-
1
-
-
14144255089
-
5-hydroxymethyl-2-furfural modifies intracellular sickle haemoglobin and inhibits sickling of red blood cells
-
Abdulmalik, O., Safo, M.K., Chen, Q., Yang, J., Brugnara, C., Ohene-Frempong, K., Abraham, D.J. & Asakura, T. (2005) 5-hydroxymethyl-2-furfural modifies intracellular sickle haemoglobin and inhibits sickling of red blood cells. British Journal of Haematology, 128, 552–561.
-
(2005)
British Journal of Haematology
, vol.128
, pp. 552-561
-
-
Abdulmalik, O.1
Safo, M.K.2
Chen, Q.3
Yang, J.4
Brugnara, C.5
Ohene-Frempong, K.6
Abraham, D.J.7
Asakura, T.8
-
2
-
-
80955136792
-
Crystallographic analysis of human hemoglobin elucidates the structural basis of the potent and dual antisickling activity of pyridyl derivatives of vanillin
-
Abdulmalik, O., Ghatge, M.S., Musayev, F.N., Parikh, A., Chen, Q., Yang, J., Nnamani, I., Danso-Danquah, R., Eseonu, D.N., Asakura, T., Abraham, D.J., Venitz, J. & Safo, M.K. (2011) Crystallographic analysis of human hemoglobin elucidates the structural basis of the potent and dual antisickling activity of pyridyl derivatives of vanillin. Acta Crystallographica Section D, D67, 920–928.
-
(2011)
Acta Crystallographica Section D
, vol.D67
, pp. 920-928
-
-
Abdulmalik, O.1
Ghatge, M.S.2
Musayev, F.N.3
Parikh, A.4
Chen, Q.5
Yang, J.6
Nnamani, I.7
Danso-Danquah, R.8
Eseonu, D.N.9
Asakura, T.10
Abraham, D.J.11
Venitz, J.12
Safo, M.K.13
-
3
-
-
0020397654
-
Kinetics of the polymerization of hemoglobin in high and low phosphate buffers
-
Adachi, K. & Asakura, T. (1982) Kinetics of the polymerization of hemoglobin in high and low phosphate buffers. Blood Cells, 8, 213–224.
-
(1982)
Blood Cells
, vol.8
, pp. 213-224
-
-
Adachi, K.1
Asakura, T.2
-
4
-
-
79960147525
-
Fetal hemoglobin in sickle cell anemia
-
Akinsheye, I., Alsultan, A., Solovieff, N., Ngo, D., Baldwin, C.T., Sebastiani, P., Chui, D.H.K. & Steinberg, M.H. (2011) Fetal hemoglobin in sickle cell anemia. Blood, 118, 19–27.
-
(2011)
Blood
, vol.118
, pp. 19-27
-
-
Akinsheye, I.1
Alsultan, A.2
Solovieff, N.3
Ngo, D.4
Baldwin, C.T.5
Sebastiani, P.6
Chui, D.H.K.7
Steinberg, M.H.8
-
5
-
-
0029895837
-
Tucaresol increases oxygen affinity and reduces haemolysis in subjects with sickle cell anaemia
-
Arya, R., Rolan, P.E., Wootton, R., Posner, J. & Bellingham, A.J. (1996) Tucaresol increases oxygen affinity and reduces haemolysis in subjects with sickle cell anaemia. British Journal of Haematology, 93, 817–821.
-
(1996)
British Journal of Haematology
, vol.93
, pp. 817-821
-
-
Arya, R.1
Rolan, P.E.2
Wootton, R.3
Posner, J.4
Bellingham, A.J.5
-
6
-
-
79952594455
-
Improvements in haemolysis and indicators of erythrocyte survival do not correlate with acute vaso-occlusive crises in patients with sickle cell disease: a phase III randomized, placebo-controlled, double-blind study of the gardos channel blocker senicapoc
-
Ataga, K.I., Reid, M., Ballas, S.K., Yasin, Z., Bigelow, C., James, L.S., Smith, W.R., Galacteros, F., Kutlar, A., Hull, J.H. & Stocker, J.W. (2011) Improvements in haemolysis and indicators of erythrocyte survival do not correlate with acute vaso-occlusive crises in patients with sickle cell disease: a phase III randomized, placebo-controlled, double-blind study of the gardos channel blocker senicapoc. British Journal of Haematology, 153, 92–104.
