AMELX (Polish Wikipedia)

Analysis of information sources in references of the Wikipedia article "AMELX" in Polish language version.

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doi.org

doi.org

  • Gibson CW, Yuan ZA, Hall B, Longenecker G, Chen E, Thyagarajan T, Sreenath T, Wright JT, Decker S, Piddington R, Harrison G, Kulkarni AB. Amelogenin-deficient mice display an amelogenesis imperfecta phenotype. „The Journal of Biological Chemistry”. 276 (34), s. 31871–5, Aug 2001. DOI: 10.1074/jbc.M104624200. PMID: 11406633. 
  • Wright JT. The molecular etiologies and associated phenotypes of amelogenesis imperfecta. „American Journal of Medical Genetics. Part A”. 140 (23), s. 2547–55, 2006-12. DOI: 10.1002/ajmg.a.31358. PMID: 16838342. PMCID: PMC1847600. 
  • Li Y, Suggs C, Wright JT, Yuan ZA, Aragon M, Fong H, Simmons D, Daly B, Golub EE, Harrison G, Kulkarni AB, Gibson CW. Partial rescue of the amelogenin null dental enamel phenotype. „The Journal of Biological Chemistry”. 283 (22), s. 15056-15062, 2008-05. DOI: 10.1074/jbc.M707992200. PMID: 18390542. 

dx.doi.org

  • Michael Beyeler i inni, Identification of a fibronectin interaction site in the extracellular matrix protein ameloblastin, t. 316, Elsevier, 2010, s. 1202-1212, DOI10.1016/j.yexcr.2009.12.019 (ang.).

nih.gov

ncbi.nlm.nih.gov

  • AceView: Gene:AMELX, a comprehensive annotation of human, mouse and worm genes with mRNAs or ESTsAceView.. National Center for Biotechnology Information, United States National Institutes of Health.
  • Salido EC, Yen PH, Koprivnikar K, Yu LC, Shapiro LJ. The human enamel protein gene amelogenin is expressed from both the X and the Y chromosomes. „American Journal of Human Genetics”. 50 (2), s. 303–316, 1992-02. PMID: 1734713. PMCID: PMC1682460. 
  • Gibson CW, Yuan ZA, Hall B, Longenecker G, Chen E, Thyagarajan T, Sreenath T, Wright JT, Decker S, Piddington R, Harrison G, Kulkarni AB. Amelogenin-deficient mice display an amelogenesis imperfecta phenotype. „The Journal of Biological Chemistry”. 276 (34), s. 31871–5, Aug 2001. DOI: 10.1074/jbc.M104624200. PMID: 11406633. 
  • Wright JT. The molecular etiologies and associated phenotypes of amelogenesis imperfecta. „American Journal of Medical Genetics. Part A”. 140 (23), s. 2547–55, 2006-12. DOI: 10.1002/ajmg.a.31358. PMID: 16838342. PMCID: PMC1847600. 
  • Li Y, Suggs C, Wright JT, Yuan ZA, Aragon M, Fong H, Simmons D, Daly B, Golub EE, Harrison G, Kulkarni AB, Gibson CW. Partial rescue of the amelogenin null dental enamel phenotype. „The Journal of Biological Chemistry”. 283 (22), s. 15056-15062, 2008-05. DOI: 10.1074/jbc.M707992200. PMID: 18390542. 

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