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Volumn 2012, Issue , 2012, Pages

Progress in pathogenesis of proteinuria

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EID: 84866154355     PISSN: 2090214X     EISSN: 20902158     Source Type: Journal    
DOI: 10.1155/2012/314251     Document Type: Review
Times cited : (38)

References (135)
  • 1
    • 56249091115 scopus 로고    scopus 로고
    • How to measure proteinuria?
    • 2-s2.0-56249091115 10.1097/MNH.0b013e328313675c
    • McIntyre N. J., Taal M. W., How to measure proteinuria? Current Opinion in Nephrology and Hypertension 2008 17 6 600 603 2-s2.0-56249091115 10.1097/MNH.0b013e328313675c
    • (2008) Current Opinion in Nephrology and Hypertension , vol.17 , Issue.6 , pp. 600-603
    • McIntyre, N.J.1    Taal, M.W.2
  • 3
    • 0029938661 scopus 로고    scopus 로고
    • The role of proteinuria in the progression of chronic renal failure
    • Burton C., Harris K. P. G., The role of proteinuria in the progression of chronic renal failure. American Journal of Kidney Diseases 1996 27 6 765 775 2-s2.0-0029938661 (Pubitemid 26169027)
    • (1996) American Journal of Kidney Diseases , vol.27 , Issue.6 , pp. 765-775
    • Burton, C.1    Harris, K.P.G.2
  • 5
    • 0034567759 scopus 로고    scopus 로고
    • Proteinuria and progression of chronic renal disease
    • 2-s2.0-0034567759
    • Wang S., LaPage J., Hirschberg R., Proteinuria and progression of chronic renal disease. Kidney & Blood Pressure Research 2000 23 35 167 169 2-s2.0-0034567759
    • (2000) Kidney & Blood Pressure Research , vol.23 , Issue.35 , pp. 167-169
    • Wang, S.1    Lapage, J.2    Hirschberg, R.3
  • 6
    • 14644398528 scopus 로고    scopus 로고
    • Renal glomerular permselectivity and vascular endothelium
    • DOI 10.1016/j.biopha.2004.06.003
    • Camici M., Renal glomerular permselectivity and vascular endothelium. Biomedicine and Pharmacotherapy 2005 59 1-2 30 37 2-s2.0-14644398528 10.1016/j.biopha.2004.06.003 (Pubitemid 40312277)
    • (2005) Biomedicine and Pharmacotherapy , vol.59 , Issue.1-2 , pp. 30-37
    • Camici, M.1
  • 7
    • 41849137193 scopus 로고    scopus 로고
    • What is the mechanism of microalbuminuria in diabetes: A role for the glomerular endothelium?
    • 2-s2.0-41849137193 10.1007/s00125-008-0961-8
    • Satchell S. C., Tooke J. E., What is the mechanism of microalbuminuria in diabetes: a role for the glomerular endothelium? Diabetologia 2008 51 5 714 725 2-s2.0-41849137193 10.1007/s00125-008-0961-8
    • (2008) Diabetologia , vol.51 , Issue.5 , pp. 714-725
    • Satchell, S.C.1    Tooke, J.E.2
  • 9
  • 10
    • 84856708866 scopus 로고    scopus 로고
    • Endothelial glycocalyx dysfunction in disease: Albuminuria and increased microvascular permeability
    • Salmon A. H., Satchell S. C., Endothelial glycocalyx dysfunction in disease: albuminuria and increased microvascular permeability. Journal of Pathology 2012 226 4 562 574
    • (2012) Journal of Pathology , vol.226 , Issue.4 , pp. 562-574
    • Salmon, A.H.1    Satchell, S.C.2
  • 11
  • 14
    • 27944496060 scopus 로고    scopus 로고
    • 1-6 chains in the glomerular basement membrane in childhood thin basement membrane disease
    • Akazawa H., Nakajima M., Nishiguchi M., Yamoto Y., Sado Y., Naito I., Yoshioka A., Quantitative immunoelectron-microscopic analysis of the type IV collagen α 1-6 chains in the glomerular basement membrane in childhood thin basement membrane disease. Clinical Nephrology 2005 64 5 329 336 2-s2.0-27944496060 (Pubitemid 41671883)
    • (2005) Clinical Nephrology , vol.64 , Issue.5 , pp. 329-336
    • Akazawa, H.1    Nakajima, M.2    Nishiguchi, M.3    Yamoto, Y.4    Sado, Y.5    Naito, I.6    Yoshioka, A.7
  • 15
    • 16644399795 scopus 로고    scopus 로고
    • The molecular basis of goodpasture and alport syndromes: Beacons for the discovery of the collagen IV family
    • DOI 10.1097/01.ASN.0000141462.00630.76
    • Hudson B. G., The molecular basis of goodpasture and alport syndromes: beacons for the discovery of the collagen IV family. Journal of the American Society of Nephrology 2004 15 10 2514 2527 2-s2.0-16644399795 10.1097/01.ASN.0000141462.00630.76 (Pubitemid 41103358)
    • (2004) Journal of the American Society of Nephrology , vol.15 , Issue.10 , pp. 2514-2527
    • Hudson, B.G.1
  • 20
    • 80053057998 scopus 로고    scopus 로고
    • Forced expression of laminin β 1 in podocytes prevents nephrotic syndrome in mice lacking laminin β 2, a model for Pierson syndrome
    • Suh J. H., Jarad G., VanDeVoorde R. G., Miner J. H., Forced expression of laminin β 1 in podocytes prevents nephrotic syndrome in mice lacking laminin β 2, a model for Pierson syndrome. Proceedings of the National Academy of Sciences of the United States 2011 108 37 15348 15353
    • (2011) Proceedings of the National Academy of Sciences of the United States , vol.108 , Issue.37 , pp. 15348-15353
    • Suh, J.H.1    Jarad, G.2    Vandevoorde, R.G.3    Miner, J.H.4
  • 21
    • 84863470574 scopus 로고    scopus 로고
    • Pierson syndrome in an adolescent girl with nephrotic range proteinuria but a normal GFR
    • Lehnhardt A., Lama A., Amann K., Pierson syndrome in an adolescent girl with nephrotic range proteinuria but a normal GFR. Pediatric Nephrology 2012 27 5 865 868
    • (2012) Pediatric Nephrology , vol.27 , Issue.5 , pp. 865-868
    • Lehnhardt, A.1    Lama, A.2    Amann, K.3
  • 22
    • 33746730496 scopus 로고    scopus 로고
    • -/- mice, implicating the glomerular basement membrane as an albumin barrier
    • DOI 10.1172/JCI28414
    • -/- mice, implicating the glomerular basement membrane as an albumin barrier. Journal of Clinical Investigation 2006 116 8 2272 2279 2-s2.0-33746730496 10.1172/JCI28414 (Pubitemid 44162337)
    • (2006) Journal of Clinical Investigation , vol.116 , Issue.8 , pp. 2272-2279
    • Jarad, G.1    Cunningham, J.2    Shaw, A.S.3    Miner, J.H.4
  • 24
    • 0036891810 scopus 로고    scopus 로고
    • Podocyte biology and response to injury
    • DOI 10.1097/01.ASN.0000039661.06947.FD
    • Mundel P., Shankland S. J., Podocyte biology and response to injury. Journal of the American Society of Nephrology 2002 13 12 3005 3015 2-s2.0-0036891810 10.1097/01.ASN.0000039661.06947.FD (Pubitemid 35386921)
    • (2002) Journal of the American Society of Nephrology , vol.13 , Issue.12 , pp. 3005-3015
    • Mundel, P.1    Shankland, S.J.2
  • 25
    • 0032730875 scopus 로고    scopus 로고
    • Unraveling the mechanisms of glomerular ultrafiltration: Nephrin, a key component of the slit diaphragm