-
(2011)
British Journal of Haematology
, vol.153
, pp. 92-104
-
-
Ataga, K.I.1
Reid, M.2
Ballas, S.K.3
Yasin, Z.4
Bigelow, C.5
James, L.S.6
Smith, W.R.7
Galacteros, F.8
Kutlar, A.9
Hull, J.H.10
Stocker, J.W.11
-
7
-
-
0021247053
-
Substituted benzaldehydes designed to increase the oxygen affinity of human haemoglobin and inhibit the sickling of sickle erythrocytes
-
Beddell, C.R., Goodford, P.J., Kneen, G., White, R.D., Wilkinson, S. & Wootton, R. (1984) Substituted benzaldehydes designed to increase the oxygen affinity of human haemoglobin and inhibit the sickling of sickle erythrocytes. British Journal of Pharmacology, 82, 397–407.
-
(1984)
British Journal of Pharmacology
, vol.82
, pp. 397-407
-
-
Beddell, C.R.1
Goodford, P.J.2
Kneen, G.3
White, R.D.4
Wilkinson, S.5
Wootton, R.6
-
8
-
-
84902131595
-
Vasculotoxic and proinflammatory effects of plasma heme: cell signaling and cytoprotective responses
-
Belcher, J., Nath, K. & Vercellotti, G. (2013) Vasculotoxic and proinflammatory effects of plasma heme: cell signaling and cytoprotective responses. ISRN Oxidative Medicine, 2013, 1–9.
-
(2013)
ISRN Oxidative Medicine
, vol.2013
, pp. 1-9
-
-
Belcher, J.1
Nath, K.2
Vercellotti, G.3
-
9
-
-
0016793039
-
Fetal hemoglobin restriction to a few erythrocytes (F cells) in normal human adults
-
Boyer, S.H., Belding, T.K., Margolet, L. & Noyes, a N. (1975) Fetal hemoglobin restriction to a few erythrocytes (F cells) in normal human adults. Science (New York, N.Y.), 188, 361–363.
-
(1975)
Science (New York, N.Y.)
, vol.188
, pp. 361-363
-
-
Boyer, S.H.1
Belding, T.K.2
Margolet, L.3
Noyes, A.N.4
-
10
-
-
77953494025
-
Hydroxyurea use in sickle cell disease: the Battle with low rates of prescription, poor patient compliance and fears of toxicities and side effects
-
Brandow, A. & Panepinto, J. (2013) Hydroxyurea use in sickle cell disease: the Battle with low rates of prescription, poor patient compliance and fears of toxicities and side effects. Expert Review Hematology, 3, 255–260.
-
(2013)
Expert Review Hematology
, vol.3
, pp. 255-260
-
-
Brandow, A.1
Panepinto, J.2
-
11
-
-
0030853711
-
Pathogenesis and treatment of sickle cell disease
-
Bunn, H.F. (1997) Pathogenesis and treatment of sickle cell disease. The New England Journal of Medicine, 337, 762–769.
-
(1997)
The New England Journal of Medicine
, vol.337
, pp. 762-769
-
-
Bunn, H.F.1
-
12
-
-
78650005938
-
myo-Inositol trispyrophosphate: a novel allosteric effector of hemoglobin with high permeation selectivity across the red blood cell plasma membrane
-
Duarte, C.D., Greferath, R., Nicolau, C. & Lehn, J.-M. (2010) myo-Inositol trispyrophosphate: a novel allosteric effector of hemoglobin with high permeation selectivity across the red blood cell plasma membrane. Chembiochem : A European Journal of Chemical Biology, 11, 2543–2548.
-
(2010)
Chembiochem : A European Journal of Chemical Biology
, vol.11
, pp. 2543-2548
-
-
Duarte, C.D.1
Greferath, R.2
Nicolau, C.3
Lehn, J.-M.4
-
13
-
-
0022183485
-
The effects in volunteers of BW12C, a compound designed to left-shift the blood-oxygen saturation curve
-
Fitzharris, P., McLean, A.E., Sparks, R.G., Weatherley, B.C., White, R.D. & Wootton, R. (1985) The effects in volunteers of BW12C, a compound designed to left-shift the blood-oxygen saturation curve. British Journal of Clinical Pharmacology, 19, 471–481.
