-
1
-
-
0015219140
-
Alpha and beta globin messenger ribonucleic acid. Different amounts and rates of initiation of translation
-
Lodish, H. F.: Alpha and beta globin messenger ribonucleic acid. Different amounts and rates of initiation of translation. J Biol Chem, 246, 7131-8 (1971).
-
(1971)
J Biol Chem
, vol.246
, pp. 7131-7138
-
-
Lodish, H.F.1
-
2
-
-
36349011460
-
α/β-Globin mRNA ratio determination by multiplex quantitative real-time reverse transcription-polymerase chain reaction as an indicator of globin gene function
-
DOI 10.1016/j.clinbiochem.2007.08.005, PII S0009912007003293
-
Chaisue, C., S. Kitcharoen, P. Wilairat, A. Jetsrisuparb, G. Fucharoen & S. Fucharoen: alpha/beta-Globin mRNA ratio determination by multiplex quantitative real-time reverse transcription-polymerase chain reaction as an indicator of globin gene function. Clin Biochem, 40, 1373-7 (2007). (Pubitemid 350151423)
-
(2007)
Clinical Biochemistry
, vol.40
, Issue.18
, pp. 1373-1377
-
-
Chaisue, C.1
Kitcharoen, S.2
Wilairat, P.3
Jetsrisuparb, A.4
Fucharoen, G.5
Fucharoen, S.6
-
3
-
-
28044444751
-
Quantitative assessment of human β-globin gene expression in vitro by TaqMan real-time reverse transcription-PCR: Comparison with competitive reverse transcription-PCR and application to mutations or deletions in noncoding regions
-
DOI 10.1373/clinchem.2005.056630
-
Irenge, L. M., A. Robert & J. L. Gala: Quantitative assessment of human beta-globin gene expression in vitro by TaqMan real-time reverse transcription-PCR: comparison with competitive reverse transcription-PCR and application to mutations or deletions in noncoding regions. Clin Chem, 51, 2395-6 (2005). (Pubitemid 41692595)
-
(2005)
Clinical Chemistry
, vol.51
, Issue.12
, pp. 2395-2396
-
-
Irenge, L.M.1
Robert, A.2
Gala, J.-L.3
-
5
-
-
0037071860
-
An abundant erythroid protein that stabilizes free α-haemoglobin
-
DOI 10.1038/nature00803
-
Kihm, A. J., Y. Kong, W. Hong, J. E. Russell, S. Rouda, K. Adachi, M. C. Simon, G. A. Blobel & M. J. Weiss: An abundant erythroid protein that stabilizes free alphahaemoglobin. Nature, 417, 758-63 (2002). (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
-
6
-
-
0035099673
-
A novel erythroidspecific marker of transmissible spongiform encephalopathies
-
Miele, G., J. Manson & M. Clinton: A novel erythroidspecific marker of transmissible spongiform encephalopathies. Nat Med, 7, 361-4 (2001).
-
(2001)
Nat Med
, vol.7
, pp. 361-364
-
-
Miele, G.1
Manson, J.2
Clinton, M.3
-
7
-
-
85047690518
-
Loss of α-hemoglobin-stabilizing protein impairs erythropoiesis and exacerbates β-thalassemia
-
DOI 10.1172/JCI200421982
-
Kong, Y., S. Zhou, A. J. Kihm, A. M. Katein, X. Yu, D. A. Gell, J. P. Mackay, K. Adachi, L. Foster-Brown, C. S. Louden, A. J. Gow & M. J. Weiss: Loss of alphahemoglobin- stabilizing protein impairs erythropoiesis and exacerbates beta-thalassemia. J Clin Invest, 114, 1457-66 (2004). (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
-
8
-
-
33644968962
-
High-yield expression in Escherichia coli of soluble human alpha-hemoglobin complexed with its molecular chaperone
-
Vasseur-Godbillon, C., D. Hamdane, M. C. Marden & V. Baudin-Creuza: High-yield expression in Escherichia coli of soluble human alpha-hemoglobin complexed with its molecular chaperone. Protein Eng Des Sel, 19, 91-7 (2006).
