메뉴 건너뛰기




Volumn 28, Issue 11, 2013, Pages 2117-2123

Diagnosis of Alport syndrome - Search for proteomic biomarkers in body fluids

Author keywords

ADAM8; Fibronectin; Matrix metalloproteinase; Myosin; Podocin

Indexed keywords

ADAM PROTEIN; BIOLOGICAL MARKER; COLLAGEN TYPE 1; COLLAGEN TYPE 4; DIPEPTIDYL CARBOXYPEPTIDASE; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; DISINTEGRIN; FIBRONECTIN; GELATINASE A; GELATINASE B; HEMOPEXIN; MYOSIN 10; MYOSIN 9; NEPHRIN; PODOCALYXIN; PODOCIN; SYNAPTOPODIN; UNCLASSIFIED DRUG;

EID: 84885960796     PISSN: 0931041X     EISSN: 1432198X     Source Type: Journal    
DOI: 10.1007/s00467-013-2533-5     Document Type: Article
Times cited : (15)

References (30)
  • 1
    • 37349123995 scopus 로고    scopus 로고
    • Inherited diseases of the glomerular basement membrane
    • 18094725 10.1038/ncpneph0671 1:CAS:528:DC%2BD1cXltlKj
    • Gubler MC (2008) Inherited diseases of the glomerular basement membrane. Nat Clin Pract Nephrol 4:24-37
    • (2008) Nat Clin Pract Nephrol , vol.4 , pp. 24-37
    • Gubler, M.C.1
  • 2
    • 70449808041 scopus 로고    scopus 로고
    • Alport syndrome. Molecular genetic aspects
    • 19728970
    • Hertz JM (2009) Alport syndrome. Molecular genetic aspects. Dan Med Bull 56:105-152
    • (2009) Dan Med Bull , vol.56 , pp. 105-152
    • Hertz, J.M.1
  • 3
    • 0038007968 scopus 로고    scopus 로고
    • Novel COL4A4 splice defect and in-frame deletion in a large consanguine family as a genetic link between benign familial haematuria and autosomal Alport syndrome
    • 12748344 10.1093/ndt/gfg157 1:CAS:528:DC%2BD3sXjvFCmtLk%3D
    • Gross O, Netzer KO, Lambrecht R, Seibold S, Weber M (2003) Novel COL4A4 splice defect and in-frame deletion in a large consanguine family as a genetic link between benign familial haematuria and autosomal Alport syndrome. Nephrol Dial Transplant 18:1122-1127
    • (2003) Nephrol Dial Transplant , vol.18 , pp. 1122-1127
    • Gross, O.1    Netzer, K.O.2    Lambrecht, R.3    Seibold, S.4    Weber, M.5
  • 4
    • 2442672631 scopus 로고    scopus 로고
    • A large tandem duplication within the COL4A5 gene is responsible for the high prevalence of Alport syndrome in French Polynesia
    • 15149316 10.1111/j.1523-1755.2004.00622.x 1:CAS:528:DC%2BD2cXltFKgsL8%3D
    • Arrondel C, Deschenes G, Le Meur Y, Viau A, Cordonnier C, Fournier A, Amadeo S, Gubler MC, Antignac C, Heidet L (2004) A large tandem duplication within the COL4A5 gene is responsible for the high prevalence of Alport syndrome in French Polynesia. Kidney Int 65:2030-2040
    • (2004) Kidney Int , vol.65 , pp. 2030-2040
    • Arrondel, C.1    Deschenes, G.2    Le Meur, Y.3    Viau, A.4    Cordonnier, C.5    Fournier, A.6    Amadeo, S.7    Gubler, M.C.8    Antignac, C.9    Heidet, L.10
  • 5
    • 0036692469 scopus 로고    scopus 로고
    • Histopathology, ultrastructure, and clinical phenotypes in thin glomerular basement membrane disease variants
    • 12203217 10.1053/hupa.2002.125374
