-
1
-
-
0037071860
-
An abundant erythroid protein that stabilizes free α-haemoglobin
-
DOI 10.1038/nature00803
-
Kihm AJ, Kong Y, Hong W, et al. An abundant erythroid protein that stabilizes free alpha-haemoglobin. Nature. 2002;417:758-763. (Pubitemid 34640631)
-
(2002)
Nature
, vol.417
, Issue.6890
, pp. 758-763
-
-
Kihm, A.J.1
Kong, Y.2
Hong, W.3
Russell, J.E.4
Rouda, S.5
Adachl, K.6
Simon, M.C.7
Blobel, G.A.8
Weiss, M.J.9
-
2
-
-
85047690518
-
Loss of α-hemoglobin-stabilizing protein impairs erythropoiesis and exacerbates β-thalassemia
-
DOI 10.1172/JCI200421982
-
Kong Y, Zhou S, Kihm AJ, et al. Loss of alpha-hemoglobin-stabilizing protein impairs erythropoiesis and exacerbates beta-thalassemia. J Clin Invest. 2004;114:1457-1466. (Pubitemid 40385576)
-
(2004)
Journal of Clinical Investigation
, vol.114
, Issue.10
, pp. 1457-1466
-
-
Kong, Y.1
Zhou, S.2
Kihm, A.J.3
Katein, A.M.4
Yu, X.5
Gell, D.A.6
Mackay, J.P.7
Adachi, K.8
Foster-Brown, L.9
Louden, C.S.10
Gow, A.J.11
Weiss, M.J.12
-
3
-
-
34447121854
-
An erythroid chaperone that facilitates folding of α-globin subunits for hemoglobin synthesis
-
DOI 10.1172/JCI31664
-
Yu X, Kong Y, Dore LC, et al. An erythroid chaperone that facilitates folding of alpha-globin subunits for hemoglobin synthesis. J Clin Invest. 2007;117:1856-1865. (Pubitemid 47036319)
-
(2007)
Journal of Clinical Investigation
, vol.117
, Issue.7
, pp. 1856-1865
-
-
Yu, X.1
Kong, Y.2
Dore, L.C.3
Abdulmalik, O.4
Katein, A.M.5
Zhou, S.6
Choi, J.K.7
Gell, D.8
Mackay, J.P.9
Gow, A.J.10
Weiss, M.J.11
-
4
-
-
33845924644
-
Biochemical fates of α hemoglobin bound to α hemoglobin-stabilizing protein AHSP
-
DOI 10.1074/jbc.M607311200
-
Zhou S, Olson JS, Fabian M, Weiss MJ, Gow AJ. Biochemical fates of alpha hemoglobin bound to alpha hemoglobin-stabilizing protein AHSP. J Biol Chem. 2006;281:32611-32618. (Pubitemid 46036816)
-
(2006)
Journal of Biological Chemistry
, vol.281
, Issue.43
, pp. 32611-32618
-
-
Zhou, S.1
Olson, J.S.2
Fabian, M.3
Weiss, M.J.4
Gow, A.J.5
-
5
-
-
39149123488
-
Reduction of AHSP synthesis in hemin-induced K562 cells and EPO-induced CD34(+) cells leads to alpha-globin precipitation, impairment of normal hemoglobin production, and increased cell death
-
Pinho FO, de Albuquerque DM, Olalla Saad ST, Costa FF. Reduction of AHSP synthesis in hemin-induced K562 cells and EPO-induced CD34(+) cells leads to alpha-globin precipitation, impairment of normal hemoglobin production, and increased cell death. Exp Hematol. 2008;36:265-272.
-
(2008)
Exp Hematol
, vol.36
, pp. 265-272
-
-
Pinho, F.O.1
De Albuquerque, D.M.2
Olalla Saad, S.T.3
Costa, F.F.4
-
6
-
-
38349170152
-
Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and function
-
dos Santos CO, Zhou S, Secolin R, et al. Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and function. Am J Hematol. 2008;83:103-108.