    • Tryggvason K., Unraveling the mechanisms of glomerular ultrafiltration: nephrin, a key component of the slit diaphragm. Journal of the American Society of Nephrology 1999 10 11 2440 2445 2-s2.0-0032730875 (Pubitemid 29501479)
    • (1999) Journal of the American Society of Nephrology , vol.10 , Issue.11 , pp. 2440-2445
    • Tryggvason, K.1
  • 26
    • 36748999500 scopus 로고    scopus 로고
    • The nephrin-based slit diaphragm: New insight into the signalling platform identifies targets for therapy
    • DOI 10.1093/ndt/gfm403
    • Aaltonen P., Holthöfer H., The nephrin-based slit diaphragm: new insight into the signalling platform identifies targets for therapy. Nephrology Dialysis Transplantation 2007 22 12 3408 3410 2-s2.0-36748999500 10.1093/ndt/gfm403 (Pubitemid 350212483)
    • (2007) Nephrology Dialysis Transplantation , vol.22 , Issue.12 , pp. 3408-3410
    • Aaltonen, P.1    Holthofer, H.2
  • 27
    • 0036144160 scopus 로고    scopus 로고
    • Focusing on the glomerular slit diaphragm: Podocin enters the picture
    • Miner J. H., Focusing on the glomerular slit diaphragm: podocin enters the picture. American Journal of Pathology 2002 160 1 3 5 2-s2.0-0036144160 (Pubitemid 34052258)
    • (2002) American Journal of Pathology , vol.160 , Issue.1 , pp. 3-5
    • Miner, J.H.1
  • 28
    • 17844376266 scopus 로고    scopus 로고
    • NPHS2 (podocin) mutations in nephrotic syndrome. Clinical spectrum and fine mechanisms
    • 2-s2.0-17844376266
    • Caridi G., Perfumo F., Ghiggeri G. M., NPHS2 (podocin) mutations in nephrotic syndrome. Clinical spectrum and fine mechanisms. Pediatric Research 2005 57 5 2-s2.0-17844376266
    • (2005) Pediatric Research , vol.57 , Issue.5
    • Caridi, G.1    Perfumo, F.2    Ghiggeri, G.M.3
  • 29
    • 0037821774 scopus 로고    scopus 로고
    • Pathogenesis of proteinuria: Lessons learned from nephrin and podocin
    • Jalanko H., Pathogenesis of proteinuria: lessons learned from nephrin and podocin. Pediatric Nephrology 2003 18 6 487 491 2-s2.0-0037821774 (Pubitemid 36790085)
    • (2003) Pediatric Nephrology , vol.18 , Issue.6 , pp. 487-491
    • Jalanko, H.1
  • 30
    • 1542318905 scopus 로고    scopus 로고
    • Podocin and Nephrotic Syndrome: Implications for the Clinician
    • DOI 10.1097/01.ASN.0000118135.00519.B0
    • Niaudet P., Podocin and nephrotic syndrome: implications for the clinician. Journal of the American Society of Nephrology 2004 15 3 832 834 2-s2.0-1542318905 10.1097/01.ASN.0000118135.00519.B0 (Pubitemid 38294817)
    • (2004) Journal of the American Society of Nephrology , vol.15 , Issue.3 , pp. 832-834
    • Niaudet, P.1
  • 31
    • 0035132759 scopus 로고    scopus 로고
    • CD2-associated protein and the kidney
    • DOI 10.1097/00041552-200101000-00004
    • Shaw A. S., Miner J. H., CD2-associated protein and the kidney. Current Opinion in Nephrology and Hypertension 2001 10 1 19 22 2-s2.0-0035132759 10.1097/00041552-200101000-00004 (Pubitemid 32102218)
    • (2001) Current Opinion in Nephrology and Hypertension , vol.10 , Issue.1 , pp. 19-22
    • Shaw, A.S.1    Miner, J.H.2
  • 32
    • 0344120816 scopus 로고    scopus 로고
    • CD2-associated protein and glomerular disease
    • DOI 10.1016/S0140-6736(03)14856-8
    • Wolf G., Stahl R. A. K., CD2-associated protein and glomerular disease. The Lancet 2003 362 9397 1746 1748 2-s2.0-0344120816 10.1016/S0140-6736(03) 14856-8 (Pubitemid 37468328)
    • (2003) Lancet , vol.362 , Issue.9397 , pp. 1746-1748
    • Wolf, G.1    Stahl, R.A.K.2
  • 33
    • 0035210324 scopus 로고    scopus 로고
    • Podocin, a raft-associated component of the glomerular slit diaphragm, interacts with CD2AP and nephrin
    • DOI 10.1172/JCI200112849
    • Schwarz K., Simons M., Reiser J., Saleem M. A., Faul C., Kriz W., Shaw A. S., Holzman L. B., Mundel P., Podocin, a raft-associated component of the glomerular slit diaphragm, interacts with CD2AP and nephrin. Journal of Clinical Investigation 2001 108 11 1621 1629 2-s2.0-0035210324 10.1172/JCI200112849 (Pubitemid 33144872)
    • (2001) Journal of Clinical Investigation , vol.108 , Issue.11 , pp. 1621-1629
    • Schwarz, K.1    Simons, M.2    Reiser, J.3    Saleem, M.A.4    Faul, C.5    Kriz, W.6    Shaw, A.S.7    Holzman, L.B.8    Mundel, P.9
  • 34
    • 44049087922 scopus 로고    scopus 로고
    • Neph1, a component of the kidney slit diaphragm, is tyrosine- phosphorylated by the Src family tyrosine kinase and modulates intracellular signaling by binding to Grb2
    • 2-s2.0-44049087922 10.1074/jbc.M707247200
    • Harita Y., Kurihara H., Kosako H., Tezuka T., Sekine T., Igarashi T., Hattori S., Neph1, a component of the kidney slit diaphragm, is tyrosine-phosphorylated by the Src family tyrosine kinase and modulates intracellular signaling by binding to Grb2. Journal of Biological Chemistry 2008 283 14 9177 9186 2-s2.0-44049087922 10.1074/jbc.M707247200
    • (2008) Journal of Biological Chemistry , vol.283 , Issue.14 , pp. 9177-9186
    • Harita, Y.1    Kurihara, H.2    Kosako, H.3    Tezuka, T.4    Sekine, T.5    Igarashi, T.6    Hattori, S.7
  • 35
    • 0042242818 scopus 로고    scopus 로고
    • Neph1 and nephrin interaction in the slit diaphragm is an important determinant of glomerular permeability
    • DOI 10.1172/JCI200318242
    • Liu G., Kaw B., Kurfis J., Rahmanuddin S., Kanwar Y. S., Chugh S. S., Neph1 and nephrin interaction in the slit diaphragm is an important determinant of glomerular permeability. Journal of Clinical Investigation 2003 112 2 209 221 2-s2.0-0042242818 10.1172/JCI200318242 (Pubitemid 38056357)
    • (2003) Journal of Clinical Investigation , vol.112 , Issue.2 , pp. 209-221
    • Liu, G.1    Kaw, B.2    Kurfis, J.3    Rahmanuddin, S.4    Kanwar, Y.S.5    Chugh, S.S.6
  • 37
    • 37549036286 scopus 로고    scopus 로고
    • Neph1 cooperates with nephrin to transduce a signal that induces actin polymerization
    • 2-s2.0-37549036286 10.1128/MCB.00948-07
    • Garg P., Verma R., Nihalani D., Johnstone D. B., Holzman L. B., Neph1 cooperates with nephrin to transduce a signal that induces actin polymerization. Molecular and Cellular Biology 2007 27 24 8698 8712 2-s2.0-37549036286 10.1128/MCB.00948-07
    • (2007) Molecular and Cellular Biology , vol.27 , Issue.24 , pp. 8698-8712
    • Garg, P.1    Verma, R.2    Nihalani, D.3    Johnstone, D.B.4    Holzman, L.B.5
  • 38
    • 0037270882 scopus 로고    scopus 로고
    • NEPH1 defines a novel family of podocin interacting proteins
    • 2-s2.0-0037270882
    • Sellin L., Huber T. B., Gerke P., Quack I., Pavenstädt H., Walz G., NEPH1 defines a novel family of podocin interacting proteins. The FASEB Journal 2003 17 1 115 117 2-s2.0-0037270882
    • (2003) The FASEB Journal , vol.17 , Issue.1 , pp. 115-117