-
(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
-
9
-
-
34447121854
-
An erythroid chaperone that facilitates folding of α-globin subunits for hemoglobin synthesis
-
DOI 10.1172/JCI31664
-
Yu, X., Y. Kong, L. C. Dore, O. Abdulmalik, A. M. Katein, S. Zhou, J. K. Choi, D. Gell, J. P. Mackay, A. J. Gow & M. J. Weiss: An erythroid chaperone that facilitates folding of alpha-globin subunits for hemoglobin synthesis. J Clin Invest, 117, 1856-65 (2007). (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
-
10
-
-
39149123488
-
Reduction of AHSP synthesis in hemininduced K562 cells and EPO-induced CD34(+) cells leads to alpha-globin precipitation, impairment of normal hemoglobin production, and increased cell death
-
Pinho, F. O., D. M. de Albuquerque, S. T. Olalla Saad & F. F. Costa: Reduction of AHSP synthesis in hemininduced K562 cells and EPO-induced CD34(+) cells leads to alpha-globin precipitation, impairment of normal hemoglobin production, and increased cell death. Exp Hematol, 36, 265-72 (2008).
-
(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
-
11
-
-
41549140910
-
Coinheritance of the different copy numbers of alpha-globin gene modifies severity of beta-thalassemia/Hb E disease
-
Sripichai, O., T. Munkongdee, C. Kumkhaek, S. Svasti, P. Winichagoon & S. Fucharoen: Coinheritance of the different copy numbers of alpha-globin gene modifies severity of beta-thalassemia/Hb E disease. Ann Hematol, 87, 375-9 (2008).
-
(2008)
Ann Hematol
, vol.87
, pp. 375-379
-
-
Sripichai, O.1
Munkongdee, T.2
Kumkhaek, C.3
Svasti, S.4
Winichagoon, P.5
Fucharoen, S.6
-
12
-
-
33746317014
-
Human red blood cell polymorphisms and malaria
-
DOI 10.1016/j.mib.2006.06.009, PII S1369527406000920
-
Williams, T. N.: Human red blood cell polymorphisms and malaria. Curr Opin Microbiol, 9, 388-94 (2006). (Pubitemid 44108720)
-
(2006)
Current Opinion in Microbiology
, vol.9
, Issue.4
, pp. 388-394
-
-
Williams, T.N.1
-
13
-
-
0037175053
-
Biophysical characterization of the alpha-globin binding protein alpha-hemoglobin stabilizing protein
-
Gell, D., Y. Kong, S. A. Eaton, M. J. Weiss & J. P. Mackay: Biophysical characterization of the alpha-globin binding protein alpha-hemoglobin stabilizing protein. J Biol Chem, 277, 40602-9 (2002).
-
(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
-
14
-
-
8844285199
-
Molecular mechanism of AHSP-mediated stabilization of α-hemoglobin
-
DOI 10.1016/j.cell.2004.11.025, PII S0092867404010438
-
Feng, L., D. A. Gell, S. Zhou, L. Gu, Y. Kong, J. Li, M. Hu, N. Yan, C. Lee, A. M. Rich, R. S. Armstrong, P. A. Lay, A. J. Gow, M. J. Weiss, J. P. Mackay & Y. Shi: Molecular mechanism of AHSP-mediated stabilization of alpha-hemoglobin. Cell, 119, 629-40 (2004). (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
-
15
-
-
4544359805
-
NMR structure of the α-hemoglobin stabilizing protein: Insights into conformational heterogeneity and binding
-
DOI 10.1074/jbc.M405016200
-
