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Number of items at this level: 43.


Acevedo, AC, Poulter, JA, Alves, PG et al. (10 more authors) (2015) Variability of systemic and oro-dental phenotype in two families with non-lethal Raine syndrome with FAM20C mutations. BMC Medical Genetics, 16. 8. 1 - 11. ISSN 1471-2350

Alkhabuli, J and High, AS (2013) Expression of Mast Cell Major Basic Protein in Oral Squamous Cell Carcinoma. Journal of Cytology and Histology, 4 (170). ISSN 2157-7099

Atkin, PA, Thomas, S, Cook, RJ et al. (9 more authors) (2018) Human Disease/Clinical Medical Sciences in Dentistry: Current state and future directions of undergraduate teaching in the UK and Ireland. European Journal of Dental Education, 22 (3). e588-e593. ISSN 1396-5883


Bingle, CD, Wilson, K, Lunn, H et al. (7 more authors) (2010) Human LPLUNC1 is a secreted product of goblet cells and minor glands of the respiratory and upper aerodigestive tracts. Histochemistry and Cell Biology, 133 (5). 505 - 515. ISSN 0948-6143

Bingle, L, Cross, SS, High, AS et al. (6 more authors) (2006) WFDC2 (HE4): A potential role in the innate immunity of the oral cavity and respiratory tract and the development of adenocarcinomas of the lung. Respiratory Research, 7. 61. ISSN 1465-9921

Brookes, SJ, Barron, MJ, Smith, CEL 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). ISSN 0964-6906

Brunton, PA, Davies, RPW, 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). ARTN E6. ISSN 0007-0610


Cottom, H, Mighell, AJ, High, A et al. (1 more author) (2015) Are plasma cell-rich inflammatory conditions of the oral mucosa manifestations of IgG4-related disease? Journal of Clinical Pathology, 68 (10). pp. 802-807. ISSN 0021-9746


De La Dure-Molla, M, Quentric, M, Yamaguti, PM et al. (6 more authors) (2014) Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations. Orphanet Journal of Rare Diseases, 9 (1). 84. ISSN 1750-1172


Fletcher, SM, Chengot, P, Dalghous, A et al. (1 more author) (2015) A granular-cell odontogenic tumour occurring alongside orofacial granulomatosis: A report of the first case. Oral Surgery, 8 (1). 42 - 47. ISSN 1752-2471


Harris, AT, Lungari, A, Needham, CJ et al. (9 more authors) (2009) Potential for Raman spectroscopy to provide cancer screening using a peripheral blood sample. Head & Neck Oncology, 1:34.

Harris, AT, Rennie, A, Waqar-Uddin, H et al. (7 more authors) (2010) Raman spectroscopy in head and neck cancer. Head and Neck Oncology, 2. 26. ISSN 1758-3284

High, AS (1978) Abscesses of Frontal Lobe of Brain Secondary to Covert Dental Sepsis. The Lancet, 8088 (2). 497 - 499. ISSN 0140-6736

High, AS (1985) Solitary Neurogenic Sarcoma of the Nose. Journal of Laryngology and Otology, 99 (11). 1151 - 1159. ISSN 0022-2151

High, AS, Eldarrat, AH, Wood, DJ et al. (1 more author) (2007) Age-related changes in ac-impedance spectroscopy studies of normal human dentine. Journal of Materials Science: Materials in Medicine, 18 (6). 1203 - 1210 (8). ISSN 0957-4530

High, AS and Hirschmann, PN (1987) Symptomatic residual radicular cysts. Journal of Oral Pathology & Medicine, 17 (2). 70 - 72 (3). ISSN 0904-2512

High, AS, Nankivell, P and MacLennan, K (2013) Tetraspanins CD9 and CD151, epidermal growth factor receptor and cyclooxegenase-2 expression predict malignant progression in oral epithelial dysplasia. British Journal of Cancer, 109 (11). 2864 - 74 (10). ISSN 0007-0920


Jaureguiberry, G, De la Dure-Molla, M, Parry, D et al. (68 more authors) (2013) Nephrocalcinosis (Enamel Renal Syndrome) Caused by Autosomal Recessive FAM20A Mutations. Nephron Physiology, 122 (1-2). pp. 1-6. ISSN 1660-8151


