The Unfolded Protein Response in Amelogenesis and Enamel Pathologies

di Brookes, Steven J., Barron, Martin J., Dixon, Michael J., Kirkham, Jennifer
Pubblicato in Front Physiol (2017)

Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia

di Barron, Martin J, McDonnell, Sinead T, MacKie, Iain, Dixon, Michael J
Pubblicazione 2008

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

di Brookes, Steven J, Kingswell, Nicola J, Barron, Martin J, Dixon, Michael J, Kirkham, Jennifer
Pubblicazione 2011

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

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

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

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

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

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

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

di 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.
Pubblicazione 2010

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

di 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
Pubblicato in J Virol (2014)

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

di 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.
Pubblicato in Hum Mol Genet (2017)

Mitochondrial DNA Defects and Selective Extraocular Muscle Involvement in CPEO

di 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.
Pubblicazione 2010

Mitochondrial DNA mutations in human colonic crypt stem cells

di 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.
Pubblicazione 2003

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

di 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.
Pubblicazione 2011

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

di 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.
Pubblicazione 2006