-
(2008)
Am J Hematol
, vol.83
, pp. 103-108
-
-
Dos Santos, C.O.1
Zhou, S.2
Secolin, R.3
-
7
-
-
1942425504
-
Evaluation of alpha hemoglobin stabilizing protein (AHSP) as a genetic modifier in patients with βthalassemia
-
DOI 10.1182/blood-2003-11-3957
-
Viprakasit V, Tanphaichitr VS, Chinchang W, Sangkla P, Weiss MJ, Higgs DR. Evaluation of alpha hemoglobin stabilizing protein (AHSP) as a genetic modifier in patients with beta thalassemia. Blood. 2004;103:3296-3299. (Pubitemid 38525654)
-
(2004)
Blood
, vol.103
, Issue.9
, pp. 3296-3299
-
-
Viprakasit, V.1
Tanphaichitr, V.S.2
Chinchang, W.3
Sangkla, P.4
Weiss, M.J.5
Higgs, D.R.6
-
8
-
-
8844285199
-
Molecular mechanism of AHSP-mediated stabilization of α-hemoglobin
-
DOI 10.1016/j.cell.2004.11.025, PII S0092867404010438
-
Feng L, Gell DA, Zhou S, et al. Molecular mechanism of AHSP-mediated stabilization of alpha-hemoglobin. Cell. 2004;119:629-640. (Pubitemid 39535751)
-
(2004)
Cell
, vol.119
, Issue.5
, pp. 629-640
-
-
Feng, L.1
Gell, D.A.2
Zhou, S.3
Gu, L.4
Kong, Y.5
Li, J.6
Hu, M.7
Yan, N.8
Lee, C.9
Rich, A.M.10
Armstrong, R.S.11
Lay, P.A.12
Gow, A.J.13
Weiss, M.J.14
MacKay, J.P.15
Shi, Y.16
-
9
-
-
20444445134
-
Structure of oxidized α-haemoglobin bound to AHSP reveals a protective mechanism for haem
-
DOI 10.1038/nature03609
-
Feng L, Zhou S, Gu L, et al. Structure of oxidized alpha-haemoglobin bound to AHSP reveals a protective mechanism for haem. Nature. 2005;435:697-701. (Pubitemid 40825516)
-
(2005)
Nature
, vol.435
, Issue.7042
, pp. 697-701
-
-
Feng, L.1
Zhou, S.2
Gu, L.3
Gell, D.A.4
Mackay, J.P.5
Weiss, M.J.6
Gow, A.J.7
Shi, Y.8
-
10
-
-
34547597988
-
Molecular characterization and origins of Hb constant spring and Hb Pakse in Southeast Asian populations
-
DOI 10.1007/s00277-007-0310-x
-
Singsanan S, Fucharoen G, Savongsy O, Sanchaisuriya K, Fucharoen S. Molecular characterization and origins of Hb Constant Spring and Hb Pakse in Southeast Asian populations. Ann Hematol. 2007;86:665-669. (Pubitemid 47193596)
-
(2007)
Annals of Hematology
, vol.86
, Issue.9
, pp. 665-669
-
-
Singsanan, S.1
Fucharoen, G.2
Savongsy, O.3
Sanchaisuriya, K.4
Fucharoen, S.5
-
11
-
-
33644868959
-
Impaired interaction of α-haemoglobin-stabilising protein with α-globin termination mutant in a yeast two-hybrid system
-
DOI 10.1111/j.1365-2141.2005.05865.x
-
Turbpaiboon C, Limjindaporn T, Wongwiwat W, et al. Impaired interaction of alpha-haemoglobin-stabilising protein with alpha-globin termination mutant in a yeast two-hybrid system. Br J Haematol. 2006;132:370-373. (Pubitemid 43381543)
-
(2006)
British Journal of Haematology
, vol.132
, Issue.3
, pp. 370-373
-
-
Turbpaiboon, C.1
Limjindaporn, T.2
Wongwiwat, W.3
U-Pratya, Y.4
Siritanaratkul, N.5
Yenchitsomanus, P.-T.6
Jitrapakdee, S.7
Wilairat, P.8
-
12
-
-
38549144245
-
Hb Foggia or alpha 117(GH5)Phe -> Ser: A new alpha 2 globin allele affecting the alpha Hb-AHSP interaction
-
Lacerra G, Scarano C, Musollino G, Flagiello A, Pucci P, Carestia C. Hb Foggia or alpha 117(GH5)Phe -> Ser: a new alpha 2 globin allele affecting the alpha Hb-AHSP interaction. Haematologica. 2008;93:141-142.