    • Sellin, L.1    Huber, T.B.2    Gerke, P.3    Quack, I.4    Pavenstädt, H.5    Walz, G.6
  • 40
    • 33748417728 scopus 로고    scopus 로고
    • FSGS-associated α-actinin-4 (K256E) impairs cytoskeletal dynamics in podocytes
    • DOI 10.1038/sj.ki.5001665, PII 5001665
    • Michaud J. L. R., Chaisson K. M., Parks R. J., Kennedy C. R. J., FSGS-associated α -actinin-4 (K256E) impairs cytoskeletal dynamics in podocytes. Kidney International 2006 70 6 1054 1061 2-s2.0-33748417728 10.1038/sj.ki.5001665 (Pubitemid 44344075)
    • (2006) Kidney International , vol.70 , Issue.6 , pp. 1054-1061
    • Michaud, J.-L.R.1    Chaisson, K.M.2    Parks, R.J.3    Kennedy, C.R.J.4
  • 41
    • 40049088125 scopus 로고    scopus 로고
    • Mice with altered α-actinin-4 expression have distinct morphologic patterns of glomerular disease
    • DOI 10.1038/sj.ki.5002751, PII 5002751
    • Henderson J. M., Al-Waheeb S., Weins A., Dandapani S. V., Pollak M. R., Mice with altered α -actinin-4 expression have distinct morphologic patterns of glomerular disease. Kidney International 2008 73 6 741 750 2-s2.0-40049088125 10.1038/sj.ki.5002751 (Pubitemid 351323257)
    • (2008) Kidney International , vol.73 , Issue.6 , pp. 741-750
    • Henderson, J.M.1    Al-Waheeb, S.2    Weins, A.3    Dandapani, S.V.4    Pollak, M.R.5
  • 42
    • 58149332840 scopus 로고    scopus 로고
    • ACTN4 gene mutations and single nucleotide polymorphisms in idiopathic focal segmental glomerulosclerosis
    • 2-s2.0-58149332840 10.1159/000191198
    • Dai S., Wang Z., Pan X., Chen X., Wang W., Ren H., Feng Q., He J. C., Han B., Chen N., ACTN4 gene mutations and single nucleotide polymorphisms in idiopathic focal segmental glomerulosclerosis. Nephron 2009 111 2 c87 c94 2-s2.0-58149332840 10.1159/000191198
    • (2009) Nephron , vol.111 , Issue.2
    • Dai, S.1    Wang, Z.2    Pan, X.3    Chen, X.4    Wang, W.5    Ren, H.6    Feng, Q.7    He, J.C.8    Han, B.9    Chen, N.10
  • 46
    • 33746491157 scopus 로고    scopus 로고
    • Essential role of integrin-linked kinase in podocyte biology: Bridging the integrin and slit diaphragm signaling
    • DOI 10.1681/ASN.2006010033
    • Dai C., Stolz D. B., Bastacky S. I., St.-Arnaud R. R., Wu C., Dedhar S., Liu Y., Essential role of integrin-linked kinase in podocyte biology: bridging the integrin and slit diaphragm signaling. Journal of the American Society of Nephrology 2006 17 8 2164 2175 2-s2.0-33746491157 10.1681/ASN.2006010033 (Pubitemid 44141906)
    • (2006) Journal of the American Society of Nephrology , vol.17 , Issue.8 , pp. 2164-2175
    • Dai, C.1    Stolz, D.B.2    Bastacky, S.I.3    St.-Arnaud, R.4    Wu, C.5    Dedhar, S.6    Liu, Y.7
  • 48
    • 28244495051 scopus 로고    scopus 로고
    • TRPC6 - A new podocyte gene involved in focal segmental glomerulosclerosis
    • DOI 10.1016/j.molmed.2005.10.001, PII S1471491405002285
    • Kriz W., TRPC6-a new podocyte gene involved in focal segmental glomerulosclerosis. Trends in Molecular Medicine 2005 11 12 527 530 2-s2.0-28244495051 10.1016/j.molmed.2005.10.001 (Pubitemid 41713992)
    • (2005) Trends in Molecular Medicine , vol.11 , Issue.12 , pp. 527-530
    • Kriz, W.1
  • 49
    • 65249099647 scopus 로고    scopus 로고
    • TRPC6 mutations associated with focal segmental glomerulosclerosis cause constitutive activation of NFAT-dependent transcription
    • 2-s2.0-65249099647 10.1152/ajpcell.00077.2008
    • Schlöndorff J., Del Camino D., Carrasquillo R., Lacey V., Pollak M. R., TRPC6 mutations associated with focal segmental glomerulosclerosis cause constitutive activation of NFAT-dependent transcription. American Journal of Physiology 2009 296 3 C558 C569 2-s2.0-65249099647 10.1152/ajpcell.00077.2008
    • (2009) American Journal of Physiology , vol.296 , Issue.3
    • Schlöndorff, J.1    Del Camino, D.2    Carrasquillo, R.3    Lacey, V.4    Pollak, M.R.5
  • 51
    • 0030410436 scopus 로고    scopus 로고
    • Molecular mechanisms of glomerular injury in rat experimental membranous nephropathy (Heymann nephritis)
    • Kerjaschki D., Neale T. J., Molecular mechanisms of glomerular injury in rat experimental membranous nephropathy (Heymann nephritis). Journal of the American Society of Nephrology 1996 7 12 2518 2526 2-s2.0-0030410436 (Pubitemid 27469557)
    • (1996) Journal of the American Society of Nephrology , vol.7 , Issue.12 , pp. 2518-2526
    • Kerjaschki, D.1    Neale, T.J.2
  • 52
    • 70349621624 scopus 로고    scopus 로고
    • Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis-A review
    • 2-s2.0-70349621624 10.1007/s00431-009-1017-x
    • Löwik M. M., Groenen P. J., Levtchenko E. N., Monnens L. A., Van Den Heuvel L. P., Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis-a review. European Journal of Pediatrics 2009 168 11 1291 1304 2-s2.0-70349621624 10.1007/s00431-009-1017-x
    • (2009) European Journal of Pediatrics , vol.168 , Issue.11 , pp. 1291-1304
    • Löwik, M.M.1    Groenen, P.J.2    Levtchenko, E.N.3    Monnens, L.A.4    Van Den Heuvel, L.P.5
  • 53
    • 33748702059 scopus 로고    scopus 로고
    • WT1 and glomerular diseases
    • DOI 10.1007/s00467-006-0208-1
    • Niaudet P., Gubler M. C., WT1 and glomerular diseases. Pediatric Nephrology 2006 21 11 1653 1660 2-s2.0-33748702059 10.1007/s00467-006-0208-1 (Pubitemid 44390829)
    • (2006) Pediatric Nephrology , vol.21 , Issue.11 , pp. 1653-1660
    • Niaudet, P.1    Gubler, M.-C.2
  • 54
    • 0027209712 scopus 로고
    • The WT1 Wilms tumor gene product: A developmentally regulated transcription factor in the kidney that functions as a tumor suppressor
    • 2-s2.0-0027209712
    • Rauscher F. J., The WT1 Wilms tumor gene product: a developmentally regulated transcription factor in the kidney that functions as a tumor suppressor. The FASEB Journal 1993 7 10 896 903 2-s2.0-0027209712
    • (1993) The FASEB Journal , vol.7 , Issue.10 , pp. 896-903
    • Rauscher, F.J.1
  • 55
    • 0037087593 scopus 로고    scopus 로고
    • WT1 is a key regulator of podocyte function: Reduced expression levels cause crescentic glomerulonephritis and mesangial sclerosis
    • Guo J. K., Menke A. L., Gubler M. C., Clarke A. R., Harrison D., Hammes A., Hastie N. D., Schedl A., WT1 is a key regulator of podocyte function: reduced expression levels cause crescentic glomerulonephritis and mesangial sclerosis. Human Molecular Genetics 2002 11 6 651 659 2-s2.0-0037087593 (Pubitemid 34285136)
    • (2002) Human Molecular Genetics , vol.11 , Issue.6 , pp. 651-659
    • Guo, J.-K.1    Menke, A.L.2    Gubler, M.-C.3    Clarke, A.R.4    Harrison, D.5    Hammes, A.6    Hastie, N.D.7    Schedl, A.8
  • 56
    • 0035839099 scopus 로고    scopus 로고
