메뉴 건너뛰기




Volumn 6, Issue 2, 2011, Pages

SOD2 deficient erythroid cells up-regulate transferrin receptor and down-regulate mitochondrial biogenesis and metabolism

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME C OXIDASE; MANGANESE SUPEROXIDE DISMUTASE; MITOCHONDRIAL DNA; PROTON TRANSPORTING ADENOSINE TRIPHOSPHATE SYNTHASE; TRANSFERRIN RECEPTOR; SUPEROXIDE DISMUTASE;

EID: 79951520304     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0016894     Document Type: Article
Times cited : (18)

References (51)
  • 1
    • 0035896748 scopus 로고    scopus 로고
    • Absence of mitochondrial superoxide dismutase results in a murine hemolytic anemia responsive to therapy with a catalytic antioxidant
    • Friedman JS, Rebel VI, Derby R, Bell K, Huang TT, et al. (2001) Absence of mitochondrial superoxide dismutase results in a murine hemolytic anemia responsive to therapy with a catalytic antioxidant. J Exp Med 193: 925-934.
    • (2001) J Exp Med , vol.193 , pp. 925-934
    • Friedman, J.S.1    Rebel, V.I.2    Derby, R.3    Bell, K.4    Huang, T.T.5
  • 2
    • 33748754872 scopus 로고    scopus 로고
    • Congenital sideroblastic anemias
    • Bottomley SS, (2006) Congenital sideroblastic anemias. Curr Hematol Rep 5: 41-49.
    • (2006) Curr Hematol Rep , vol.5 , pp. 41-49
    • Bottomley, S.S.1
  • 4
    • 0036799489 scopus 로고    scopus 로고
    • The genetics of inherited sideroblastic anemias
    • Fleming MD, (2002) The genetics of inherited sideroblastic anemias. Semin Hematol 39: 270-281.
    • (2002) Semin Hematol , vol.39 , pp. 270-281
    • Fleming, M.D.1
  • 6
    • 0028148438 scopus 로고
    • X-linked sideroblastic anemia: identification of the mutation in the erythroid-specific delta-aminolevulinate synthase gene (ALAS2) in the original family described by Cooley
    • Cotter PD, Rucknagel DL, Bishop DF, (1994) X-linked sideroblastic anemia: identification of the mutation in the erythroid-specific delta-aminolevulinate synthase gene (ALAS2) in the original family described by Cooley. Blood 84: 3915-3924.
    • (1994) Blood , vol.84 , pp. 3915-3924
    • Cotter, P.D.1    Rucknagel, D.L.2    Bishop, D.F.3
  • 7
    • 0032920837 scopus 로고    scopus 로고
    • Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A)
    • Allikmets R, Raskind WH, Hutchinson A, Schueck ND, Dean M, et al. (1999) Mutation of a putative mitochondrial iron transporter gene (ABC7) in X-linked sideroblastic anemia and ataxia (XLSA/A). Hum Mol Genet 8: 743-749.
    • (1999) Hum Mol Genet , vol.8 , pp. 743-749
    • Allikmets, R.1    Raskind, W.H.2    Hutchinson, A.3    Schueck, N.D.4    Dean, M.5
  • 8
    • 2442691791 scopus 로고    scopus 로고
    • Missense mutation in pseudouridine synthase 1 (PUS1) causes mitochondrial myopathy and sideroblastic anemia (MLASA)
    • Bykhovskaya Y, Casas K, Mengesha E, Inbal A, Fischel-Ghodsian N, (2004) Missense mutation in pseudouridine synthase 1 (PUS1) causes mitochondrial myopathy and sideroblastic anemia (MLASA). Am J Hum Genet 74: 1303-1308.
    • (2004) Am J Hum Genet , vol.74 , pp. 1303-1308
    • Bykhovskaya, Y.1    Casas, K.2    Mengesha, E.3    Inbal, A.4    Fischel-Ghodsian, N.5
  • 9
    • 21244449941 scopus 로고    scopus 로고
    • Mitochondrial myopathy and sideroblastic anemia (MLASA): missense mutation in the pseudouridine synthase 1 (PUS1) gene is associated with the loss of tRNA pseudouridylation
    • Patton JR, Bykhovskaya Y, Mengesha E, Bertolotto C, Fischel-Ghodsian N, (2005) Mitochondrial myopathy and sideroblastic anemia (MLASA): missense mutation in the pseudouridine synthase 1 (PUS1) gene is associated with the loss of tRNA pseudouridylation. J Biol Chem 280: 19823-19828.