-
(1985)
British Journal of Clinical Pharmacology
, vol.19
, pp. 471-481
-
-
Fitzharris, P.1
McLean, A.E.2
Sparks, R.G.3
Weatherley, B.C.4
White, R.D.5
Wootton, R.6
-
14
-
-
0017641722
-
Participation of hemoglobins A and F in polymerization of sickle hemoglobin
-
Goldberg, M.A., Husson, M.A. & Bunn, H.F. (1977) Participation of hemoglobins A and F in polymerization of sickle hemoglobin. The Journal of Biological Chemistry, 252, 3414–3421.
-
(1977)
The Journal of Biological Chemistry
, vol.252
, pp. 3414-3421
-
-
Goldberg, M.A.1
Husson, M.A.2
Bunn, H.F.3
-
15
-
-
59049098921
-
Haemoglobinopathies with high oxygen affinity. Experience of Erythropathology Cooperative Spanish Group
-
González Fernández, F.A., Villegas, A., Ropero, P., Carreño, M.D., Anguita, E., Polo, M., Pascual, A. & Henández, A. (2009) Haemoglobinopathies with high oxygen affinity. Experience of Erythropathology Cooperative Spanish Group. Annals of Hematology, 88, 235–238.
-
(2009)
Annals of Hematology
, vol.88
, pp. 235-238
-
-
González Fernández, F.A.1
Villegas, A.2
Ropero, P.3
Carreño, M.D.4
Anguita, E.5
Polo, M.6
Pascual, A.7
Henández, A.8
-
16
-
-
0028817948
-
Performance characteristics of Hemox-Analyzer for assessment of the hemoglobin dissociation curve
-
Guarnone, R., Centenara, E. & Barosi, G. (1995) Performance characteristics of Hemox-Analyzer for assessment of the hemoglobin dissociation curve. Haematologica, 80, 426–430.
-
(1995)
Haematologica
, vol.80
, pp. 426-430
-
-
Guarnone, R.1
Centenara, E.2
Barosi, G.3
-
17
-
-
0037098945
-
A high-throughput microplate method for assessing aggregation of deoxygenated hemoglobin s heterotetramers in vitro
-
He, Z. & Russell, J.E. (2002) A high-throughput microplate method for assessing aggregation of deoxygenated hemoglobin s heterotetramers in vitro. Analytical Biochemistry, 306, 349–352.
-
(2002)
Analytical Biochemistry
, vol.306
, pp. 349-352
-
-
He, Z.1
Russell, J.E.2
-
18
-
-
0035124017
-
Detection of haemoglobin variants and inference of their functional properties using complete oxygen dissociation curve measurements
-
Imai, K., Tientadakul, P., Opartkiattikul, N., Luenee, P., Winichagoon, P., Svasti, J. & Fucharoen, S. (2001) Detection of haemoglobin variants and inference of their functional properties using complete oxygen dissociation curve measurements. British Journal of Haematology, 112, 483–487.
-
(2001)
British Journal of Haematology
, vol.112
, pp. 483-487
-
-
Imai, K.1
Tientadakul, P.2
Opartkiattikul, N.3
Luenee, P.4
Winichagoon, P.5
Svasti, J.6
Fucharoen, S.7
-
19
-
-
84978313365
-
Phase 1 clinical trial of the candidate anti-sickling agent Aes-103 in adults with sickle cell anemia
-
Kato, G.J., Lawrence, M.P., Mendelsohn, L.G., Saiyed, R., Wang, X., Ph, D., Conrey, A.K., Starling, J.M., Pharm, D., Grimes, G., Taylor, J.G., Mckew, J., Minniti, P. & Stern, W. (2013) Phase 1 clinical trial of the candidate anti-sickling agent Aes-103 in adults with sickle cell anemia. Blood, 122, 1009.
-
(2013)
Blood
, vol.122
, pp. 1009
-
-
Kato, G.J.1
Lawrence, M.P.2
Mendelsohn, L.G.3
Saiyed, R.4
Wang, X.5
Ph, D.6
Conrey, A.K.7
Starling, J.M.8
Pharm, D.9
Grimes, G.10
Taylor, J.G.11
Mckew, J.12
Minniti, P.13
Stern, W.14
-
20
-
-
0036265634
-
Comparison of mechanisms of anemia in mice with sickle cell disease and β-thalassemia: peripheral destruction, ineffective erythropoiesis, and phospholipid scramblase-mediated phosphatidylserine exposure
-
Kean, L.S., Brown, L.E., Nichols, J.W., Mohandas, N., Archer, D.R. & Hsu, L.L. (2002) Comparison of mechanisms of anemia in mice with sickle cell disease and β-thalassemia: peripheral destruction, ineffective erythropoiesis, and phospholipid scramblase-mediated phosphatidylserine exposure. Experimental Hematology, 30, 394–402.
