메뉴 건너뛰기




Volumn 62, Issue 3, 2015, Pages 389-394

Endothelial nitric oxide synthase gene intron 4 VNTR polymorphism in sickle cell disease: Relation to vasculopathy and disease severity

Author keywords

Endothelial dysfunction; Nitric oxide synthase gene polymorphism; SCD

Indexed keywords

ENDOTHELIAL NITRIC OXIDE SYNTHASE; LACTATE DEHYDROGENASE; NITRIC OXIDE; FERRITIN; FIBRIN DEGRADATION PRODUCT; FIBRIN FRAGMENT D; HYDROLYASE; LACTATE DEHYDRATASE; NOS3 PROTEIN, HUMAN; VON WILLEBRAND ANTIGEN; VON WILLEBRAND FACTOR;

EID: 84921361762     PISSN: 15455009     EISSN: 15455017     Source Type: Journal    
DOI: 10.1002/pbc.25234     Document Type: Article
Times cited : (16)

References (50)
  • 1
    • 65949124657 scopus 로고    scopus 로고
    • Mechanisms of vasculopathy in sickle cell disease and thalassemia
    • Morris CR. Mechanisms of vasculopathy in sickle cell disease and thalassemia. Hematology Am Soc Hematol Educ Program 2008; 2008:177-185.
    • (2008) Hematology Am Soc Hematol Educ Program , vol.2008 , pp. 177-185
    • Morris, C.R.1
  • 2
    • 15944398355 scopus 로고    scopus 로고
    • The clinical sequelae of intravascular hemolysis and extracellular plasma hemoglobin: A novel mechanism of human disease
    • Rother RP, Bell L, Hillmen P, et al. The clinical sequelae of intravascular hemolysis and extracellular plasma hemoglobin: A novel mechanism of human disease. JAMA 2005; 293:1653-1662.
    • (2005) JAMA , vol.293 , pp. 1653-1662
    • Rother, R.P.1    Bell, L.2    Hillmen, P.3
  • 3
    • 33646231295 scopus 로고    scopus 로고
    • Cardiopulmonary complications of sickle cell disease: Role of nitric oxide and hemolytic anemia
    • Gladwin MT, Kato GJ. Cardiopulmonary complications of sickle cell disease: Role of nitric oxide and hemolytic anemia. Hematology Am Soc Hematol Educ Program 2005; 2005:51-57.
    • (2005) Hematology Am Soc Hematol Educ Program , vol.2005 , pp. 51-57
    • Gladwin, M.T.1    Kato, G.J.2
  • 4
    • 0025883342 scopus 로고
    • Nitric oxide: Physiology, pathophysiology, and pharmacology
    • Moncada S, Palmer RM, Higgs EA. Nitric oxide: Physiology, pathophysiology, and pharmacology. Pharmacol Rev 1991; 43:109-142.
    • (1991) Pharmacol Rev , vol.43 , pp. 109-142
    • Moncada, S.1    Palmer, R.M.2    Higgs, E.A.3
  • 6
    • 0030808466 scopus 로고    scopus 로고
    • Biosynthesis and homeostatic roles of nitric oxide in the normal kidney
    • Kone BC, Baylis C. Biosynthesis and homeostatic roles of nitric oxide in the normal kidney. Am J Physiol 1997; 272:F561-F578.
    • (1997) Am J Physiol , vol.272 , pp. F561-F578
    • Kone, B.C.1    Baylis, C.2
  • 7
    • 0028233602 scopus 로고
    • Gene structure, polymorphism and mapping of the human endothelial nitric oxide synthase gene
    • Nadaud S, Bonnardeaux A, Lathrop M, et al. Gene structure, polymorphism and mapping of the human endothelial nitric oxide synthase gene. Biochem Biophys Res Commun 1994; 198:1027-1033.
    • (1994) Biochem Biophys Res Commun , vol.198 , pp. 1027-1033
    • Nadaud, S.1    Bonnardeaux, A.2    Lathrop, M.3
  • 8
    • 0035882208 scopus 로고    scopus 로고
    • Molecular biology of natriuretic peptides and nitric oxide synthase
    • Kone BC. Molecular biology of natriuretic peptides and nitric oxide synthase. Cardiovasc Res 2001; 51:429-441.
