메뉴 건너뛰기




Volumn 18, Issue R2, 2009, Pages

Genetics of nephrotic syndrome: Connecting molecular genetics to podocyte physiology

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL; CELL MEMBRANE; GENETICS; HUMAN; LYSOSOME; MITOCHONDRION; MOLECULAR BIOLOGY; NEPHROTIC SYNDROME; PATHOLOGY; PATHOPHYSIOLOGY; PHYSIOLOGY; PODOCYTE; REVIEW;

EID: 77950515351     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddp328     Document Type: Article
Times cited : (106)

References (94)
  • 1
    • 42149122041 scopus 로고    scopus 로고
    • Properties of the glomerular barrier and mechanisms of proteinuria
    • Haraldsson, B., Nystrom, J. and Deen, W.M. (2008) Properties of the glomerular barrier and mechanisms of proteinuria. Physiol. Rev., 88, 451-487.
    • (2008) Physiol. Rev. , vol.88 , pp. 451-487
    • Haraldsson, B.1    Nystrom, J.2    Deen, W.M.3
  • 2
    • 23944442318 scopus 로고    scopus 로고
    • Three-dimensional reconstruction of glomeruli by electron microscopy reveals a distinct restrictive urinary subpodocyte space
    • Neal, C.R., Crook, H., Bell, E., Harper, S.J. and Bates, D.O. (2005) Three-dimensional reconstruction of glomeruli by electron microscopy reveals a distinct restrictive urinary subpodocyte space. J. Am. Soc. Nephrol., 16, 1223-1235.
    • (2005) J. Am. Soc. Nephrol. , vol.16 , pp. 1223-1235
    • Neal, C.R.1    Crook, H.2    Bell, E.3    Harper, S.J.4    Bates, D.O.5
  • 3
    • 0028278929 scopus 로고
    • Plasmapheresis reduces proteinuria and serum capacity to injure glomeruli in patients with recurrent focal glomerulosclerosis
    • Artero, M.L., Sharma, R., Savin, V.J. and Vincenti, F. (1994) Plasmapheresis reduces proteinuria and serum capacity to injure glomeruli in patients with recurrent focal glomerulosclerosis. Am. J. Kidney Dis., 23, 574-581.
    • (1994) Am. J. Kidney Dis. , vol.23 , pp. 574-581
    • Artero, M.L.1    Sharma, R.2    Savin, V.J.3    Vincenti, F.4
  • 5
    • 0031750931 scopus 로고    scopus 로고
    • Antihuman immunoglobulin affinity immunoadsorption strongly decreases proteinuria in patients with relapsing nephrotic syndrome
    • Dantal, J., Godfrin, Y., Koll, R., Perretto, S., Naulet, J., Bouhours, J.F. and Soulillou, J.P. (1998) Antihuman immunoglobulin affinity immunoadsorption strongly decreases proteinuria in patients with relapsing nephrotic syndrome. J. Am. Soc. Nephrol., 9, 1709-1715.
    • (1998) J. Am. Soc. Nephrol. , vol.9 , pp. 1709-1715
    • Dantal, J.1    Godfrin, Y.2    Koll, R.3    Perretto, S.4    Naulet, J.5    Bouhours, J.F.6    Soulillou, J.P.7
  • 7
    • 30944431921 scopus 로고    scopus 로고
    • Renal macrophage activation and Th2 polarization precedes the development of nephrotic syndrome in Buffalo/Mna rats
    • Le Berre, L., Herve, C., Buzelin, F., Usal, C., Soulillou, J.P. and Dantal, J. (2005) Renal macrophage activation and Th2 polarization precedes the development of nephrotic syndrome in Buffalo/Mna rats. Kidney Int., 68, 2079-2090.
    • (2005) Kidney Int. , vol.68 , pp. 2079-2090
    • Le Berre, L.1    Herve, C.2    Buzelin, F.3    Usal, C.4    Soulillou, J.P.5    Dantal, J.6
  • 8
    • 3242795082 scopus 로고    scopus 로고
    • NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence
    • Weber, S., Gribouval, O., Esquivel, E.L., Moriniere, V., Tete, M.J., Legendre, C., Niaudet, P. and Antignac, C. (2004) NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence. Kidney Int., 66, 571-579.