    • Two splice variants of the wilms' tumor 1 gene have distinct functions during sex determination and nephron formation
    • DOI 10.1016/S0092-8674(01)00453-6
    • Hammes A., Guo J. K., Lutsch G., Leheste J. R., Landrock D., Ziegler U., Gubler M. C., Schedl A., Two splice variants of the wilms' tumor 1 gene have distinct functions during sex determination and nephron formation. Cell 2001 106 3 319 329 2-s2.0-0035839099 10.1016/S0092-8674(01)00453-6 (Pubitemid 32772616)
    • (2001) Cell , vol.106 , Issue.3 , pp. 319-329
    • Hammes, A.1    Guo, J.-K.2    Lutsch, G.3    Leheste, J.-R.4    Landrock, D.5    Ziegler, U.6    Gubler, M.-C.7    Schedl, A.8
  • 57
    • 0032921040 scopus 로고    scopus 로고
    • WT1 and PAX-2 podocyte expression in Denys-Drash syndrome and isolated diffuse mesangial sclerosis
    • Yang Y., Jeanpierre C., Dressler G. R., Lacoste M., Niaudet P., Gubler M. C., WT1 and PAX-2 podocyte expression in Denys-Drash syndrome and isolated diffuse mesangial sclerosis. American Journal of Pathology 1999 154 1 181 192 2-s2.0-0032921040 (Pubitemid 29031625)
    • (1999) American Journal of Pathology , vol.154 , Issue.1 , pp. 181-192
    • Yang, Y.1    Jeanpierre, C.2    Dressler, G.R.3    Lacoste, M.4    Niaudet, P.5    Gubler, M.-C.6
  • 59
    • 0035059468 scopus 로고    scopus 로고
    • Clinical spectrum of Denys-Drash and Frasier syndrome
    • DOI 10.1007/s004670000541
    • McTaggart S. J., Algar E., Chow C. W., Powell H. R., Jones C. L., Clinical spectrum of Denys-Drash and Frasier syndrome. Pediatric Nephrology 2001 16 4 335 339 2-s2.0-0035059468 10.1007/s004670000541 (Pubitemid 32366667)
    • (2001) Pediatric Nephrology , vol.16 , Issue.4 , pp. 335-339
    • McTaggart, S.J.1    Algar, E.2    Chow, C.W.3    Powell, H.R.4    Jones, C.L.5
  • 60
    • 0032786044 scopus 로고    scopus 로고
    • Nephrotic syndrome and end-stage renal disease with WT1 mutation detected at 3 years
    • 2-s2.0-0032786044 10.1007/s004670050702
    • Ito S., Ikeda M., Takata A., Kikuchi H., Hata J. I., Honda M., Nephrotic syndrome and end-stage renal disease with WT1 mutation detected at 3 years. Pediatric Nephrology 1999 13 9 790 791 2-s2.0-0032786044 10.1007/s004670050702
    • (1999) Pediatric Nephrology , vol.13 , Issue.9 , pp. 790-791
    • Ito, S.1    Ikeda, M.2    Takata, A.3    Kikuchi, H.4    Hata, J.I.5    Honda, M.6
  • 61
    • 84857123332 scopus 로고    scopus 로고
    • Urinary exosomal WT1 in childhood nephrotic syndrome
    • Lee H., Han K. H., Lee S. E., Urinary exosomal WT1 in childhood nephrotic syndrome. Pediatric Nephrology 2012 27 2 317 320
    • (2012) Pediatric Nephrology , vol.27 , Issue.2 , pp. 317-320
    • Lee, H.1    Han, K.H.2    Lee, S.E.3
  • 62
    • 9644281578 scopus 로고    scopus 로고
    • The major podocyte protein nephrin is transcriptionally activated by the Wilms' tumor suppressor WT1
    • DOI 10.1097/01.ASN.0000146687.99058.25
    • Wagner N., Wagner K. D., Xing Y., Scholz H., Schedl A., The major podocyte protein nephrin is transcriptionally activated by the Wilms' tumor suppressor WT1. Journal of the American Society of Nephrology 2004 15 12 3044 3051 2-s2.0-9644281578 10.1097/01.ASN.0000146687.99058.25 (Pubitemid 39578836)
    • (2004) Journal of the American Society of Nephrology , vol.15 , Issue.12 , pp. 3044-3051
    • Wagner, N.1    Wagner, K.-D.2    Xing, Y.3    Scholz, H.4    Schedl, A.5
  • 63
    • 0035856480 scopus 로고    scopus 로고
    • WT1 regulates the expression of the major glomerular podocyte membrane protein Podocalyxin
    • DOI 10.1016/S0960-9822(01)00560-7
    • Palmer R. E., Kotsianti A., Cadman B., Boyd T., Gerald W., Haber D. A., WT1 regulates the expression of the major glomerular podocyte membrane protein Podocalyxin. Current Biology 2001 11 22 1805 1809 2-s2.0-0035856480 10.1016/S0960-9822(01)00560-7 (Pubitemid 33092171)
    • (2001) Current Biology , vol.11 , Issue.22 , pp. 1805-1809
    • Palmer, R.E.1    Kotsianti, A.2    Cadman, B.3    Boyd, T.4    Gerald, W.5    Haber, D.A.6
  • 64
    • 49949109926 scopus 로고    scopus 로고
    • New insights into the function of the Wilms tumor suppressor gene WT1 in podocytes
    • 2-s2.0-49949109926 10.1152/ajprenal.00597.2007
    • Morrison A. A., Viney R. L., Saleem M. A., Ladomery M. R., New insights into the function of the Wilms tumor suppressor gene WT1 in podocytes. American Journal of Physiology 2008 295 1 F12 F17 2-s2.0-49949109926 10.1152/ajprenal. 00597.2007
    • (2008) American Journal of Physiology , vol.295 , Issue.1
    • Morrison, A.A.1    Viney, R.L.2    Saleem, M.A.3    Ladomery, M.R.4
  • 66
    • 33751540445 scopus 로고    scopus 로고
    • A new piece in the nephrotic puzzle
    • DOI 10.1038/ng1206-1360, PII NG12061360
    • Quaggin S. E., A new piece in the nephrotic puzzle. Nature Genetics 2006 38 12 1360 1361 2-s2.0-33751540445 10.1038/ng1206-1360 (Pubitemid 44837553)
    • (2006) Nature Genetics , vol.38 , Issue.12 , pp. 1360-1361
    • Quaggin, S.E.1
  • 67
    • 34547851696 scopus 로고    scopus 로고
    • Familial nephrotic syndrome: PLCE1 enters the fray
    • DOI 10.1093/ndt/gfm098
    • Jefferson J. A., Shankland S. J., Familial nephrotic syndrome: PLCE1 enters the fray. Nephrology Dialysis Transplantation 2007 22 7 1849 1852 2-s2.0-34547851696 10.1093/ndt/gfm098 (Pubitemid 47244751)
    • (2007) Nephrology Dialysis Transplantation , vol.22 , Issue.7 , pp. 1849-1852
    • Jefferson, J.A.1    Shankland, S.J.2
  • 68
    • 38349026841 scopus 로고    scopus 로고
    • Identification of BRAF as a new interactor of PLC ε 1, the protein mutated in nephrotic syndrome type 3
    • 2-s2.0-38349026841 10.1152/ajprenal.00345.2007
    • Chaib H., Hoskins B. E., Ashraf S., Goyal M., Wiggins R. C., Hildebrandt F., Identification of BRAF as a new interactor of PLC ε 1, the protein mutated in nephrotic syndrome type 3. American Journal of Physiology 2008 294 1 F93 F99 2-s2.0-38349026841 10.1152/ajprenal.00345.2007
    • (2008) American Journal of Physiology , vol.294 , Issue.1
    • Chaib, H.1    Hoskins, B.E.2    Ashraf, S.3    Goyal, M.4    Wiggins, R.C.5    Hildebrandt, F.6
  • 69
    • 70350656203 scopus 로고    scopus 로고
    • Kidney disease in nail-patella syndrome
    • 2-s2.0-70350656203 10.1007/s00467-008-0836-8
    • Lemley K. V., Kidney disease in nail-patella syndrome. Pediatric Nephrology 2009 24 12 2345 2354 2-s2.0-70350656203 10.1007/s00467-008-0836-8
    • (2009) Pediatric Nephrology , vol.24 , Issue.12 , pp. 2345-2354
    • Lemley, K.V.1
  • 70
    • 0037338559 scopus 로고    scopus 로고
    • Nail patella syndrome: A review of the phenotype aided by developmental biology