    • (2005) J Biol Chem , vol.280 , pp. 19823-19828
    • Patton, J.R.1    Bykhovskaya, Y.2    Mengesha, E.3    Bertolotto, C.4    Fischel-Ghodsian, N.5
  • 10
    • 34249008188 scopus 로고    scopus 로고
    • Pleiotropic effects and compensation mechanisms determine tissue specificity in mitochondrial myopathy and sideroblastic anemia (MLASA)
    • Bykhovskaya Y, Mengesha E, Fischel-Ghodsian N, (2007) Pleiotropic effects and compensation mechanisms determine tissue specificity in mitochondrial myopathy and sideroblastic anemia (MLASA). Mol Genet Metab 91: 148-156.
    • (2007) Mol Genet Metab , vol.91 , pp. 148-156
    • Bykhovskaya, Y.1    Mengesha, E.2    Fischel-Ghodsian, N.3
  • 11
    • 0018712317 scopus 로고
    • A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction
    • Pearson HA, Lobel JS, Kocoshis SA, Naiman JL, Windmiller J, et al. (1979) A new syndrome of refractory sideroblastic anemia with vacuolization of marrow precursors and exocrine pancreatic dysfunction. J Pediatr 95: 976-984.
    • (1979) J Pediatr , vol.95 , pp. 976-984
    • Pearson, H.A.1    Lobel, J.S.2    Kocoshis, S.A.3    Naiman, J.L.4    Windmiller, J.5
  • 12
    • 34548013116 scopus 로고    scopus 로고
    • The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload
    • Camaschella C, Campanella A, De Falco L, Boschetto L, Merlini R, et al. (2007) The human counterpart of zebrafish shiraz shows sideroblastic-like microcytic anemia and iron overload. Blood 110: 1353-1358.
    • (2007) Blood , vol.110 , pp. 1353-1358
    • Camaschella, C.1    Campanella, A.2    De Falco, L.3    Boschetto, L.4    Merlini, R.5
  • 13
    • 67349267792 scopus 로고    scopus 로고
    • Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia
    • Guernsey DL, Jiang H, Campagna DR, Evans SC, Ferguson M, et al. (2009) Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia. Nat Genet 41: 651-653.
    • (2009) Nat Genet , vol.41 , pp. 651-653
    • Guernsey, D.L.1    Jiang, H.2    Campagna, D.R.3    Evans, S.C.4    Ferguson, M.5
  • 14
    • 74849109450 scopus 로고    scopus 로고
    • Systematic molecular genetic analysis of congenital sideroblastic anemia: Evidence for genetic heterogeneity and identification of novel mutations
    • Bergmann AK, Campagna DR, McLoughlin EM, Agarwal S, Fleming MD, et al. (2009) Systematic molecular genetic analysis of congenital sideroblastic anemia: Evidence for genetic heterogeneity and identification of novel mutations. Pediatr Blood Cancer.
    • (2009) Pediatr Blood Cancer
    • Bergmann, A.K.1    Campagna, D.R.2    McLoughlin, E.M.3    Agarwal, S.4    Fleming, M.D.5
  • 15
    • 0031467871 scopus 로고    scopus 로고
    • Heteroplasmic point mutations of mitochondrial DNA affecting subunit I of cytochrome c oxidase in two patients with acquired idiopathic sideroblastic anemia
    • Gattermann N, Retzlaff S, Wang YL, Hofhaus G, Heinisch J, et al. (1997) Heteroplasmic point mutations of mitochondrial DNA affecting subunit I of cytochrome c oxidase in two patients with acquired idiopathic sideroblastic anemia. Blood 90: 4961-4972.
    • (1997) Blood , vol.90 , pp. 4961-4972
    • Gattermann, N.1    Retzlaff, S.2    Wang, Y.L.3    Hofhaus, G.4    Heinisch, J.5
  • 16
    • 0842285640 scopus 로고    scopus 로고
    • Ineffective hematopoiesis linked with a mitochondrial tRNA mutation (G3242A) in a patient with myelodysplastic syndrome
    • Gattermann N, Wulfert M, Junge B, Germing U, Haas R, et al. (2004) Ineffective hematopoiesis linked with a mitochondrial tRNA mutation (G3242A) in a patient with myelodysplastic syndrome. Blood 103: 1499-1502.
