A comprehensive functional analysis of PTEN mutations: implications in tumor- and autism-related syndromes

By Rodríguez-Escudero Isabel   Oliver María D.   Andrés-Pons Amparo   Molina María   Cid Víctor J.   Pulido Rafael  

Human Molecular Genetics, Vol. 20, Iss. 21, 2011-11 ,pp. : 4132-4142

Oxford University Press

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Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan–Zonana syndrome, two hamartoma syndromes with germline PTEN mutation

By Lin A.Y.  

Human Molecular Genetics, Vol. 7, Iss. 3, 1998-03 ,pp. : 507-515

Oxford University Press

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Mutations and impaired function of LKB1 in familial and non-familial Peutz–Jeghers syndrome and a sporadic testicular cancer

By Markie D.  

Human Molecular Genetics, Vol. 8, Iss. 1, 1999-01 ,pp. : 45-51

Oxford University Press

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Functional analysis of Peutz–Jeghers mutations reveals that the LKB1 C-terminal region exerts a crucial role in regulating both the AMPK pathway and the cell polarity

By Forcet Christelle  

Human Molecular Genetics, Vol. 14, Iss. 10, 2005-05 ,pp. : 1283-1292

Oxford University Press

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Functional characterization of the CgPGS1 gene reveals a link between mitochondrial phospholipid homeostasis and drug resistance in Candida glabrata

By Batova Monika   Borecka-Melkusova Silvia   Simockova Maria   Dzugasova Vladimira   Goffa Eduard   Subik Julius  

Current Genetics, Vol. 53, Iss. 5, 2008-05 ,pp. : 313-322

Springer Publishing Company

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