    • (2001) Cardiovasc Res , vol.51 , pp. 429-441
    • Kone, B.C.1
  • 9
    • 34247135939 scopus 로고    scopus 로고
    • Endothelial nitric oxide synthase gene intron4 VNTR polymorphism in patients with coronary artery disease in Iran
    • Salimi S, Firoozrai M, Nourmohammadi I, et al. Endothelial nitric oxide synthase gene intron4 VNTR polymorphism in patients with coronary artery disease in Iran. Indian J Med Res 2006; 124:683-688.
    • (2006) Indian J Med Res , vol.124 , pp. 683-688
    • Salimi, S.1    Firoozrai, M.2    Nourmohammadi, I.3
  • 10
    • 80052082567 scopus 로고    scopus 로고
    • Endothelial nitric oxide synthase gene intron4 VNTR polymorphism in patients with chronic kidney disease
    • Elshamaa MF, Sabry S, Badr A, et al. Endothelial nitric oxide synthase gene intron4 VNTR polymorphism in patients with chronic kidney disease. Blood Coagul Fibrinolysis 2011; 22:487-492.
    • (2011) Blood Coagul Fibrinolysis , vol.22 , pp. 487-492
    • Elshamaa, M.F.1    Sabry, S.2    Badr, A.3
  • 11
    • 0032753416 scopus 로고    scopus 로고
    • Endothelial nitric oxide synthase gene polymorphism in intron 4 affects the progression of renal failure in nondiabetic renal diseases
    • Wang Y, Kikuchi S, Suzuki H, et al. Endothelial nitric oxide synthase gene polymorphism in intron 4 affects the progression of renal failure in nondiabetic renal diseases. Nephrol Dial Transplant 1999; 14:2898-2902.
    • (1999) Nephrol Dial Transplant , vol.14 , pp. 2898-2902
    • Wang, Y.1    Kikuchi, S.2    Suzuki, H.3
  • 12
    • 0031902667 scopus 로고    scopus 로고
    • Endothelial nitric oxide synthase gene is positively associated with essential hypertension
    • Miyamoto Y, Saito Y, Kajiyama N, et al. Endothelial nitric oxide synthase gene is positively associated with essential hypertension. Hypertension 1998; 32:3-8.
    • (1998) Hypertension , vol.32 , pp. 3-8
    • Miyamoto, Y.1    Saito, Y.2    Kajiyama, N.3
  • 13
    • 0031704975 scopus 로고    scopus 로고
    • Endothelial nitric oxide synthase gene polymorphism and acute myocardial infarction
    • Hibi K, Ishigami T, Tamura K, et al. Endothelial nitric oxide synthase gene polymorphism and acute myocardial infarction. Hypertension 1998; 32:521-526.
    • (1998) Hypertension , vol.32 , pp. 521-526
    • Hibi, K.1    Ishigami, T.2    Tamura, K.3
  • 14
    • 67649649581 scopus 로고    scopus 로고
    • A new electrophoresis technique to separate microsatellite alleles
    • Wang X, Rinehart TA, Wadl PA, et al. A new electrophoresis technique to separate microsatellite alleles. J Biotechnol 2009; 8:2432-2436.
    • (2009) J Biotechnol , vol.8 , pp. 2432-2436
    • Wang, X.1    Rinehart, T.A.2    Wadl, P.A.3
  • 15
    • 69249118680 scopus 로고    scopus 로고
    • Screening for expanded alleles of the FMR1 gene in blood spots from newborn males in a Spanish population
    • Fernandez-Carvajal I, Walichiewicz P, Xiaosen X, et al. Screening for expanded alleles of the FMR1 gene in blood spots from newborn males in a Spanish population. J Mol Diagn 2009; 11:324-329.
    • (2009) J Mol Diagn , vol.11 , pp. 324-329
    • Fernandez-Carvajal, I.1    Walichiewicz, P.2    Xiaosen, X.3
  • 16
    • 0034283465 scopus 로고    scopus 로고
    • Sickle cell disease in childhood: Part I. Laboratory diagnosis, pathophysiology and health maintenance
    • Wethers DL. Sickle cell disease in childhood: Part I. Laboratory diagnosis, pathophysiology and health maintenance. Am Fam Physician 2000; 62:1013-1020.
    • (2000) Am Fam Physician , vol.62 , pp. 1013-1020
    • Wethers, D.L.1
  • 17
    • 0025770390 scopus 로고
    • Pain in sickle cell disease. Rates and risk factors
    • Platt OS, Thorington BD, Brambilla DJ, et al. Pain in sickle cell disease. Rates and risk factors. N Engl J Med 1991; 325:11-16.
