Items where authors include "Brookes, SJ"

Article

Nikolopoulos, G orcid.org/0000-0003-3166-8372, Smith, CEL orcid.org/0000-0001-8320-5105, Brookes, SJ et al. (7 more authors) (2020) New missense variants in RELT causing hypomineralised amelogenesis imperfecta. Clinical Genetics, 97 (5). pp. 688-695. ISSN 0009-9163

Smith, CEL orcid.org/0000-0001-8320-5105, Poulter, JA orcid.org/0000-0003-2048-5693, Brookes, SJ orcid.org/0000-0002-9097-7311 et al. (8 more authors) (2019) Phenotype and variant spectrum in the LAMB3 form of amelogenesis imperfecta. Journal of Dental Research, 98 (6). pp. 698-704. ISSN 0022-0345

Brookes, SJ orcid.org/0000-0002-9097-7311, Berdal, A, Vieira, AR et al. (2 more authors) (2018) Editorial: Tooth Enamel: Frontiers in Mineral Chemistry and Biochemistry, Integrative Cell Biology and Genetics. Frontiers in Physiology, 9. ARTN 1153. ISSN 1664-042X

Pechlivani, N orcid.org/0000-0001-5041-5763, Devine, DA orcid.org/0000-0002-8037-9254, Marsh, PD et al. (2 more authors) (2018) Novel methodology for determining the effect of adsorbates on human enamel acid dissolution. Archives of Oral Biology, 85. pp. 46-50. ISSN 0003-9969

Brookes, SJ orcid.org/0000-0002-9097-7311, Barron, MJ, Dixon, MJ et al. (1 more author) (2017) The Unfolded Protein Response in Amelogenesis and Enamel Pathologies. Frontiers in Physiology, 8. 653. ISSN 1664-042X

Smith, CEL orcid.org/0000-0001-8320-5105, Whitehouse, LLE, Poulter, JA orcid.org/0000-0003-2048-5693 et al. (6 more authors) (2017) Defects in the acid phosphatase ACPT cause recessive hypoplastic amelogenesis imperfecta. European Journal of Human Genetics, 25 (8). pp. 1015-1019. ISSN 1018-4813

Kirkham, J, Brookes, SJ orcid.org/0000-0002-9097-7311, Diekwisch, TGH et al. (3 more authors) (2017) Enamel research: Priorities and future directions. Frontiers in Physiology, 8. 513. ISSN 1664-042X

Smith, CEL orcid.org/0000-0001-8320-5105, Poulter, JA orcid.org/0000-0003-2048-5693, Antanaviciute, A et al. (4 more authors) (2017) Amelogenesis Imperfecta; Genes, Proteins And Pathways. Frontiers in Physiology, 8. 435. ISSN 1664-042X

Gabe, CM, Brookes, SJ orcid.org/0000-0002-9097-7311 and Kirkham, J (2017) Preparative SDS PAGE as an Alternative to His–Tag Purification of Recombinant Amelogenin. Frontiers in Physiology, 8. 424. ISSN 1664-042X

Smith, CEL orcid.org/0000-0001-8320-5105, Kirkham, J, Day, PF orcid.org/0000-0001-9711-9638 et al. (6 more authors) (2017) A Fourth KLK4 Mutation Is Associated with Enamel Hypomineralisation and Structural Abnormalities. Frontiers in Physiology, 8. 333. ISSN 1664-042X

Brookes, SJ orcid.org/0000-0002-9097-7311, Barron, MJ, Smith, CEL orcid.org/0000-0001-8320-5105 et al. (7 more authors) (2017) Amelogenesis Imperfecta caused by N-Terminal Enamelin Point Mutations in Mice and Men is driven by Endoplasmic Reticulum Stress. Human Molecular Genetics, 26 (10). pp. 1863-1876. ISSN 0964-6906

Ma, P, Yan, W, Tian, Y et al. (3 more authors) (2016) The Importance of Serine Phosphorylation of Ameloblastin on Enamel Formation. Journal of Dental Research, 95 (12). pp. 1408-1414. ISSN 0022-0345

Smith, CEL orcid.org/0000-0001-8320-5105, Poulter, JA orcid.org/0000-0003-2048-5693, Levin, AV et al. (9 more authors) (2016) Spectrum of PEX1 and PEX6 variants in Heimler syndrome. European Journal of Human Genetics, 24 (11). pp. 1565-1571. ISSN 1018-4813

Smith, CEL orcid.org/0000-0001-8320-5105, Murillo, G, Brookes, SJ orcid.org/0000-0002-9097-7311 et al. (5 more authors) (2016) Deletion of amelotin exons 3-6 is associated with amelogenesis imperfecta. Human Molecular Genetics, 25 (16). pp. 3578-3587. ISSN 0964-6906

Villa, O, Wohlfahrt, JC, Koldsland, OC et al. (4 more authors) (2016) EMD in periodontal regenerative surgery modulates cytokine profiles: A randomised controlled clinical trial. Scientific Reports, 6. p. 23060. ISSN 2045-2322

Villa, O, Brookes, SJ, Thiede, B et al. (3 more authors) (2015) Subfractions of enamel matrix derivative differentially influence cytokine secretion from human oral fibroblasts. Journal of tissue engineering, 6. ISSN 2041-7314

Poulter, JA orcid.org/0000-0003-2048-5693, Murillo, G, Brookes, SJ orcid.org/0000-0002-9097-7311 et al. (6 more authors) (2014) Deletion of ameloblastin exon 6 is associated with amelogenesis imperfecta. Human Molecular Genetics, 23 (20). pp. 5317-5324. ISSN 0964-6906

Jacques, J, Hotton, D, De La Dure-Molla, M et al. (7 more authors) (2014) Tracking Endogenous Amelogenin and Ameloblastin In Vivo. PLoS One, 9 (6). e99626. ISSN 1932-6203

Poulter, JA, Brookes, SJ, Shore, RC et al. (5 more authors) (2014) A missense mutation in ITGB6 causes pitted hypomineralized amelogenesis imperfecta. Human Molecular Genetics, 23 (8). 2189 - 2197. ISSN 0964-6906

Brookes, SJ, Barron, MJ, Boot-Handford, R et al. (2 more authors) (2013) Endoplasmic reticulum stress in amelogenesis imperfecta and phenotypic rescue using 4-phenylbutyrate. Human Molecular Genetics, 23 (9). 2468 - 2480. ISSN 0964-6906

Brunton, PA, Davies, RPW orcid.org/0000-0002-9135-9320, Burke, JL et al. (4 more authors) (2013) Treatment of early caries lesions using biomimetic self-assembling peptides – a clinical safety trial. British Dental Journal, 215 (4). E6. ISSN 0007-0610

Jedeon, K, De La Dure-Molla, M, Brookes, SJ et al. (9 more authors) (2013) Enamel defects reflect perinatal exposure to bisphenol A. American Journal of Pathology, 183 (1). 108 - 118. ISSN 1525-2191

Parry, DA, Brookes, SJ, Logan, CV et al. (19 more authors) (2012) Mutations in C4orf26, encoding a peptide with in vitro hydroxyapatite crystal nucleation and growth activity, cause amelogenesis imperfecta. American Journal of Human Genetics, 91 (3). 565 - 571. ISSN 0002-9297