Dr Lee Parry - PhD
Wilson C, Idziaszczyk S, Parry L, Guy C, Griffiths DFR, Lazda E, Bayne RAL, Smith AJH, Sampson JR, Cheadle JP. 2005. A mouse model of tuberous sclerosis 1 showing background specific early post-natal mortality and metastatic renal cell carcinoma. Hum. Mol. Genet., Jul 2005; 14: 1839 – 1850.
Kirby DM, Salemi R, Sugiana C, Ohtake A, Parry L, Bell KM, Kirk EP, Boneh A, Taylor RW, Dahl HH, Ryan MT, Thorburn DR. 2004. NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency. J Clin Invest 114(6):837-45.
Hodges AK, Li S, Maynard JH, Parry L, Nellist M, Cheadle JP, Sampson JR. 2001. Pathological mutations in TSC1 and TSC2 affect the interaction between hamartin and tuberin. Hum Mol Gen 10: 2899-905
Parry L, Maynard JH, Patel A, Clifford SC, Maher ER, Cheadle JP, Sampson JR. 2001. Analysis of the TSC1 and TSC2 genes in sporadic renal cell carcinomas. Brit J Cancer 85: 1226-1230
Parry L, Maynard JH, Patel A, Hodges AK, von Deimling A, Sampson JR, Cheadle JP. 2000. Molecular analysis of the TSC1 and TSC2 tumour suppressor genes in sporadic glial and glioneuronal tumours. Hum Genet 107: 350-356