    • Sweeney E., Fryer A., Mountford R., Green A., McIntosh I., Nail patella syndrome: a review of the phenotype aided by developmental biology. Journal of Medical Genetics 2003 40 3 153 162 2-s2.0-0037338559 (Pubitemid 36315385)
    • (2003) Journal of Medical Genetics , vol.40 , Issue.3 , pp. 153-162
    • Sweeney, E.1    Fryer, A.2    Mountford, R.3    Green, A.4    McIntosh, I.5
  • 72
    • 0014890909 scopus 로고
    • Ultrastructure of the kidney in the nephropathy of the nailpatella syndrome
    • 2-s2.0-0014890909
    • Del Pozo E., Lapp H., Ultrastructure of the kidney in the nephropathy of the nailpatella syndrome. American Journal of Clinical Pathology 1970 54 6 845 851 2-s2.0-0014890909
    • (1970) American Journal of Clinical Pathology , vol.54 , Issue.6 , pp. 845-851
    • Del Pozo, E.1    Lapp, H.2
  • 73
    • 0036120564 scopus 로고    scopus 로고
    • Transcriptional induction of slit diaphragm genes by Lmx1b is required in podocyte differentiation
    • DOI 10.1172/JCI200213954
    • Miner J. H., Morello R., Andrews K. L., Li C., Antignac C., Shaw A. S., Lee B., Transcriptional induction of slit diaphragm genes by Lmx1b is required in podocyte differentiation. Journal of Clinical Investigation 2002 109 8 1065 1072 2-s2.0-0036120564 10.1172/JCI200213954 (Pubitemid 34408581)
    • (2002) Journal of Clinical Investigation , vol.109 , Issue.8 , pp. 1065-1072
    • Miner, J.H.1    Morello, R.2    Andrews, K.L.3    Li, C.4    Antignac, C.5    Shaw, A.S.6    Lee, B.7
  • 74
    • 0031747153 scopus 로고    scopus 로고
    • Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndrome
    • DOI 10.1038/ng0598-51
    • Chen H., Lun Y., Ovchinnikov D., Kokubo H., Oberg K. C., Pepicelli C. V., Gan L., Lee B., Johnson R. L., Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndrome. Nature Genetics 1998 19 1 51 55 2-s2.0-0031747153 10.1038/ng0598-51 (Pubitemid 28242022)
    • (1998) Nature Genetics , vol.19 , Issue.1 , pp. 51-55
    • Chen, H.1    Lun, Y.2    Ovchinnikov, D.3    Kokubo, H.4    Oberg, K.C.5    Pepicelli, C.V.6    Gan, L.7    Lee, B.8    Johnson, R.L.9
  • 75
    • 70349914303 scopus 로고    scopus 로고
    • The transcriptional regulation of podocin (NPHS2) by Lmx1b and a promoter single nucleotide polymorphism
    • 2-s2.0-70349914303 10.2478/s11658-009-0026-0
    • Harendza S., Stahl R. A. K., Schneider A., The transcriptional regulation of podocin (NPHS2) by Lmx1b and a promoter single nucleotide polymorphism. Cellular and Molecular Biology Letters 2009 14 4 679 691 2-s2.0-70349914303 10.2478/s11658-009-0026-0
    • (2009) Cellular and Molecular Biology Letters , vol.14 , Issue.4 , pp. 679-691
    • Harendza, S.1    Stahl, R.A.K.2    Schneider, A.3
  • 77
    • 0038512591 scopus 로고    scopus 로고
    • Podocyte differentiation and hereditary proteinuria/nephrotic syndromes
    • supplement 1 2-s2.0-0038512591
    • Gubler M. C., Podocyte differentiation and hereditary proteinuria/nephrotic syndromes. Journal of the American Society of Nephrology 2003 14 supplement 1 S22 S26 2-s2.0-0038512591
    • (2003) Journal of the American Society of Nephrology , vol.14
    • Gubler, M.C.1
  • 78
    • 28444490314 scopus 로고    scopus 로고
    • R561C missense mutation in the SMARCAL1 gene associated with mild Schimke immuno-osseous dysplasia
    • DOI 10.1007/s00467-005-2047-x
    • Bökenkamp A., deJong M., van Wijk J. A., Block D., van Hagen J. M., Ludwig M., R561C missense mutation in the SMARCAL1 gene associated with mild Schimke immuno-osseous dysplasia. Pediatric Nephrology 2005 20 12 1724 1728 2-s2.0-28444490314 10.1007/s00467-005-2047-x (Pubitemid 41722955)
    • (2005) Pediatric Nephrology , vol.20 , Issue.12 , pp. 1724-1728
    • Bokenkamp, A.1    De Jong, M.2    Van Wijk, J.A.3    Block, D.4    Van Hagen, J.M.5    Ludwig, M.6
  • 79
    • 41349106442 scopus 로고    scopus 로고
    • Schimke immuno-osseous dysplasia: Expression of SMARCAL1 in blood and kidney provides novel insight into disease phenotype
    • DOI 10.1203/PDR.0b013e31816721cc, PII 0000645020080400000012
    • Dekel B., Metsuyanim S., Goldstein N., Pode-Shakked N., Kovalski Y., Cohen Y., Davidovits M., Anikster Y., Schimke immuno-osseous dysplasia: expression of SMARCAL1 in blood and kidney provides novel insight into disease phenotype. Pediatric Research 2008 63 4 398 403 2-s2.0-41349106442 10.1203/PDR.0b013e31816721cc (Pubitemid 351450586)
    • (2008) Pediatric Research , vol.63 , Issue.4 , pp. 398-403
    • Dekel, B.1    Metsuyanim, S.2    Goldstein, N.3    Pode-Shakked, N.4    Kovalski, Y.5    Cohen, Y.6    Davidovits, M.7    Anikster, Y.8
  • 80
    • 69049119143 scopus 로고    scopus 로고
    • SMARCAL1 mutations: A cause of prepubertal idiopathic steroid-resistant nephrotic syndrome
    • 2-s2.0-69049119143 10.1203/PDR.0b013e3181998a74
    • Zivicnjak M., Franke D., Zenker M., Hoyer J., Lücke T., Pape L., Ehrich J. H. H., SMARCAL1 mutations: a cause of prepubertal idiopathic steroid-resistant nephrotic syndrome. Pediatric Research 2009 65 5 564 568 2-s2.0-69049119143 10.1203/PDR.0b013e3181998a74
    • (2009) Pediatric Research , vol.65 , Issue.5 , pp. 564-568
    • Zivicnjak, M.1    Franke, D.2    Zenker, M.3    Hoyer, J.4    Lücke, T.5    Pape, L.6    Ehrich, J.H.H.7
  • 81
    • 84861121701 scopus 로고    scopus 로고
    • Penetrance of biallelic SMARCAL1 mutations is associated with environmental and genetic disturbances of gene expression
    • Baradaran-Heravi A., Cho K. S., Tolhuis B., Penetrance of biallelic SMARCAL1 mutations is associated with environmental and genetic disturbances of gene expression. Human Molecular Genetics 2012 21 11 2575 2587
    • (2012) Human Molecular Genetics , vol.21 , Issue.11 , pp. 2575-2587
    • Baradaran-Heravi, A.1    Cho, K.S.2    Tolhuis, B.3
  • 84
    • 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., Grünfeld J., Gubler M., Antignac C., Heidet L., Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndromes. Journal of the American Society of Nephrology 2002 13 1 65 74 2-s2.0-0036138503 (Pubitemid 34042012)
    • (2002) Journal of the American Society of Nephrology , vol.13 , Issue.1 , pp. 65-74
    • Arrondel, C.1    Vodovar, N.2    Knebelmann, B.3    Grunfeld, J.4    Gubler, M.5    Antignac, C.6    Heidet, L.7
  • 85
    • 0024209817 scopus 로고
    • Ultrastructural organization of contractile and cytoskeletal proteins in glomerular podocytes of chicken, rat, and man
    • Drenckhahn D., Franke R. P., Ultrastructural organization of contractile and cytoskeletal proteins in glomerular podocytes of chicken, rat, and man. Laboratory Investigation 1988 59 5 673 682 2-s2.0-0024209817 (Pubitemid 19009729)
    • (1988) Laboratory Investigation , vol.59 , Issue.5 , pp. 673-682
