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Steven J Brookes

Showing results (21-30 of 31) with videos related to

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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 Oral Sciences|January 17, 2012
Enamel matrix derivative stimulates expression and secretion of resistin in mesenchymal cellsMaria V Obregon-Whittle, Astrid K Stunes, Sofia Almqvist, et al.
Human Molecular Genetics|January 14, 2010
A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfectaMartin J Barron, Steven J Brookes, Jennifer Kirkham, et al.
Frontiers in Physiology|June 15, 2017
A Fourth <i>KLK4</i> Mutation Is Associated with Enamel Hypomineralisation and Structural AbnormalitiesClaire E L Smith, Jennifer Kirkham, Peter F Day, 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.
Clinical Genetics|February 14, 2020
New missense variants in RELT causing hypomineralised amelogenesis imperfectaGeorgios Nikolopoulos, Claire E L Smith, Steven J Brookes, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 10, 2012
Adaptor protein complex 2-mediated, clathrin-dependent endocytosis, and related gene activities, are a prominent feature during maturation stage amelogenesisRodrigo S Lacruz, Steven J Brookes, Xin Wen, et al.
The American Journal of Pathology|June 15, 2013
Enamel defects reflect perinatal exposure to bisphenol AKatia Jedeon, Muriel De la Dure-Molla, Steven J Brookes, et al.
American Journal of Human Genetics|February 5, 2013
Identification of mutations in SLC24A4, encoding a potassium-dependent sodium/calcium exchanger, as a cause of amelogenesis imperfectaDavid A Parry, James A Poulter, Clare V Logan, et al.
European Journal of Human Genetics : EJHG|June 16, 2016
Spectrum of PEX1 and PEX6 variants in Heimler syndromeClaire E L Smith, James A Poulter, Alex V Levin, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
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 Oral Sciences|January 17, 2012
Enamel matrix derivative stimulates expression and secretion of resistin in mesenchymal cellsMaria V Obregon-Whittle, Astrid K Stunes, Sofia Almqvist, et al.
Human Molecular Genetics|January 14, 2010
A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfectaMartin J Barron, Steven J Brookes, Jennifer Kirkham, et al.
Frontiers in Physiology|June 15, 2017
A Fourth <i>KLK4</i> Mutation Is Associated with Enamel Hypomineralisation and Structural AbnormalitiesClaire E L Smith, Jennifer Kirkham, Peter F Day, 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.
Clinical Genetics|February 14, 2020
New missense variants in RELT causing hypomineralised amelogenesis imperfectaGeorgios Nikolopoulos, Claire E L Smith, Steven J Brookes, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 10, 2012
Adaptor protein complex 2-mediated, clathrin-dependent endocytosis, and related gene activities, are a prominent feature during maturation stage amelogenesisRodrigo S Lacruz, Steven J Brookes, Xin Wen, et al.
The American Journal of Pathology|June 15, 2013
Enamel defects reflect perinatal exposure to bisphenol AKatia Jedeon, Muriel De la Dure-Molla, Steven J Brookes, et al.
American Journal of Human Genetics|February 5, 2013
Identification of mutations in SLC24A4, encoding a potassium-dependent sodium/calcium exchanger, as a cause of amelogenesis imperfectaDavid A Parry, James A Poulter, Clare V Logan, et al.
European Journal of Human Genetics : EJHG|June 16, 2016
Spectrum of PEX1 and PEX6 variants in Heimler syndromeClaire E L Smith, James A Poulter, Alex V Levin, et al.
Pageof 4