-
(2008)
Haematologica
, vol.93
, pp. 141-142
-
-
Lacerra, G.1
Scarano, C.2
Musollino, G.3
Flagiello, A.4
Pucci, P.5
Carestia, C.6
-
13
-
-
33750908580
-
Impaired binding of AHSP to α chain variants: Hb Groene Hart illustrates a mechanism leading to unstable hemoglobins with α thalassemic like syndrome
-
DOI 10.1016/j.bcmd.2006.09.002, PII S1079979606001951
-
Vasseur-Godbillon C, Marden MC, Giordano P, Wajcman H, Baudin-Creuza V. Impaired binding of AHSP to alpha chain variants: Hb Groene Hart illustrates a mechanism leading to unstable hemoglobins with alpha thalassemic like syndrome. Blood Cells Mol Dis. 2006;37:173-179. (Pubitemid 44724949)
-
(2006)
Blood Cells, Molecules, and Diseases
, vol.37
, Issue.3
, pp. 173-179
-
-
Vasseur-Godbillon, C.1
Marden, M.C.2
Giordano, P.3
Wajcman, H.4
Baudin-Creuza, V.5
-
14
-
-
0037175053
-
Biophysical characterization of the alpha-globin binding protein alpha-hemoglobin stabilizing protein
-
Gell D, Kong Y, Eaton SA, Weiss MJ, Mackay JP. Biophysical characterization of the alpha-globin binding protein alpha-hemoglobin stabilizing protein. J Biol Chem. 2002;277:40602-40609.
-
(2002)
J Biol Chem
, vol.277
, pp. 40602-40609
-
-
Gell, D.1
Kong, Y.2
Eaton, S.A.3
Weiss, M.J.4
Mackay, J.P.5
-
15
-
-
0019738499
-
Preparation of isolated chains of human hemoglobin
-
Antonini E, Luigi R-B, Chiancone E, eds. New York, NY: Academic Press
-
Bucci E. Preparation of isolated chains of human hemoglobin. In: Antonini E, Luigi R-B, Chiancone E, eds. Methods in Enzymology. Vol.76. New York, NY: Academic Press; 1981:97-105.
-
(1981)
Methods in Enzymology
, vol.76
, pp. 97-105
-
-
Bucci, E.1
-
16
-
-
0028308978
-
Production of human hemoglobin in Escherichia coli using cleavable fusion protein expression vector
-
DOI 10.1016/0076-6879(94)31024-6
-
Jessen TH, Komiyama NH, Tame J, et al. Production of human hemoglobin in Escherichia coli using cleavable fusion protein expression vector. Methods Enzymol. 1994;231:347-364. (Pubitemid 24169852)
-
(1994)
Methods in Enzymology
, vol.231
, pp. 347-364
-
-
Jessen, T.-H.1
Komiyama, N.H.2
Tame, J.3
Pagnier, J.4
Shih, D.5
Luisi, B.6
Fermi, G.7
Nagai, K.8
-
17
-
-
33845363586
-
Speciation and structure of ferriprotoporphyrin IX in aqueous solution: Spectroscopic and diffusion measurements demonstrate dimerization, but not mu-oxo dimer formation
-
de Villiers KA, Kaschula CH, Egan TJ, Marques HM. Speciation and structure of ferriprotoporphyrin IX in aqueous solution: spectroscopic and diffusion measurements demonstrate dimerization, but not mu-oxo dimer formation. J Biol Inorg Chem. 2007;12:101-117.