    • (2004) Blood , vol.103 , pp. 1499-1502
    • Gattermann, N.1    Wulfert, M.2    Junge, B.3    Germing, U.4    Haas, R.5
  • 17
    • 0034142678 scopus 로고    scopus 로고
    • From sideroblastic anemia to the role of mitochondrial DNA mutations in myelodysplastic syndromes
    • Gattermann N, (2000) From sideroblastic anemia to the role of mitochondrial DNA mutations in myelodysplastic syndromes. Leuk Res 24: 141-151.
    • (2000) Leuk Res , vol.24 , pp. 141-151
    • Gattermann, N.1
  • 18
    • 0030001270 scopus 로고    scopus 로고
    • A heteroplasmic point mutation of mitochondrial tRNALeu(CUN) in non- lymphoid haemopoietic cell lineages from a patient with acquired idiopathic sideroblastic anaemia
    • Gattermann N, Retzlaff S, Wang YL, Berneburg M, Heinisch J, et al. (1996) A heteroplasmic point mutation of mitochondrial tRNALeu(CUN) in non- lymphoid haemopoietic cell lineages from a patient with acquired idiopathic sideroblastic anaemia. Br J Haematol 93: 845-855.
    • (1996) Br J Haematol , vol.93 , pp. 845-855
    • Gattermann, N.1    Retzlaff, S.2    Wang, Y.L.3    Berneburg, M.4    Heinisch, J.5
  • 19
    • 0032888986 scopus 로고    scopus 로고
    • The MERRF mutation of mitochondrial DNA in the bone marrow of a patient with acquired idiopathic sideroblastic anemia
    • Wang YL, Choi HK, Aul C, Gattermann N, Heinisch J, (1999) The MERRF mutation of mitochondrial DNA in the bone marrow of a patient with acquired idiopathic sideroblastic anemia. Am J Hematol 60: 83-84.
    • (1999) Am J Hematol , vol.60 , pp. 83-84
    • Wang, Y.L.1    Choi, H.K.2    Aul, C.3    Gattermann, N.4    Heinisch, J.5
  • 20
    • 0038281403 scopus 로고    scopus 로고
    • Mitochondrial DNA mutations in patients with myelodysplastic syndromes
    • Shin MG, Kajigaya S, Levin BC, Young NS, (2003) Mitochondrial DNA mutations in patients with myelodysplastic syndromes. Blood 101: 3118-3125.
    • (2003) Blood , vol.101 , pp. 3118-3125
    • Shin, M.G.1    Kajigaya, S.2    Levin, B.C.3    Young, N.S.4
  • 21
    • 0014042534 scopus 로고
    • Reversible sideroblastic anemia caused by chloramphenicol
    • Beck EA, Ziegler G, Schmid R, Ludin H, (1967) Reversible sideroblastic anemia caused by chloramphenicol. Acta Haematol 38: 1-10.
    • (1967) Acta Haematol , vol.38 , pp. 1-10
    • Beck, E.A.1    Ziegler, G.2    Schmid, R.3    Ludin, H.4
  • 22
    • 0025612762 scopus 로고
    • Anti-tuberculous drugs and sideroblastic anaemia
    • Sharp RA, Lowe JG, Johnston RN, (1990) Anti-tuberculous drugs and sideroblastic anaemia. Br J Clin Pract 44: 706-707.
    • (1990) Br J Clin Pract , vol.44 , pp. 706-707
    • Sharp, R.A.1    Lowe, J.G.2    Johnston, R.N.3
  • 23
    • 0019072006 scopus 로고
    • Drug-induced mitochondrial damage and sideroblastic change
    • Yunis AA, Salem Z, (1980) Drug-induced mitochondrial damage and sideroblastic change. Clin Haematol 9: 607-619.
    • (1980) Clin Haematol , vol.9 , pp. 607-619
    • Yunis, A.A.1    Salem, Z.2
  • 24
    • 0028827252 scopus 로고
    • Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase
    • Li Y, Huang TT, Carlson EJ, Melov S, Ursell PC, et al. (1995) Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase. Nat Genet 11: 376-381.
