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Mechanisms of Development|October 1, 2003
Expression of mOb1, a novel atypical 73 amino acid K50-homeodomain protein, during mouse developmentJimi Adu, Fong T Leong, Neil R Smith, et al.Frontiers in Physiology|July 12, 2017
Amelogenesis Imperfecta; Genes, Proteins, and PathwaysClaire E L Smith, James A Poulter, Agne Antanaviciute, et al.Human Molecular Genetics|July 15, 2016
Deletion of amelotin exons 3-6 is associated with amelogenesis imperfectaClaire E L Smith, Gina Murillo, Steven J Brookes, et al.Human Molecular Genetics|December 10, 2013
A missense mutation in ITGB6 causes pitted hypomineralized amelogenesis imperfectaJames A Poulter, Steven J Brookes, Roger C Shore, et al.Human Molecular Genetics|May 27, 2014
Deletion of ameloblastin exon 6 is associated with amelogenesis imperfectaJames A Poulter, Gina Murillo, Steven J Brookes, et al.European Journal of Human Genetics : EJHG|May 18, 2017
Defects in the acid phosphatase ACPT cause recessive hypoplastic amelogenesis imperfectaClaire El Smith, Laura LE Whitehouse, James A Poulter, et al.Orphanet Journal of Rare Diseases|June 15, 2014
Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutationsMuriel de la Dure-Molla, Mickael Quentric, Paulo Marcio Yamaguti, et al.Frontiers in Physiology|June 15, 2017
A Fourth KLK4 Mutation Is Associated with Enamel Hypomineralisation and Structural AbnormalitiesClaire E L Smith, Jennifer Kirkham, Peter F Day, et al.American Journal of Human Genetics|October 27, 2009
Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfectaWalid El-Sayed, David A Parry, Roger C Shore, et al.Human Molecular Genetics|March 24, 2017
Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stressSteven J Brookes, Martin J Barron, Claire E L Smith, et al.Pageof 4