메뉴 건너뛰기




Volumn 63, Issue 4, 2003, Pages 1220-1229

Delayed cystogenesis and increased ciliogenesis associated with the re-expression of polaris in Tg737 mutant mice

Author keywords

Autosomal recessive polycystic kidney disease; Cilia; orpk; Polaris; Tg737

Indexed keywords

MUTANT PROTEIN; PROTEIN ORPK; UNCLASSIFIED DRUG;

EID: 0037377655     PISSN: 00852538     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1523-1755.2003.00863.x     Document Type: Article
Times cited : (46)

References (22)
  • 1
    • 0032949167 scopus 로고    scopus 로고
    • New insights into the molecular pathophysiology of polycystic kidney disease
    • MURCIA NS, SWEENEY WE, AVNER ED: New insights into the molecular pathophysiology of polycystic kidney disease. Kidney Int 55:1187-1197, 1999
    • (1999) Kidney Int , vol.55 , pp. 1187-1197
    • Murcia, N.S.1    Sweeney, W.E.2    Avner, E.D.3
  • 2
    • 0035083551 scopus 로고    scopus 로고
    • The genetics and physiology of polycystic kidney disease
    • CALVET JP, GRANTHAM JJ: The genetics and physiology of polycystic kidney disease. Semin Nephrol 21:107-123, 2001
    • (2001) Semin Nephrol , vol.21 , pp. 107-123
    • Calvet, J.P.1    Grantham, J.J.2
  • 3
    • 0035127256 scopus 로고    scopus 로고
    • Molecular genetics and pathogenesis of autosomal dominant polycystic kidney disease
    • ARNAOUT MA: Molecular genetics and pathogenesis of autosomal dominant polycystic kidney disease. Annu Rev Med 52:93-123, 2001
    • (2001) Annu Rev Med , vol.52 , pp. 93-123
    • Arnaout, M.A.1
  • 4
    • 0034844158 scopus 로고    scopus 로고
    • Can progression of autosomal dominant and autosomal recessive polycystic kidney disease be prevented?
    • DAVIS ID, MACRAE DELL K, SWEENEY WE, AVNER ED: Can progression of autosomal dominant and autosomal recessive polycystic kidney disease be prevented? Semin Nephrol 21:430-440, 2001
    • (2001) Semin Nephrol , vol.21 , pp. 430-440
    • Davis, I.D.1    Macrae Dell, K.2    Sweeney, W.E.3    Avner, E.D.4
  • 5
    • 0034042763 scopus 로고    scopus 로고
    • The Oak Ridge Polycystic Kidney (orpk) disease gene is required for left-right axis determination
    • MURCIA NS, RICHARDS WG, YODER BK, et al: The Oak Ridge Polycystic Kidney (orpk) disease gene is required for left-right axis determination. Development 127:2347-2355, 2000
    • (2000) Development , vol.127 , pp. 2347-2355
    • Murcia, N.S.1    Richards, W.G.2    Yoder, B.K.3
  • 6
    • 0034735526 scopus 로고    scopus 로고
    • Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg 737, are required for assembly of cilia and flagella
    • PAZOUR GJ, DICKERT BL, VUCICA Y, et al: Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella. J Cell Biol 151:709-718, 2000
    • (2000) J Cell Biol , vol.151 , pp. 709-718
    • Pazour, G.J.1    Dickert, B.L.2    Vucica, Y.3
  • 7
    • 0028322016 scopus 로고
    • Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice
    • MOYER JH, LEE-TISCHLER MJ, KWON HY, et al: Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice. Science 264:1329-1333, 1994
    • (1994) Science , vol.264 , pp. 1329-1333
    • Moyer, J.H.1    Lee-Tischler, M.J.2    Kwon, H.Y.3
  • 8
    • 0035159015 scopus 로고    scopus 로고
    • Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia
    • TAULMAN PD, HAYCRAFT CJ, BALKOVETZ DF, YODER BK: polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia. Mol Biol Cell 12:589-599, 2001
    • (2001) Mol Biol Cell , vol.12 , pp. 589-599
    • Taulman, P.D.1    Haycraft, C.J.2    Balkovetz, D.F.3    Yoder, B.K.4
  • 9
    • 0030971669 scopus 로고    scopus 로고
    • Differential rescue of the renal and hepatic disease in an autosomal recessive polycystic kidney disease mouse mutant: A new model to study the liver lesion
    • YODER BK, RICHARDS WG, SOMMARDAHL C, et al: Differential rescue of the renal and hepatic disease in an autosomal recessive polycystic kidney disease mouse mutant: A new model to study the liver lesion. Am J Pathol 150:2231-2241, 1997
    • (1997) Am J Pathol , vol.150 , pp. 2231-2241
    • Yoder, B.K.1    Richards, W.G.2    Sommardahl, C.3
  • 10
    • 0035095710 scopus 로고    scopus 로고
    • Expression of the orpk disease gene during kidney development and maturation
    • NAKANISHI K, SWEENEY WE, AVNER ED, MURCIA NS: Expression of the orpk disease gene during kidney development and maturation. Ped Nephrol 16:219-226, 2001
    • (2001) Ped Nephrol , vol.16 , pp. 219-226
    • Nakanishi, K.1    Sweeney, W.E.2    Avner, E.D.3    Murcia, N.S.4
  • 11
    • 0028936982 scopus 로고
    • Tyrosine kinase activity of the EGF receptor in murine metanephric organ culture