    • (2004) Kidney Int. , vol.66 , pp. 571-579
    • Weber, S.1    Gribouval, O.2    Esquivel, E.L.3    Moriniere, V.4    Tete, M.J.5    Legendre, C.6    Niaudet, P.7    Antignac, C.8
  • 10
    • 48049090083 scopus 로고    scopus 로고
    • 2007 Young Investigator Award: TRP'ing into a new era for glomerular disease
    • Winn, M.P. (2008) 2007 Young Investigator Award: TRP'ing into a new era for glomerular disease. J. Am. Soc. Nephrol., 19, 1071-1075.
    • (2008) J. Am. Soc. Nephrol. , vol.19 , pp. 1071-1075
    • Winn, M.P.1
  • 14
    • 0038136885 scopus 로고    scopus 로고
    • CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility
    • Kim, J.M., Wu, H., Green, G., Winkler, C.A., Kopp, J.B., Miner, J.H., Unanue, E.R. and Shaw, A.S. (2003) CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility. Science, 300, 1298-1300.
    • (2003) Science , vol.300 , pp. 1298-1300
    • Kim, J.M.1    Wu, H.2    Green, G.3    Winkler, C.A.4    Kopp, J.B.5    Miner, J.H.6    Unanue, E.R.7    Shaw, A.S.8
  • 16
    • 34548526982 scopus 로고    scopus 로고
    • Nephrin-a unique structural and signaling protein of the kidney filter
    • Patrakka, J. and Tryggvason, K. (2007) Nephrin-a unique structural and signaling protein of the kidney filter. Trends Mol. Med., 13, 396-403.
    • (2007) Trends Mol. Med. , vol.13 , pp. 396-403
    • Patrakka, J.1    Tryggvason, K.2
  • 18
    • 37549036286 scopus 로고    scopus 로고
    • Neph1 cooperates with nephrin to transduce a signal that induces actin polymerization
    • Garg, P., Verma, R., Nihalani, D., Johnstone, D.B. and Holzman, L.B. (2007) Neph1 cooperates with nephrin to transduce a signal that induces actin polymerization. Mol. Cell. Biol., 27, 8698-8712.
    • (2007) Mol. Cell. Biol. , vol.27 , pp. 8698-8712
    • Garg, P.1    Verma, R.2    Nihalani, D.3    Johnstone, D.B.4    Holzman, L.B.5
  • 22
    • 34848907421 scopus 로고    scopus 로고
    • Actin up: regulation of podocyte structure and function by components of the actin cytoskeleton
    • Faul, C., Asanuma, K., Yanagida-Asanuma, E., Kim, K. and Mundel, P. (2007) Actin up: regulation of podocyte structure and function by components of the actin cytoskeleton. Trends Cell. Biol., 17, 428-437.
    • (2007) Trends Cell. Biol. , vol.17 , pp. 428-437
    • Faul, C.1    Asanuma, K.2    Yanagida-Asanuma, E.3    Kim, K.4    Mundel, P.5
  • 29
    • 0037084569 scopus 로고    scopus 로고
    • Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration
    • Koziell, A., Grech, V., Hussain, S., Lee, G., Lenkkeri, U., Tryggvason, K. and Scambler, P. (2002) Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration. Hum. Mol. Genet., 11, 379-388.
    • (2002) Hum. Mol. Genet. , vol.11 , pp. 379-388
    • Koziell, A.1    Grech, V.2    Hussain, S.3    Lee, G.4    Lenkkeri, U.5    Tryggvason, K.6    Scambler, P.7
  • 31
    • 0035510132 scopus 로고    scopus 로고
    • Defective nephrin trafficking caused by missense mutations in the NPHS1 gene: insight into the mechanisms of congenital nephrotic syndrome
    • Liu, L., Done, S.C., Khoshnoodi, J., Bertorello, A., Wartiovaara, J., Berggren, P.O. and Tryggvason, K. (2001) Defective nephrin trafficking caused by missense mutations in the NPHS1 gene: insight into the mechanisms of congenital nephrotic syndrome. Hum. Mol. Genet., 10, 2637-2644.
