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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

280 related articles for article (PubMed ID: 12714618)

  • 21. Chronic wound state exacerbated by oxidative stress in Pax6+/- aniridia-related keratopathy.
    Ou J; Walczysko P; Kucerova R; Rajnicek AM; McCaig CD; Zhao M; Collinson JM
    J Pathol; 2008 Aug; 215(4):421-30. PubMed ID: 18491289
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities.
    Dansault A; David G; Schwartz C; Jaliffa C; Vieira V; de la Houssaye G; Bigot K; Catin F; Tattu L; Chopin C; Halimi P; Roche O; Van Regemorter N; Munier F; Schorderet D; Dufier JL; Marsac C; Ricquier D; Menasche M; Penfornis A; Abitbol M
    Mol Vis; 2007 Apr; 13():511-23. PubMed ID: 17417613
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Genetic dissection of Pax6 dosage requirements in the developing mouse eye.
    Davis-Silberman N; Kalich T; Oron-Karni V; Marquardt T; Kroeber M; Tamm ER; Ashery-Padan R
    Hum Mol Genet; 2005 Aug; 14(15):2265-76. PubMed ID: 15987699
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Primary defects in the lens underlie complex anterior segment abnormalities of the Pax6 heterozygous eye.
    Collinson JM; Quinn JC; Buchanan MA; Kaufman MH; Wedden SE; West JD; Hill RE
    Proc Natl Acad Sci U S A; 2001 Aug; 98(17):9688-93. PubMed ID: 11481423
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Familial peripheral keratopathy without PAX6 mutation.
    Smith WM; Lange JM; Sturm AC; Tanner SM; Mauger TF
    Cornea; 2012 Feb; 31(2):130-3. PubMed ID: 22146551
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Transcription Factor PAX6 (Paired Box 6) Controls Limbal Stem Cell Lineage in Development and Disease.
    Li G; Xu F; Zhu J; Krawczyk M; Zhang Y; Yuan J; Patel S; Wang Y; Lin Y; Zhang M; Cai H; Chen D; Zhang M; Cao G; Yeh E; Lin D; Su Q; Li WW; Sen GL; Afshari N; Chen S; Maas RL; Fu XD; Zhang K; Liu Y; Ouyang H
    J Biol Chem; 2015 Aug; 290(33):20448-54. PubMed ID: 26045558
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Early phenotypic features of aniridia-associated keratopathy and association with PAX6 coding mutations.
    Lagali N; Wowra B; Fries FN; Latta L; Moslemani K; Utheim TP; Wylegala E; Seitz B; Käsmann-Kellner B
    Ocul Surf; 2020 Jan; 18(1):130-140. PubMed ID: 31734509
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Experimental transplantation of corneal epithelium-like cells induced by Pax6 gene transfection of mouse embryonic stem cells.
    Ueno H; Kurokawa MS; Kayama M; Homma R; Kumagai Y; Masuda C; Takada E; Tsubota K; Ueno S; Suzuki N
    Cornea; 2007 Dec; 26(10):1220-7. PubMed ID: 18043180
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Human aniridia limbal epithelial cells lack expression of keratins K3 and K12.
    Latta L; Viestenz A; Stachon T; Colanesi S; Szentmáry N; Seitz B; Käsmann-Kellner B
    Exp Eye Res; 2018 Feb; 167():100-109. PubMed ID: 29162348
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The roles of calcium signaling and ERK1/2 phosphorylation in a Pax6+/- mouse model of epithelial wound-healing delay.
    Leiper LJ; Walczysko P; Kucerova R; Ou J; Shanley LJ; Lawson D; Forrester JV; McCaig CD; Zhao M; Collinson JM
    BMC Biol; 2006 Aug; 4():27. PubMed ID: 16914058
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Corneal epithelial stem cells: deficiency and regulation.
    Secker GA; Daniels JT
    Stem Cell Rev; 2008 Sep; 4(3):159-68. PubMed ID: 18622724
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A case of aniridia with unilateral Peters anomaly.
    Sawada M; Sato M; Hikoya A; Wang C; Minoshima S; Azuma N; Hotta Y
    J AAPOS; 2011 Feb; 15(1):104-6. PubMed ID: 21397818
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Reduced expression of Pax6 in lens and cornea of mutant mice leads to failure of chamber angle development and juvenile glaucoma.
    Kroeber M; Davis N; Holzmann S; Kritzenberger M; Shelah-Goraly M; Ofri R; Ashery-Padan R; Tamm ER
    Hum Mol Genet; 2010 Sep; 19(17):3332-42. PubMed ID: 20538882
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Gene expression of the mouse corneal crystallin Aldh3a1: activation by Pax6, Oct1, and p300.
    Davis J; Davis D; Norman B; Piatigorsky J
    Invest Ophthalmol Vis Sci; 2008 May; 49(5):1814-26. PubMed ID: 18436815
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Reduction of lens size in PAX6-related aniridia.
    Duncan MK; Daruich A; Valleix S; Bremond-Gignac D
    Exp Eye Res; 2024 Jan; 238():109746. PubMed ID: 38056551
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Microphthalmia, late onset keratitis, and iris coloboma/aniridia in a family with a novel PAX6 mutation.
    Xiao X; Li S; Zhang Q
    Ophthalmic Genet; 2012 Jun; 33(2):119-21. PubMed ID: 22171686
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Modeling of Aniridia-Related Keratopathy by CRISPR/Cas9 Genome Editing of Human Limbal Epithelial Cells and Rescue by Recombinant PAX6 Protein.
    Roux LN; Petit I; Domart R; Concordet JP; Qu J; Zhou H; Joliot A; Ferrigno O; Aberdam D
    Stem Cells; 2018 Sep; 36(9):1421-1429. PubMed ID: 29808941
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mutational analysis and genotype-phenotype correlations in southern Indian patients with sporadic and familial aniridia.
    Dubey SK; Mahalaxmi N; Vijayalakshmi P; Sundaresan P
    Mol Vis; 2015; 21():88-97. PubMed ID: 25678763
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Production and Limbal Lineage Commitment of Aniridia Patient-Derived Induced Pluripotent Stem Cells.
    Ilmarinen T; Vattulainen M; Kandhavelu J; Bremond-Gignac D; Aberdam D; Skottman H
    Stem Cells; 2023 Dec; 41(12):1133-1141. PubMed ID: 37632794
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Congenital aniridia variant: minimally abnormal irides with severe limbal stem cell deficiency.
    Skeens HM; Brooks BP; Holland EJ
    Ophthalmology; 2011 Jul; 118(7):1260-4. PubMed ID: 21376398
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.