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Volumn 273, Issue 5 42-5, 1997, Pages

cDNA cloning and localization of OCRL-1 in rabbit kidney

Author keywords

Fanconi's syndrome; Inositol polyphosphate 5 phosphatase; Lowe's syndrome; Nephron segment reverse transcription polymerase chain reaction

Indexed keywords

COMPLEMENTARY DNA; INOSITOL POLYPHOSPHATE;

EID: 0030669453     PISSN: 1931857X     EISSN: 15221466     Source Type: Journal    
DOI: 10.1152/ajprenal.1997.273.5.f790     Document Type: Article
Times cited : (13)

References (18)
  • 2
    • 0026742127 scopus 로고
    • The Lowe's oculocerebrorenal syndrome gene encodes a protein highly ho mologous to inositol polyphosphate-5-phosphatase
    • Attree, O., I. M. Olivos, I. Okabe, L. C. Bailey, D. L. Nelson, R. A. Lewis, R. R. McInnes, and R. L. Nussbaum. The Lowe's oculocerebrorenal syndrome gene encodes a protein highly ho mologous to inositol polyphosphate-5-phosphatase. Nature 358: 239-242, 1992.
    • (1992) Nature , vol.358 , pp. 239-242
    • Attree, O.1    Olivos, I.M.2    Okabe, I.3    Bailey, L.C.4    Nelson, D.L.5    Lewis, R.A.6    McInnes, R.R.7    Nussbaum, R.L.8
  • 3
    • 0027142022 scopus 로고
    • ADP-ribosylation factor, a small GTP-dependent regulatory protein stimulates phospholipase D activity
    • Brown, H. A., S. Gutowski, C. R. Moomaw, C. Slaughter, and P. C. Sternweis. ADP-ribosylation factor, a small GTP-dependent regulatory protein stimulates phospholipase D activity. Cell 75: 1137-1144, 1993.
    • (1993) Cell , vol.75 , pp. 1137-1144
    • Brown, H.A.1    Gutowski, S.2    Moomaw, C.R.3    Slaughter, C.4    Sternweis, P.C.5
  • 4
    • 0025876473 scopus 로고
    • Clinical and laboratory findings in the oculocerebrorenal syndrome of Lowe, with special reference to growth and renal function
    • Charnas, L. R., I. Bernardini, D. Rader, J. M. Hoeg, and W. A. Gaul. Clinical and laboratory findings in the oculocerebrorenal syndrome of Lowe, with special reference to growth and renal function. N. Engl. J. Med. 324: 1318-1325, 1991.
    • (1991) N. Engl. J. Med. , vol.324 , pp. 1318-1325
    • Charnas, L.R.1    Bernardini, I.2    Rader, D.3    Hoeg, J.M.4    Gaul, W.A.5
  • 5
    • 0029968296 scopus 로고    scopus 로고
    • Phosphoinositides as regulators in membrane traffic
    • De Camilli, P., S. D. Emr, P. S. McPherson, and P. Novick. Phosphoinositides as regulators in membrane traffic. Science 271: 1533-1539, 1996.
    • (1996) Science , vol.271 , pp. 1533-1539
    • De Camilli, P.1    Emr, S.D.2    McPherson, P.S.3    Novick, P.4
  • 6
    • 0026623115 scopus 로고
    • ADP-ribosylation factor, a small GTP-binding protein, is required for binding of the coatomer protein β-COP to Golgi membranes
    • Donaldson, J. G., D. Cassel, R. A. Kahn, and R. D. Klausner. ADP-ribosylation factor, a small GTP-binding protein, is required for binding of the coatomer protein β-COP to Golgi membranes. Proc. Natl. Acad. Sci. USA 89: 6408-6412, 1992.
    • (1992) Proc. Natl. Acad. Sci. USA , vol.89 , pp. 6408-6412
    • Donaldson, J.G.1    Cassel, D.2    Kahn, R.A.3    Klausner, R.D.4
  • 8
    • 0027138873 scopus 로고
    • ARF signaling: A potential role for phospholipase D in membrane traffic
    • Kahn, R. A., J. K. Yucel, and V. Malhotra. ARF signaling: a potential role for phospholipase D in membrane traffic. Cell 75: 1045-1048, 1993.
    • (1993) Cell , vol.75 , pp. 1045-1048
    • Kahn, R.A.1    Yucel, J.K.2    Malhotra, V.3
  • 9
    • 0027457372 scopus 로고
