Literature DB >> 2857230

Detection of phenylalanine hydroxylase messenger RNA in liver biopsy samples from patients with phenylketonuria.

A G DiLella, F D Ledley, F Rey, A Munnich, S L Woo.   

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Year:  1985        PMID： 2857230     DOI： 10.1016/s0140-6736(85)91925-7

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  6 in total

Review 1.  Heterogeneity of phenylketonuria at the clinical, protein and DNA levels.

Authors:  R G Cotton
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

2.  Clinical and molecular heterogeneity of phenylalanine hydroxylase deficiencies in France.

Authors:  F Rey; M Berthelon; C Caillaud; S Lyonnet; V Abadie; F Blandin-Savoja; J Feingold; J M Saudubray; J Frézal; A Munnich
Journal:  Am J Hum Genet       Date:  1988-12       Impact factor: 11.025

3.  Molecular genetics of PKU.

Authors:  F Güttler; S L Woo
Journal:  J Inherit Metab Dis       Date:  1986       Impact factor: 4.982

4.  Molecular genetics of phenylketonuria in Mediterranean countries: a mutation associated with partial phenylalanine hydroxylase deficiency.

Authors:  S Lyonnet; C Caillaud; F Rey; M Berthelon; J Frézal; J Rey; A Munnich
Journal:  Am J Hum Genet       Date:  1989-04       Impact factor: 11.025

5.  Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria.

Authors:  R Chakraborty; A S Lidsky; S P Daiger; F Güttler; S Sullivan; A G Dilella; S L Woo
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

6.  Molecular mechanisms of McArdle's disease (muscle glycogen phosphorylase deficiency). RNA and DNA analysis.

Authors:  S Gautron; D Daegelen; F Mennecier; D Dubocq; A Kahn; J C Dreyfus
Journal:  J Clin Invest       Date:  1987-01       Impact factor: 14.808
  6 in total

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