Browsing publications by Dr Alison Trainer

Newcastle AuthorsTitleYearFull text
Dr Alison Trainer
Moira Crosier
Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome2010
Dr Neil Rajan
Dr Alison Trainer
Professor Sir John Burn
Dr James Langtry
Familial cylindromatosis and brooke-spiegler syndrome: A review of current therapeutic approaches and the surgical challenges posed by two affected families2009
Dr Neil Rajan
Dr James Langtry
Pamela Chapman
Professor Sir John Burn
Dr Alison Trainer
et al.
Tumor Mapping in 2 Large Multigenerational Families With CYLD Mutations: Implications for Disease Management and Tumor Induction2009
Dr Alison Trainer
The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity2008
Dr Catherine Arden
Dr Alison Trainer
Dr Kathleen Scougall
Professor James Shaw
Professor Loranne Agius
et al.
Cell biology assessment of glucokinase mutations V62M and G72R in pancreatic β-cells: Evidence for cellular instability of catalytic activity2007
Dr Alison Trainer
Roberts syndrome-SC phocomeliia: Clinical and molecular findings2007
Moira Crosier
Dr Alison Trainer
Esco1, a candidate gene for TAR syndrome2006
Dr Alison Trainer
Molecular tumor profiling: Translating genomic insights into clinical advances2004
Dr Alison Trainer
De novo translocation (1; 2)(q32; p25) associated with bilateral renal dysplasia2003
Dr Miranda Splitt
Dr Alison Trainer
Clinical studies on submicroscopic subtelomeric rearrangements: a checklist2001
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