    • (1991) N Engl J Med , vol.325 , pp. 11-16
    • Platt, O.S.1    Thorington, B.D.2    Brambilla, D.J.3
  • 18
    • 70449382364 scopus 로고    scopus 로고
    • CURAMA study group. Circulating erythrocyte-derived microparticles are associated with coagulation activation in sickle cell disease
    • van Beers EJ, Schaap MCL, Berkmans RJ, et al. CURAMA study group. Circulating erythrocyte-derived microparticles are associated with coagulation activation in sickle cell disease. Haematologica 2009; 94:1513-1519.
    • (2009) Haematologica , vol.94 , pp. 1513-1519
    • van Beers, E.J.1    Schaap, M.C.L.2    Berkmans, R.J.3
  • 19
    • 84855643775 scopus 로고    scopus 로고
    • Markers of severe vaso-occlusive painful episode frequency in children and adolescents with sickle cell anemia
    • Darbari DS, Onyekwere O, Nouraie M, et al. Markers of severe vaso-occlusive painful episode frequency in children and adolescents with sickle cell anemia. J Pediatr 2012; 160:286-290.
    • (2012) J Pediatr , vol.160 , pp. 286-290
    • Darbari, D.S.1    Onyekwere, O.2    Nouraie, M.3
  • 20
    • 42949169561 scopus 로고    scopus 로고
    • Prevalence and risk factors of elevated pulmonary artery pressures in children with sickle cell disease
    • Pashankar FD, Carbonella J, Bazzy-Asaad A, et al. Prevalence and risk factors of elevated pulmonary artery pressures in children with sickle cell disease. Pediatrics 2008; 121:777-782.
    • (2008) Pediatrics , vol.121 , pp. 777-782
    • Pashankar, F.D.1    Carbonella, J.2    Bazzy-Asaad, A.3
  • 21
    • 80053647695 scopus 로고    scopus 로고
    • Thalassemia Clinical Research Network. Risk factors and mortality associated with an elevated tricuspid regurgitant jet velocity measured by Doppler-echocardiography in thalassemia: A Thalassemia Clinical Research Network report
    • Morris CR, Kim HY, Trachtenberg F, et al. Thalassemia Clinical Research Network. Risk factors and mortality associated with an elevated tricuspid regurgitant jet velocity measured by Doppler-echocardiography in thalassemia: A Thalassemia Clinical Research Network report. Blood 2011; 118:3794-3802.
    • (2011) Blood , vol.118 , pp. 3794-3802
    • Morris, C.R.1    Kim, H.Y.2    Trachtenberg, F.3
  • 22
    • 0032211192 scopus 로고    scopus 로고
    • Beneficial effect of intravenous dexamethasone in children with mild to moderately severe acute chest syndrome complicating sickle cell disease
    • Bernini JC, Rogers ZR, Sandler ES, et al. Beneficial effect of intravenous dexamethasone in children with mild to moderately severe acute chest syndrome complicating sickle cell disease. Blood 1998; 92:3082-3089.
    • (1998) Blood , vol.92 , pp. 3082-3089
    • Bernini, J.C.1    Rogers, Z.R.2    Sandler, E.S.3
  • 23
    • 0035458340 scopus 로고    scopus 로고
    • Does microalbuminuria predict diabetic nephropathy
    • Tabaei BP, Al-Kassab AS, llag LL, et al. Does microalbuminuria predict diabetic nephropathy? Diabetes Care 2001; 24:1560-1566.
    • (2001) Diabetes Care , vol.24 , pp. 1560-1566
    • Tabaei, B.P.1    Al-Kassab, A.S.2    Llag, L.L.3
  • 24
    • 0029141969 scopus 로고
    • Double-stranded DNA analysis by capillary electrophoresis with laser-induced fluorescence using thidium bromide as an intercalator
    • Liu MS, Zang J, Evangelista RA, et al. Double-stranded DNA analysis by capillary electrophoresis with laser-induced fluorescence using thidium bromide as an intercalator. Biotechniques 1995; 18:316-323.
