Literature DB >> 18773304

Connecting mutant phenylalanine hydroxylase with phenylketonuria.

Shaomin Yan1, Guang Wu.   

Abstract

OBJECTIVE: The building of a quantitative relationship between genotype and phenotype would be great helpful for better clinical monitoring, diagnosis, prognosis and treatment. As the phenylketonuria is an autosomal recessive disorder caused by mutations in the phenylalanine hydroxylase, in this study we build a descriptively quantitative relationship between mutant phenylalanine hydroxylase and classifications of phenylketonuria.
METHODS: The amino-acid distribution probability is used to quantify the phenylalanine hydroxylase and its mutants, the cross-impact analysis is used to couple mutant phenylalanine hydroxylase and classifications of phenylketonuria, and the Bayesian equation is used to compute the probability that the phenylketonuria can be classified under mutations.
RESULTS: The results show that the patient has more than 0.9 chance of being phenylketonuria when a new mutation occurs in phenylalanine hydroxylase.
CONCLUSIONS: The built relationship paves the way for modeling of this type relationship for better clinical monitoring, diagnosis, prognosis and treatment.

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Year:  2008        PMID: 18773304     DOI: 10.1007/s10877-008-9139-7

Source DB:  PubMed          Journal:  J Clin Monit Comput        ISSN: 1387-1307            Impact factor:   2.502


  46 in total

1.  Prediction of mutations in H1 neuraminidases from North America influenza A virus engineered by internal randomness.

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2.  Application of cross-impact analysis to the relationship between aldehyde dehydrogenase 2 allele and the flushing syndrome.

Authors:  G Wu
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3.  The discovery of phenylketonuria: the story of a young couple, two retarded children, and a scientist.

Authors:  S A Centerwall; W R Centerwall
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4.  Five novel missense mutations of the phenylalanine hydroxylase gene in phenylketonuria.

Authors:  P Bénit; F Rey; D Melle; A Munnich; J Rey
Journal:  Hum Mutat       Date:  1994       Impact factor: 4.878

5.  Mutations of the phenylalanine hydroxylase (PAH) gene in Brazilian patients with phenylketonuria.

Authors:  A Acosta; W Silva; T Carvalho; M Gomes; M Zago
Journal:  Hum Mutat       Date:  2001-02       Impact factor: 4.878

6.  Tetrahydrobiopterin responsiveness in patients with phenylketonuria.

Authors:  Belén Pérez-Dueñas; Maria Antonia Vilaseca; Anna Mas; Nilo Lambruschini; Rafael Artuch; Lilian Gómez; Julia Pineda; Alejandra Gutiérrez; Montse Mila; Jaume Campistol
Journal:  Clin Biochem       Date:  2004-12       Impact factor: 3.281

7.  Timing of mutation in influenza A virus hemagglutinins by means of amino-acid distribution rank and fast Fourier transform.

Authors:  Guang Wu; Shaomin Yan
Journal:  Protein Pept Lett       Date:  2006       Impact factor: 1.890

8.  Long-term development of intelligence (IQ) and EEG in 34 children with phenylketonuria treated early.

Authors:  J Pietz; C Benninger; H Schmidt; D Scheffner; H Bickel
Journal:  Eur J Pediatr       Date:  1988-05       Impact factor: 3.183

9.  Meta-analysis of neuropsychological symptoms of adolescents and adults with PKU.

Authors:  J J Moyle; A M Fox; M Arthur; M Bynevelt; J R Burnett
Journal:  Neuropsychol Rev       Date:  2007-04-05       Impact factor: 7.444

Review 10.  Mutation trend of hemagglutinin of influenza A virus: a review from a computational mutation viewpoint.

Authors:  Guang Wu; Shao-Min Yan
Journal:  Acta Pharmacol Sin       Date:  2006-05       Impact factor: 6.150

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