Santiveri, C. M., J. M. Perez-Canadillas, M. K. Vadivelu, M. D. Allen, T. J. Rutherford, N. A. Watkins & M. Bycroft: NMR structure of the alpha-hemoglobin stabilizing protein: insights into conformational heterogeneity and binding. J Biol Chem, 279, 34963-70 (2004). (Pubitemid 39318133)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.33
, pp. 34963-34970
-
-
Santiveri, C.M.1
Perez-Canadillas, J.M.2
Vadivelu, M.K.3
Allen, M.D.4
Rutherford, T.J.5
Watkins, N.A.6
Bycroft, M.7
-
16
-
-
4344601600
-
Transfer of human α- to β-hemoglobin via its chaperone protein: Evidence for a new state
-
DOI 10.1074/jbc.M405389200
-
Baudin-Creuza, V., C. Vasseur-Godbillon, C. Pato, C. Prehu, H. Wajcman & M. C. Marden: Transfer of human alpha- to beta-hemoglobin via its chaperone protein: evidence for a new state. J Biol Chem, 279, 36530-3 (2004). (Pubitemid 39128994)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.35
, pp. 36530-36533
-
-
Baudin-Creuza, V.1
Vasseur-Godbillon, C.2
Pato, C.3
Prehu, C.4
Wajcman, H.5
Marden, M.C.6
-
17
-
-
33845924644
-
Biochemical fates of α hemoglobin bound to α hemoglobin-stabilizing protein AHSP
-
DOI 10.1074/jbc.M607311200
-
Zhou, S., J. S. Olson, M. Fabian, M. J. Weiss & A. J. Gow: Biochemical fates of alpha hemoglobin bound to alpha hemoglobin-stabilizing protein AHSP. J Biol Chem, 281, 32611-8 (2006). (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
-
18
-
-
20444445134
-
Structure of oxidized α-haemoglobin bound to AHSP reveals a protective mechanism for haem
-
DOI 10.1038/nature03609
-
Feng, L., S. Zhou, L. Gu, D. A. Gell, J. P. Mackay, M. J. Weiss, A. J. Gow & Y. Shi: Structure of oxidized alpha-haemoglobin bound to AHSP reveals a protective mechanism for haem. Nature, 435, 697-701 (2005). (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
-
19
-
-
34250369650
-
Reversible hexacoordination of α-Hemoglobin-stabilizing Protein (AHSP)/α-hemoglobin versus pressure: Evidence for protection of the α-chains by their chaperone
-
DOI 10.1074/jbc.M610543200
-
Hamdane, D., C. Vasseur-Godbillon, V. Baudin-Creuza, G. H. Hoa & M. C. Marden: Reversible hexacoordination of alpha-hemoglobin-stabilizing protein (AHSP)/alpha-hemoglobin Versus pressure. Evidence for protection of the alpha-chains by their chaperone. J Biol Chem, 282, 6398-404 (2007). (Pubitemid 47100835)
-
(2007)
Journal of Biological Chemistry
, vol.282
, Issue.9
, pp. 6398-6404
-
-
Hamdane, D.1
Vasseur-Godbillon, C.2
Baudin-Creuza, V.3
Hoa, G.H.B.4
Marden, M.C.5
-
20
-
-
0842287506
-
Expression of α-hemoglobin stabilizing protein gene during human erythropoiesis
-
DOI 10.1016/j.exphem.2003.11.002
-
dos Santos, C. O., A. S. Duarte, S. T. Saad & F. F. Costa: Expression of alpha-hemoglobin stabilizing protein gene during human erythropoiesis. Exp Hematol, 32, 157- 62 (2004). (Pubitemid 38177641)
-
(2004)
Experimental Hematology
, vol.32
, Issue.2
, pp. 157-162
-
-
Dos Santos, C.O.1
Duarte, A.S.S.2
Olalla Saad, S.T.3
Costa, F.F.4
-
21
-
-
28244472034
-
GATA-1 and Oct-1 are required for expression of the human α-hemoglobin-stabilizing protein gene
-
DOI 10.1074/jbc.M506062200
-
