The Unfolded Protein Response in Amelogenesis and Enamel Pathologies

Por Brookes, Steven J., Barron, Martin J., Dixon, Michael J., Kirkham, Jennifer
Publicado no Front Physiol (2017)

Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia

Por Barron, Martin J, McDonnell, Sinead T, MacKie, Iain, Dixon, Michael J
Publicado em 2008

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 em 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 em 2014

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 em 2008

Defects in multiple complexes of the respiratory chain are present in ageing human colonic crypts

Por Greaves, Laura C., Barron, Martin J., Plusa, Stefan, Kirkwood, Thomas B., Mathers, John C., Taylor, Robert W., Turnbull, Doug M.
Publicado em 2010

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 em 2010

Entry Mechanisms of Herpes Simplex Virus 1 into Murine Epidermis: Involvement of Nectin-1 and Herpesvirus Entry Mediator as Cellular Receptors

Por Petermann, Philipp, Thier, Katharina, Rahn, Elena, Rixon, Frazer J., Bloch, Wilhelm, Özcelik, Semra, Krummenacher, Claude, Barron, Martin J., Dixon, Michael J., Scheu, Stefanie, Pfeffer, Klaus, Knebel-Mörsdorf, Dagmar
Publicado no J Virol (2014)

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 no Hum Mol Genet (2017)

Mitochondrial DNA Defects and Selective Extraocular Muscle Involvement in CPEO

Por Greaves, Laura C., Yu-Wai-Man, Patrick, Blakely, Emma L., Krishnan, Kim J., Beadle, Nina E., Kerin, Jamie, Barron, Martin J., Griffiths, Philip G., Dickinson, Alison J., Turnbull, Douglass M., Taylor, Robert W.
Publicado em 2010

Mitochondrial DNA mutations in human colonic crypt stem cells

Por Taylor, Robert W., Barron, Martin J., Borthwick, Gillian M., Gospel, Amy, Chinnery, Patrick F., Samuels, David C., Taylor, Geoffrey A., Plusa, Stefan M., Needham, Stephanie J., Greaves, Laura C., Kirkwood, Thomas B.L., Turnbull, Douglass M.
Publicado em 2003

Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome

Por O'Sullivan, James, Bitu, Carolina C., Daly, Sarah B., Urquhart, Jill E., Barron, Martin J., Bhaskar, Sanjeev S., Martelli-Júnior, Hercilio, dos Santos Neto, Pedro Eleuterio, Mansilla, Maria A., Murray, Jeffrey C., Coletta, Ricardo D., Black, Graeme C.M., Dixon, Michael J.
Publicado em 2011

Mitochondrial DNA mutations are established in human colonic stem cells, and mutated clones expand by crypt fission

Por Greaves, Laura C., Preston, Sean L., Tadrous, Paul J., Taylor, Robert W., Barron, Martin J., Oukrif, Dahmane, Leedham, Simon J., Deheragoda, Maesha, Sasieni, Peter, Novelli, Marco R., Jankowski, Janusz A. Z., Turnbull, Douglass M., Wright, Nicholas A., McDonald, Stuart A. C.
Publicado em 2006