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 *

361 related articles for article (PubMed ID: 10498698)

  • 1. Dosage requirement of Pitx2 for development of multiple organs.
    Gage PJ; Suh H; Camper SA
    Development; 1999 Oct; 126(20):4643-51. PubMed ID: 10498698
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Pitx2 regulates lung asymmetry, cardiac positioning and pituitary and tooth morphogenesis.
    Lin CR; Kioussi C; O'Connell S; Briata P; Szeto D; Liu F; Izpisúa-Belmonte JC; Rosenfeld MG
    Nature; 1999 Sep; 401(6750):279-82. PubMed ID: 10499586
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in zebrafish pitx2 model congenital malformations in Axenfeld-Rieger syndrome but do not disrupt left-right placement of visceral organs.
    Ji Y; Buel SM; Amack JD
    Dev Biol; 2016 Aug; 416(1):69-81. PubMed ID: 27297886
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pitx2 and cardiac development: a molecular link between left/right signaling and congenital heart disease.
    Campione M; Acosta L; Martínez S; Icardo JM; Aránega A; Franco D
    Cold Spring Harb Symp Quant Biol; 2002; 67():89-95. PubMed ID: 12858528
    [No 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. Rieger syndrome: a clinical, molecular, and biochemical analysis.
    Amendt BA; Semina EV; Alward WL
    Cell Mol Life Sci; 2000 Oct; 57(11):1652-66. PubMed ID: 11092457
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Disruption of foxc1 genes in zebrafish results in dosage-dependent phenotypes overlapping Axenfeld-Rieger syndrome.
    Ferre-Fernández JJ; Sorokina EA; Thompson S; Collery RF; Nordquist E; Lincoln J; Semina EV
    Hum Mol Genet; 2020 Sep; 29(16):2723-2735. PubMed ID: 32720677
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A role of the cryptic gene in the correct establishment of the left-right axis.
    Gaio U; Schweickert A; Fischer A; Garratt AN; Müller T; Ozcelik C; Lankes W; Strehle M; Britsch S; Blum M; Birchmeier C
    Curr Biol; 1999 Nov; 9(22):1339-42. PubMed ID: 10574770
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pitx2 is required at multiple stages of pituitary organogenesis: pituitary primordium formation and cell specification.
    Suh H; Gage PJ; Drouin J; Camper SA
    Development; 2002 Jan; 129(2):329-37. PubMed ID: 11807026
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mouse Pitx2 deficiency leads to anomalies of the ventral body wall, heart, extra- and periocular mesoderm and right pulmonary isomerism.
    Kitamura K; Miura H; Miyagawa-Tomita S; Yanazawa M; Katoh-Fukui Y; Suzuki R; Ohuchi H; Suehiro A; Motegi Y; Nakahara Y; Kondo S; Yokoyama M
    Development; 1999 Dec; 126(24):5749-58. PubMed ID: 10572050
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes.
    Idrees F; Bloch-Zupan A; Free SL; Vaideanu D; Thompson PJ; Ashley P; Brice G; Rutland P; Bitner-Glindzicz M; Khaw PT; Fraser S; Sisodiya SM; Sowden JC
    Am J Med Genet B Neuropsychiatr Genet; 2006 Mar; 141B(2):184-91. PubMed ID: 16389592
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. The homeobox gene Pitx2: mediator of asymmetric left-right signaling in vertebrate heart and gut looping.
    Campione M; Steinbeisser H; Schweickert A; Deissler K; van Bebber F; Lowe LA; Nowotschin S; Viebahn C; Haffter P; Kuehn MR; Blum M
    Development; 1999 Mar; 126(6):1225-34. PubMed ID: 10021341
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Homeodomain factor Nkx2-5 in heart development and disease.
    Harvey RP; Lai D; Elliott D; Biben C; Solloway M; Prall O; Stennard F; Schindeler A; Groves N; Lavulo L; Hyun C; Yeoh T; Costa M; Furtado M; Kirk E
    Cold Spring Harb Symp Quant Biol; 2002; 67():107-14. PubMed ID: 12858530
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. Differential expression and functional analysis of Pitx2 isoforms in regulation of heart looping in the chick.
    Yu X; St Amand TR; Wang S; Li G; Zhang Y; Hu YP; Nguyen L; Qiu MS; Chen YP
    Development; 2001 Mar; 128(6):1005-13. PubMed ID: 11222154
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesis.
    Berry FB; Lines MA; Oas JM; Footz T; Underhill DA; Gage PJ; Walter MA
    Hum Mol Genet; 2006 Mar; 15(6):905-19. PubMed ID: 16449236
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.