    • (1995) Nat Genet , vol.11 , pp. 376-381
    • Li, Y.1    Huang, T.T.2    Carlson, E.J.3    Melov, S.4    Ursell, P.C.5
  • 25
    • 4944225788 scopus 로고    scopus 로고
    • SOD2 Deficiency Anemia: Protein Oxidation and Altered Protein Expression Reveal Targets of Damage, Stress Response and Anti-oxidant Responsiveness
    • Friedman JS, Lopez MF, Fleming MD, Rivera A, Martin FM, et al. (2004) SOD2 Deficiency Anemia: Protein Oxidation and Altered Protein Expression Reveal Targets of Damage, Stress Response and Anti-oxidant Responsiveness. Blood 104: 2565-2573.
    • (2004) Blood , vol.104 , pp. 2565-2573
    • Friedman, J.S.1    Lopez, M.F.2    Fleming, M.D.3    Rivera, A.4    Martin, F.M.5
  • 27
    • 33746783738 scopus 로고    scopus 로고
    • SOD2-deficiency sideroblastic anemia and red blood cell oxidative stress
    • Martin FM, Bydlon G, Friedman JS, (2006) SOD2-deficiency sideroblastic anemia and red blood cell oxidative stress. Antioxid Redox Signal 8: 1217-1225.
    • (2006) Antioxid Redox Signal , vol.8 , pp. 1217-1225
    • Martin, F.M.1    Bydlon, G.2    Friedman, J.S.3
  • 28
    • 54049135327 scopus 로고    scopus 로고
    • Purification and Characterization of Sideroblasts from Patients with Acquired and Hereditary Sideroblastic Anemia
    • British Journal of Haematology in press
    • Martin FM, Prchal J, Nieva J, Saven A, Andrey J, et al. (2008) Purification and Characterization of Sideroblasts from Patients with Acquired and Hereditary Sideroblastic Anemia. British Journal of Haematology in press.
    • (2008)
    • Martin, F.M.1    Prchal, J.2    Nieva, J.3    Saven, A.4    Andrey, J.5
  • 29
    • 0035760889 scopus 로고    scopus 로고
    • Ineffective erythropoiesis in Stat5a(-/-)5b(-/-) mice due to decreased survival of early erythroblasts
    • Socolovsky M, Nam H, Fleming MD, Haase VH, Brugnara C, et al. (2001) Ineffective erythropoiesis in Stat5a(-/-)5b(-/-) mice due to decreased survival of early erythroblasts. Blood 98: 3261-3273.
    • (2001) Blood , vol.98 , pp. 3261-3273
    • Socolovsky, M.1    Nam, H.2    Fleming, M.D.3    Haase, V.H.4    Brugnara, C.5
  • 30
    • 0344826470 scopus 로고    scopus 로고
    • Role of Ras signaling in erythroid differentiation of mouse fetal liver cells: functional analysis by a flow cytometry-based novel culture system
    • Zhang J, Socolovsky M, Gross AW, Lodish HF, (2003) Role of Ras signaling in erythroid differentiation of mouse fetal liver cells: functional analysis by a flow cytometry-based novel culture system. Blood 102: 3938-3946.
    • (2003) Blood , vol.102 , pp. 3938-3946
    • Zhang, J.1    Socolovsky, M.2    Gross, A.W.3    Lodish, H.F.4
  • 31
    • 0034069495 scopus 로고    scopus 로고
    • Gene ontology: tool for the unification of biology. The Gene Ontology Consortium
    • Ashburner M, Ball CA, Blake JA, Botstein D, Butler H, et al. (2000) Gene ontology: tool for the unification of biology. The Gene Ontology Consortium. Nat Genet 25: 25-29.
    • (2000) Nat Genet , vol.25 , pp. 25-29
    • Ashburner, M.1    Ball, C.A.2    Blake, J.A.3    Botstein, D.4    Butler, H.5
  • 32
    • 0037263812 scopus 로고    scopus 로고
    • MAPPFinder: using Gene Ontology and GenMAPP to create a global gene-expression profile from microarray data
    • Doniger SW, Salomonis N, Dahlquist KD, Vranizan K, Lawlor SC, et al. (2003) MAPPFinder: using Gene Ontology and GenMAPP to create a global gene-expression profile from microarray data. Genome Biol 4: R7.