-
(2007)
J Biol Inorg Chem
, vol.12
, pp. 101-117
-
-
De Villiers, K.A.1
Kaschula, C.H.2
Egan, T.J.3
Marques, H.M.4
-
18
-
-
0037134465
-
Assembly of human hemoglobin (Hb) β- and γ-globin chains expressed in a cell-free system with α-globin chains to form Hb a and Hb F
-
DOI 10.1074/jbc.M200857200
-
Adachi K, Zhao Y, Surrey S. Assembly of human hemoglobin (Hb) beta- and gamma-globin chains expressed in a cell-free system with alpha-globin chains to form Hb A and Hb F. J Biol Chem. 2002;277:13415-13420. (Pubitemid 34967935)
-
(2002)
Journal of Biological Chemistry
, vol.277
, Issue.16
, pp. 13415-13420
-
-
Adachi, K.1
Zhao, Y.2
Surrey, S.3
-
19
-
-
0037405439
-
Effects of heme addition on formation of stable human globin chains and hemoglobin subunit assembly in a cell-free system
-
DOI 10.1016/S0003-9861(03)00089-4
-
Adachi K, Zhao Y, Surrey S. Effects of heme addition on formation of stable human globin chains and hemoglobin subunit assembly in a cell-free system. Arch Biochem Biophys. 2003;413:99-106. (Pubitemid 36434356)
-
(2003)
Archives of Biochemistry and Biophysics
, vol.413
, Issue.1
, pp. 99-106
-
-
Adachi, K.1
Zhao, Y.2
Surrey, S.3
-
20
-
-
0022429238
-
Folding of thermolysin fragments: Identification of the minimum size of a carboxyl-terminal fragment that can fold into a stable native-like structure
-
Dalzoppo D, Vita C, Fontana A. Folding of thermolysin fragments: identification of the minimum size of a carboxyl-terminal fragment that can fold into a stable native-like structure. J Mol Biol. 1985;182:331-340.
-
(1985)
J Mol Biol
, vol.182
, pp. 331-340
-
-
Dalzoppo, D.1
Vita, C.2
Fontana, A.3
-
21
-
-
0025147605
-
Expression of fully functional tetrameric human hemoglobin in Escherichia coli
-
Hoffman SJ, Looker DL, Roehrich JM, et al. Expression of fully functional tetrameric human hemoglobin in Escherichia coli. Proc Natl Acad Sci U S A. 1990;87:8521-8525. (Pubitemid 20373123)
-
(1990)
Proceedings of the National Academy of Sciences of the United States of America
, vol.87
, Issue.21
, pp. 8521-8525
-
-
Hoffman, S.J.1
Looker, D.L.2
Roehrich, J.M.3
Cozart, P.E.4
Durfee, S.L.5
Tedesco, J.L.6
Stetler, G.L.7
-
22
-
-
33644968962
-
High-yield expression in Escherichia coli of soluble human alpha-hemoglobin complexed with its molecular chaperone
-
Vasseur-Godbillon C, Hamdane D, Marden MC, Baudin-Creuza V. High-yield expression in Escherichia coli of soluble human alpha-hemoglobin complexed with its molecular chaperone. Protein Eng Des Sel. 2006;19:91-97.