-
(2002)
Experimental Hematology
, vol.30
, pp. 394-402
-
-
Kean, L.S.1
Brown, L.E.2
Nichols, J.W.3
Mohandas, N.4
Archer, D.R.5
Hsu, L.L.6
-
21
-
-
84995573689
-
GBT440, a Potent Anti-Sickling Hemoglobin Modifier Reduces Hemolysis, Improves Anemia and Nearly Eliminates Sickle Cells in Peripheral Blood of Patients with Sickle Cell Disease
-
Lehrer-Graiwer, J., Howard, J., Hemmaway, C.J., Awogbade, M., Telfer, P., Layton, M., Mant, T., Dufu, K., Hutchaleelaha, A., Koller, T., Oksenberg, D., Patel, M. & Ramos, E. (2015) GBT440, a Potent Anti-Sickling Hemoglobin Modifier Reduces Hemolysis, Improves Anemia and Nearly Eliminates Sickle Cells in Peripheral Blood of Patients with Sickle Cell Disease. Blood, 126, 542.
-
(2015)
Blood
, vol.126
, pp. 542
-
-
Lehrer-Graiwer, J.1
Howard, J.2
Hemmaway, C.J.3
Awogbade, M.4
Telfer, P.5
Layton, M.6
Mant, T.7
Dufu, K.8
Hutchaleelaha, A.9
Koller, T.10
Oksenberg, D.11
Patel, M.12
Ramos, E.13
-
22
-
-
84891121208
-
Vaso-occlusion in sickle cell disease : pathophysiology and novel targeted therapies
-
Manwani, D. & Frenette, P.S. (2013) Vaso-occlusion in sickle cell disease : pathophysiology and novel targeted therapies. Blood, 122, 3892–3898.
-
(2013)
Blood
, vol.122
, pp. 3892-3898
-
-
Manwani, D.1
Frenette, P.S.2
-
23
-
-
0031012328
-
Quantitative analysis of erythrocytes containing fetal hemoglobin (F cells) in children with sickle cell disease
-
Marcus, S.J., Kinney, T.R., Schultz, W.H., O'Branski, E.E. & Ware, R.E. (1997) Quantitative analysis of erythrocytes containing fetal hemoglobin (F cells) in children with sickle cell disease. American Journal of Hematology, 54, 40–46.
-
(1997)
American Journal of Hematology
, vol.54
, pp. 40-46
-
-
Marcus, S.J.1
Kinney, T.R.2
Schultz, W.H.3
O'Branski, E.E.4
Ware, R.E.5
-
24
-
-
0017855570
-
Irreversibly sickled cells and red cell survival in sickle cell anemia
-
McCurdy, P.R. & Sherman, A.S. (1978) Irreversibly sickled cells and red cell survival in sickle cell anemia. The American Journal of Medicine, 64, 253–258.
-
(1978)
The American Journal of Medicine
, vol.64
, pp. 253-258
-
-
McCurdy, P.R.1
Sherman, A.S.2
-
25
-
-
0023195612
-
Delay time of hemoglobin S polymerization prevents most cells from sickling in vivo
-
Mozzarelli, A., Hofrichter, J. & Eaton, W. (1987) Delay time of hemoglobin S polymerization prevents most cells from sickling in vivo. Science (New York, N.Y.), 237, 500–506.
-
(1987)
Science (New York, N.Y.)
, vol.237
, pp. 500-506
-
-
Mozzarelli, A.1
Hofrichter, J.2
Eaton, W.3
-
26
-
-
0023859033
-
Levels of fetal hemoglobin necessary for treatment of sickle cell disease
-
Noguchi, C.T., Rodgers, G.P., Serjeant, G. & Schechter, A.N. (1988) Levels of fetal hemoglobin necessary for treatment of sickle cell disease. The New England Journal of Medicine, 318, 96–99.