    • Liapis H, Gokden N, Hmiel P, Miner JH (2002) Histopathology, ultrastructure, and clinical phenotypes in thin glomerular basement membrane disease variants. Hum Pathol 33:836-845
    • (2002) Hum Pathol , vol.33 , pp. 836-845
    • Liapis, H.1    Gokden, N.2    Hmiel, P.3    Miner, J.H.4
  • 9
    • 0345258070 scopus 로고    scopus 로고
    • Cystic and inherited kidney diseases
    • 14655206 10.1053/j.ajkd.2003.10.002
    • Rizk D, Chapman AB (2003) Cystic and inherited kidney diseases. Am J Kidney Dis 42:1305-1317
    • (2003) Am J Kidney Dis , vol.42 , pp. 1305-1317
    • Rizk, D.1    Chapman, A.B.2
  • 10
    • 78649283144 scopus 로고    scopus 로고
    • Genetic disorders of glomerular basement membranes
    • 21071975 10.1159/000320876
    • Kashtan CE, Segal Y (2011) Genetic disorders of glomerular basement membranes. Nephron Clin Pract 118:c9-c18
    • (2011) Nephron Clin Pract , vol.118
    • Kashtan, C.E.1    Segal, Y.2
  • 11
    • 84856555625 scopus 로고    scopus 로고
    • Renal diseases associated with hematuria in children and adolescents: A brief tutorial
    • 22292732 10.3109/01913123.2011.620731
    • Hicks J, Mierau G, Wartchow E, Eldin K (2012) Renal diseases associated with hematuria in children and adolescents: a brief tutorial. Ultrastruct Pathol 36:1-18
    • (2012) Ultrastruct Pathol , vol.36 , pp. 1-18
    • Hicks, J.1    Mierau, G.2    Wartchow, E.3    Eldin, K.4
  • 13
    • 1642299073 scopus 로고    scopus 로고
    • Familial hematuria due to type IV collagen mutations: Alport syndrome and thin basement membrane nephropathy
    • 15021198 10.1097/00008480-200404000-00011
    • Kashtan CE (2004) Familial hematuria due to type IV collagen mutations: Alport syndrome and thin basement membrane nephropathy. Curr Opin Pediatr 16:177-181
    • (2004) Curr Opin Pediatr , vol.16 , pp. 177-181
    • Kashtan, C.E.1
  • 15
    • 34247898894 scopus 로고    scopus 로고
    • Diagnosis of Alport syndrome without biopsy?
    • 17143627 10.1007/s00467-006-0376-z
    • Gubler MC (2007) Diagnosis of Alport syndrome without biopsy? Pediatr Nephrol 22:621-625
    • (2007) Pediatr Nephrol , vol.22 , pp. 621-625
    • Gubler, M.C.1
  • 16
    • 34250630898 scopus 로고    scopus 로고
    • Alport syndrome and thin basement membrane nephropathy
    • 17570934 10.1159/000101802 1:CAS:528:DC%2BD2sXmsVOisrs%3D
    • Thorner PS (2007) Alport syndrome and thin basement membrane nephropathy. Nephron Clin Pract 106:c82-c88
    • (2007) Nephron Clin Pract , vol.106
    • Thorner, P.S.1
  • 17
    • 84870405692 scopus 로고    scopus 로고
    • Clinical practice recommendations for the treatment of Alport syndrome: A statement of the Alport Syndrome Research Collaborative
    • 22461141 10.1007/s00467-012-2138-4
    • Kashtan CE, Ding J, Gregory M, Gross O, Heidet L, Knebelmann B, Rheault M, Licht C (2013) Clinical practice recommendations for the treatment of Alport syndrome: a statement of the Alport Syndrome Research Collaborative. Pediatr Nephrol 28:5-11
    • (2013) Pediatr Nephrol , vol.28 , pp. 5-11