    • (2003) Genome Biol , vol.4
    • Doniger, S.W.1    Salomonis, N.2    Dahlquist, K.D.3    Vranizan, K.4    Lawlor, S.C.5
  • 34
    • 33947580628 scopus 로고    scopus 로고
    • Cytosolic phosphoenolpyruvate carboxykinase does not solely control the rate of hepatic gluconeogenesis in the intact mouse liver
    • Burgess SC, He T, Yan Z, Lindner J, Sherry AD, et al. (2007) Cytosolic phosphoenolpyruvate carboxykinase does not solely control the rate of hepatic gluconeogenesis in the intact mouse liver. Cell Metab 5: 313-320.
    • (2007) Cell Metab , vol.5 , pp. 313-320
    • Burgess, S.C.1    He, T.2    Yan, Z.3    Lindner, J.4    Sherry, A.D.5
  • 35
    • 0033525773 scopus 로고    scopus 로고
    • Mitochondrial diseases in man and mouse
    • Wallace DC, (1999) Mitochondrial diseases in man and mouse. Science 283: 1482-1488.
    • (1999) Science , vol.283 , pp. 1482-1488
    • Wallace, D.C.1
  • 36
    • 0035234813 scopus 로고    scopus 로고
    • A mitochondrial paradigm for degenerative diseases and ageing
    • discussion 263-246
    • Wallace DC, (2001) A mitochondrial paradigm for degenerative diseases and ageing. Novartis Found Symp 235: 247-263; discussion 263-246.
    • (2001) Novartis Found Symp , vol.235 , pp. 247-263
    • Wallace, D.C.1
  • 37
    • 0035016566 scopus 로고    scopus 로고
    • Pgc-1-related coactivator, a novel, serum-inducible coactivator of nuclear respiratory factor 1-dependent transcription in mammalian cells
    • Andersson U, Scarpulla RC, (2001) Pgc-1-related coactivator, a novel, serum-inducible coactivator of nuclear respiratory factor 1-dependent transcription in mammalian cells. Mol Cell Biol 21: 3738-3749.
    • (2001) Mol Cell Biol , vol.21 , pp. 3738-3749
    • Andersson, U.1    Scarpulla, R.C.2
  • 38
    • 42049114034 scopus 로고    scopus 로고
    • Transcriptional paradigms in mammalian mitochondrial biogenesis and function
    • Scarpulla RC, (2008) Transcriptional paradigms in mammalian mitochondrial biogenesis and function. Physiol Rev 88: 611-638.
    • (2008) Physiol Rev , vol.88 , pp. 611-638
    • Scarpulla, R.C.1
  • 39
    • 38449092832 scopus 로고    scopus 로고
    • Transcriptional control of mitochondrial energy metabolism through the PGC1 coactivators
    • discussion 63-69
    • Spiegelman BM, (2007) Transcriptional control of mitochondrial energy metabolism through the PGC1 coactivators. Novartis Found Symp 287: 60-63; discussion 63-69.
    • (2007) Novartis Found Symp , vol.287 , pp. 60-63
    • Spiegelman, B.M.1
  • 40
    • 39449110058 scopus 로고    scopus 로고
    • Rb intrinsically promotes erythropoiesis by coupling cell cycle exit with mitochondrial biogenesis
    • Sankaran VG, Orkin SH, Walkley CR, (2008) Rb intrinsically promotes erythropoiesis by coupling cell cycle exit with mitochondrial biogenesis. Genes Dev 22: 463-475.
    • (2008) Genes Dev , vol.22 , pp. 463-475
    • Sankaran, V.G.1    Orkin, S.H.2    Walkley, C.R.3
  • 41
    • 0031930319 scopus 로고    scopus 로고
    • Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice
    • Larsson NG, Wang J, Wilhelmsson H, Oldfors A, Rustin P, et al. (1998) Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice. Nat Genet 18: 231-236.
    • (1998) Nat Genet , vol.18 , pp. 231-236
    • Larsson, N.G.1    Wang, J.2    Wilhelmsson, H.3    Oldfors, A.4    Rustin, P.5
  • 42
    • 0027452550 scopus 로고
    • Regulating the fate of mRNA: the control of cellular iron metabolism
    • Klausner RD, Rouault TA, Harford JB, (1993) Regulating the fate of mRNA: the control of cellular iron metabolism. Cell 72: 19-28.
    • (1993) Cell , vol.72 , pp. 19-28
    • Klausner, R.D.1    Rouault, T.A.2    Harford, J.B.3
  • 43
    • 33746361251 scopus 로고    scopus 로고
    • The role of iron regulatory proteins in mammalian iron homeostasis and disease
    • Rouault TA, (2006) The role of iron regulatory proteins in mammalian iron homeostasis and disease. Nat Chem Biol 2: 406-414.
