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Journal Abstract Search

122 related items for PubMed ID: 8894705

  • 1. The gene for schnyder's crystalline corneal dystrophy maps to human chromosome 1p34.1-p36.
    Shearman AM, Hudson TJ, Andresen JM, Wu X, Sohn RL, Haluska F, Housman DE, Weiss JS.
    Hum Mol Genet; 1996 Oct; 5(10):1667-72. PubMed ID: 8894705
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  • 2. Fine mapping of the Schnyder's crystalline corneal dystrophy locus.
    Theendakara V, Tromp G, Kuivaniemi H, White PS, Panchal S, Cox J, Winters RS, Riebeling P, Tost F, Hoeltzenbein M, Tervo TM, Henn W, Denniger E, Krause M, Koksal M, Kargi S, Ugurbas SH, Latvala T, Shearman AM, Weiss JS.
    Hum Genet; 2004 May; 114(6):594-600. PubMed ID: 15034782
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  • 3. [Schnyder's crystalline corneal dystrophy. Further narrowing of the linkage interval at chromosome 1p34.1-p36?].
    Riebeling P, Polz S, Tost F, Weiss JS, Kuivaniemi H, Hoeltzenbein M.
    Ophthalmologe; 2003 Nov; 100(11):979-83. PubMed ID: 14669035
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  • 6. Panstromal Schnyder's corneal dystrophy. Ultrastructural and histochemical studies.
    Weiss JS, Rodrigues MM, Kruth HS, Rajagopalan S, Rader DJ, Kachadoorian H.
    Ophthalmology; 1992 Jul; 99(7):1072-81. PubMed ID: 1495786
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  • 8. [Schnyder corneal dystrophy and juvenile, systemic hypercholesteremia].
    Kohnen T, Pelton RW, Jones DB.
    Klin Monbl Augenheilkd; 1997 Aug; 211(2):135-7. PubMed ID: 9379642
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  • 9. Accumulation of HDL apolipoproteins accompanies abnormal cholesterol accumulation in Schnyder's corneal dystrophy.
    Gaynor PM, Zhang WY, Weiss JS, Skarlatos SI, Rodrigues MM, Kruth HS.
    Arterioscler Thromb Vasc Biol; 1996 Aug; 16(8):992-9. PubMed ID: 8696964
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  • 10. Mutations in the UBIAD1 gene on chromosome short arm 1, region 36, cause Schnyder crystalline corneal dystrophy.
    Weiss JS, Kruth HS, Kuivaniemi H, Tromp G, White PS, Winters RS, Lisch W, Henn W, Denninger E, Krause M, Wasson P, Ebenezer N, Mahurkar S, Nickerson ML.
    Invest Ophthalmol Vis Sci; 2007 Nov; 48(11):5007-12. PubMed ID: 17962451
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  • 11. Functional study of SCCD pathogenic gene UBIAD1 (Review).
    Xie J, Li L.
    Mol Med Rep; 2021 Oct; 24(4):. PubMed ID: 34368857
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  • 12. Linkage analysis in granular corneal dystrophy (Groenouw I), Schnyder's crystalline corneal dystrophy, and Reis-Bücklers' corneal dystrophy.
    Kömpf J, Ritter H, Lisch W, Weidle EG, Baur MP.
    Graefes Arch Clin Exp Ophthalmol; 1989 Oct; 227(6):538-40. PubMed ID: 2625210
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  • 13. Linkage mapping of Thiel-Behnke corneal dystrophy (CDB2) to chromosome 10q23-q24.
    Yee RW, Sullivan LS, Lai HT, Stock EL, Lu Y, Khan MN, Blanton SH, Daiger SP.
    Genomics; 1997 Nov 15; 46(1):152-4. PubMed ID: 9403072
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  • 15. Mutations in the UBIAD1 gene, encoding a potential prenyltransferase, are causal for Schnyder crystalline corneal dystrophy.
    Orr A, Dubé MP, Marcadier J, Jiang H, Federico A, George S, Seamone C, Andrews D, Dubord P, Holland S, Provost S, Mongrain V, Evans S, Higgins B, Bowman S, Guernsey D, Samuels M.
    PLoS One; 2007 Aug 01; 2(8):e685. PubMed ID: 17668063
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  • 16. Unesterified cholesterol in Schnyder's corneal crystalline dystrophy.
    Rodrigues MM, Kruth HS, Krachmer JH, Willis R.
    Am J Ophthalmol; 1987 Aug 15; 104(2):157-63. PubMed ID: 3303946
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  • 17. Posterior polymorphous corneal dystrophy in Czech families maps to chromosome 20 and excludes the VSX1 gene.
    Gwilliam R, Liskova P, Filipec M, Kmoch S, Jirsova K, Huckle EJ, Stables CL, Bhattacharya SS, Hardcastle AJ, Deloukas P, Ebenezer ND.
    Invest Ophthalmol Vis Sci; 2005 Dec 15; 46(12):4480-4. PubMed ID: 16303937
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  • 18. Replication and refinement of linkage of posterior polymorphous corneal dystrophy to the posterior polymorphous corneal dystrophy 1 locus on chromosome 20.
    Yellore VS, Papp JC, Sobel E, Khan MA, Rayner SA, Farber DB, Aldave AJ.
    Genet Med; 2007 Apr 15; 9(4):228-34. PubMed ID: 17438387
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  • 19. Analysis of fifteen positional candidate genes for Schnyder crystalline corneal dystrophy.
    Aldave AJ, Rayner SA, Principe AH, Affeldt JA, Katsev D, Yellore VS.
    Mol Vis; 2005 Sep 02; 11():713-6. PubMed ID: 16163269
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