Publications by authors named "Steven Brookes"

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New missense variants in RELT causing hypomineralised amelogenesis imperfecta.
Georgios Nikolopoulos, Claire E L Smith, Steven J Brookes, Mohammed E El-Asrag, Catriona J Brown

Clin Genet· May 2020

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Purification of Developing Enamel Matrix Proteins Using Preparative SDS-PAGE.
Steven J Brookes, Claire M Gabe

Methods Mol Biol· June 2019

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Using ImageJ (Fiji) to Analyze and Present X-Ray CT Images of Enamel.
Steven J Brookes

Methods Mol Biol· June 2019

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Editorial: Tooth Enamel: Frontiers in Mineral Chemistry and Biochemistry, Integrative Cell Biology and Genetics.
Steven J Brookes, Ariane Berdal, Alexandre R Vieira, Sylvie Babajko, Jennifer Kirkham

Front Physiol· August 2018

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The Unfolded Protein Response in Amelogenesis and Enamel Pathologies.
Steven J Brookes, Martin J Barron, Michael J Dixon, Jennifer Kirkham

Front Physiol· September 2017

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Defects in the acid phosphatase ACPT cause recessive hypoplastic amelogenesis imperfecta.
Claire El Smith, Laura LE Whitehouse, James A Poulter, Steven J Brookes, Peter F Day

Eur J Hum Genet· August 2017

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Enamel Research: Priorities and Future Directions.
Jennifer Kirkham, Steven J Brookes, Thomas G H Diekwisch, Henry C Margolis, Ariane Berdal

Front Physiol· July 2017

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Preparative SDS PAGE as an Alternative to His-Tag Purification of Recombinant Amelogenin.
Claire M Gabe, Steven J Brookes, Jennifer Kirkham

Front Physiol· June 2017

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Amelogenesis Imperfecta; Genes, Proteins, and Pathways.
Claire E L Smith, James A Poulter, Agne Antanaviciute, Jennifer Kirkham, Steven J Brookes

Front Physiol· June 2017

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Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stress.
Steven J Brookes, Martin J Barron, Claire E L Smith, James A Poulter, Alan J Mighell

Hum Mol Genet· May 2017

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A Fourth Mutation Is Associated with Enamel Hypomineralisation and Structural Abnormalities.
Claire E L Smith, Jennifer Kirkham, Peter F Day, Francesca Soldani, Esther J McDerra, Steven J Brookes

Front Physiol· May 2017

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Spectrum of PEX1 and PEX6 variants in Heimler syndrome.
Claire E L Smith, James A Poulter, Alex V Levin, Jenina E Capasso, Susan Price, Steven J Brookes

Eur J Hum Genet· November 2016

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Deletion of amelotin exons 3-6 is associated with amelogenesis imperfecta.
Claire E L Smith, Gina Murillo, Steven J Brookes, James A Poulter, Sandra Silva

Hum Mol Genet· August 2016

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EMD in periodontal regenerative surgery modulates cytokine profiles: A randomised controlled clinical trial.
Oscar Villa, Johan C Wohlfahrt, Odd Carsten Koldsland, Steven J Brookes, Staale P Lyngstadaas

Sci Rep· March 2016

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Tracking endogenous amelogenin and ameloblastin in vivo.
Jaime Jacques, Dominique Hotton, Muriel De la Dure-Molla, Stephane Petit, Audrey Asselin, Steven Joseph Brookes

PLoS One· October 2015

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Subfractions of enamel matrix derivative differentially influence cytokine secretion from human oral fibroblasts.
Oscar Villa, Steven J Brookes, Bernd Thiede, Lars Heijl, Staale P Lyngstadaas

J Tissue Eng· June 2015

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Deletion of ameloblastin exon 6 is associated with amelogenesis imperfecta.
James A Poulter, Gina Murillo, Steven J Brookes, Claire E L Smith, David A Parry

Hum Mol Genet· October 2014

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Endoplasmic reticulum stress in amelogenesis imperfecta and phenotypic rescue using 4-phenylbutyrate.
Steven J Brookes, Martin J Barron, Ray Boot-Handford, Jennifer Kirkham, Michael J Dixon

Hum Mol Genet· May 2014

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A missense mutation in ITGB6 causes pitted hypomineralized amelogenesis imperfecta.
James A Poulter, Steven J Brookes, Roger C Shore, Claire E L Smith, Layal Abi Farraj

Hum Mol Genet· April 2014

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Enamel defects reflect perinatal exposure to bisphenol A.
Katia Jedeon, Muriel De la Dure-Molla, Steven J Brookes, Sophia Loiodice, Clémence Marciano

Am J Pathol· July 2013

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Cellular uptake and processing of enamel matrix derivative by human periodontal ligament fibroblasts.
James D Lees, Colin Robinson, Roger C Shore, Michael L Paine, Steven J Brookes

Arch Oral Biol· April 2013

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Adaptor protein complex 2-mediated, clathrin-dependent endocytosis, and related gene activities, are a prominent feature during maturation stage amelogenesis.
Rodrigo S Lacruz, Steven J Brookes, Xin Wen, Jaime M Jimenez, Susanna Vikman

J Bone Miner Res· March 2013

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Identification of mutations in SLC24A4, encoding a potassium-dependent sodium/calcium exchanger, as a cause of amelogenesis imperfecta.
David A Parry, James A Poulter, Clare V Logan, Steven J Brookes, Hussain Jafri

Am J Hum Genet· February 2013

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Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta.
David A Parry, Steven J Brookes, Clare V Logan, James A Poulter, Walid El-Sayed

Am J Hum Genet· September 2012

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Enamel matrix derivative stimulates expression and secretion of resistin in mesenchymal cells.
Maria V Obregon-Whittle, Astrid K Stunes, Sofia Almqvist, Steven J Brookes, James D Lees

Eur J Oral Sci· December 2011

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