-
(1988)
The New England Journal of Medicine
, vol.318
, pp. 96-99
-
-
Noguchi, C.T.1
Rodgers, G.P.2
Serjeant, G.3
Schechter, A.N.4
-
27
-
-
0031059866
-
Processing of X-ray diffraction data collected in oscillation mode
-
In, (ed. by, J.N. Abelson, M.I. Simon, C.W. CarterJr, &, R.M. Sweet, Academic Press, New York
-
Otwinowski, Z. & Minor, W. (1997) Processing of X-ray diffraction data collected in oscillation mode. In: Macromolecular Crystallography, Part A, (ed. by J.N. Abelson, M.I. Simon, C.W. CarterJr & R.M. Sweet), pp. 307–326. Academic Press, New York.
-
(1997)
Macromolecular Crystallography, Part A
, pp. 307-326
-
-
Otwinowski, Z.1
Minor, W.2
-
29
-
-
22844451604
-
COHbC and COHbS crystallize in the R2 quaternary state at neutral pH in the presence of PEG 4000. Acta crystallographica
-
Patskovska, L.N., Patskovsky, Y.V., Almo, S.C. & Hirsch, R.E. (2005) COHbC and COHbS crystallize in the R2 quaternary state at neutral pH in the presence of PEG 4000. Acta crystallographica. Section D, Biological Crystallography, 61, 566–573.
-
(2005)
Section D, Biological Crystallography
, vol.61
, pp. 566-573
-
-
Patskovska, L.N.1
Patskovsky, Y.V.2
Almo, S.C.3
Hirsch, R.E.4
-
30
-
-
78650179046
-
Sickle-cell disease
-
Rees, D.C., Williams, T.N. & Gladwin, M.T. (2010) Sickle-cell disease. Lancet, 376, 2018–2031.
-
(2010)
Lancet
, vol.376
, pp. 2018-2031
-
-
Rees, D.C.1
Williams, T.N.2
Gladwin, M.T.3
-
31
-
-
0027466298
-
The pharmacokinetics, tolerability and pharmacodynamics of tucaresol (589C80; 4[2-formyl-3-hydroxyphenoxymethyl] benzoic acid), a potential anti-sickling agent, following oral administration to healthy subjects
-
Rolan, P.E., Parker, J.E., Gray, S.J., Weatherley, B.C., Ingram, J., Leavens, W., Wootton, R. & Posner, J. (1993) The pharmacokinetics, tolerability and pharmacodynamics of tucaresol (589C80; 4[2-formyl-3-hydroxyphenoxymethyl] benzoic acid), a potential anti-sickling agent, following oral administration to healthy subjects. British Journal of Clinical Pharmacology, 35, 419–425.
-
(1993)
British Journal of Clinical Pharmacology
, vol.35
, pp. 419-425
-
-
Rolan, P.E.1
Parker, J.E.2
Gray, S.J.3
Weatherley, B.C.4
Ingram, J.5
Leavens, W.6
Wootton, R.7
Posner, J.8
-
32
-
-
0028917476
-
Pharmacokinetics and pharmacodynamics of tucaresol, an antisickling agent, in healthy volunteers
-
Rolan, P.E., Mercer, A.J., Wootton, R. & Posner, J. (1995) Pharmacokinetics and pharmacodynamics of tucaresol, an antisickling agent, in healthy volunteers. British Journal of Clinical Pharmacology, 39, 375–380.
-
(1995)
British Journal of Clinical Pharmacology
, vol.39
, pp. 375-380
-
-
Rolan, P.E.1
Mercer, A.J.2
Wootton, R.3
Posner, J.4
-
33
-
-
84896734559
-
Therapeutic strategies to alter the oxygen affinity of sickle hemoglobin
-
Safo, M.K. & Kato, G.J. (2014) Therapeutic strategies to alter the oxygen affinity of sickle hemoglobin. Hematology/Oncology Clinics of North America, 28, 217–231.
-
(2014)
Hematology/Oncology Clinics of North America
, vol.28
, pp. 217-231
-
-
Safo, M.K.1
Kato, G.J.2
-
35
-
-
85028262243
-
Pharmacological Modulation of Fetal Hemoglobin
-
Steinberg, M.H. & Rodgers, G.P. (2001) Pharmacological Modulation of Fetal Hemoglobin. Medicine, 74, 301–304.
-
(2001)
Medicine
, vol.74
, pp. 301-304
-
-
Steinberg, M.H.1
Rodgers, G.P.2
-
36
-
-
0030893396
-
Fetal hemoglobin in sickle cell anemia: determinants of response to hydroxyurea. Multicenter Study of Hydroxyurea
-
Steinberg, M.H., Lu, Z.H., Barton, F.B., Terrin, M.L., Charache, S. & Dover, G.J. (1997) Fetal hemoglobin in sickle cell anemia: determinants of response to hydroxyurea. Multicenter Study of Hydroxyurea. Blood, 89, 1078–1088.
