Amelogenesis Imperfecta; Genes, Proteins, and Pathways
Smith, Claire E L, Poulter, James A, Antanaviciute, Agne, Kirkham, Jennifer, Brookes, Steven J, Inglehearn, Chris F, Mighell, Alan J
Published in Frontiers in physiology (26.06.2017)
Published in Frontiers in physiology (26.06.2017)
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Journal Article
Identification of Mutations in SLC24A4, Encoding a Potassium-Dependent Sodium/Calcium Exchanger, as a Cause of Amelogenesis Imperfecta
Parry, David A., Poulter, James A., Logan, Clare V., Brookes, Steven J., Jafri, Hussain, Ferguson, Christopher H., Anwari, Babra M., Rashid, Yasmin, Zhao, Haiqing, Johnson, Colin A., Inglehearn, Chris F., Mighell, Alan J.
Published in American journal of human genetics (07.02.2013)
Published in American journal of human genetics (07.02.2013)
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Journal Article
Spectrum of PEX1 and PEX6 variants in Heimler syndrome
Smith, Claire E L, Poulter, James A, Levin, Alex V, Capasso, Jenina E, Price, Susan, Ben-Yosef, Tamar, Sharony, Reuven, Newman, William G, Shore, Roger C, Brookes, Steven J, Mighell, Alan J, Inglehearn, Chris F
Published in European journal of human genetics : EJHG (01.11.2016)
Published in European journal of human genetics : EJHG (01.11.2016)
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Journal Article
Preparative SDS PAGE as an Alternative to His-Tag Purification of Recombinant Amelogenin
Gabe, Claire M, Brookes, Steven J, Kirkham, Jennifer
Published in Frontiers in physiology (16.06.2017)
Published in Frontiers in physiology (16.06.2017)
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Journal Article
Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta
Parry, David A., Brookes, Steven J., Logan, Clare V., Poulter, James A., El-Sayed, Walid, Al-Bahlani, Suhaila, Al Harasi, Sharifa, Sayed, Jihad, Raïf, El Mostafa, Shore, Roger C., Dashash, Mayssoon, Barron, Martin, Morgan, Joanne E., Carr, Ian M., Taylor, Graham R., Johnson, Colin A., Aldred, Michael J., Dixon, Michael J., Wright, J. Tim, Kirkham, Jennifer, Inglehearn, Chris F., Mighell, Alan J.
Published in American journal of human genetics (07.09.2012)
Published in American journal of human genetics (07.09.2012)
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Journal Article
The Unfolded Protein Response in Amelogenesis and Enamel Pathologies
Brookes, Steven J, Barron, Martin J, Dixon, Michael J, Kirkham, Jennifer
Published in Frontiers in physiology (08.09.2017)
Published in Frontiers in physiology (08.09.2017)
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Journal Article
Adaptor protein complex 2–mediated, clathrin‐dependent endocytosis, and related gene activities, are a prominent feature during maturation stage amelogenesis
Lacruz, Rodrigo S, Brookes, Steven J, Wen, Xin, Jimenez, Jaime M, Vikman, Susanna, Hu, Ping, White, Shane N, Lyngstadaas, S Petter, Okamoto, Curtis T, Smith, Charles E, Paine, Michael L
Published in Journal of bone and mineral research (01.03.2013)
Published in Journal of bone and mineral research (01.03.2013)
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Journal Article
Enamel Research: Priorities and Future Directions
Kirkham, Jennifer, Brookes, Steven J, Diekwisch, Thomas G H, Margolis, Henry C, Berdal, Ariane, Hubbard, Michael J
Published in Frontiers in physiology (20.07.2017)
Published in Frontiers in physiology (20.07.2017)
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Journal Article
A Fourth KLK4 Mutation Is Associated with Enamel Hypomineralisation and Structural Abnormalities
Smith, Claire E L, Kirkham, Jennifer, Day, Peter F, Soldani, Francesca, McDerra, Esther J, Poulter, James A, Inglehearn, Christopher F, Mighell, Alan J, Brookes, Steven J
Published in Frontiers in physiology (29.05.2017)
Published in Frontiers in physiology (29.05.2017)
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Journal Article
Ameloblastin expression and putative autoregulation in mesenchymal cells suggest a role in early bone formation and repair
Tamburstuen, Margareth V, Reseland, Janne E, Spahr, Axel, Brookes, Steven J, Kvalheim, Gunnar, Slaby, Ivan, Snead, Malcolm L, Lyngstadaas, S. Petter
Published in Bone (New York, N.Y.) (01.02.2011)
Published in Bone (New York, N.Y.) (01.02.2011)
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Journal Article
A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta
Barron, Martin J., Brookes, Steven J., Kirkham, Jennifer, Shore, Roger C., Hunt, Charlotte, Mironov, Aleksandr, Kingswell, Nicola J., Maycock, Joanne, Shuttleworth, C. Adrian, Dixon, Michael J.
Published in Human molecular genetics (01.04.2010)
Published in Human molecular genetics (01.04.2010)
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Journal Article
A missense mutation in ITGB6 causes pitted hypomineralized amelogenesis imperfecta
Poulter, James A., Brookes, Steven J., Shore, Roger C., Smith, Claire E. L., Abi Farraj, Layal, Kirkham, Jennifer, Inglehearn, Chris F., Mighell, Alan J.
Published in Human molecular genetics (15.04.2014)
Published in Human molecular genetics (15.04.2014)
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Journal Article
Is the 32-kDa fragment the functional enamelin unit in all species?
Brookes, Steven J., Kingswell, Nicola J., Barron, Martin J., Dixon, Michael J., Kirkham, Jennifer
Published in European journal of oral sciences (01.12.2011)
Published in European journal of oral sciences (01.12.2011)
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Journal Article
Determination of protein regions responsible for interactions of amelogenin with CD63 and LAMP1
Zou, YanMing, Wang, HongJun, Shapiro, Jason L, Okamoto, Curtis T, Brookes, Steven J, Lyngstadaas, S Petter, Snead, Malcolm L, Paine, Michael L
Published in Biochemical journal (15.12.2007)
Published in Biochemical journal (15.12.2007)
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Journal Article
Subfractions of enamel matrix derivative differentially influence cytokine secretion from human oral fibroblasts
Villa, Oscar, Brookes, Steven J, Thiede, Bernd, Heijl, Lars, Lyngstadaas, Staale P, Reseland, Janne E
Published in Journal of tissue engineering (01.01.2015)
Published in Journal of tissue engineering (01.01.2015)
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Journal Article
Enamel Defects Reflect Perinatal Exposure to Bisphenol A
Jedeon, Katia, De la Dure-Molla, Muriel, Brookes, Steven J, Loiodice, Sophia, Marciano, Clémence, Kirkham, Jennifer, Canivenc-Lavier, Marie-Chantal, Boudalia, Sofiane, Bergès, Raymond, Harada, Hidemitsu, Berdal, Ariane, Babajko, Sylvie
Published in The American journal of pathology (01.07.2013)
Published in The American journal of pathology (01.07.2013)
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Journal Article
Deletion of ameloblastin exon 6 is associated with amelogenesis imperfecta
Poulter, James A, Murillo, Gina, Brookes, Steven J, Smith, Claire E L, Parry, David A, Silva, Sandra, Kirkham, Jennifer, Inglehearn, Chris F, Mighell, Alan J
Published in Human molecular genetics (15.10.2014)
Published in Human molecular genetics (15.10.2014)
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Journal Article