Homomeric and Heteromeric Interactions between Wild-Type and Mutant Phenylalanine Hydroxylase Subunits: Evaluation of Two-Hybrid Approaches for Functional Analysis of Mutations Causing Hyperphenylalaninemia-Reference-Cited by-同舟云学术

Homomeric and Heteromeric Interactions between Wild-Type and Mutant Phenylalanine Hydroxylase Subunits: Evaluation of Two-Hybrid Approaches for Functional Analysis of Mutations Causing Hyperphenylalaninemia

Published:2001-07 Issue:3 Volume:73 Page:230-238
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Waters Paula J.,Scriver Charles R.,Parniak Michael A.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference26 articles.

1. Hyperphenylalaninemia: Phenylalanine hydroxylase deficiency;Scriver,2001

2. PAHdb, Phenylalanine Hydroxylase Locus Knowledgebase, http://www.mcgill.ca/pahdb.

3. PAHdb: A locus-specific knowledgebase;Scriver;Hum Mutat,2000

4. In vitro expression analysis of mutations in phenylalanine hydroxylase: Linking genotype to phenotype and structure to function;Waters;Hum Mutat,1998

5. PKU mutation G46S is associated with increased aggregation and degradation of the phenylalanine hydroxylase enzyme;Eiken;Hum Mutat,1996

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