These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

111 related items for PubMed ID: 16163269

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Central corneal mosaic opacities in Schnyder's crystalline dystrophy.
    Wu CW, Lin PY, Liu YF, Liu TC, Lin MW, Chen WM, Lee FL, Lee SM, Hsu WM.
    Ophthalmology; 2005 Apr 02; 112(4):650-3. PubMed ID: 15808257
    [Abstract] [Full Text] [Related]

  • 4. Identification of mutations in UBIAD1 following exclusion of coding mutations in the chromosome 1p36 locus for Schnyder crystalline corneal dystrophy.
    Yellore VS, Khan MA, Bourla N, Rayner SA, Chen MC, Sonmez B, Momi RS, Sampat KM, Gorin MB, Aldave AJ.
    Mol Vis; 2007 Sep 24; 13():1777-82. PubMed ID: 17960116
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Molecular genetic analysis of two functional candidate genes in the autosomal recessive retinitis pigmentosa, RP25, locus.
    Abd El-Aziz MM, El-Ashry MF, Barragan I, Marcos I, Borrego S, Antiñolo G, Bhattacharya SS.
    Curr Eye Res; 2005 Dec 24; 30(12):1081-7. PubMed ID: 16354621
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Genetic analysis of 14 families with Schnyder crystalline corneal dystrophy reveals clues to UBIAD1 protein function.
    Weiss JS, Kruth HS, Kuivaniemi H, Tromp G, Karkera J, Mahurkar S, Lisch W, Dupps WJ, White PS, Winters RS, Kim C, Rapuano CJ, Sutphin J, Reidy J, Hu FR, Lu DW, Ebenezer N, Nickerson ML.
    Am J Med Genet A; 2008 Feb 01; 146A(3):271-83. PubMed ID: 18176953
    [Abstract] [Full Text] [Related]

  • 11. Four mutations (three novel, one founder) in TACSTD2 among Iranian GDLD patients.
    Alavi A, Elahi E, Tehrani MH, Amoli FA, Javadi MA, Rafati N, Chiani M, Banihosseini SS, Bayat B, Kalhor R, Amini SS.
    Invest Ophthalmol Vis Sci; 2007 Oct 01; 48(10):4490-7. PubMed ID: 17898270
    [Abstract] [Full Text] [Related]

  • 12. [Molecular genetic analysis of the BIGH3 gene in lattice type I (Biber-Haab-Dimmer) and granular type II (Avellino) corneal dystrophy: is indirect mutation analysis for hot spots recommended?].
    Grünauer-Kloevekorn C, Bräutigam S, Wolter-Roessler M, Tost F, Weidle E, Froster U, Duncker GI.
    Klin Monbl Augenheilkd; 2005 Dec 01; 222(12):1017-23. PubMed ID: 16380889
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Novel L558P mutation of the TGFBI gene found in Ukrainian families with atypical corneal dystrophy.
    Pampukha VM, Kravchenko SA, Tereshchenko FA, Livshits LA, Drozhyna GI.
    Ophthalmologica; 2009 Dec 01; 223(3):207-14. PubMed ID: 19221447
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Exclusion of positional candidate gene coding region mutations in the common posterior polymorphous corneal dystrophy 1 candidate gene interval.
    Aldave AJ, Yellore VS, Vo RC, Kamal KM, Rayner SA, Plaisier CL, Chen MC, Damani MR, Pham MN, Gorin MB, Sobel E, Papp J.
    Cornea; 2009 Aug 01; 28(7):801-7. PubMed ID: 19574904
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. 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 01; 48(11):5007-12. PubMed ID: 17962451
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.