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Number of items at this level: 29.

A

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

B

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

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. 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

C

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

D

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

F

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

H

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

N

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

P

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. Elsevier.

Parry, DA, Smith, CEL orcid.org/0000-0001-8320-5105, 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

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). 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.

S

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). 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 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

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

W

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 May 1 03:41:13 2017 BST.