    • (2001) Hum. Mol. Genet. , vol.10 , pp. 2637-2644
    • Liu, L.1    Done, S.C.2    Khoshnoodi, J.3    Bertorello, A.4    Wartiovaara, J.5    Berggren, P.O.6    Tryggvason, K.7
  • 32
    • 0742289582 scopus 로고    scopus 로고
    • Plasma membrane targeting of podocin through the classical exocytic pathway: effect of NPHS2 mutations
    • Roselli, S., Moutkine, I., Gribouval, O., Benmerah, A. and Antignac, C. (2004) Plasma membrane targeting of podocin through the classical exocytic pathway: effect of NPHS2 mutations. Traffic, 5, 37-44.
    • (2004) Traffic , vol.5 , pp. 37-44
    • Roselli, S.1    Moutkine, I.2    Gribouval, O.3    Benmerah, A.4    Antignac, C.5
  • 33
    • 0037361663 scopus 로고    scopus 로고
    • Intracellular mislocalization of mutant podocin and correction by chemical chaperones
    • Ohashi, T., Uchida, K., Uchida, S., Sasaki, S. and Nihei, H. (2003) Intracellular mislocalization of mutant podocin and correction by chemical chaperones. Histochem. Cell Biol., 119, 257-264.
    • (2003) Histochem. Cell Biol. , vol.119 , pp. 257-264
    • Ohashi, T.1    Uchida, K.2    Uchida, S.3    Sasaki, S.4    Nihei, H.5
  • 35
    • 68049095269 scopus 로고    scopus 로고
    • Predisposition to relapsing nephrotic syndrome by a nephrin mutation that interferes with assembly of functioning microdomains
    • Shono, A., Tsukaguchi, H., Kitamura, A., Hiramoto, R., Qin, X.S., Doi, T. and Iijima, K. (2009) Predisposition to relapsing nephrotic syndrome by a nephrin mutation that interferes with assembly of functioning microdomains. Hum. Mol. Genet., 18, 2943-2956.
    • (2009) Hum. Mol. Genet. , vol.18 , pp. 2943-2956
    • Shono, A.1    Tsukaguchi, H.2    Kitamura, A.3    Hiramoto, R.4    Qin, X.S.5    Doi, T.6    Iijima, K.7
  • 39
    • 33751540445 scopus 로고    scopus 로고
    • A new piece in the nephrotic puzzle
    • Quaggin, S.E. (2006) A new piece in the nephrotic puzzle. Nat. Genet., 38, 1360-1361.
    • (2006) Nat. Genet. , vol.38 , pp. 1360-1361
    • Quaggin, S.E.1
  • 49
    • 0042242818 scopus 로고    scopus 로고
    • Neph1 and nephrin interaction in the slit diaphragm is an important determinant of glomerular permeability
    • Liu, G., Kaw, B., Kurfis, J., Rahmanuddin, S., Kanwar, Y.S. and Chugh, S.S. (2003) Neph1 and nephrin interaction in the slit diaphragm is an important determinant of glomerular permeability. J. Clin. Invest., 112, 209-221.
    • (2003) J. Clin. Invest. , vol.112 , pp. 209-221
    • Liu, G.1    Kaw, B.2    Kurfis, J.3    Rahmanuddin, S.4    Kanwar, Y.S.5    Chugh, S.S.6
  • 51
    • 39349104907 scopus 로고    scopus 로고
    • Nephrin mediates actin reorganization via phosphoinositide 3-kinase in podocytes
    • Zhu, J., Sun, N., Aoudjit, L., Li, H., Kawachi, H., Lemay, S. and Takano, T. (2008) Nephrin mediates actin reorganization via phosphoinositide 3-kinase in podocytes. Kidney Int., 73, 556-566.
