Literature DB >> 8304187

Expression of wild type and mutant forms of human phenylalanine hydroxylase in E. coli.

M Knappskog1, H G Eiken, A Martinez, S Olafsdotti, J Haavik, T Flatmark, J Apold.   

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Year:  1993        PMID： 8304187     DOI： 10.1007/978-1-4615-2960-6_11

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN： 0065-2598            Impact factor:   2.622


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  4 in total

1.  A model of human phenylalanine metabolism in normal subjects and in phenylketonuric patients.

Authors:  S Kaufman
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-16       Impact factor: 11.205

2.  Phenylketonuria genotypes correlated to metabolic phenotype groups in Norway.

Authors:  H G Eiken; P M Knappskog; K Motzfeldt; H Boman; J Apold
Journal:  Eur J Pediatr       Date:  1996-07       Impact factor: 3.183

3.  Expression of recombinant human phenylalanine hydroxylase as fusion protein in Escherichia coli circumvents proteolytic degradation by host cell proteases. Isolation and characterization of the wild-type enzyme.

Authors:  A Martinez; P M Knappskog; S Olafsdottir; A P Døskeland; H G Eiken; R M Svebak; M Bozzini; J Apold; T Flatmark
Journal:  Biochem J       Date:  1995-03-01       Impact factor: 3.857

4.  The PKU mutation S349P causes complete loss of catalytic activity in the recombinant phenylalanine hydroxylase enzyme.

Authors:  P M Knappskog; H G Eiken; A Martinez; T Flatmark; J Apold
Journal:  Hum Genet       Date:  1995-02       Impact factor: 4.132
  4 in total

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