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 *

205 related articles for article (PubMed ID: 10502778)

  • 1. Threading analysis of the Pitx2 homeodomain: predicted structural effects of mutations causing Rieger syndrome and iridogoniodysgenesis.
    Banerjee-Basu S; Baxevanis AD
    Hum Mutat; 1999; 14(4):312-9. PubMed ID: 10502778
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Solution structure of the K50 class homeodomain PITX2 bound to DNA and implications for mutations that cause Rieger syndrome.
    Chaney BA; Clark-Baldwin K; Dave V; Ma J; Rance M
    Biochemistry; 2005 May; 44(20):7497-511. PubMed ID: 15895993
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
    Vieira V; David G; Roche O; de la Houssaye G; Boutboul S; Arbogast L; Kobetz A; Orssaud C; Camand O; Schorderet DF; Munier F; Rossi A; Delezoide AL; Marsac C; Ricquier D; Dufier JL; Menasche M; Abitbol M
    Mol Vis; 2006 Dec; 12():1448-60. PubMed ID: 17167399
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Threading analysis of prospero-type homeodomains.
    Banerjee-Basu S; Landsman D; Baxevanis AD
    In Silico Biol; 1999; 1(3):163-73. PubMed ID: 11471237
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of mutations of the PITX2 transcription factor found in patients with Axenfeld-Rieger syndrome.
    Footz T; Idrees F; Acharya M; Kozlowski K; Walter MA
    Invest Ophthalmol Vis Sci; 2009 Jun; 50(6):2599-606. PubMed ID: 19218601
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Pitx2 protein in mouse development.
    Hjalt TA; Semina EV; Amendt BA; Murray JC
    Dev Dyn; 2000 May; 218(1):195-200. PubMed ID: 10822271
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Function of Rieger syndrome gene in left-right asymmetry and craniofacial development.
    Lu MF; Pressman C; Dyer R; Johnson RL; Martin JF
    Nature; 1999 Sep; 401(6750):276-8. PubMed ID: 10499585
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel mutations of FOXC1 and PITX2 in patients with Axenfeld-Rieger malformations.
    Weisschuh N; Dressler P; Schuettauf F; Wolf C; Wissinger B; Gramer E
    Invest Ophthalmol Vis Sci; 2006 Sep; 47(9):3846-52. PubMed ID: 16936096
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic dissection of Pitx2 in craniofacial development uncovers new functions in branchial arch morphogenesis, late aspects of tooth morphogenesis and cell migration.
    Liu W; Selever J; Lu MF; Martin JF
    Development; 2003 Dec; 130(25):6375-85. PubMed ID: 14623826
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Structural effect of the L16Q, K50E, and R53P mutations on homeodomain of pituitary homeobox protein 2.
    Rajasekaran M; Chen C
    Int J Biol Macromol; 2012 Oct; 51(3):305-13. PubMed ID: 22584078
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations.
    Strungaru MH; Dinu I; Walter MA
    Invest Ophthalmol Vis Sci; 2007 Jan; 48(1):228-37. PubMed ID: 17197537
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The human BARX2 gene: genomic structure, chromosomal localization, and single nucleotide polymorphisms.
    Hjalt TA; Murray JC
    Genomics; 1999 Dec; 62(3):456-9. PubMed ID: 10644443
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome.
    Semina EV; Reiter R; Leysens NJ; Alward WL; Small KW; Datson NA; Siegel-Bartelt J; Bierke-Nelson D; Bitoun P; Zabel BU; Carey JC; Murray JC
    Nat Genet; 1996 Dec; 14(4):392-9. PubMed ID: 8944018
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The pitx2 homeobox protein is required early for endoderm formation and nodal signaling.
    Faucourt M; Houliston E; Besnardeau L; Kimelman D; Lepage T
    Dev Biol; 2001 Jan; 229(2):287-306. PubMed ID: 11203696
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cloning, characterization, localization, and mutational screening of the human BARX1 gene.
    Gould DB; Walter MA
    Genomics; 2000 Sep; 68(3):336-42. PubMed ID: 10995576
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Exclusion of PITX2 mutations as a major cause of CHARGE association.
    Martin DM; Probst FJ; Fox SE; Schimmenti LA; Semina EV; Hefner MA; Belmont JW; Camper SA
    Am J Med Genet; 2002 Jul; 111(1):27-30. PubMed ID: 12124729
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of the first intragenic deletion of the PITX2 gene causing an Axenfeld-Rieger Syndrome: case report.
    de la Houssaye G; Bieche I; Roche O; Vieira V; Laurendeau I; Arbogast L; Zeghidi H; Rapp P; Halimi P; Vidaud M; Dufier JL; Menasche M; Abitbol M
    BMC Med Genet; 2006 Nov; 7():82. PubMed ID: 17134502
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Current molecular understanding of Axenfeld-Rieger syndrome.
    Hjalt TA; Semina EV
    Expert Rev Mol Med; 2005 Nov; 7(25):1-17. PubMed ID: 16274491
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cytogenetically invisible microdeletions involving PITX2 in Rieger syndrome.
    Engenheiro E; Saraiva J; Carreira I; Ramos L; Ropers HH; Silva E; Tommerup N; Tümer Z
    Clin Genet; 2007 Nov; 72(5):464-70. PubMed ID: 17850355
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Construction and analysis of a sequence-ready map in 4q25: Rieger syndrome can be caused by haploinsufficiency of RIEG, but also by chromosome breaks approximately 90 kb upstream of this gene.
    Flomen RH; Vatcheva R; Gorman PA; Baptista PR; Groet J; Barisić I; Ligutic I; Nizetić D
    Genomics; 1998 Feb; 47(3):409-13. PubMed ID: 9480756
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.