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British Dental Journal|October 14, 2022
The changing face of a dental school: a Leeds perspectiveAlan J Mighell
British Journal of Hospital Medicine (London, England : 2005)|January 19, 2010
So you want to be ... an oral medicine physicianAnne M Hegarty, Alan J Mighell
Biochemical and Biophysical Research Communications|April 14, 2020
A missense mutation of Leu74Pro of OGR1 found in familial amelogenesis imperfecta actually causes the loss of the pH-sensing mechanismKoichi Sato, Chihiro Mogi, Alan J Mighell, et al.
BMJ Case Reports|June 14, 2018
Dentin dysplasia: diagnostic challengesAhmed Alhilou, Hannah P Beddis, Alan J Mighell, et al.
Journal of Clinical Pathology|June 10, 2015
Are plasma cell-rich inflammatory conditions of the oral mucosa manifestations of IgG4-related disease?Hannah Cottom, Alan J Mighell, Alec High, et al.
Molecular Carcinogenesis|December 22, 2005
Phenotypic changes associated with DYNACTIN-2 (DCTN2) over expression characterise SJSA-1 osteosarcoma cellsKieran L Bransfield, Jon M Askham, Jack P Leek, et al.
European Journal of Human Genetics : EJHG|May 2, 2013
Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfectaJames A Poulter, Walid El-Sayed, Roger C Shore, et al.
Gene Expression Patterns : GEP|March 6, 2003
Expression of mOb1, a novel atypical 73 amino acid K50-homeodomain protein, during mouse developmentJimi Adu, Fong T Leong, Neil R Smith, et al.
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