-
(2006)
Protein Eng des Sel
, vol.19
, pp. 91-97
-
-
Vasseur-Godbillon, C.1
Hamdane, D.2
Marden, M.C.3
Baudin-Creuza, V.4
-
23
-
-
52049094782
-
Hb(alphaalpha,betabeta): A novel fusion construct for a dimeric, four-domain hemoglobin
-
Panetta G, Arcovito A, Morea V, Bellelli A, Miele AE. Hb(alphaalpha,betabeta): a novel fusion construct for a dimeric, four-domain hemoglobin. Biochim Biophys Acta. 2008;1784:1462-1470.
-
(2008)
Biochim Biophys Acta
, vol.1784
, pp. 1462-1470
-
-
Panetta, G.1
Arcovito, A.2
Morea, V.3
Bellelli, A.4
Miele, A.E.5
-
24
-
-
20244389684
-
Notch1 expression in early lymphopoiesis influences B versus T lineage determination
-
DOI 10.1016/S1074-7613(00)80105-3
-
Pui JC, Allman D, Xu L, et al. Notch1 expression in early lymphopoiesis influences B versus T lineage determination. Immunity. 1999;11:299-308. (Pubitemid 29463238)
-
(1999)
Immunity
, vol.11
, Issue.3
, pp. 299-308
-
-
Pui, J.C.1
Allman, D.2
Xu, L.3
Derocco, S.4
Karnell, F.G.5
Bakkour, S.6
Lee, J.Y.7
Kadesch, T.8
Hardy, R.R.9
Aster, J.C.10
Pear, W.S.11
-
25
-
-
0026544859
-
A new alpha chain variant, Hb Turriff [alpha 99(G6)Lys - Glu]: The interference of abnormal hemoglobins in Hb A1c determination
-
Langdown JV, Davidson RJ, Williamson D. A new alpha chain variant, Hb Turriff [alpha 99(G6)Lys - Glu]: the interference of abnormal hemoglobins in Hb A1c determination. Hemoglobin. 1992;16:11-17.
-
(1992)
Hemoglobin
, vol.16
, pp. 11-17
-
-
Langdown, J.V.1
Davidson, R.J.2
Williamson, D.3
-
26
-
-
0026708724
-
HB Prato [alpha 31(B12)Arg - Ser] in a Calabrian family
-
De Marco EV, Crescibene L, Pasqua A, Brancati C, Bria M, Qualtieri A. HB Prato [alpha 31(B12)Arg - Ser] in a Calabrian family. Hemoglobin. 1992;16:275-279.
-
(1992)
Hemoglobin
, vol.16
, pp. 275-279
-
-
De Marco, E.V.1
Crescibene, L.2
Pasqua, A.3
Brancati, C.4
Bria, M.5
Qualtieri, A.6
-
27
-
-
0018772224
-
A new abnormal human hemoglobin: Hb Prato (alpha 2 31 (B12) Arg leads to Ser beta 2)
-
Marinucci M, Mavilio F, Massa A, et al. A new abnormal human hemoglobin: Hb Prato (alpha 2 31 (B12) Arg leads to Ser beta 2). Biochim Biophys Acta. 1979;578:534-540.
-
(1979)
Biochim Biophys Acta
, vol.578
, pp. 534-540
-
-
Marinucci, M.1
Mavilio, F.2
Massa, A.3
-
28
-
-
0037283908
-
Hb Prato [alpha31(B12)Arg → Ser (A2)] and alpha-thalassemia in a Taiwanese
-
Shih MC, Peng CT, Chang JY, Liu SC, Kuo PL, Chang JG. Hb Prato [alpha31(B12)Arg → Ser (A2)] and alpha-thalassemia in a Taiwanese. Hemoglobin. 2003;27:45-47.
-
(2003)
Hemoglobin
, vol.27
, pp. 45-47
-
-
Shih, M.C.1
Peng, C.T.2
Chang, J.Y.3
Liu, S.C.4
Kuo, P.L.5
Chang, J.G.6
-
29
-
-
1342345048
-
Two new alpha chain variants: Hb Die [alpha93(FG5)Val → Ala (alpha1)] and Hb Beziers [alpha99(G6)Lys → Asn (alpha1)]
-
Lacan P, Aubry M, Couprie N, Francina A. Two new alpha chain variants: Hb Die [alpha93(FG5)Val → Ala (alpha1)] and Hb Beziers [alpha99(G6)Lys → Asn (alpha1)]. Hemoglobin. 2004;28:59-63.
