,
Kantoninas, Z, Nikolaidou, A, Savopoulos, C, Pidonia, I, and Alexiou, S.
2007. Discrimination indices as screening tests for β-thalassemic trait. Ann
Hematol 2007, 86: 487-491
70
Universitas Sumatera Utara
Dewajanthi, A.M. Identifikasi Adanya Kelainan Gen Protein Pita 3 pada
Membran Sel Darah Merah Penderita Thalassemia β di Pusat Thalassemia
RSCM/ FKUI. 2004.
Weatherall, D.J. and Provan, A.B. Red Cells I : Inherited anaemias. The Lancet
2000, 355: 1169-75.
Murray, R.K., Granner, D.K., Mayes, P.A. and Rodwell, V.W. Biokimia Harper
(Terjemahan) Ed.24. EGC Jakarta 1997.
Yuwono. Resistensi sel darah merah dengan southeast asian ovalositosis (SAO)
terhadap malaria: variasi resistensi yang berhubungan dengan etnis dan
geografis. Tesis Magister Program Studi Ilmu Biomedik, Fakultas
Kedokteran Universitas Indonesia 2002.
Muladno. Seputar teknologi rekayasa genetika. Penerbit Pustaka Wirausaha
Muda, Bogor 2002.
71
Universitas Sumatera Utara
[FK UI] Fakultas Kedokteran Universitas Indonesia, Bagian Ilmu Kesehatan
Anak. 1985. Buku Kuliah Ilmu Kesehatan Anak 1. Percetakan Infomedika,
Jakarta.A
Suryohudoyo, P. 2000. Kapita Selekta : Ilmu Kedokteran Molekuler.
Shinar, E, Shalev, O, Rachmilewitz, E.A. and Schrier, S.L. Erythrocyte membrane
skeleton abnormalities in severe β thalassemia. Blood 1987 70: 158-64.
Rachmilewitz, E.A. Pathologic changes of red blood cell membranes in
Thalassemia. Birth Defects : Original Article Series 1987 18: 219-22.
Rachmilewitz, E.A, Shinar, R, Shalev, O,. and Schrier, S.L. Erythrocyte
membrane alteration in β-thalassemia. Clinical Haematology 1985 14: 163182.
Chasis, J.A., Mohandas, N. Erythrocyte membrane deformability and stability :
two distinct membrane properties that are independently regulated by
skeletal protein associations. J Cell Biology 1986 103: 343-350.
Passow, H. The band 3 proteins. An introduction. Progress in Cell Research 1992
2: 1-6.
Tanner, M.J.A. Molecular and cellular biology of the erythrocyte anion exchanger
(AE1). Semin Hematology 1993 30(1): 34-57.
Yuan, J, Bunyaratvej, A, Fucharoen, S, Fung, C, Shinar, E and Schrier, S.L. The
instability of the membrane skeleton in thalassemic red blood cells. Blood
1995 86: 3945-3950
68
Universitas Sumatera Utara
Voet, D, Voet, J.G. 1995. Biochemistry. Ed2. John Wiley & Sons, Inc., New
York.
Hamasaki, N. The role of band 3 protein in oxygen delivery by red blood cells.
Indian Journal of Clinical Biochemistry 1999 14(1): 49-58.
Wang, D.N. Band 3 protein : structure, flexibility and function. FEBS Letters
346(1994) : 26-31.
Dhermy, D, Bournier, O, Bourgeois, M and Grandchamp, B. The red blood cell
band 3 variant associated with dominant hereditary spherocytosis causes
defective membrane targeting of the molecule and a dominant negative
effect. Molecular Membrane Biology 1999, 16: 305-312.
Mohandas, N, Winardi, R, Knowles, D, Leung, A, Parra, M, George, E, Conboy,
J, and Chasis, J. Molecular basis for membrane rigidity of hereditary
ovalocytosis, a novel mechanism involving the cytoplasmic domain of band
3. J Clin Invest 1992, 89: 686-692.
Jarolim, P, Palek, J, Amato, D, Hassan, K, Sapak, P, Nurse, G.T., Rubin, H.L.,
Sen Zhai, Shar, K.E., Chun Liu, S. Deletion in erythrocyte band 3 gene in
malaria-resistant southeast asian ovalositosis. Proc Nati Acad Sci 1991, 88:
11022-11026.
Kuma, H, Inoue, K, Fu, G, Ando, S, Lee, S, Sugihara, G and Hamasaki, N.
Secondary structures of synthetic peptides corresponding to the first
membrane-contact portion of normal band 3 and its deletion mutant
(southeast asian ovalocytosis). J. Biochem 1998, 124: 509-518.
Kurniati. 2000. Analisis pola protein membran sel darah merah normal dan
talasemia secara elektroforesis. Tesis Magister Program Studi Ilmu
Biomedik, FK UI.
69
Universitas Sumatera Utara
Cappellini, M.D., Tavazzi, D, Duca, L, Graziadei, G, Mannu, F, Turrini, F, Arese,
P and Fiorelli, G. Metabolic indicators of oxidative stress correlate with
haemichrome attachment
to
membrane, band
3
aggregation and
erythrophagocytosis in β-thalassemia intermedia. British Journal of
Haematology 1999, 104: 504-512.
Olivieri, N.F. The β-thalassemias. The New England Journal of Medicine,
vol.341, number 2: 99-109.
Rund, D, Rachmilewitz, E. β thalassemia. The New England Journal of Medicine
2005, 353: 1135-1146.
Weatherall, D.J. The thalassemias. British Medical Journal 1997, 314: 1675-1678.
Shinar, E, Rachmilewitz, E.A. Oxidative denaturation of red blood cells in
thalassemia. Semin Hematology 1990, 27: 70-82.
Weatherall, D.J. and Clegg, J.B.,contribution by Gibbons, R, Higgs, D.R., Old,
J.M., Olivieri, N.F., Thein, S.L., Wood, W.G. 2001. The thalassemia
syndromes. 4th ed.
Popov, M, Li, J and Reithmeier, A.F. Transmembrane folding of the human
erythrocyte anion exchanger (AE1, Band3) determined by scanning and
insertional N-glycosylation mutagenesis. Biochem. J. 1999, 339: 269-279.
Ntaois, G., Chatzinikolaou, A, Saouli, Z, Girtovitis, F, Tsapanidou, M, Kaiafa, G,
Kantoninas, Z, Nikolaidou, A, Savopoulos, C, Pidonia, I, and Alexiou, S.
2007. Discrimination indices as screening tests for β-thalassemic trait. Ann
Hematol 2007, 86: 487-491
70
Universitas Sumatera Utara
Dewajanthi, A.M. Identifikasi Adanya Kelainan Gen Protein Pita 3 pada
Membran Sel Darah Merah Penderita Thalassemia β di Pusat Thalassemia
RSCM/ FKUI. 2004.
Weatherall, D.J. and Provan, A.B. Red Cells I : Inherited anaemias. The Lancet
2000, 355: 1169-75.
Murray, R.K., Granner, D.K., Mayes, P.A. and Rodwell, V.W. Biokimia Harper
(Terjemahan) Ed.24. EGC Jakarta 1997.
Yuwono. Resistensi sel darah merah dengan southeast asian ovalositosis (SAO)
terhadap malaria: variasi resistensi yang berhubungan dengan etnis dan
geografis. Tesis Magister Program Studi Ilmu Biomedik, Fakultas
Kedokteran Universitas Indonesia 2002.
Muladno. Seputar teknologi rekayasa genetika. Penerbit Pustaka Wirausaha
Muda, Bogor 2002.
71
Universitas Sumatera Utara