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Volumn 21, Issue 1, 2004, Pages 54-57

Eruptive Vellus Hair Cysts in a Patient with Lowe Syndrome

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; LYSOSOME ENZYME; PHOSPHATASE; PHOSPHATIDYLINOSITOL;

EID: 1342281808     PISSN: 07368046     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.0736-8046.2004.21112.x     Document Type: Article
Times cited : (28)

References (16)
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    • Lowe CU, Terrey M, MacLachlan EA. Organic aciduria, decreased renal ammonia production, hydrophthalmos and mental retardation: a clinical study. Am J Dis Child 1952;83:164-184.
    • (1952) Am J Dis Child , vol.83 , pp. 164-184
    • Lowe, C.U.1    Terrey, M.2    MacLachlan, E.A.3
  • 2
    • 1342293258 scopus 로고    scopus 로고
    • Online Mendelian Inheritance in Man. Available at http://www.ncbi.nlm.nih.gov/Omim.
  • 3
    • 0023089666 scopus 로고
    • Mapping the Lowe oculocerebrorenal syndrome to Xq24-q26 by the use of restriction fragment length polymorphism
    • Silver DN, Lewis RA, Nussbaum RL. Mapping the Lowe oculocerebrorenal syndrome to Xq24-q26 by the use of restriction fragment length polymorphism. J Clin Invest 1987;79:282-285.
    • (1987) J Clin Invest , vol.79 , pp. 282-285
    • Silver, D.N.1    Lewis, R.A.2    Nussbaum, R.L.3
  • 4
    • 0031914642 scopus 로고    scopus 로고
    • Cell lines from kidney proximal tubules of a patient with Lowe syndrome lack OCRL inositol polyphosphate 5-phosphatase and accumulate phosphatidylinositol 4,5 bisphosphate
    • Zhang X, Hartz PA, Philip E, Racusen LC, Majerus PW. Cell lines from kidney proximal tubules of a patient with Lowe syndrome lack OCRL inositol polyphosphate 5-phosphatase and accumulate phosphatidylinositol 4,5 bisphosphate. J Biol Chem 1998;273:1574-1582.
    • (1998) J Biol Chem , vol.273 , pp. 1574-1582
    • Zhang, X.1    Hartz, P.A.2    Philip, E.3    Racusen, L.C.4    Majerus, P.W.5
  • 5
    • 0032486078 scopus 로고    scopus 로고
    • Oculocerebrorenal syndrome of Lowe: Three mutations of the OCRL1 gene derived from three patients with different phenotypes
    • Kawano T, Indo Y, Nakazato H, Shimadzu M, Matsuda I. Oculocerebrorenal syndrome of Lowe: three mutations of the OCRL1 gene derived from three patients with different phenotypes. Am J Med Genet 1998;77:348-355.
    • (1998) Am J Med Genet , vol.77 , pp. 348-355
    • Kawano, T.1    Indo, Y.2    Nakazato, H.3    Shimadzu, M.4    Matsuda, I.5
  • 6
    • 0030067977 scopus 로고    scopus 로고
    • Eruptive vellus hair cyst and steatocystoma multiplex: Hybrid cysts
    • Hurlimann AF, Panizzon RG, Burg G. Eruptive vellus hair cyst and steatocystoma multiplex: hybrid cysts. Dermatology 1996;192:64-66.
    • (1996) Dermatology , vol.192 , pp. 64-66
    • Hurlimann, A.F.1    Panizzon, R.G.2    Burg, G.3
  • 8
    • 0018650093 scopus 로고
    • Eruptive vellus hair cyst: Clinical and histological findings
    • Lee S, Kim JG. Eruptive vellus hair cyst: clinical and histological findings. Arch Dermatol 1979;115:744-746.
    • (1979) Arch Dermatol , vol.115 , pp. 744-746
    • Lee, S.1    Kim, J.G.2
  • 9
    • 0030902811 scopus 로고    scopus 로고
    • Expression of keratins (K10 and K17) in steatocystoma multiplex, eruptive vellus hair cysts, and epidermoid and trichilemmal cysts
    • Tomkova H, Fujimoto W, Arata J. Expression of keratins (K10 and K17) in steatocystoma multiplex, eruptive vellus hair cysts, and epidermoid and trichilemmal cysts. Am J Dermatopathol 1997;19:250-253.
    • (1997) Am J Dermatopathol , vol.19 , pp. 250-253
    • Tomkova, H.1    Fujimoto, W.2    Arata, J.3
  • 12
    • 0026625565 scopus 로고
    • Relationship between steatocystoma multiplex and eruptive vellus hair cysts
    • Ohtake N, Kubota Y, Takayama O, Shimada S, Tamaki K. Relationship between steatocystoma multiplex and eruptive vellus hair cysts. J Am Acad Dermatol 1992;26:876-879.
    • (1992) J Am Acad Dermatol , vol.26 , pp. 876-879
    • Ohtake, N.1    Kubota, Y.2    Takayama, O.3    Shimada, S.4    Tamaki, K.5
  • 13
    • 0029060795 scopus 로고
    • The protein deficient in Lowe syndrome is a phosphatidylinositol 4,5-bisphosphate-5-phosphatase
    • Zhang X, Jefferson AB, Auethavekiat V, Majerus PW. The protein deficient in Lowe syndrome is a phosphatidylinositol 4,5-bisphosphate-5-phosphatase. Proc Natl Acad Sci USA 1995;92:4853-4856.
    • (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
  • 14
    • 0032042095 scopus 로고    scopus 로고
    • Phosphatidylinositol signaling reactions
    • Zhang X, Majerus P. Phosphatidylinositol signaling reactions. Semin Cell Dev Biol 1998;9:153-160.
    • (1998) Semin Cell Dev Biol , vol.9 , pp. 153-160
    • Zhang, X.1    Majerus, P.2
  • 15
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    • The oculocerebrorenal syndrome gene product is a 105-kD protein localized to the Golgi complex
    • Olivos-Glander IM, Janne PA, Nussbaum RL. The oculocerebrorenal syndrome gene product is a 105-kD protein localized to the Golgi complex. Am J Hum Genet 1995;57:817-823.
    • (1995) Am J Hum Genet , vol.57 , pp. 817-823
    • Olivos-Glander, I.M.1    Janne, P.A.2    Nussbaum, R.L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.