    • Drenckhahn, D.1    Franke, R.-P.2
  • 86
    • 79956071512 scopus 로고    scopus 로고
    • Podocyte-specific deletion of Myh9 encoding nonmuscle myosin heavy chain 2A predisposes mice to glomerulopathy
    • 2-s2.0-79956071512 10.1128/MCB.05234-11
    • Johnstone D. B., Zhang J., George B., Léon C., Gachet C., Wong H., Parekh R., Holzman L. B., Podocyte-specific deletion of Myh9 encoding nonmuscle myosin heavy chain 2A predisposes mice to glomerulopathy. Molecular and Cellular Biology 2011 31 10 2162 2170 2-s2.0-79956071512 10.1128/MCB.05234-11
    • (2011) Molecular and Cellular Biology , vol.31 , Issue.10 , pp. 2162-2170
    • Johnstone, D.B.1    Zhang, J.2    George, B.3    Léon, C.4    Gachet, C.5    Wong, H.6    Parekh, R.7    Holzman, L.B.8
  • 87
    • 84859946262 scopus 로고    scopus 로고
    • Glomerular MYH9 expression is reduced by HIV-1
    • Hays T., D'Agati V. D., Garellek J. A., Glomerular MYH9 expression is reduced by HIV-1. AIDS 2012 26 7 797 803
    • (2012) AIDS , vol.26 , Issue.7 , pp. 797-803
    • Hays, T.1    D'Agati, V.D.2    Garellek, J.A.3
  • 88
    • 84859314693 scopus 로고    scopus 로고
    • Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans
    • 10.1093/ndt/gfr522
    • Cooke J. N., Bostrom M. A., Hicks P. J., Polymorphisms in MYH9 are associated with diabetic nephropathy in European Americans. Nephrology Dialysis Transplantation 2012 27 4 1505 1511 10.1093/ndt/gfr522
    • (2012) Nephrology Dialysis Transplantation , vol.27 , Issue.4 , pp. 1505-1511
    • Cooke, J.N.1    Bostrom, M.A.2    Hicks, P.J.3
  • 90
    • 80053570634 scopus 로고    scopus 로고
    • Progressive myoclonus epilepsy with nephropathy C1q due to SCARB2/LIMP-2 deficiency: Clinical report of two siblings
    • 2-s2.0-79960380325 10.1016/j.seizure.2011.06.018
    • Chaves J., Beirão I., Balreira A., Gaspar P., Caiola D., Sá M. C., Lima J. L., Progressive myoclonus epilepsy with nephropathy C1q due to SCARB2/LIMP-2 deficiency: clinical report of two siblings. Seizure 2011 20 9 738 740 2-s2.0-79960380325 10.1016/j.seizure.2011.06.018
    • (2011) Seizure , vol.20 , Issue.9 , pp. 738-740
    • Chaves, J.1    Beirão, I.2    Balreira, A.3    Gaspar, P.4    Caiola, D.5    Sá, M.C.6    Lima, J.L.7
  • 91
    • 46249129691 scopus 로고    scopus 로고
    • A nonsense mutation in the LIMP-2 gene associated with progressive myoclonic epilepsy and nephrotic syndrome
    • DOI 10.1093/hmg/ddn124
    • Balreira A., Gaspar P., Caiola D., Chaves J., Beirão I., Lima J. L., Azevedo J. E., Miranda M. C. S., A nonsense mutation in the LIMP-2 gene associated with progressive myoclonic epilepsy and nephrotic syndrome. Human Molecular Genetics 2008 17 14 2238 2243 2-s2.0-46249129691 10.1093/hmg/ddn124 (Pubitemid 351911989)
    • (2008) Human Molecular Genetics , vol.17 , Issue.14 , pp. 2238-2243
    • Balreira, A.1    Gaspar, P.2    Caiola, D.3    Chaves, J.4    Beirao, I.5    Lima, J.L.6    Azevedo, J.E.7    Miranda, M.C.S.8
  • 92
    • 36048935960 scopus 로고    scopus 로고
    • LIMP-2 Is a Receptor for Lysosomal Mannose-6-Phosphate-Independent Targeting of β-Glucocerebrosidase
    • DOI 10.1016/j.cell.2007.10.018, PII S0092867407012901
    • Reczek D., Schwake M., Schröder J., Hughes H., Blanz J., Jin X., Brondyk W., Van Patten S., Edmunds T., Saftig P., LIMP-2 is a receptor for lysosomal mannose-6-phosphate-independent targeting of β -glucocerebrosidase. Cell 2007 131 4 770 783 2-s2.0-36048935960 10.1016/j.cell.2007.10.018 (Pubitemid 350087202)
    • (2007) Cell , vol.131 , Issue.4 , pp. 770-783
    • Reczek, D.1    Schwake, M.2    Schroder, J.3    Hughes, H.4    Blanz, J.5    Jin, X.6    Brondyk, W.7    Van Patten, S.8    Edmunds, T.9    Saftig, P.10
  • 94
    • 80054927374 scopus 로고    scopus 로고
    • Novel SCARB2 mutation in action myoclonus-renal failure syndrome and evaluation of SCARB2 mutations in isolated AMRF features
    • 10.1186/1471-2377-11-134
    • Hopfner F., Schormair B., Knauf F., Novel SCARB2 mutation in action myoclonus-renal failure syndrome and evaluation of SCARB2 mutations in isolated AMRF features. BMC Neurology 2011 11 134 10.1186/1471-2377-11-134
    • (2011) BMC Neurology , vol.11 , pp. 134
    • Hopfner, F.1    Schormair, B.2    Knauf, F.3
  • 97
    • 79960881464 scopus 로고    scopus 로고
    • MYO1E, focal segmental glomerulosclerosis, and the cytoskeleton
    • 2-s2.0-79960881464 10.1056/NEJMe1106093
    • Ingelfinger J. R., MYO1E, focal segmental glomerulosclerosis, and the cytoskeleton. New England Journal of Medicine 2011 365 4 368 369 2-s2.0-79960881464 10.1056/NEJMe1106093
    • (2011) New England Journal of Medicine , vol.365 , Issue.4 , pp. 368-369
    • Ingelfinger, J.R.1
  • 99
    • 84864378898 scopus 로고    scopus 로고
    • Implication of CD38 gene in podocyte epithelial-to-mesenchymal transition and glomerular sclerosis
    • In press 10.1111/j.1582-4934.2011.01462.x
    • Boini K. M., Xia M., Xiong J., Implication of CD38 gene in podocyte epithelial-to-mesenchymal transition and glomerular sclerosis. Journal of Cellular and Molecular Medicine. In press 10.1111/j.1582-4934.2011.01462.x
    • Journal of Cellular and Molecular Medicine
    • Boini, K.M.1    Xia, M.2    Xiong, J.3
  • 100
    • 84855433172 scopus 로고    scopus 로고
    • Blood pressure influences end-stage renal disease of Cd151 knockout mice
    • 10.1172/JCI58878
    • Sachs N., Claessen N., Aten J., Blood pressure influences end-stage renal disease of Cd151 knockout mice. Journal of Clinical Investigation 2012 122 1 348 358 10.1172/JCI58878
    • (2012) Journal of Clinical Investigation , vol.122 , Issue.1 , pp. 348-358
    • Sachs, N.1    Claessen, N.2    Aten, J.3
  • 101
    • 4444324996 scopus 로고    scopus 로고
    • Progressive nephropathy associated with mitochondrial tRNA gene mutation
    • Dinour D., Mini S., Polak-Charcon S., Lotan D., Holtzman E. J., Progressive nephropathy associated with mitochondrial tRNA gene mutation. Clinical Nephrology 2004 62 2 149 154 2-s2.0-4444324996 (Pubitemid 39162768)
    • (2004) Clinical Nephrology , vol.62 , Issue.2 , pp. 149-154
    • Dinour, D.1    Mini, S.2    Polak-Charcon, S.3    Lotan, D.4    Holtzman, E.J.5
  • 102
    • 34248195476 scopus 로고    scopus 로고
    • Endogenous synthesis of coenzyme Q in eukaryotes
    • DOI 10.1016/j.mito.2007.03.007, PII S1567724907000645, The Roled of Coenzyme Q in Cellular Metabolism: Current Biological and Clinical Aspects
    • Tran U. C., Clarke C. F., Endogenous synthesis of coenzyme Q in eukaryotes. Mitochondrion 2007 7 S62 S71 2-s2.0-34248195476 10.1016/j.mito.2007. 03.007 (Pubitemid 46712237)
    • (2007) Mitochondrion , vol.7 , Issue.SUPPL.
