Preparative SDS PAGE as an Alternative to His-Tag Purification of Recombinant Amelogenin

por Gabe, Claire M., Brookes, Steven J., Kirkham, Jennifer
Publicado 2017

The Unfolded Protein Response in Amelogenesis and Enamel Pathologies

por Brookes, Steven J., Barron, Martin J., Dixon, Michael J., Kirkham, Jennifer
Publicado 2017

Editorial: Tooth Enamel: Frontiers in Mineral Chemistry and Biochemistry, Integrative Cell Biology and Genetics

por Brookes, Steven J., Berdal, Ariane, Vieira, Alexandre R., Babajko, Sylvie, Kirkham, Jennifer
Publicado 2018

Is the 32-kDa fragment the functional enamelin unit in all species?

por Brookes, Steven J, Kingswell, Nicola J, Barron, Martin J, Dixon, Michael J, Kirkham, Jennifer
Publicado 2011

Endoplasmic reticulum stress in amelogenesis imperfecta and phenotypic rescue using 4-phenylbutyrate

por Brookes, Steven J., Barron, Martin J., Boot-Handford, Ray, Kirkham, Jennifer, Dixon, Michael J.
Publicado 2014

Subfractions of enamel matrix derivative differentially influence cytokine secretion from human oral fibroblasts

por Villa, Oscar, Brookes, Steven J, Thiede, Bernd, Heijl, Lars, Lyngstadaas, Staale P, Reseland, Janne E
Publicado 2015

Enamel Research: Priorities and Future Directions

por Kirkham, Jennifer, Brookes, Steven J., Diekwisch, Thomas G. H., Margolis, Henry C., Berdal, Ariane, Hubbard, Michael J.
Publicado 2017

The cell adhesion molecule nectin-1 is critical for normal enamel formation in mice

por Barron, Martin J., Brookes, Steven J., Draper, Clare E., Garrod, David, Kirkham, Jennifer, Shore, Roger C., Dixon, Michael J.
Publicado 2008

EMD in periodontal regenerative surgery modulates cytokine profiles: A randomised controlled clinical trial

por Villa, Oscar, Wohlfahrt, Johan C., Koldsland, Odd Carsten, Brookes, Steven J., Lyngstadaas, Staale P., Aass, Anne M., Reseland, Janne E.
Publicado 2016

Amelogenesis Imperfecta; Genes, Proteins, and Pathways

por Smith, Claire E. L., Poulter, James A., Antanaviciute, Agne, Kirkham, Jennifer, Brookes, Steven J., Inglehearn, Chris F., Mighell, Alan J.
Publicado 2017

Deletion of amelotin exons 3–6 is associated with amelogenesis imperfecta

por Smith, Claire E.L., Murillo, Gina, Brookes, Steven J., Poulter, James A., Silva, Sandra, Kirkham, Jennifer, Inglehearn, Chris F., Mighell, Alan J.
Publicado 2016

A missense mutation in ITGB6 causes pitted hypomineralized amelogenesis imperfecta

por Poulter, James A., Brookes, Steven J., Shore, Roger C., Smith, Claire E. L., Abi Farraj, Layal, Kirkham, Jennifer, Inglehearn, Chris F., Mighell, Alan J.
Publicado 2014

Deletion of ameloblastin exon 6 is associated with amelogenesis imperfecta

por 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.
Publicado 2014

Defects in the acid phosphatase ACPT cause recessive hypoplastic amelogenesis imperfecta

por Smith, Claire EL, Whitehouse, Laura LE, Poulter, James A, Brookes, Steven J, Day, Peter F, Soldani, Francesca, Kirkham, Jennifer, Inglehearn, Chris F, Mighell, Alan J
Publicado 2017

A mutation in the mouse Amelx tri-tyrosyl domain results in impaired secretion of amelogenin and phenocopies human X-linked amelogenesis imperfecta

por 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.
Publicado 2010

A Fourth KLK4 Mutation Is Associated with Enamel Hypomineralisation and Structural Abnormalities

por 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.
Publicado 2017

Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stress

por Brookes, Steven J., Barron, Martin J., Smith, Claire E.L., Poulter, James A., Mighell, Alan J., Inglehearn, Chris F., Brown, Catriona J., Rodd, Helen, Kirkham, Jennifer, Dixon, Michael J.
Publicado 2017

New missense variants in RELT causing hypomineralised amelogenesis imperfecta

por Nikolopoulos, Georgios, Smith, Claire E.L., Brookes, Steven J., El‐Asrag, Mohammed E., Brown, Catriona J., Patel, Anesha, Murillo, Gina, O'Connell, Mary J., Inglehearn, Chris F., Mighell, Alan J.
Publicado 2020

Spectrum of PEX1 and PEX6 variants in Heimler syndrome

por 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
Publicado 2016