-
(2004)
Hemoglobin
, vol.28
, pp. 59-63
-
-
Lacan, P.1
Aubry, M.2
Couprie, N.3
Francina, A.4
-
30
-
-
18444396272
-
Four new variants of the alpha2-globin gene without clinical or hematologic effects: Hb Park Ridge [alpha9(alpha7)Asn → Lys (alpha2)], Hb Norton [alpha72(EF1)His → Asp (alpha2)], Hb Lombard [alpha103(G10)His → Tyr (alpha2)], and Hb San Antonio [A113(GH2)Leu → Arg (A2)]
-
Hoyer JD, McCormick DJ, Snow K, et al. Four new variants of the alpha2-globin gene without clinical or hematologic effects: Hb Park Ridge [alpha9(alpha7)Asn → Lys (alpha2)], Hb Norton [alpha72(EF1)His → Asp (alpha2)], Hb Lombard [alpha103(G10)His → Tyr (alpha2)], and Hb San Antonio [A113(GH2)Leu → Arg (A2)]. Hemoglobin. 2002;26:175-179.
-
(2002)
Hemoglobin
, vol.26
, pp. 175-179
-
-
Hoyer, J.D.1
McCormick, D.J.2
Snow, K.3
-
31
-
-
0021240710
-
The characterization of hemoglobin Manitoba or alpha (2)102(G9)Ser - Arg beta 2 and hemoglobin Contaldo or alpha (2)103(G10)His - Arg beta 2 by high performance liquid chromatography
-
Sciarratta GV, Ivaldi G, Molaro GL, et al. The characterization of hemoglobin Manitoba or alpha (2)102(G9)Ser - Arg beta 2 and hemoglobin Contaldo or alpha (2)103(G10)His - Arg beta 2 by high performance liquid chromatography. Hemoglobin. 1984;8:169-181.
-
(1984)
Hemoglobin
, vol.8
, pp. 169-181
-
-
Sciarratta, G.V.1
Ivaldi, G.2
Molaro, G.L.3
-
32
-
-
34248206669
-
The first case of Hb Groene Hart [alpha119(H2)Pro → Ser, CCT → TCT (alpha1)] homozygosity confirms that a thalassemia phenotype is associated with this abnormal hemoglobin variant
-
Giordano PC, Zweegman S, Akkermans N, et al. The first case of Hb Groene Hart [alpha119(H2)Pro → Ser, CCT → TCT (alpha1)] homozygosity confirms that a thalassemia phenotype is associated with this abnormal hemoglobin variant. Hemoglobin. 2007;31:179-182.
-
(2007)
Hemoglobin
, vol.31
, pp. 179-182
-
-
Giordano, P.C.1
Zweegman, S.2
Akkermans, N.3
-
33
-
-
18644385340
-
Hb Groene Hart: A new Pro → Ser amino acid substitution at position 119 of the alpha1-globin chain is associated with a mild alpha-thalassemia phenotype
-
Harteveld CL, van Delft P, Plug R, et al. Hb Groene Hart: a new Pro → Ser amino acid substitution at position 119 of the alpha1-globin chain is associated with a mild alpha-thalassemia phenotype. Hemoglobin. 2002;26:255-260.