    • Tran, U.C.1    Clarke, C.F.2
  • 105
    • 57349192861 scopus 로고    scopus 로고
    • Coenzyme Q10 supplementation rescues renal disease in Pdss2 kd/kd mice with mutations in prenyl diphosphate synthase subunit 2
    • 2-s2.0-57349192861 10.1152/ajprenal.90445.2008
    • Saiki R., Lunceford A. L., Shi Y., Marbois B., King R., Pachuski J., Kawamukai M., Gasser D. L., Clarke C. F., Coenzyme Q10 supplementation rescues renal disease in Pdss2 kd/kd mice with mutations in prenyl diphosphate synthase subunit 2. American Journal of Physiology 2008 295 5 F1535 F1544 2-s2.0-57349192861 10.1152/ajprenal.90445.2008
    • (2008) American Journal of Physiology , vol.295 , Issue.5
    • Saiki, R.1    Lunceford, A.L.2    Shi, Y.3    Marbois, B.4    King, R.5    Pachuski, J.6    Kawamukai, M.7    Gasser, D.L.8    Clarke, C.F.9
  • 106
    • 84856239775 scopus 로고    scopus 로고
    • Ubiquinone (coenzyme Q10) prevents renal mitochondrial dysfunction in an experimental model of type 2 diabetes
    • 10.1016/j.freeradbiomed.2011.11.017
    • Sourris K. C., Harcourt B. E., Tang P. H., Ubiquinone (coenzyme Q10) prevents renal mitochondrial dysfunction in an experimental model of type 2 diabetes. Free Radical Biology & Medicine 2012 52 3 716 723 10.1016/j.freeradbiomed.2011.11.017
    • (2012) Free Radical Biology & Medicine , vol.52 , Issue.3 , pp. 716-723
    • Sourris, K.C.1    Harcourt, B.E.2    Tang, P.H.3
  • 107
    • 84862528769 scopus 로고    scopus 로고
    • Coenzyme Q10 prevents GDP-sensitive mitochondrial uncoupling, glomerular hyperfiltration and proteinuria in kidneys from db/db mice as a model of type 2 diabetes
    • Persson M. F., Franzen S., Catrina S. B., Coenzyme Q10 prevents GDP-sensitive mitochondrial uncoupling, glomerular hyperfiltration and proteinuria in kidneys from db/db mice as a model of type 2 diabetes. Diabetologia 2012 55 5 1535 1543
    • (2012) Diabetologia , vol.55 , Issue.5 , pp. 1535-1543
    • Persson, M.F.1    Franzen, S.2    Catrina, S.B.3
  • 108
    • 0011818676 scopus 로고    scopus 로고
    • MELAS as an example of a mitochondrial disease
    • Piechota J., Mroczek K., Bartnik E., MELAS as an example of a mitochondrial disease. Journal of Applied Genetics 2001 42 3 351 358 2-s2.0-0011818676 (Pubitemid 33681392)
    • (2001) Journal of Applied Genetics , vol.42 , Issue.3 , pp. 351-358
    • Piechota, J.1    Mroczek, K.2    Bartnik, E.3
  • 109
    • 0032976998 scopus 로고    scopus 로고
    • Functional and morphological abnormalities of mitochondria harbouring the tRNA(Leu(UUR)) mutation in mitochondrial DNA derived from patients with maternally inherited diabetes and deafness (MIDD) and progressive kidney disease
    • DOI 10.1007/s001250051183
    • Van Den Ouweland J. M. W., Maechler P., Wollheim C. B., Attardi G., Maassen J. A., Functional and morphological abnormalities of mitochondria harbouring the tRNA(Leu(UUR)) mutation in mitochondrial DNA derived from patients with maternally inherited diabetes and deafness (MIDD) and progressive kidney disease. Diabetologia 1999 42 4 485 492 2-s2.0-0032976998 10.1007/s001250051183 (Pubitemid 29148409)
    • (1999) Diabetologia , vol.42 , Issue.4 , pp. 485-492
    • Van Den Ouweland, J.M.W.1    Maechler, P.2    Wollheim, C.B.3    Attardi, G.4    Maassen, J.A.5
  • 111
    • 0347268935 scopus 로고    scopus 로고
    • A boy with mitochondrial disease: Asymptomatic proteinuria without neuromyopathy
    • DOI 10.1007/s00467-003-1318-7
    • Ueda Y., Ando A., Nagata T., Yanagida H., Yagi K., Sugimoto K., Okada M., Takemura T., A boy with mitochondrial disease: asymptomatic proteinuria without neuromyopathy. Pediatric Nephrology 2004 19 1 107 110 2-s2.0-0347268935 10.1007/s00467-003-1318-7 (Pubitemid 38088261)
    • (2004) Pediatric Nephrology , vol.19 , Issue.1 , pp. 107-110
    • Ueda, Y.1    Ando, A.2    Nagata, T.3    Yanagida, H.4    Yagi, K.5    Sugimoto, K.6    Okada, M.7    Takemura, T.8
  • 112
    • 70350425652 scopus 로고    scopus 로고
    • Cardiomyopathy and kidney disease in a patient with maternally inherited diabetes and deafness caused by the 3243A>G mutation of mitochondrial DNA
    • 2-s2.0-70350425652 10.1159/000252811
    • Azevedo O., Vilarinho L., Almeida F., Ferreira F., Guardado J., Ferreira M., Lourenço A., Medeiros R., Almeida J., Cardiomyopathy and kidney disease in a patient with maternally inherited diabetes and deafness caused by the 3243A>G mutation of mitochondrial DNA. Cardiology 2009 115 1 71 74 2-s2.0-70350425652 10.1159/000252811
    • (2009) Cardiology , vol.115 , Issue.1 , pp. 71-74
    • Azevedo, O.1    Vilarinho, L.2    Almeida, F.3    Ferreira, F.4    Guardado, J.5    Ferreira, M.6    Lourenço, A.7    Medeiros, R.8    Almeida, J.9
  • 113
    • 0242594752 scopus 로고    scopus 로고
    • Tyr Gene Associated with Atypical Mitochondrial Cytopathy Presenting with Focal Segmental Glomerulosclerosis
    • Scaglia F., Vogel H., Hawkins E. P., Vladutiu G. D., Liu L. L., Wong L. J. C., Novel homoplasmic mutation in the mitochondrial tRNATyr gene associated with atypical mitochondrial cytopathy presenting with focal segmental glomerulosclerosis. American Journal of Medical Genetics 2003 123 2 172 178 2-s2.0-0242594752 (Pubitemid 37429599)
    • (2003) American Journal of Medical Genetics , vol.123 , Issue.2 A , pp. 172-178
    • Scaglia, F.1    Vogel, H.2    Hawkins, E.P.3    Vladutiu, G.D.4    Liu, L.-L.5    Wong, L.-J.C.6
  • 116
    • 0346656642 scopus 로고    scopus 로고
    • Angiotensin II-induced proteinuria and expression of the podocyte slit pore membrane protein, nephrin [3]
    • DOI 10.1093/ndt/gfg509
    • Langham R. G., Kelly D. J., Cox A. J., Gow R. M., Holthofer H., Gilbert R. E., Angiotensin II-induced proteinuria and expression of the podocyte slit pore membrane protein, nephrin [3]. Nephrology Dialysis Transplantation 2004 19 1 262 263 2-s2.0-0346656642 10.1093/ndt/gfg509 (Pubitemid 38072650)
    • (2004) Nephrology Dialysis Transplantation , vol.19 , Issue.1 , pp. 262-263
    • Langham, R.G.1    Kelly, D.J.2    Cox, A.J.3    Gow, R.M.4    Holthofer, H.5    Gilbert, R.E.6
  • 117
    • 79952767139 scopus 로고    scopus 로고
    • Role of angiotensin II in the development of nephropathy and podocytopathy of diabetes
    • 2-s2.0-79952767139