    • Kashtan, C.E.1    Ding, J.2    Gregory, M.3    Gross, O.4    Heidet, L.5    Knebelmann, B.6    Rheault, M.7    Licht, C.8
  • 18
    • 79961074073 scopus 로고    scopus 로고
    • Efficacy and safety of losartan in children with Alport syndrome-results from a subgroup analysis of a prospective, randomized, placebo- or amlodipine-controlled trial
    • 21285125 10.1093/ndt/gfq797 1:CAS:528:DC%2BC3MXps1ykt70%3D
    • Webb NJ, Lam C, Shahinfar S, Strehlau J, Wells TG, Gleim GW, Le Bailly De Tilleghem C (2011) Efficacy and safety of losartan in children with Alport syndrome-results from a subgroup analysis of a prospective, randomized, placebo- or amlodipine-controlled trial. Nephrol Dial Transplant 26:2521-2526
    • (2011) Nephrol Dial Transplant , vol.26 , pp. 2521-2526
    • Webb, N.J.1    Lam, C.2    Shahinfar, S.3    Strehlau, J.4    Wells, T.G.5    Gleim, G.W.6    Le Bailly De Tilleghem, C.7
  • 19
    • 84863983649 scopus 로고    scopus 로고
    • Glomerular pathology in Alport syndrome: A molecular perspective
    • 21455721 10.1007/s00467-011-1868-z
    • Cosgrove D (2012) Glomerular pathology in Alport syndrome: a molecular perspective. Pediatr Nephrol 27:885-890
    • (2012) Pediatr Nephrol , vol.27 , pp. 885-890
    • Cosgrove, D.1
  • 20
    • 0037248954 scopus 로고    scopus 로고
    • Preemptive ramipril therapy delays renal failure and reduces renal fibrosis in COL4A3-knockout mice with Alport syndrome
    • 12631109 10.1046/j.1523-1755.2003.00779.x 1:CAS:528:DC%2BD3sXht1yrs7w%3D
    • Gross O, Beirowski B, Koepke ML, Kuck J, Reiner M, Addicks K, Smyth N, Schulze-Lohoff E, Weber M (2003) Preemptive ramipril therapy delays renal failure and reduces renal fibrosis in COL4A3-knockout mice with Alport syndrome. Kidney Int 63:438-446
    • (2003) Kidney Int , vol.63 , pp. 438-446
    • Gross, O.1    Beirowski, B.2    Koepke, M.L.3    Kuck, J.4    Reiner, M.5    Addicks, K.6    Smyth, N.7    Schulze-Lohoff, E.8    Weber, M.9
  • 21
    • 0030730063 scopus 로고    scopus 로고
    • Treatment of X-linked hereditary nephritis in Samoyed dogs with angiotensin converting enzyme (ACE) inhibitor
    • 9447482 10.1016/S0021-9975(97)80016-3 1:CAS:528:DyaK1cXjsFaquw%3D%3D
    • Grodecki KM, Gains MJ, Baumal R, Osmond DH, Cotter B, Valli VE, Jacobs RM (1997) Treatment of X-linked hereditary nephritis in Samoyed dogs with angiotensin converting enzyme (ACE) inhibitor. J Comp Pathol 117:209-225
    • (1997) J Comp Pathol , vol.117 , pp. 209-225
    • Grodecki, K.M.1    Gains, M.J.2    Baumal, R.3    Osmond, D.H.4    Cotter, B.5    Valli, V.E.6    Jacobs, R.M.7
  • 23
    • 84870961210 scopus 로고    scopus 로고
    • Safety and efficacy of the ACE-inhibitor ramipril in Alport syndrome: The Double-Blind, Randomized, Placebo-Controlled. Multicenter Phase III EARLY PRO-TECT Alport Trial in Pediatric Patients
    • 10.5402/2012/436046 22811928
    • Gross O, Friede T, Hilgers R, Gorlitz A, Gavenis K, Ahmed R, Durr U (2012) Safety and efficacy of the ACE-inhibitor ramipril in Alport syndrome: The Double-Blind, Randomized, Placebo-Controlled. Multicenter Phase III EARLY PRO-TECT Alport Trial in Pediatric Patients ISRN Pediatr 2012:436046 doi: 10.5402/2012/436046
