In Vitro Expression of 34 Naturally Occurring Mutant Variants of Phenylalanine Hydroxylase: Correlation with Metabolic Phenotypes and Susceptibility toward Protein Aggregation

By Gjetting T.   Petersen M.   Guldberg P.   Güttler F.  

Molecular Genetics and Metabolism, Vol. 72, Iss. 2, 2001-02 ,pp. : 132-143

Academic Press

Access to resources Recommend Favorite

The V388M Mutation Results in a Kinetic Variant Form of Phenylalanine Hydroxylase

By Leandro P.   Rivera I.   Lechner M.C.   de Almeida I.T.   Konecki D.  

Molecular Genetics and Metabolism, Vol. 69, Iss. 3, 2000-03 ,pp. : 204-212

Academic Press

Access to resources Recommend Favorite

Impaired Arachidonic (20:4n-6) and Docosahexaenoic (22:6n-3) Acid Synthesis by Phenylalanine Metabolites as Etiological Factors in the Neuropathology of Phenylketonuria

By Infante J.P.   Huszagh V.A.  

Molecular Genetics and Metabolism, Vol. 72, Iss. 3, 2001-03 ,pp. : 185-198

Academic Press

Access to resources Recommend Favorite

The Hemochromatosis N144H Mutation of SLC11A3 Gene in Patients with Type 2 Diabetes

By Njajou O.T.   Vaessen N.   Oostra B.   Heutink P.   van Duijn C.M.  

Molecular Genetics and Metabolism, Vol. 75, Iss. 3, 2002-03 ,pp. : 290-291

Academic Press

Access to resources Recommend Favorite

A Murine Model for Juvenile NCL: Gene Targeting of Mouse Cln3

By Greene N.D.E.   Bernard D.L.   Taschner P.E.M.   Lake B.D.   de Vos N.   Breuning M.H.   Gardiner R.M.   Mole S.E.   Nussbaum R.L.   Mitchison H.M.  

Molecular Genetics and Metabolism, Vol. 66, Iss. 4, 1999-04 ,pp. : 309-313

Academic Press

Access to resources Recommend Favorite