Items where authors include "Brown, C.J."

Article

Mustoe, C.L., Turner, A.J., Urwin, S.J. et al. (46 more authors) (2025) Quality by digital design to accelerate sustainable medicines development. International Journal of Pharmaceutics, 681. 125625. ISSN 0378-5173

Hany, U., Watson, C.M. orcid.org/0000-0003-2371-1844, Liu, L. et al. (16 more authors) (2025) Genetic Screening of a Nonsyndromic Amelogenesis Imperfecta Patient Cohort Using a Custom smMIP Reagent for Selective Enrichment of Target Loci. Human Mutation, 2025. 8942542. ISSN 1059-7794

Hany, U. orcid.org/0000-0002-4486-1625, Watson, C.M. orcid.org/0000-0003-2371-1844, Liu, L. orcid.org/0009-0008-3593-8409 et al. (16 more authors) (2025) Genetic Screening of a nonsyndromic amelogenesis imperfecta patient cohort using a custom smMIP reagent for selective enrichment of target loci. Human Mutation, 2025 (1). 8942542. ISSN 1059-7794

Slobodian, L. orcid.org/0009-0009-0229-5125, Buelow, C.A., Baker, S.C. et al. (18 more authors) (2025) Quantifying the presence and potential of national legal frameworks for global mangrove protection. Cell Reports Sustainability. 100430. ISSN 2949-7906

Zhu, I.Y. orcid.org/0009-0004-2407-0297, Lloyd, A., Critchley, W.R. orcid.org/0000-0002-2707-4080 et al. (7 more authors) (2025) Structure and function of MDM2 and MDM4 in health and disease. The Biochemical journal, 482 (04). pp. 241-262. ISSN 0264-6021

Hany, U. orcid.org/0000-0002-4486-1625, Watson, C.M. orcid.org/0000-0003-2371-1844, Liu, L. et al. (17 more authors) (2024) Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta. Journal of Medical Genetics, 61 (4). pp. 347-355. ISSN 0022-2593

Hany, U. orcid.org/0000-0002-4486-1625, Watson, C.M. orcid.org/0000-0003-2371-1844, Liu, L. et al. (17 more authors) (2024) Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta. Journal of Medical Genetics, 61 (4). pp. 347-355. ISSN 0022-2593

Brown, C.J., McGinty, J., Islam, M.T. et al. (19 more authors) (2024) Integrated continuous process design for crystallisation, spherical agglomeration, and filtration of lovastatin. Journal of Pharmaceutical Innovation, 19. 9. ISSN 1872-5120

Hany, U. orcid.org/0000-0002-4486-1625, Watson, C.M. orcid.org/0000-0003-2371-1844, Liu, L. et al. (11 more authors) (2024) Novel Ameloblastin Variants, Contrasting Amelogenesis Imperfecta Phenotypes. Journal of Dental Research, 103 (1). pp. 22-30. ISSN 0022-0345

Hany, U. orcid.org/0000-0002-4486-1625, Watson, C.M. orcid.org/0000-0003-2371-1844, Liu, L. et al. (11 more authors) (2024) Novel ameloblastin variants, contrasting amelogenesis imperfecta phenotypes. Journal of Dental Research, 103 (1). pp. 22-30. ISSN 0022-0345

Brown, C.J., Webb, T.L. orcid.org/0000-0001-9320-0068, Robinson, M.A. et al. (1 more author) (2019) Athletes’ retirement from elite sport: A qualitative study of parents and partners’ experiences. Psychology of Sport and Exercise, 40. pp. 51-60. ISSN 1469-0292

Brown, C.J., Webb, T.L. orcid.org/0000-0001-9320-0068, Robinson, M.A. et al. (1 more author) (2018) Athletes' experiences of social support during their transition out of elite sport: An interpretive phenomenological analysis. Psychology of Sport and Exercise, 36. pp. 71-80. ISSN 1469-0292

Brookes, S.J., Barron, M.J., Smith, C.E.L. 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