    • (2012) ISRN Pediatr
    • Gross, O.1    Friede, T.2    Hilgers, R.3    Gorlitz, A.4    Gavenis, K.5    Ahmed, R.6    Durr, U.7
  • 24
    • 0017891936 scopus 로고
    • Urinary excretion of glomerular basement membrane antigens in Alport's syndrome. A new diagnostic approach
    • 666354 10.1136/adc.53.5.401 1:STN:280:DyaE1c3gvFGmuw%3D%3D
    • Lubec G, Balzar E, Weissenbacher G, Syré G (1978) Urinary excretion of glomerular basement membrane antigens in Alport's syndrome. A new diagnostic approach. Arch Dis Child 53:401-406
    • (1978) Arch Dis Child , vol.53 , pp. 401-406
    • Lubec, G.1    Balzar, E.2    Weissenbacher, G.3    Syré, G.4
  • 25
    • 0018937541 scopus 로고
    • Harnausscheidung von sauren Glykosaminoglykanen und Glomerulumbasalmembranantigenen bei Patienten mit Alport Syndrom
    • 7192341 10.1055/s-2008-1035624 1:STN:280:DyaL3M%2FntlWlsA%3D%3D
    • Lubec G, Legenstein E, Meznik E (1980) Harnausscheidung von sauren Glykosaminoglykanen und Glomerulumbasalmembranantigenen bei Patienten mit Alport Syndrom. Klin Pädiatr 192:453-456
    • (1980) Klin Pädiatr , vol.192 , pp. 453-456
    • Lubec, G.1    Legenstein, E.2    Meznik, E.3
  • 27
    • 0141533033 scopus 로고    scopus 로고
    • ADAMs: Modulators of cell-cell and cell-matrix interactions
    • 14519395 10.1016/j.ceb.2003.08.001 1:CAS:528:DC%2BD3sXnslSqsbs%3D
    • White JM (2003) ADAMs: modulators of cell-cell and cell-matrix interactions. Curr Opin Cell Biol 15:598-606
    • (2003) Curr. Opin. Cell Biol. , vol.15 , pp. 598-606
    • White, J.M.1
  • 28
    • 84860233616 scopus 로고    scopus 로고
    • The role of ADAM-mediated shedding in vascular biology
    • 22138087 10.1016/j.ejcb.2011.09.003 1:CAS:528:DC%2BC38XlvFyqs7k%3D
    • Dreymueller D, Pruessmeyer J, Groth E, Ludwig A (2012) The role of ADAM-mediated shedding in vascular biology. Eur J Cell Biol 91:472-485
    • (2012) Eur J Cell Biol , vol.91 , pp. 472-485
    • Dreymueller, D.1    Pruessmeyer, J.2    Groth, E.3    Ludwig, A.4
  • 29
    • 84878638745 scopus 로고    scopus 로고
    • An update on the pathomechanisms and future therapies of Alport syndrome
    • 22903660 10.1007/s00467-012-2272-z
    • Noone D, Licht C (2012) An update on the pathomechanisms and future therapies of Alport syndrome. Pediatr Nephrol 28:1025-1036
    • (2012) Pediatr Nephrol , vol.28 , pp. 1025-1036
    • Noone, D.1    Licht, C.2
  • 30
    • 73949113843 scopus 로고    scopus 로고
    • Unravelling the genetic basis of renal diseases; From single gene to multifactorial disorders
    • 19882676 1:CAS:528:DC%2BC3cXht1Onsbk%3D
    • McKnight AJ, Currie D, Maxwell AP (2010) Unravelling the genetic basis of renal diseases; from single gene to multifactorial disorders. J Pathol 220:198-216
    • (2010) J Pathol , vol.220 , pp. 198-216
    • McKnight, A.J.1    Currie, D.2    Maxwell, A.P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.