    • Nonsense mutations in the OCRL-1 gene in patients with the oculocerebrorenal syndrome of Lowe
    • Leahey, A.-M., L. R. Charnas, and R. L. Nussbaum. Nonsense mutations in the OCRL-1 gene in patients with the oculocerebrorenal syndrome of Lowe. Hum. Mol. Genet. 2: 461-463, 1993.
    • (1993) Hum. Mol. Genet. , vol.2 , pp. 461-463
    • Leahey, A.-M.1    Charnas, L.R.2    Nussbaum, R.L.3
  • 10
    • 0000623605 scopus 로고
    • Organic-aciduria, decreased renal ammonia production, hydrophthalmos, and mental retardation
    • Lowe, C. U., M. Terrey, and E. A. MacLachlan. Organic-aciduria, decreased renal ammonia production, hydrophthalmos, and mental retardation. Am. J. Dis. Child. 83: 164-184, 1952.
    • (1952) Am. J. Dis. Child. , vol.83 , pp. 164-184
    • Lowe, C.U.1    Terrey, M.2    MacLachlan, E.A.3
  • 11
    • 0026690390 scopus 로고
    • Isolation of cDNA sequences around the chromosomal breakpoint in a female with Lowe syndrome by direct screening of cDNA libraries with yeast artificial chromosomes
    • Okabe, I., O. Attree, L. C. Bailey, D. L. Nelson, and R. L. Nussbaum. Isolation of cDNA sequences around the chromosomal breakpoint in a female with Lowe syndrome by direct screening of cDNA libraries with yeast artificial chromosomes. J. Inherit. Metab. Dis. 15: 526-531, 1992.
    • (1992) J. Inherit. Metab. Dis. , vol.15 , pp. 526-531
    • Okabe, I.1    Attree, O.2    Bailey, L.C.3    Nelson, D.L.4    Nussbaum, R.L.5
  • 13
    • 0026695623 scopus 로고
    • 2+ exchanger
    • Renal Fluid Electrolyte Physiol. 31
    • 2+ exchanger. Am. J. Physiol. 262 (Renal Fluid Electrolyte Physiol. 31): F1105-F1109, 1992.
    • (1992) Am. J. Physiol. , vol.262
    • Reilly, R.F.1    Shugrue, C.A.2
  • 14
  • 15
    • 1542370372 scopus 로고
    • Lowe's syndrome: Abnormalities in renal tubular function in combination with other congenital defects
    • Schoen, E. J. Lowe's syndrome: abnormalities in renal tubular function in combination with other congenital defects. Am. J. Med. 27: 781-792, 1959.
    • (1959) Am. J. Med. , vol.27 , pp. 781-792
    • Schoen, E.J.1
  • 16
    • 0028945343 scopus 로고
    • Hypercalciuria and nephrocalcinosis in the oculocerebrorenal syndrome
    • Sliman, G. A., W. D. Winters, D. W. Shaw, and E. D. Avner. Hypercalciuria and nephrocalcinosis in the oculocerebrorenal syndrome. J. Urol. 153: 1244-1246, 1995.
    • (1995) J. Urol. , vol.153 , pp. 1244-1246
    • Sliman, G.A.1    Winters, W.D.2    Shaw, D.W.3    Avner, E.D.4
  • 17
    • 0028880052 scopus 로고
    • Lowe syndrome, a deficiency of a phosphatidylinositol 4,5-bisphosphate 5-phosphatase in the Golgi apparatus
    • Suchy, S. F., I. M. Olivos-Glander, and R. L. Nussbaum. Lowe syndrome, a deficiency of a phosphatidylinositol 4,5-bisphosphate 5-phosphatase in the Golgi apparatus. Hum. Mol. Genet. 4: 2245-2250, 1995.
    • (1995) Hum. Mol. Genet. , vol.4 , pp. 2245-2250
    • Suchy, S.F.1    Olivos-Glander, I.M.2    Nussbaum, R.L.3
  • 18
    • 0029060795 scopus 로고
    • The protein deficient in Lowe syndrome is a phosphatidylinositol-4,5-bisphosphate 5-phosphatase
    • Zhang, X., A. B. Jefferson, V. Auethavekiat, and P. W. Majerus. The protein deficient in Lowe syndrome is a phosphatidylinositol-4,5-bisphosphate 5-phosphatase. Proc. Natl. Acad. Sci. USA 92: 4853-4856, 1995.
    • (1995) Proc. Natl. Acad. Sci. USA , vol.92 , pp. 4853-4856
    • Zhang, X.1    Jefferson, A.B.2    Auethavekiat, V.3    Majerus, P.W.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.