-
(1997)
Blood
, vol.89
, pp. 1078-1088
-
-
Steinberg, M.H.1
Lu, Z.H.2
Barton, F.B.3
Terrin, M.L.4
Charache, S.5
Dover, G.J.6
-
37
-
-
0018199125
-
Requirement for therapeutic inhibition of sickle haemoglobin gelation
-
Sunshine, H.R., Hofrichter, J. & Eaton, W.A. (1978) Requirement for therapeutic inhibition of sickle haemoglobin gelation. Nature, 275, 238–240.
-
(1978)
Nature
, vol.275
, pp. 238-240
-
-
Sunshine, H.R.1
Hofrichter, J.2
Eaton, W.A.3
-
38
-
-
84928492198
-
Randomized phase 2 study of GMI-1070 in SCD : reduction in time to resolution of vaso-occlusive events and decreased opioid use
-
Telen, M.J., Wun, T., Mccavit, T.L., De Castro, L.M., Krishnamurti, L., Lanzkron, S., Hsu, L.L., Smith, W.R., Rhee, S., Magnani, J.L. & Thackray, H. (2015) Randomized phase 2 study of GMI-1070 in SCD : reduction in time to resolution of vaso-occlusive events and decreased opioid use. Blood, 125, 2656–2665.
-
(2015)
Blood
, vol.125
, pp. 2656-2665
-
-
Telen, M.J.1
Wun, T.2
Mccavit, T.L.3
De Castro, L.M.4
Krishnamurti, L.5
Lanzkron, S.6
Hsu, L.L.7
Smith, W.R.8
Rhee, S.9
Magnani, J.L.10
Thackray, H.11
-
39
-
-
16644364842
-
REFMAC5 dictionary: organization of prior chemical knowledge and guidelines for its use
-
Vagin, A.A., Steiner, R.A., Lebedev, A.A., Potterton, L., McNicholas, S., Long, F. & Murshudov, G.N. (2004) REFMAC5 dictionary: organization of prior chemical knowledge and guidelines for its use. Acta Crystallographica Section D, Biological Crystallography, 60, 2184–2195.
-
(2004)
Acta Crystallographica Section D, Biological Crystallography
, vol.60
, pp. 2184-2195
-
-
Vagin, A.A.1
Steiner, R.A.2
Lebedev, A.A.3
Potterton, L.4
McNicholas, S.5
Long, F.6
Murshudov, G.N.7
-
40
-
-
62849129028
-
Current issues in blood transfusion for sickle cell disease
-
Wahl, S. & Quirolo, K.C. (2009) Current issues in blood transfusion for sickle cell disease. Current Opinion in Pediatrics, 21, 15–21.
-
(2009)
Current Opinion in Pediatrics
, vol.21
, pp. 15-21
-
-
Wahl, S.1
Quirolo, K.C.2
-
41
-
-
0026080846
-
Allosteric modifiers of hemoglobin. 2. Crystallographically determined binding sites and hydrophobic binding/interaction analysis of novel hemoglobin oxygen effectors
-
Wireko, F.C., Kellogg, G.E. & Abraham, D.J. (1991) Allosteric modifiers of hemoglobin. 2. Crystallographically determined binding sites and hydrophobic binding/interaction analysis of novel hemoglobin oxygen effectors. Journal of Medicinal Chemistry, 34, 758–767.
-
(1991)
Journal of Medicinal Chemistry
, vol.34
, pp. 758-767
-
-
Wireko, F.C.1
Kellogg, G.E.2
Abraham, D.J.3
-
42
-
-
33747152507
-
Correction of sickle cell disease by homologous recombination in embryonic stem cells
-
Wu, L.-C., Sun, C.-W., Ryan, T.M., Pawlik, K.M., Ren, J. & Townes, T.M. (2006) Correction of sickle cell disease by homologous recombination in embryonic stem cells. Blood, 108, 1183–1188.
-
(2006)
Blood
, vol.108
, pp. 1183-1188
-
-
Wu, L.-C.1
Sun, C.-W.2
Ryan, T.M.3
Pawlik, K.M.4
Ren, J.5
Townes, T.M.6
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