    • (2008) Kidney Int. , vol.73 , pp. 556-566
    • Zhu, J.1    Sun, N.2    Aoudjit, L.3    Li, H.4    Kawachi, H.5    Lemay, S.6    Takano, T.7
  • 53
    • 0036783544 scopus 로고    scopus 로고
    • CD2-associated protein directly interacts with the actin cytoskeleton
    • Lehtonen, S., Zhao, F. and Lehtonen, E. (2002) CD2-associated protein directly interacts with the actin cytoskeleton. Am. J. Physiol. Renal Physiol., 283, F734-F743.
    • (2002) Am. J. Physiol. Renal Physiol. , vol.283
    • Lehtonen, S.1    Zhao, F.2    Lehtonen, E.3
  • 56
    • 0025291522 scopus 로고
    • An interaction between alpha-actinin and the beta 1 integrin subunit in vitro
    • Otey, C.A., Pavalko, F.M. and Burridge, K. (1990) An interaction between alpha-actinin and the beta 1 integrin subunit in vitro. J. Cell. Biol., 111, 721-729.
    • (1990) J. Cell. Biol. , vol.111 , pp. 721-729
    • Otey, C.A.1    Pavalko, F.M.2    Burridge, K.3
  • 58
    • 2342514426 scopus 로고    scopus 로고
    • PLC-epsilon: a shared effector protein in Ras-, Rho-, and G alpha beta gamma-mediated signaling
    • Wing, M.R., Bourdon, D.M. and Harden, T.K. (2003) PLC-epsilon: a shared effector protein in Ras-, Rho-, and G alpha beta gamma-mediated signaling. Mol. Interv., 3, 273-280.
    • (2003) Mol. Interv. , vol.3 , pp. 273-280
    • Wing, M.R.1    Bourdon, D.M.2    Harden, T.K.3
  • 59
    • 22244466451 scopus 로고    scopus 로고
    • Cell junction-associated proteins IQGAP1, MAGI-2, CASK, spectrins, and alpha-actinin are components of the nephrin multiprotein complex
    • Lehtonen, S., Ryan, J.J., Kudlicka, K., Iino, N., Zhou, H. and Farquhar, M.G. (2005) Cell junction-associated proteins IQGAP1, MAGI-2, CASK, spectrins, and alpha-actinin are components of the nephrin multiprotein complex. Proc. Natl. Acad. Sci. U.S.A., 102, 9814-9819.
    • (2005) Proc. Natl. Acad. Sci. U.S.A. , vol.102 , pp. 9814-9819
    • Lehtonen, S.1    Ryan, J.J.2    Kudlicka, K.3    Iino, N.4    Zhou, H.5    Farquhar, M.G.6
  • 60
    • 33846807748 scopus 로고    scopus 로고
    • Transient receptor potential cation channels in disease
    • Nilius, B., Owsianik, G., Voets, T. and Peters, J.A. (2007) Transient receptor potential cation channels in disease. Physiol. Rev., 87, 165-217.
    • (2007) Physiol. Rev. , vol.87 , pp. 165-217
    • Nilius, B.1    Owsianik, G.2    Voets, T.3    Peters, J.A.4
  • 61
    • 33750802650 scopus 로고    scopus 로고
    • A common mechanism underlies stretch activation and receptor activation of TRPC6 channels
    • Spassova, M.A., Hewavitharana, T., Xu, W., Soboloff, J. and Gill, D.L. (2006) A common mechanism underlies stretch activation and receptor activation of TRPC6 channels. Proc. Natl. Acad. Sci. U.S.A., 103, 16586-16591.
    • (2006) Proc. Natl. Acad. Sci. U.S.A. , vol.103 , pp. 16586-16591
    • Spassova, M.A.1    Hewavitharana, T.2    Xu, W.3    Soboloff, J.4    Gill, D.L.5
  • 62
    • 34447136072 scopus 로고    scopus 로고
    • Podocin organizes ion channel-lipid supercomplexes: implications for mechanosensation at the slit diaphragm
    • Huber, T.B., Schermer, B. and Benzing, T. (2007) Podocin organizes ion channel-lipid supercomplexes: implications for mechanosensation at the slit diaphragm. Nephron. Exp. Nephrol., 106, e27-e31.