Gallagher, P. G., R. I. Liem, E. Wong, M. J. Weiss & D. M. Bodine: GATA-1 and Oct-1 are required for expression of the human alpha-hemoglobin- stabilizing protein gene. J Biol Chem, 280, 39016-23 (2005). (Pubitemid 41713851)
-
(2005)
Journal of Biological Chemistry
, vol.280
, Issue.47
, pp. 39016-39023
-
-
Gallagher, P.G.1
Liem, R.I.2
Wong, E.3
Weiss, M.J.4
Bodine, D.M.5
-
22
-
-
20344364878
-
The erythroid phenotype of EKLF-null mice: Defects in hemoglobin metabolism and membrane stability
-
DOI 10.1128/MCB.25.12.5205-5214.2005
-
Drissen, R., M. von Lindern, A. Kolbus, S. Driegen, P. Steinlein, H. Beug, F. Grosveld & S. Philipsen: The erythroid phenotype of EKLF-null mice: defects in hemoglobin metabolism and membrane stability. Mol Cell Biol, 25, 5205-14 (2005). (Pubitemid 40781118)
-
(2005)
Molecular and Cellular Biology
, vol.25
, Issue.12
, pp. 5205-5214
-
-
Drissen, R.1
Von Lindern, M.2
Kolbus, A.3
Driegen, S.4
Steinlein, P.5
Beug, H.6
Grosveld, F.7
Philipsen, S.8
-
23
-
-
33845473296
-
Genomic organisation and regulation of murine alpha haemoglobin stabilising protein by erythroid Kruppel-like factor
-
DOI 10.1111/j.1365-2141.2006.06381.x
-
Keys, J. R., M. R. Tallack, D. J. Hodge, S. O. Cridland, R. David & A. C. Perkins: Genomic organisation and regulation of murine alpha haemoglobin stabilising protein by erythroid Kruppel-like factor. Br J Haematol, 136, 150- 7 (2007). (Pubitemid 44912602)
-
(2007)
British Journal of Haematology
, vol.136
, Issue.1
, pp. 150-157
-
-
Keys, J.R.1
Tallack, M.R.2
Hodge, D.J.3
Cridland, S.O.4
David, R.5
Perkins, A.C.6
-
24
-
-
33646873303
-
Alterations in expression and chromatin configuration of the alpha hemoglobin-stabilizing protein gene in erythroid Krüppel-like factor-deficient mice
-
DOI 10.1128/MCB.02216-05
-
Pilon, A. M., D. G. Nilson, D. Zhou, J. Sangerman, T. M. Townes, D. M. Bodine & P. G. Gallagher: Alterations in expression and chromatin configuration of the alpha hemoglobin-stabilizing protein gene in erythroid Kruppellike factor-deficient mice. Mol Cell Biol, 26, 4368-77 (2006). (Pubitemid 43788035)
-
(2006)
Molecular and Cellular Biology
, vol.26
, Issue.11
, pp. 4368-4377
-
-
Pilon, A.M.1
Nilson, D.G.2
Zhou, D.3
Sangerman, J.4
Townes, T.M.5
Bodine, D.M.6
Gallagher, P.G.7
-
25
-
-
55249087434
-
An iron responsive element-like stem-loop regulates alpha hemoglobin stabilizing protein mRNA
-
Dos Santos, C. O., L. C. Dore, E. Valentine, S. G. Shelat, R. C. Hardison, M. Ghosh, W. Wang, R. S. Eisenstein, F. F. Costa & M. J. Weiss: An iron responsive element-like stem-loop regulates alpha hemoglobin stabilizing protein mRNA. J Biol Chem, 283, 26956-64 (2008).
-
(2008)
J Biol Chem
, vol.283
, pp. 26956-26964
-
-
Dos Santos, C.O.1
Dore, L.C.2
Valentine, E.3
Shelat, S.G.4
Hardison, R.C.5
Ghosh, M.6
Wang, W.7
Eisenstein, R.S.8
Costa, F.F.9
Weiss, M.J.10
-
26
-
-
0034321997
-
Genetic factors affecting clinical severity in betathalassemia syndromes
-
Winichagoon, P., S. Fucharoen, P. Chen & P. Wasi: Genetic factors affecting clinical severity in betathalassemia syndromes. J Pediatr Hematol Oncol, 22, 573- 80 (2000).
