Literature DB >> 6796764

Observations indicating the nature of the mutation in phenylketonuria.

K H Choo, R G Cotton, I G Jennings, D M Danks.   

Abstract

Rabbit antiserum was prepared against purified normal human liver phenylalanine hydroxylase. This was used to test for cross-reacting material in crude extracts of livers from patients with classical phenylketonuria (PKU); the samples from patients were two livers obtained at autopsy and a needle biopsy core. None of these enzymically inactive livers contained detectable cross-reacting material capable of neutralizing antibody activity in double immunodiffusion and/or enzyme inhibition experiments. In an earlier study, no phenylalanine hydroxylase was found in the two autopsy PKU livers by an affinity chromatography method or by the use of a specific antiserum raised against purified monkey liver phenylalanine hydroxylase (Choo et al., 1979a). This evidence suggests that mutations in th PKU patients studied may be regulatory in nature.

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Year:  1980        PMID: 6796764     DOI: 10.1007/BF01805662

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  12 in total

Review 1.  The HPRT locus.

Authors:  C T Caskey; G D Kruh
Journal:  Cell       Date:  1979-01       Impact factor: 41.582

2.  Genetics of the mammalian phenylalanine hydroxylase system. II. Immunological and two-dimensional gel electrophoretic studies of phenylalanine hydroxylase in cultured normal and mutant rat hepatoma cells.

Authors:  K H Choo; R G Cotton
Journal:  Biochem Genet       Date:  1979-10       Impact factor: 1.890

3.  Purification of inactive phenylalanine hydroxylase protein from liver in classical phenylketonuria.

Authors:  R G Cotton; D M Danks
Journal:  Nature       Date:  1976-03-04       Impact factor: 49.962

4.  Reappearance of murine hypoxanthine guanine phosphoribosyl transferase activity in mouse A9 cells after attempted hybridisation with human cell lines.

Authors:  B Watson; I P Gormley; S E Gardiner; H J Evans; H Harris
Journal:  Exp Cell Res       Date:  1972-12       Impact factor: 3.905

5.  Genetics of the mammalian phenylalanine hydroxylase system. Studies of human liver phenylalanine hydroxylase subunit structure and of mutations in phenylketonuria.

Authors:  K H Choo; R G Cotton; D M Danks; I G Jennings
Journal:  Biochem J       Date:  1979-08-01       Impact factor: 3.857

6.  Genetics of mammalian phenylalanine hydroxylase system. IV. Evidence of phenylalanine hydroxylase in a cultured human hepatoma cell line.

Authors:  K H Choo; R G Cotton; I G Jennings; K Fowler; D M Danks
Journal:  Biochem Genet       Date:  1980-10       Impact factor: 1.890

7.  Detection of hepatic phenylalanine 4-hydroxylase in classical phenylketonuria.

Authors:  P A Friedman; D B Fisher; E S Kang; S Kaufman
Journal:  Proc Natl Acad Sci U S A       Date:  1973-02       Impact factor: 11.205

8.  Reexpression of the rat hypoxanthine phosphoribosyltransferase gene in rat-human hybrids.

Authors:  C M Croce; B Bakay; W L Nyhan; H Koprowski
Journal:  Proc Natl Acad Sci U S A       Date:  1973-09       Impact factor: 11.205

9.  Nature of mutations conferring resistance to 8-azaguanine in mouse cell lines.

Authors:  S I Shin
Journal:  J Cell Sci       Date:  1974-03       Impact factor: 5.285

10.  Reversion in expression of hypoxanthine-guanine phosphoribosyl transferase following cell hybridization.

Authors:  B Bakay; W L Nyhan; C M Croce; H Koprowski
Journal:  J Cell Sci       Date:  1975-05       Impact factor: 5.285

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  7 in total

1.  Functional analysis of the effect of monoclonal antibodies on monkey liver phenylalanine hydroxylase.

Authors:  I G Jennings; R G Russell; W L Armarego; R G Cotton
Journal:  Biochem J       Date:  1986-04-01       Impact factor: 3.857

2.  Comparative studies of four monoclonal antibodies to phenylalanine hydroxylase exhibiting different properties with respect to substrate-dependence, species-specificity and a range of effects on enzyme activity.

Authors:  K H Choo; I G Jennings; R G Cotton
Journal:  Biochem J       Date:  1981-12-01       Impact factor: 3.857

3.  GT to AT transition at a splice donor site causes skipping of the preceding exon in phenylketonuria.

Authors:  J Marvit; A G DiLella; K Brayton; F D Ledley; K J Robson; S L Woo
Journal:  Nucleic Acids Res       Date:  1987-07-24       Impact factor: 16.971

Review 4.  A prefrontal dysfunction model of early-treated phenylketonuria.

Authors:  M C Welsh
Journal:  Eur J Pediatr       Date:  1996-07       Impact factor: 3.183

5.  Genetics of mammalian phenylalanine hydroxylase system. IV. Evidence of phenylalanine hydroxylase in a cultured human hepatoma cell line.

Authors:  K H Choo; R G Cotton; I G Jennings; K Fowler; D M Danks
Journal:  Biochem Genet       Date:  1980-10       Impact factor: 1.890

6.  Studies on the molecular defect in phenylketonuria and hyperphenylalaninaemia using antibodies against phenylalanine hydroxylase.

Authors:  K Bartholomé; A Dresel
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

7.  Isolation and characterization of a myeloma--spleen-cell hybrid producing antibody to phenylalanine hydroxylase.

Authors:  R G Cotton; I G Jennings; K H Choo; K Fowler
Journal:  Biochem J       Date:  1980-12-01       Impact factor: 3.857

  7 in total

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