    • (2007) Nephron. Exp. Nephrol. , vol.106
    • Huber, T.B.1    Schermer, B.2    Benzing, T.3
  • 64
    • 65249099647 scopus 로고    scopus 로고
    • TRPC6 mutations associated with focal segmental glomerulosclerosis cause constitutive activation of NFAT-dependent transcription
    • Schlondorff, J., Del Camino, D., Carrasquillo, R., Lacey, V. and Pollak, M.R. (2009) TRPC6 mutations associated with focal segmental glomerulosclerosis cause constitutive activation of NFAT-dependent transcription. Am. J. Physiol. Cell Physiol., 296, C558-C569.
    • (2009) Am. J. Physiol. Cell Physiol. , vol.296
    • Schlondorff, J.1    Del Camino, D.2    Carrasquillo, R.3    Lacey, V.4    Pollak, M.R.5
  • 65
    • 1842509188 scopus 로고    scopus 로고
    • Laminin: the crux of basement membrane assembly
    • Sasaki, T., Fassler, R. and Hohenester, E. (2004) Laminin: the crux of basement membrane assembly. J. Cell. Biol., 164, 959-963.
    • (2004) J. Cell. Biol. , vol.164 , pp. 959-963
    • Sasaki, T.1    Fassler, R.2    Hohenester, E.3
  • 71
    • 33750006320 scopus 로고    scopus 로고
    • A syndrome comprising childhood-onset glomerular kidney disease and ocular abnormalities with progressive loss of vision is caused by mutated LAMB2
    • Matejas, V., Al-Gazali, L., Amirlak, I. and Zenker, M. (2006) A syndrome comprising childhood-onset glomerular kidney disease and ocular abnormalities with progressive loss of vision is caused by mutated LAMB2. Nephrol. Dial. Transplant., 21, 3283-3286.
    • (2006) Nephrol. Dial. Transplant. , vol.21 , pp. 3283-3286
    • Matejas, V.1    Al-Gazali, L.2    Amirlak, I.3    Zenker, M.4
  • 74
    • 34248195476 scopus 로고    scopus 로고
    • Endogenous synthesis of coenzyme Q in eukaryotes
    • Tran, U.C. and Clarke, C.F. (2007) Endogenous synthesis of coenzyme Q in eukaryotes. Mitochondrion, 7 (suppl), S62-S71.
    • (2007) Mitochondrion , vol.7 , Issue.SUPPL.
    • Tran, U.C.1    Clarke, C.F.2
  • 77
    • 0034822296 scopus 로고    scopus 로고
    • Neonatal presentation of coenzyme Q10 deficiency
    • Rahman, S., Hargreaves, I., Clayton, P. and Heales, S. (2001) Neonatal presentation of coenzyme Q10 deficiency. J. Pediatr., 139, 456-458.
    • (2001) J. Pediatr. , vol.139 , pp. 456-458
    • Rahman, S.1    Hargreaves, I.2    Clayton, P.3    Heales, S.4
  • 78
    • 4544375641 scopus 로고    scopus 로고
    • Isolation and functional expression of human COQ2, a gene encoding a polyprenyl transferase involved in the synthesis of CoQ
    • Forsgren, M., Attersand, A., Lake, S., Grunler, J., Swiezewska, E., Dallner, G. and Climent, I. (2004) Isolation and functional expression of human COQ2, a gene encoding a polyprenyl transferase involved in the synthesis of CoQ. Biochem. J., 382, 519-526.
    • (2004) Biochem. J. , vol.382 , pp. 519-526
    • Forsgren, M.1    Attersand, A.2    Lake, S.3    Grunler, J.4    Swiezewska, E.5    Dallner, G.6    Climent, I.7
  • 80
    • 33845232634 scopus 로고    scopus 로고
    • Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations
    • Lopez, L.C., Schuelke, M., Quinzii, C.M., Kanki, T., Rodenburg, R.J., Naini, A., Dimauro, S. and Hirano, M. (2006) Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations. Am. J. Hum. Genet., 79, 1125-1129.