Mann, L and Moore, R (2017) Paraesthesia of the lower lip as the presenting symptom of an acoustic neuroma: a case report. Oral Surgery, 10 (2). pp. 105-108. ISSN 1752-2471

McDowall, F, Kenny, K, Mighell, AJ et al. (1 more author) (2018) Genetic testing for amelogenesis imperfecta: knowledge and attitudes of paediatric dentists. British Dental Journal, 225 (4). pp. 335-339. ISSN 0007-0610

Montgomery-Cranny, J, Edmondson, M, Reid, J et al. (3 more authors) (2017) Development of a managed clinical network in oral medicine. British Dental Journal, 223 (9). pp. 719-725. ISSN 0007-0610

Moore, RJ (2018) Social Media - What dentists need to be aware of. Dental Update, 45 (1). pp. 5-6. ISSN 0305-5000


Nankivell, P, Williams, H, Webster, K et al. (7 more authors) (2013) Investigation of p16INK4a as a prognostic biomarker in oral epithelial dysplasia. Journal Of Oral Pathology and Medicine. ISSN 0904-2512


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

Parry, DA, Holmes, TD, Gamper, N et al. (12 more authors) (2016) A homozygous STIM1 mutation impairs store-operated calcium entry and natural killer cell effector function without clinical immunodeficiency. Journal of Allergy and Clinical Immunology, 137 (3). pp. 955-957. ISSN 0091-6749

Parry, DA, Smith, CEL, El-Sayed, W et al. (17 more authors) (2016) Mutations in the pH Sensing G-protein Coupled Receptor GPR68 cause Amelogenesis Imperfecta. American Journal of Human Genetics, 99 (4). pp. 984-990. ISSN 0002-9297

Pechlivani, N, Devine, DA, 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

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

Poulter, JA, El-Sayed, W, Shore, RC et al. (3 more authors) (2013) Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta. European Journal of Human Genetics, 22. 132 - 135. ISSN 1018-4813

Poulter, JA, Murillo, G, Brookes, SJ 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

Poulter, JA, Smith, CEL, Murrillo, G et al. (9 more authors) (2015) A distinctive oral phenotype points to FAM20A mutations not identified by Sanger sequencing. Molecular Genetics & Genomic Medicine, 3 (6). pp. 543-549.


Samman, M, Wood, H, Conway, C et al. (11 more authors) (2014) Next-generation sequencing analysis for detecting human papillomavirus in oral verrucous carcinoma. Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology, 118 (1). 117 - 125. ISSN 2212-4403

Samman, M, Wood, HM, Conway, C et al. (18 more authors) (2015) A novel genomic signature reclassifies an oral cancer subtype. International Journal of Cancer, 137 (10). pp. 2364-2373. ISSN 0020-7136

Siddique, I, Chengot, P, Frewer, J et al. (1 more author) (2015) A rare case of gingival metastases from papillary thyroid carcinoma. International Journal of Surgery Case Reports, 7. 82 - 84. ISSN 2210-2612

Smith, CEL, Kirkham, J, Day, PF 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

Smith, CEL, Murillo, G, Brookes, SJ 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

Smith, CEL, Poulter, JA, Antanaviciute, A et al. (4 more authors) (2017) Amelogenesis Imperfecta; Genes, Proteins And Pathways. Frontiers in Physiology, 8. 435. ISSN 1664-042X

Smith, CEL, Poulter, JA, Brookes, SJ 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

Smith, CEL, Poulter, JA, 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, Whitehouse, LLE, Poulter, JA 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


Wanis, C, Jawad, H, Moore, RJ et al. (1 more author) (2019) Accidental administration of auto-injectable adrenaline into a digit. Dental update. ISSN 0305-5000 (In Press)

Whitehouse, LLE, Smith, CEL, Poulter, JA et al. (10 more authors) (2019) Novel DLX3 variants in amelogenesis imperfecta with attenuated tricho‐dento‐osseous syndrome. Oral Diseases, 25 (1). pp. 182-191. ISSN 1354-523X

Wood, HM, Conway, C, Daly, C et al. (13 more authors) (2015) The clonal relationships between pre-cancer and cancer revealed by ultra-deep sequencing. Journal of Pathology, 237 (3). 296 - 306. ISSN 0022-3417

This list was generated on Mon Jun 17 04:03:15 2019 BST.