    • (1995) Biotechniques , vol.18 , pp. 316-323
    • Liu, M.S.1    Zang, J.2    Evangelista, R.A.3
  • 25
    • 59249083671 scopus 로고    scopus 로고
    • Nitric oxide and arginine dysregulation: A novel pathway to pulmonary hypertension in hemolytic disorders
    • Morris CR, Gladwin MT, Kato GJ. Nitric oxide and arginine dysregulation: A novel pathway to pulmonary hypertension in hemolytic disorders. Curr Mol Med 2008; 8:620-632.
    • (2008) Curr Mol Med , vol.8 , pp. 620-632
    • Morris, C.R.1    Gladwin, M.T.2    Kato, G.J.3
  • 26
    • 33846279380 scopus 로고    scopus 로고
    • Deconstructing sickle cell disease: Reappraisal of the role of hemolysis in the development of clinical subphenotypes
    • Kato GJ, Gladwin MT, Steinberg MH. Deconstructing sickle cell disease: Reappraisal of the role of hemolysis in the development of clinical subphenotypes. Blood Rev 2007; 21:37-47.
    • (2007) Blood Rev , vol.21 , pp. 37-47
    • Kato, G.J.1    Gladwin, M.T.2    Steinberg, M.H.3
  • 27
    • 0031459896 scopus 로고    scopus 로고
    • Genetic contribution of endothelial constitutive nitric oxide synthase gene to plasma nitric oxide levels
    • Wang XL, Mahaney MC, Sim AS, et al. Genetic contribution of endothelial constitutive nitric oxide synthase gene to plasma nitric oxide levels. Arterioscler Thromb Vasc Biol 1997; 17:3147-3153.
    • (1997) Arterioscler Thromb Vasc Biol , vol.17 , pp. 3147-3153
    • Wang, X.L.1    Mahaney, M.C.2    Sim, A.S.3
  • 28
    • 4544225997 scopus 로고    scopus 로고
    • Endothelial nitric oxide synthase gene intron 4 polymorphism in patients with end-stage renal disease
    • Buraczynska M, Ksiazek P, Zaluska W, et al. Endothelial nitric oxide synthase gene intron 4 polymorphism in patients with end-stage renal disease. Nephrol Dial Transplant 2004; 19:2302-2306.
    • (2004) Nephrol Dial Transplant , vol.19 , pp. 2302-2306
    • Buraczynska, M.1    Ksiazek, P.2    Zaluska, W.3
  • 29
    • 3042545771 scopus 로고    scopus 로고
    • Relation of endothelial nitric oxide synthase gene to plasma nitric oxide level, endothelial function and blood pressure in African Americans
    • Li R, Lyn D, Lapu-Bula R, et al. Relation of endothelial nitric oxide synthase gene to plasma nitric oxide level, endothelial function and blood pressure in African Americans. Am J Hypertens 2004; 17:560-567.
    • (2004) Am J Hypertens , vol.17 , pp. 560-567
    • Li, R.1    Lyn, D.2    Lapu-Bula, R.3
  • 30
    • 27944453568 scopus 로고    scopus 로고
    • Polymorphisms of chemokine receptors and eNOS in Brazilian patients with sickle cell disease
    • Vargas AE, da Silva MA, Silla L, et al. Polymorphisms of chemokine receptors and eNOS in Brazilian patients with sickle cell disease. Tissue Antigens 2005; 66:683-690.
    • (2005) Tissue Antigens , vol.66 , pp. 683-690
    • Vargas, A.E.1    da Silva, M.A.2    Silla, L.3
  • 31
    • 41549136868 scopus 로고    scopus 로고
    • Sickle cell disease vasculopathy: A state of nitric oxide resistance
    • Wood KC, Hsu LL, Gladwin MT. Sickle cell disease vasculopathy: A state of nitric oxide resistance. Free Radic Biol Med 2008; 44:1506-1528.
    • (2008) Free Radic Biol Med , vol.44 , pp. 1506-1528
    • Wood, K.C.1    Hsu, L.L.2    Gladwin, M.T.3
  • 32
    • 33644860603 scopus 로고    scopus 로고
    • Hydrolysis of phosphatidylserine-exposing red blood cells by secretory phospholipase A2 generates lysophosphatidic acid and results in vascular dysfunction
    • Neidlinger NA, Larkin SK, Bhagat A, et al. Hydrolysis of phosphatidylserine-exposing red blood cells by secretory phospholipase A2 generates lysophosphatidic acid and results in vascular dysfunction. J Biol Chem 2006; 281:775-781.