    • (2006) Am. J. Hum. Genet. , vol.79 , pp. 1125-1129
    • Lopez, L.C.1    Schuelke, M.2    Quinzii, C.M.3    Kanki, T.4    Rodenburg, R.J.5    Naini, A.6    Dimauro, S.7    Hirano, M.8
  • 82
    • 45949099527 scopus 로고    scopus 로고
    • Early coenzyme Q10 supplementation in primary coenzyme Q10 deficiency
    • Montini, G., Malaventura, C. and Salviati, L. (2008) Early coenzyme Q10 supplementation in primary coenzyme Q10 deficiency. N. Engl. J. Med., 358, 2849-2850.
    • (2008) N. Engl. J. Med. , vol.358 , pp. 2849-2850
    • Montini, G.1    Malaventura, C.2    Salviati, L.3
  • 83
    • 0025666322 scopus 로고
    • A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
    • Goto, Y., Nonaka, I. and Horai, S. (1990) A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. Nature, 348, 651-653.
    • (1990) Nature , vol.348 , pp. 651-653
    • Goto, Y.1    Nonaka, I.2    Horai, S.3
  • 85
    • 0031774828 scopus 로고    scopus 로고
    • A case of mitochondrial cytopathy with a typical point mutation for MELAS, presenting with severe focal-segmental glomerulosclerosis as main clinical manifestation
    • Kurogouchi, F., Oguchi, T., Mawatari, E., Yamaura, S., Hora, K., Takei, M., Sekijima, Y., Ikeda, S. and Kiyosawa, K. (1998) A case of mitochondrial cytopathy with a typical point mutation for MELAS, presenting with severe focal-segmental glomerulosclerosis as main clinical manifestation. Am. J. Nephrol., 18, 551-556.
    • (1998) Am. J. Nephrol. , vol.18 , pp. 551-556
    • Kurogouchi, F.1    Oguchi, T.2    Mawatari, E.3    Yamaura, S.4    Hora, K.5    Takei, M.6    Sekijima, Y.7    Ikeda, S.8    Kiyosawa, K.9
  • 88
    • 0036138503 scopus 로고    scopus 로고
    • Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes
    • Arrondel, C., Vodovar, N., Knebelmann, B., Grunfeld, J.P., Gubler, M.C., Antignac, C. and Heidet, L. (2002) Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes. J. Am. Soc. Nephrol., 13, 65-74.
    • (2002) J. Am. Soc. Nephrol. , vol.13 , pp. 65-74
    • Arrondel, C.1    Vodovar, N.2    Knebelmann, B.3    Grunfeld, J.P.4    Gubler, M.C.5    Antignac, C.6    Heidet, L.7
  • 89
    • 0024209817 scopus 로고
    • Ultrastructural organization of contractile and cytoskeletal proteins in glomerular podocytes of chicken, rat, and man
    • Drenckhahn, D. and Franke, R.P. (1988) Ultrastructural organization of contractile and cytoskeletal proteins in glomerular podocytes of chicken, rat, and man. Lab. Invest., 59, 673-682.
    • (1988) Lab. Invest. , vol.59 , pp. 673-682
    • Drenckhahn, D.1    Franke, R.P.2
  • 91
    • 34247897032 scopus 로고    scopus 로고
    • Familial steroid-sensitive nephrotic syndrome in Southern Israel: clinical and genetic observations
    • Landau, D., Oved, T., Geiger, D., Abizov, L., Shalev, H. and Parvari, R. (2007) Familial steroid-sensitive nephrotic syndrome in Southern Israel: clinical and genetic observations. Pediatr. Nephrol., 22, 661-669.
    • (2007) Pediatr. Nephrol. , vol.22 , pp. 661-669
    • Landau, D.1    Oved, T.2    Geiger, D.3    Abizov, L.4    Shalev, H.5    Parvari, R.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.