-
(2002)
Hemoglobin
, vol.26
, pp. 255-260
-
-
Harteveld, C.L.1
Van Delft, P.2
Plug, R.3
-
34
-
-
28844434222
-
3.7 deletion
-
DOI 10.1080/03630260500308053
-
Siala H, Ouali F, Messaoud T, Sfar R, Fattoum S. First description in Tunisia of a point mutation at codon 119 (CCT → TCT) in the alpha1-globin gene: Hb Groene Hart in association with the -alpha3.7 deletion. Hemoglobin. 2005;29:263-268. (Pubitemid 41780126)
-
(2005)
Hemoglobin
, vol.29
, Issue.4
, pp. 263-268
-
-
Siala, H.1
Ouali, F.2
Messaoud, T.3
Sfar, R.4
Fattoum, S.5
-
35
-
-
0026641219
-
Hb Yuda or alpha 130(H13)Ala - Asp; a new alpha chain variant with low oxygen affinity
-
Fujisawa K, Hattori Y, Ohba Y, Ando S. Hb Yuda or alpha 130(H13)Ala - Asp; a new alpha chain variant with low oxygen affinity. Hemoglobin. 1992;16:435-439.
-
(1992)
Hemoglobin
, vol.16
, pp. 435-439
-
-
Fujisawa, K.1
Hattori, Y.2
Ohba, Y.3
Ando, S.4
-
36
-
-
70449388508
-
Hemolytic anemias: Intracorpuscular defects IV. Thalassemia
-
Harmening DM, ed. F.A. Davis: Philadelphia
-
Harrison CR. Hemolytic anemias: Intracorpuscular defects IV. Thalassemia. In: Harmening DM, ed. Clinical Hematology and Fundamentals of Hemostasis. F.A. Davis: Philadelphia; 1997:193-210.
-
(1997)
Clinical Hematology and Fundamentals of Hemostasis
, pp. 193-210
-
-
Harrison, C.R.1
-
37
-
-
0022978460
-
Human alpha-globin gene expression: The dominant role of the alpha 2-locus in mRNA and protein synthesis
-
Liebhaber SA, Cash FE, Ballas SK. Human alpha-globin gene expression: the dominant role of the alpha 2-locus in mRNA and protein synthesis. J Biol Chem. 1986;261:15327-15333.
-
(1986)
J Biol Chem
, vol.261
, pp. 15327-15333
-
-
Liebhaber, S.A.1
Cash, F.E.2
Ballas, S.K.3
-
38
-
-
0023179675
-
The kinetics of assembly of normal and variant human oxyhemoglobins
-
McDonald MJ, Turci SM, Mrabet NT, Himelstein BP, Bunn HF. The kinetics of assembly of normal and variant human oxyhemoglobins. J Biol Chem. 1987;262:5951-5956. (Pubitemid 17103029)
-
(1987)
Journal of Biological Chemistry
, vol.262
, Issue.13
, pp. 5951-5956
-
-
McDonald, M.J.1
Turci, S.M.2
Mrabet, N.T.3
-
40
-
-
0026550785
-
A human recombinant haemoglobin designed for use as a blood substitute
-
Looker D, Abbott-Brown D, Cozart P, et al. A human recombinant haemoglobin designed for use as a blood substitute. Nature. 1992;356:258-260.
-
(1992)
Nature
, vol.356
, pp. 258-260
-
-
Looker, D.1
Abbott-Brown, D.2
Cozart, P.3
-
41
-
-
0037570781
-
The mutation of Hb Turriff [alpha99(G6)Lys → Glu (AAG → GAG)] is carried by the alpha1-globin gene in a Japanese (Hb Turriff-I)
-
Harano T, Harano K, Hong YF, Than AM, Suetsugu Y, Ohba K. The mutation of Hb Turriff [alpha99(G6)Lys → Glu (AAG → GAG)] is carried by the alpha1-globin gene in a Japanese (Hb Turriff-I). Hemoglobin. 2003;27:123-127.
-
(2003)
Hemoglobin
, vol.27
, pp. 123-127
-
-
Harano, T.1
Harano, K.2
Hong, Y.F.3
Than, A.M.4
Suetsugu, Y.5
Ohba, K.6
|