    • (2006) J Biol Chem , vol.281 , pp. 775-781
    • Neidlinger, N.A.1    Larkin, S.K.2    Bhagat, A.3
  • 33
    • 10744233940 scopus 로고    scopus 로고
    • Pulmonary hypertension as a risk factor for death in patients with sickle cell disease
    • Gladwin M, Sachdev V, Jison M, et al. Pulmonary hypertension as a risk factor for death in patients with sickle cell disease. N Engl J Med 2004; 350:22-31.
    • (2004) N Engl J Med , vol.350 , pp. 22-31
    • Gladwin, M.1    Sachdev, V.2    Jison, M.3
  • 34
    • 0036908599 scopus 로고    scopus 로고
    • Cell-free hemoglobin limits nitric oxide bioavailability in sickle cell disease
    • Reiter C, Wang X, Tanus-Santos J, et al. Cell-free hemoglobin limits nitric oxide bioavailability in sickle cell disease. Nat Med 2002; 8:1383-1389.
    • (2002) Nat Med , vol.8 , pp. 1383-1389
    • Reiter, C.1    Wang, X.2    Tanus-Santos, J.3
  • 35
    • 21444441271 scopus 로고    scopus 로고
    • Dysregulated arginine metabolism, hemolysis-associated pulmonary hypertension and mortality in sickle cell disease
    • Morris CR, Kato GJ, Poljakovic M, et al. Dysregulated arginine metabolism, hemolysis-associated pulmonary hypertension and mortality in sickle cell disease. JAMA 2005; 294:81-90.
    • (2005) JAMA , vol.294 , pp. 81-90
    • Morris, C.R.1    Kato, G.J.2    Poljakovic, M.3
  • 36
    • 26444579276 scopus 로고    scopus 로고
    • Pulmonary hypertension in sickle cell disease: Mechanisms, diagnosis, and management
    • Castro O, Gladwin MT. Pulmonary hypertension in sickle cell disease: Mechanisms, diagnosis, and management. Hematol Oncol Clin North Am 2005; 19:881-896.
    • (2005) Hematol Oncol Clin North Am , vol.19 , pp. 881-896
    • Castro, O.1    Gladwin, M.T.2
  • 37
    • 40949158038 scopus 로고    scopus 로고
    • Pulmonary hypertension in children and adolescents with sickle cell disease
    • Onyekwere OC, Campbell A, Teshome M, et al. Pulmonary hypertension in children and adolescents with sickle cell disease. Pediatr Cardiol 2008; 29:309-312.
    • (2008) Pediatr Cardiol , vol.29 , pp. 309-312
    • Onyekwere, O.C.1    Campbell, A.2    Teshome, M.3
  • 38
    • 3242792093 scopus 로고    scopus 로고
    • The endothelial biology of sickle cell disease: Inflammation and a chronic vasculopathy
    • Hebbel RP, Osarogiagbon KD. The endothelial biology of sickle cell disease: Inflammation and a chronic vasculopathy. Microcirculation 2004; 11:129-151.
    • (2004) Microcirculation , vol.11 , pp. 129-151
    • Hebbel, R.P.1    Osarogiagbon, K.D.2
  • 39
    • 84890907794 scopus 로고    scopus 로고
    • Endothelial nitric oxide synthase gene polymorphism is associated with sickle cell disease patients in India
    • Nishank SS, Singh MP, Yadav R, et al. Endothelial nitric oxide synthase gene polymorphism is associated with sickle cell disease patients in India. J Hum Genet 2013; 58:775-779.
    • (2013) J Hum Genet , vol.58 , pp. 775-779
    • Nishank, S.S.1    Singh, M.P.2    Yadav, R.3
  • 40
    • 1642458091 scopus 로고    scopus 로고
    • Association of T-786C eNOS gene polymorphism with increased susceptibility to acute chest syndrome in females with sickle cell disease
    • Sharan K, Surrey S, Ballas S, et al. Association of T-786C eNOS gene polymorphism with increased susceptibility to acute chest syndrome in females with sickle cell disease. Br J Haematol 2004; 124:240-243.
    • (2004) Br J Haematol , vol.124 , pp. 240-243
    • Sharan, K.1    Surrey, S.2    Ballas, S.3
  • 41
    • 34247193669 scopus 로고    scopus 로고
    • Physician-diagnosed asthma and acute chest syndrome: Associations with NOS polymorphisms
    • Duckworth L, Hsu L, Feng H, et al. Physician-diagnosed asthma and acute chest syndrome: Associations with NOS polymorphisms. Pediatr Pulmonol 2007; 42:332-338.