    • (2006) Nat Chem Biol , vol.2 , pp. 406-414
    • Rouault, T.A.1
  • 44
    • 0023430885 scopus 로고
    • A cis-acting element is necessary and sufficient for translational regulation of human ferritin expression in response to iron
    • Hentze MW, Rouault TA, Caughman SW, Dancis A, Harford JB, et al. (1987) A cis-acting element is necessary and sufficient for translational regulation of human ferritin expression in response to iron. Proc Natl Acad Sci U S A 84: 6730-6734.
    • (1987) Proc Natl Acad Sci U S A , vol.84 , pp. 6730-6734
    • Hentze, M.W.1    Rouault, T.A.2    Caughman, S.W.3    Dancis, A.4    Harford, J.B.5
  • 45
    • 44849143798 scopus 로고    scopus 로고
    • The role of the iron transporter ABCB7 in refractory anemia with ring sideroblasts
    • Boultwood J, Pellagatti A, Nikpour M, Pushkaran B, Fidler C, et al. (2008) The role of the iron transporter ABCB7 in refractory anemia with ring sideroblasts. PLoS ONE 3: e1970.
    • (2008) PLoS ONE , vol.3
    • Boultwood, J.1    Pellagatti, A.2    Nikpour, M.3    Pushkaran, B.4    Fidler, C.5
  • 46
    • 35148812715 scopus 로고    scopus 로고
    • Structure of the yeast WD40 domain protein Cia1, a component acting late in iron-sulfur protein biogenesis
    • Srinivasan V, Netz DJ, Webert H, Mascarenhas J, Pierik AJ, et al. (2007) Structure of the yeast WD40 domain protein Cia1, a component acting late in iron-sulfur protein biogenesis. Structure 15: 1246-1257.
    • (2007) Structure , vol.15 , pp. 1246-1257
    • Srinivasan, V.1    Netz, D.J.2    Webert, H.3    Mascarenhas, J.4    Pierik, A.J.5
  • 47
    • 28544450863 scopus 로고    scopus 로고
    • The essential WD40 protein Cia1 is involved in a late step of cytosolic and nuclear iron-sulfur protein assembly
    • Balk J, Aguilar Netz DJ, Tepper K, Pierik AJ, Lill R, (2005) The essential WD40 protein Cia1 is involved in a late step of cytosolic and nuclear iron-sulfur protein assembly. Mol Cell Biol 25: 10833-10841.
    • (2005) Mol Cell Biol , vol.25 , pp. 10833-10841
    • Balk, J.1    Aguilar Netz, D.J.2    Tepper, K.3    Pierik, A.J.4    Lill, R.5
  • 48
    • 10544256600 scopus 로고    scopus 로고
    • Expression monitoring by hybridization to high-density oligonucleotide arrays
    • Lockhart DJ, Dong H, Byrne MC, Follettie MT, Gallo MV, et al. (1996) Expression monitoring by hybridization to high-density oligonucleotide arrays. Nat Biotechnol 14: 1675-1680.
    • (1996) Nat Biotechnol , vol.14 , pp. 1675-1680
    • Lockhart, D.J.1    Dong, H.2    Byrne, M.C.3    Follettie, M.T.4    Gallo, M.V.5
  • 49
    • 0001677717 scopus 로고
    • Controlling the false discovery rate: a practical and powerful approach to multiple testing
    • Benjamini Y, Hochberg Y, (1995) Controlling the false discovery rate: a practical and powerful approach to multiple testing. J Roy Stat Soc B 57: 289-300.
    • (1995) J Roy Stat Soc B , vol.57 , pp. 289-300
    • Benjamini, Y.1    Hochberg, Y.2
  • 50
    • 0025066941 scopus 로고
    • More powerful procedures for multiple significance testing
    • Hochberg Y, Benjamini Y, (1990) More powerful procedures for multiple significance testing. Stat Med 9: 811-818.
    • (1990) Stat Med , vol.9 , pp. 811-818
    • Hochberg, Y.1    Benjamini, Y.2
  • 51
    • 0035710746 scopus 로고    scopus 로고
    • Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method
    • Livak KJ, Schmittgen TD, (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods 25: 402-408.
    • (2001) Methods , vol.25 , pp. 402-408
    • Livak, K.J.1    Schmittgen, T.D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.