-
(2000)
J Pediatr Hematol Oncol
, vol.22
, pp. 573-580
-
-
Winichagoon, P.1
Fucharoen, S.2
Chen, P.3
Wasi, P.4
-
27
-
-
1942425504
-
Evaluation of alpha hemoglobin stabilizing protein (AHSP) as a genetic modifier in patients with β thalassemia
-
DOI 10.1182/blood-2003-11-3957
-
Viprakasit, V., V. S. Tanphaichitr, W. Chinchang, P. Sangkla, M. J. Weiss & D. R. Higgs: Evaluation of alpha hemoglobin stabilizing protein (AHSP) as a genetic modifier in patients with beta thalassemia. Blood, 103, 3296-9 (2004). (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
-
28
-
-
25844494542
-
Sick chaperones, cellular stress, and disease
-
DOI 10.1056/NEJMra050111
-
Macario, A. J. L. & E. Conway de Macario: Sick chaperones, cellular stress and disease. New Eng J Med 353, 1489-501 (2005). (Pubitemid 41400923)
-
(2005)
New England Journal of Medicine
, vol.353
, Issue.14
, pp. 1489-1501
-
-
Macario, A.J.L.1
Conway De Macario, E.2
-
29
-
-
35548998775
-
Chaperonopathies by defect, excess, or mistake
-
DOI 10.1196/annals.1391.009, Stress Responses
-
Macario, A. J. L. & E. Conway de Macario: Chaperonopathies by defect, excess, or mistake. Ann New York Acad Sci, 1113, 178-91 (2007). (Pubitemid 350015008)
-
(2007)
Annals of the New York Academy of Sciences
, vol.1113
, pp. 178-191
-
-
Macario, A.J.L.1
De Macario, E.C.2
-
30
-
-
34347238198
-
Genetics of human longevity with emphasis on the relevance of HSP70 as candidate genes
-
Singh, R., S. Kolvraa & S. I. S. Rattan: Genetics of human longevity with emphasis on the relevance of HSP70 as candidate genes. Front Biosci 12, 4504-13 (2007). http://www.bioscience.org/2007/v12/af/2405/fulltext.htm.
-
(2007)
Front Biosci
, vol.12
, pp. 4504-4513
-
-
Singh, R.1
Kolvraa, S.2
Rattan, S.I.S.3
-
31
-
-
33646689318
-
α-haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of β-thalassaemia
-
DOI 10.1111/j.1365-2141.2006.06075.x
-
Lai, M. I., J. Jiang, N. Silver, S. Best, S. Menzel, A. Mijovic, S. Colella, J. Ragoussis, C. Garner, M. J. Weiss & S. L. Thein: Alpha-haemoglobin stabilising protein is a quantitative trait gene that modifies the phenotype of betathalassaemia. Br J Haematol, 133, 675-82 (2006). (Pubitemid 43742786)
-
(2006)
British Journal of Haematology
, vol.133
, Issue.6
, pp. 675-682
-
-
Lai, M.I.1
Jiang, J.2
Silver, N.3
Best, S.4
Menzel, S.5
Mijovic, A.6
Colella, S.7
Ragoussis, J.8
Garner, C.9
Weiss, M.J.10
Thein, S.L.11
-
32
-
-
38349170152
-
Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and function
-
dos Santos, C. O., S. Zhou, R. Secolin, X. Wang, A. F. Cunha, D. R. Higgs, J. L. Kwiatkowski, S. L. Thein, P. G. Gallagher, F. F. Costa & M. J. Weiss: Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and function. Am J Hematol, 83, 103-8 (2008).
-
(2008)
Am J Hematol
, vol.83
, pp. 103-108
-
-
Dos Santos, C.O.1
Zhou, S.2
Secolin, R.3
Wang, X.4
Cunha, A.F.5
Higgs, D.R.6
Kwiatkowski, J.L.7
Thein, S.L.8
Gallagher, P.G.9
Costa, F.F.10
Weiss, M.J.11
-
33
-
-
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., T. Limjindaporn, W. Wongwiwat, U. P. Y, N. Siritanaratkul, P. T. Yenchitsomanus, S. Jitrapakdee & P. Wilairat: Impaired interaction of alphahaemoglobin-stabilising protein with alpha-globin termination mutant in a yeast two-hybrid system. Br J Haematol, 132, 370-3 (2006). (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
-
34
-
-
0028148498
-
Erythroid cell-specific determinants of α-globin mRNA stability
-
Weiss, I. M. & S. A. Liebhaber: Erythroid cell-specific determinants of alpha-globin mRNA stability. Mol Cell Biol, 14, 8123-32 (1994). (Pubitemid 24373561)
-
(1994)
Molecular and Cellular Biology
, vol.14
, Issue.12
, pp. 8123-8132
-
-
Weiss, I.M.1
Liebhaber, S.A.2
-
35
-
-
0008151168
-
Presence of alpha CS-globin on membrane of red cell containing hemoglobin Constant Spring (CS)
-
Peerapittayamongkol, C., L. F. Bernini & P. Wilairat: Presence of alphaCS-globin on membrane of red cell containing hemoglobin Constant Spring (CS). J Sci Soc Thailand 22, 117-20 (1996).