    • (2007) Pediatr Pulmonol , vol.42 , pp. 332-338
    • Duckworth, L.1    Hsu, L.2    Feng, H.3
  • 42
    • 0037114210 scopus 로고    scopus 로고
    • Low exhaled nitric oxide and a polymorphism in the NOS I gene is associated with acute chest syndrome
    • Sullivan KJ, Kissoon N, Duckworth LJ, et al. Low exhaled nitric oxide and a polymorphism in the NOS I gene is associated with acute chest syndrome. Am J Respir Crit Care Med 2001; 164:2186-2190.
    • (2001) Am J Respir Crit Care Med , vol.164 , pp. 2186-2190
    • Sullivan, K.J.1    Kissoon, N.2    Duckworth, L.J.3
  • 43
    • 33748780631 scopus 로고    scopus 로고
    • ET-1 and ecNOS gene polymorphisms and susceptibility to acute chest syndrome and painful vaso-occlusive crises in children with sickle cell anemia
    • Chaar V, Tarer V, Etienne-Julan M, et al. ET-1 and ecNOS gene polymorphisms and susceptibility to acute chest syndrome and painful vaso-occlusive crises in children with sickle cell anemia. Haematologica 2006; 91:1277-1278.
    • (2006) Haematologica , vol.91 , pp. 1277-1278
    • Chaar, V.1    Tarer, V.2    Etienne-Julan, M.3
  • 45
    • 0034105690 scopus 로고    scopus 로고
    • Renal abnormalities in sickle cell disease
    • Ataga KI, Orringer EP. Renal abnormalities in sickle cell disease. Am J Hematol 2000; 63:205-211.
    • (2000) Am J Hematol , vol.63 , pp. 205-211
    • Ataga, K.I.1    Orringer, E.P.2
  • 46
    • 33745263204 scopus 로고    scopus 로고
    • Early markers of renal dysfunction in patients with sickle cell/b-thalassemia
    • Voskaridou E, Terpos E, Michail S, et al. Early markers of renal dysfunction in patients with sickle cell/b-thalassemia. Kidney Int 2006; 69:2037-2042.
    • (2006) Kidney Int , vol.69 , pp. 2037-2042
    • Voskaridou, E.1    Terpos, E.2    Michail, S.3
  • 47
    • 80655135449 scopus 로고    scopus 로고
    • Chronic kidney disease and albuminuria in children with sickle cell disease
    • McPherson Yee M, Jabbar SF, Osunkwo I, et al. Chronic kidney disease and albuminuria in children with sickle cell disease. Clin J Am Soc Nephrol 2011; 6:2628-2633.
    • (2011) Clin J Am Soc Nephrol , vol.6 , pp. 2628-2633
    • McPherson Yee, M.1    Jabbar, S.F.2    Osunkwo, I.3
  • 48
    • 45449117083 scopus 로고    scopus 로고
    • Endothelial nitric oxide synthase gene haplotypes and diabetic nephropathy among Asian Indians
    • Ahluwalia TS, Ahuja M, Rai TS, et al. Endothelial nitric oxide synthase gene haplotypes and diabetic nephropathy among Asian Indians. Mol Cell Biochem 2008; 314:9-17.
    • (2008) Mol Cell Biochem , vol.314 , pp. 9-17
    • Ahluwalia, T.S.1    Ahuja, M.2    Rai, T.S.3
  • 49
    • 0033996626 scopus 로고    scopus 로고
    • Renal abnormalities in sickle cell disease
    • Pham PT, Pham PC, Wilkinson AH, et al. Renal abnormalities in sickle cell disease. Kidney Int 2000; 57:1-8.
    • (2000) Kidney Int , vol.57 , pp. 1-8
    • Pham, P.T.1    Pham, P.C.2    Wilkinson, A.H.3
  • 50
    • 67651159347 scopus 로고    scopus 로고
    • Novel small molecule therapeutics for sickle cell disease: Nitric oxide, carbon monoxide, nitrite, and apolipoprotein A-I
    • Kato GJ. Novel small molecule therapeutics for sickle cell disease: Nitric oxide, carbon monoxide, nitrite, and apolipoprotein A-I. Hematology Am Soc Hematol Educ Program 2008; 186-192.
    • (2008) Hematology Am Soc Hematol Educ Program , pp. 186-192
    • Kato, G.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.