42 results on '"Mighell, Alan J"'
Search Results
2. Review of 1.75 million referrals over 34 months identifies the disruptive impact of the SARS-CoV-2 pandemic on oral surgery care in England: a service evaluation
3. The changing face of a dental school: a Leeds perspective
4. An evaluation of referrer factors for 98,671 referrals made to the West Yorkshire oral surgery managed clinical network over a three-year period
5. Spectrum of pathogenic variants and founder effects in amelogenesis imperfecta associated with MMP20
6. Spectrum of pathogenic variants and multiple founder effects in amelogenesis imperfecta associated with MMP20
7. A missense mutation of Leu74Pro of OGR1 found in familial amelogenesis imperfecta actually causes the loss of the pH-sensing mechanism
8. A missense variant in specificity protein 6 (SP6) is associated with amelogenesis imperfecta
9. New missense variants in RELT causing hypomineralised amelogenesis imperfecta
10. NovelDLX3variants in amelogenesis imperfecta with attenuated tricho‐dento‐osseous syndrome
11. Dentin dysplasia: diagnostic challenges
12. Amelogenesis Imperfecta; Genes, Proteins, and Pathways
13. A Fourth KLK4 Mutation Is Associated with Enamel Hypomineralisation and Structural Abnormalities
14. Defects in the acid phosphatase ACPT cause recessive hypoplastic amelogenesis imperfecta
15. Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stress
16. Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta
17. Deletion of amelotin exons 3–6 is associated with amelogenesis imperfecta
18. Spectrum of PEX1 and PEX6 variants in Heimler syndrome
19. A homozygous STIM1 mutation impairs store-operated calcium entry and natural killer cell effector function without clinical immunodeficiency
20. A distinctive oral phenotype points to FAM 20A mutations not identified by S anger sequencing
21. Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6
22. Are plasma cell-rich inflammatory conditions of the oral mucosa manifestations of IgG4-related disease?
23. Variability of systemic and oro-dental phenotype in two families with non-lethal Raine syndrome with FAM20C mutations
24. Deletion of ameloblastin exon 6 is associated with amelogenesis imperfecta
25. OI0390 UK and Ireland National Oral Medicine Specialty Training Forum
26. Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations
27. A missense mutation in ITGB6 causes pitted hypomineralized amelogenesis imperfecta
28. Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta
29. Identification of Mutations in SLC24A4, Encoding a Potassium-Dependent Sodium/Calcium Exchanger, as a Cause of Amelogenesis Imperfecta
30. Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta
31. So you want to be … an oral medicine physician
32. Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta
33. Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta
34. Phenotypic changes associated with DYNACTIN‐2 (DCTN2) over expression characterise SJSA‐1 osteosarcoma cells
35. Expression of mOb1, a novel atypical 73 amino acid K50-homeodomain protein, during mouse development
36. RETRACTED: Expression of mOb1, a novel atypical 73 amino acid K50-homeodomain protein, during mouse development
37. Identification of Microcephalin, a Protein Implicated in Determining the Size of the Human Brain
38. Human tenascin-C: Identification of a novel type III repeat in oral cancer and of novel splice variants in normal, malignant and reactive oral mucosae
39. Histochemical and immunohistochemical localisation of elastic system fibres in focal reactive overgrowths of oral mucosa
40. PCNA and Ki‐67 immunoreactivity in multinucleated cells of giant cell fibroma and peripheral giant cell granuloma
41. Immunolocalisation of tenascin-C in focal reactive overgrowths of oral mucosa
42. Periosteal fasciitis of the mandible
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