-
(1996)
J Sci Soc Thailand
, vol.22
, pp. 117-120
-
-
Peerapittayamongkol, C.1
Bernini, L.F.2
Wilairat, P.3
-
36
-
-
0031032788
-
The unusual pathobiology of hemoglobin constant spring red blood cells
-
Schrier, S. L., A. Bunyaratvej, A. Khuhapinant, S. Fucharoen, M. Aljurf, L. M. Snyder, C. R. Keifer, L. Ma & N. Mohandas: The unusual pathobiology of hemoglobin constant spring red blood cells. Blood, 89, 1762-9 (1997). (Pubitemid 27097472)
-
(1997)
Blood
, vol.89
, Issue.5
, pp. 1762-1769
-
-
Schrier, S.L.1
Bunyaratvej, A.2
Khuhapinant, A.3
Fucharoen, S.4
Aljurf, M.5
Snyder, L.M.6
Keifer, C.R.7
Ma, L.8
Mohandas, N.9
-
37
-
-
4444286637
-
Hemoglobin Pakse: Presence on red blood cell membrane and detection by polymerase chain reaction - Single-strand conformational polymorphism
-
DOI 10.1532/IJH97.A20402
-
Turbpaiboon, C., A. Siritantikorn, W. Thongnoppakhun, D. Bunditworapoom, C. Limwongse, P. T. Yenchitsomanus, N. Siritanaratkul & P. Wilairat: Hemoglobin Pakse: presence on red blood cell membrane and detection by polymerase chain reaction-single-strand conformational polymorphism. Int J Hematol, 80, 136-9 (2004). (Pubitemid 39201566)
-
(2004)
International Journal of Hematology
, vol.80
, Issue.2
, pp. 136-139
-
-
Turbpaiboon, C.1
Siritantikorn, A.2
Thongnoppakhun, W.3
Bunditworapoom, D.4
Limwongse, C.5
Yenchitsomanus, P.-T.6
Siritanaratkul, N.7
Wilairat, P.8
-
38
-
-
1342302434
-
0 Thalassemia Associated with Transfusion-Dependent Hb H Disease
-
DOI 10.1002/ajh.10479
-
Viprakasit, V., V. S. Tanphaichitr, G. Veerakul, W. Chinchang, S. Petrarat, P. Pung-Amritt & D. R. Higgs: Coinheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H disease. Am J Hematol, 75, 157-63 (2004). (Pubitemid 38263825)
-
(2004)
American Journal of Hematology
, vol.75
, Issue.3
, pp. 157-163
-
-
Viprakasit, V.1
Tanphaichitr, V.S.2
Veerakul, G.3
Chinchang, W.4
Petrarat, S.5
Pung-Amritt, P.6
Higgs, D.R.7
-
39
-
-
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., M. C. Marden, P. Giordano, H. Wajcman & V. Baudin-Creuza: 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, 37, 173-9 (2006). (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
-
40
-
-
47949117716
-
Unstable and thalassemic alpha chain hemoglobin variants: A cause of Hb H disease and thalassemia intermedia
-
Wajcman, H., J. Traeger-Synodinos, I. Papassotiriou, P. C. Giordano, C. L. Harteveld, V. Baudin-Creuza & J. Old: Unstable and thalassemic alpha chain hemoglobin variants: a cause of Hb H disease and thalassemia intermedia. Hemoglobin, 32, 327-49 (2008).
-
(2008)
Hemoglobin
, vol.32
, pp. 327-349
-
-
Wajcman, H.1
Traeger-Synodinos, J.2
Papassotiriou, I.3
Giordano, P.C.4
Harteveld, C.L.5
Baudin-Creuza, V.6
Old, J.7
-
41
-
-
67651100891
-
Analysis of human alpha globin gene mutations that impair binding to the alpha hemoglobin stabilizing protein
-
Xiang Yu, X., T. L. Mollan, A. Butler, A. J. Gow, J. S. Olson & M. J. Weiss: Analysis of human alpha globin gene mutations that impair binding to the alpha hemoglobin stabilizing protein. Blood, 113, 5961-69 (2009).
-
(2009)
Blood
, vol.113
, pp. 5961-5969
-
-
Xiang Yu, X.1
Mollan, T.L.2
Butler, A.3
Gow, A.J.4
Olson, J.S.5
Weiss, M.J.6
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