    • PUGH JL, SWEENEY WE, AVNER ED: Tyrosine kinase activity of the EGF receptor in murine metanephric organ culture. Kidney Int 47:774-781, 1995
    • (1995) Kidney Int , vol.47 , pp. 774-781
    • Pugh, J.L.1    Sweeney, W.E.2    Avner, E.D.3
  • 12
    • 0032030918 scopus 로고    scopus 로고
    • Epidermal growth factor receptor activity mediates renal cyst formation in polycystic kidney disease
    • RICHARDS WG, SWEENEY WE, YODER BK, et al: Epidermal growth factor receptor activity mediates renal cyst formation in polycystic kidney disease. J Clin Invest 101:935-939, 1998
    • (1998) J Clin Invest , vol.101 , pp. 935-939
    • Richards, W.G.1    Sweeney, W.E.2    Yoder, B.K.3
  • 13
    • 0032807280 scopus 로고    scopus 로고
    • In vitro modulation of cyst formation by a novel tyrosine kinase inhibitor
    • SWEENEY WE, FUTEY L, FROST P, AVNER D: In vitro modulation of cyst formation by a novel tyrosine kinase inhibitor. Kidney Int 56:406-413, 1999
    • (1999) Kidney Int , vol.56 , pp. 406-413
    • Sweeney, W.E.1    Futey, L.2    Frost, P.3    Avner, D.4
  • 14
    • 0033995015 scopus 로고    scopus 로고
    • Treatment of polycystic kidney disease with a novel tyrosine kinase inhibitor
    • SWEENEY WE, CHEN Y, NAKANlSHI K, et al: Treatment of polycystic kidney disease with a novel tyrosine kinase inhibitor. Kidney Int 57:33-40, 2000
    • (2000) Kidney Int , vol.57 , pp. 33-40
    • Sweeney, W.E.1    Chen, Y.2    Nakanishi, K.3
  • 15
    • 0001305632 scopus 로고
    • High-resolution scanning electron microscopy of milk products: A new sample preparation procedure
    • MCMANUS WR, MCMAHON DJ, OBERG CJ: High-resolution scanning electron microscopy of milk products: A new sample preparation procedure. Food Struct 12:475-482, 1993
    • (1993) Food Struct , vol.12 , pp. 475-482
    • Mcmanus, W.R.1    Mcmahon, D.J.2    Oberg, C.J.3
  • 17
    • 0021381028 scopus 로고
    • A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
    • FEINBERG AP, VOGELSTEIN B: A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem 137:266-267, 1984
    • (1984) Anal Biochem , vol.137 , pp. 266-267
    • Feinberg, A.P.1    Vogelstein, B.2
  • 18
    • 0029842984 scopus 로고    scopus 로고
    • Functional correction of renal defects in a mouse model for ARPKD through expression of the cloned wild-type Tg737 cDNA
    • YODER BK, RICHARDS WG, SOMMARDAHL C, et al: Functional correction of renal defects in a mouse model for ARPKD through expression of the cloned wild-type Tg737 cDNA. Kidney Int 50:1240-1248, 1996
    • (1996) Kidney Int , vol.50 , pp. 1240-1248
    • Yoder, B.K.1    Richards, W.G.2    Sommardahl, C.3
  • 19
    • 0036086844 scopus 로고    scopus 로고
    • Polaris, a protein disrupted in orpk mutant mice, is required for assembly of renal cilium
    • YODER BK, TOUSSON A, MILLICAN L, et al: polaris, a protein disrupted in orpk mutant mice, is required for assembly of renal cilium. Am J Physiol Renal Physiol 282:F541-552, 2002
    • (2002) Am J Physiol Renal Physiol , vol.282
    • Yoder, B.K.1    Tousson, A.2    Millican, L.3
  • 20
    • 0034987372 scopus 로고    scopus 로고
    • The C. elegans homolog of the murine cystic kidney disease gene Tg737 functions in a ciliogenic pathway and is disrupted in osm-5 mutant worms
    • HAYCRAFT CJ, SWOBODA P, TAULMAN PD, et al: The C. elegans homolog of the murine cystic kidney disease gene Tg737 functions in a ciliogenic pathway and is disrupted in osm-5 mutant worms. Development 128:1493-1505, 2001
    • (2001) Development , vol.128 , pp. 1493-1505
    • Haycraft, C.J.1    Swoboda, P.2    Taulman, P.D.3
  • 21
    • 0035916823 scopus 로고    scopus 로고
    • An autosomal recessive polycystic kidney disease gene homolog is involved in intraflagellar transport in C. elegans ciliated sensory neurons
    • QIN H, ROSENBAUM JL, BARR MM: An autosomal recessive polycystic kidney disease gene homolog is involved in intraflagellar transport in C. elegans ciliated sensory neurons. Curr Biol 11:457-461, 2001
    • (2001) Curr Biol , vol.11 , pp. 457-461
    • Qin, H.1    Rosenbaum, J.L.2    Barr, M.M.3
  • 22
    • 0036544554 scopus 로고    scopus 로고
    • The intraflagellar transport protein, IFT 88, is essential for vertebrate photoreceptor assembly and maintenance
    • PAZOUR GJ, BAKER SA, DEANE JA, et al: The intraflagellar transport protein, IFT88, is essential for vertebrate photoreceptor assembly and maintenance. J Cell Biol 157:103-113, 2002
    • (2002) J Cell Biol , vol.157 , pp. 103-113
    • Pazour, G.J.1    Baker, S.A.2    Deane, J.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.