    • Campbell K. N., Raij L., Mundel P., Role of angiotensin II in the development of nephropathy and podocytopathy of diabetes. Current Diabetes Reviews 2011 7 1 3 7 2-s2.0-79952767139
    • (2011) Current Diabetes Reviews , vol.7 , Issue.1 , pp. 3-7
    • Campbell, K.N.1    Raij, L.2    Mundel, P.3
  • 118
    • 46649084424 scopus 로고    scopus 로고
    • Reduction of proteinuria with angiotensin receptor blockers
    • DOI 10.1038/ncpcardio0806, PII NCPCARDIO0806
    • Galle J., Reduction of proteinuria with angiotensin receptor blockers. Nature Clinical Practice Cardiovascular Medicine 2008 5 supplement 1 S36 S43 (Pubitemid 351935845)
    • (2008) Nature Clinical Practice Cardiovascular Medicine , vol.5 , Issue.SUPPL. 1
    • Galle, J.1
  • 119
    • 2442621619 scopus 로고    scopus 로고
    • Discovery and development of bevacizumab, an anti-VEGF antibody for treating cancer
    • Ferrara N., Hillan K. J., Gerber H. P., Novotny W., Discovery and development of bevacizumab, an anti-VEGF antibody for treating cancer. Nature Reviews Drug Discovery 2004 3 5 391 400 2-s2.0-2442621619 (Pubitemid 38618122)
    • (2004) Nature Reviews Drug Discovery , vol.3 , Issue.5 , pp. 391-400
    • Ferrara, N.1    Hillan, K.J.2    Gerber, H.-P.3    Novotny, W.4
  • 120
    • 0037631361 scopus 로고    scopus 로고
    • Neutralization of circulating vascular endothelial growth factor (VEGF) by anti-VEGF antibodies and soluble VEGF receptor 1 (sFlt-1) induces proteinuria
    • DOI 10.1074/jbc.C300012200
    • Sugimoto H., Hamanog Y., Charytan D., Cosgrove D., Kieran M., Sudhakar A., Kalluri R., Neutralization of circulating vascular endothelial growth factor (VEGF) by anti-VEGF antibodies and soluble VEGF receptor 1 (sFlt-1) induces proteinuria. Journal of Biological Chemistry 2003 278 15 12605 12608 2-s2.0-0037631361 10.1074/jbc.C300012200 (Pubitemid 36800018)
    • (2003) Journal of Biological Chemistry , vol.278 , Issue.15 , pp. 12605-12608
    • Sugimoto, H.1    Hamanog, Y.2    Charytan, D.3    Cosgrove, D.4    Kieran, M.5    Sudhakar, A.6
  • 121
    • 79954525448 scopus 로고    scopus 로고
    • Circulating FGF21 levels are progressively increased from the early to end stages of chronic kidney diseases and are associated with renal function in Chinese
    • 2-s2.0-79954525448 10.1371/journal.pone.0018398 e18398
    • Lin Z., Zhou Z., Liu Y., Gong Q., Yan X., Xiao J., Wang X., Lin S., Feng W., Li X., Circulating FGF21 levels are progressively increased from the early to end stages of chronic kidney diseases and are associated with renal function in Chinese. PLoS ONE 2011 6 4 2-s2.0-79954525448 10.1371/journal.pone.0018398 e18398
    • (2011) PLoS ONE , vol.6 , Issue.4
    • Lin, Z.1    Zhou, Z.2    Liu, Y.3    Gong, Q.4    Yan, X.5    Xiao, J.6    Wang, X.7    Lin, S.8    Feng, W.9    Li, X.10
  • 124
    • 79959238107 scopus 로고    scopus 로고
    • Mitochondrial dysfunction mediates aldosterone-induced podocyte damage: A therapeutic target of PPAR γ
    • Zhu C., Huang S., Yuan Y., Mitochondrial dysfunction mediates aldosterone-induced podocyte damage: a therapeutic target of PPAR γ American Journal of Pathology 2011 178 5 2020 2031
    • (2011) American Journal of Pathology , vol.178 , Issue.5 , pp. 2020-2031
    • Zhu, C.1    Huang, S.2    Yuan, Y.3
  • 125
    • 37349107870 scopus 로고    scopus 로고
    • The mTOR inhibitor everolimus induces proteinuria and renal deterioration in the remnant kidney model in the rat
    • DOI 10.1097/01.tp.0000282866.92367.99, PII 0000789020071215000016
    • Vogelbacher R., Wittmann S., Braun A., Daniel C., Hugo C., The mTOR inhibitor everolimus induces proteinuria and renal deterioration in the remnant kidney model in the rat. Transplantation 2007 84 11 1492 1499 2-s2.0-37349107870 10.1097/01.tp.0000282866.92367.99 (Pubitemid 350294725)
    • (2007) Transplantation , vol.84 , Issue.11 , pp. 1492-1499
    • Vogelbacher, R.1    Wittmann, S.2    Braun, A.3    Daniel, C.4    Hugo, C.5
  • 126
    • 79957894759 scopus 로고    scopus 로고
    • The targeted podocyte
    • 2-s2.0-79957894759 10.1172/JCI57935
    • Fogo A. B., The targeted podocyte. Journal of Clinical Investigation 2011 121 6 2142 2145 2-s2.0-79957894759 10.1172/JCI57935
    • (2011) Journal of Clinical Investigation , vol.121 , Issue.6 , pp. 2142-2145
    • Fogo, A.B.1
  • 128
    • 79957881425 scopus 로고    scopus 로고
    • Role of mTOR in podocyte function and diabetic nephropathy in humans and mice
    • 10.1172/JCI44774
    • Godel M., Hartleben B., Herbach N., Role of mTOR in podocyte function and diabetic nephropathy in humans and mice. Journal of Clinical Investigation 2011 121 6 2197 2209 10.1172/JCI44774
    • (2011) Journal of Clinical Investigation , vol.121 , Issue.6 , pp. 2197-2209
    • Godel, M.1    Hartleben, B.2    Herbach, N.3
  • 129
    • 84857243208 scopus 로고    scopus 로고
    • Cell biology and pathology of podocytes
    • Greka A., Mundel P., Cell biology and pathology of podocytes. Annual Review of Physiology 2012 74 299 323
    • (2012) Annual Review of Physiology , vol.74 , pp. 299-323
    • Greka, A.1    Mundel, P.2
  • 130
    • 80555134770 scopus 로고    scopus 로고
    • Balancing calcium signals through TRPC5 and TRPC6 in podocytes
    • Greka A., Mundel P., Balancing calcium signals through TRPC5 and TRPC6 in podocytes. Journal of the American Society of Nephrology 2011 22 11 1969 1980
    • (2011) Journal of the American Society of Nephrology , vol.22 , Issue.11 , pp. 1969-1980
    • Greka, A.1    Mundel, P.2
  • 132
    • 0037069690 scopus 로고    scopus 로고
    • Rho GTPases in cell biology
    • DOI 10.1038/nature01148
    • Etienne-Manneville S., Hall A., Rho GTPases in cell biology. Nature 2002 420 6916 629 635 2-s2.0-0037069690 10.1038/nature01148 (Pubitemid 36764489)
    • (2002) Nature , vol.420 , Issue.6916 , pp. 629-635
    • Etienne-Manneville, S.1    Hall, A.2
  • 133
    • 84862777971 scopus 로고    scopus 로고
    • Mechanisms of the proteinuria induced by Rho GTPases
    • Wang L., Ellis M. J., Gomez J. A., Mechanisms of the proteinuria induced by Rho GTPases. Kidney International 2012 81 11 1075 1085
    • (2012) Kidney International , vol.81 , Issue.11 , pp. 1075-1085
    • Wang, L.1    Ellis, M.J.2    Gomez, J.A.3


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