Hochschulschrift
A new approach to mutational analysis at the human phenylalanine hydroxylase locus : application of in vitro DNA amplification to the study of mutations resulting in phenylalanine hydroxylase deficiency in man
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Dimensions
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30 cm
- Extent
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174 Bl.
- Language
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Englisch
- Notes
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Ill., graph. Darst.
Heidelberg, Univ., Diss., 1989 (Nicht f.d. Austausch)
- Creator
- Table of contents
- Rights
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Bei diesem Objekt liegt nur das Inhaltsverzeichnis digital vor. Der Zugriff darauf ist unbeschränkt möglich.
- Last update
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11.06.2025, 1:53 PM CEST
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Object type
- Hochschulschrift
Associated
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Deubiquitinase USP19 extends the residual enzymatic activity of phenylalanine hydroxylase variants
Birth prevalence of phenylalanine hydroxylase deficiency: a systematic literature review and meta-analysis
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Mutational and phenotypic spectrum of phenylalanine hydroxylase deficiency in Zhejiang Province, China
Characterization of phenylalanine hydroxylase gene variants and analysis of genotype–phenotype correlation in patients with phenylalanine hydroxylase deficiency from Fujian Province, Southeastern China
Engineered Escherichia coli platforms for tyrosine-derivative production from phenylalanine using phenylalanine hydroxylase and tetrahydrobiopterin-regeneration system
Deubiquitinase USP19 extends the residual enzymatic activity of phenylalanine hydroxylase variants
Birth prevalence of phenylalanine hydroxylase deficiency: a systematic literature review and meta-analysis
Suspected pterin-4a-carbinolamine dehydratase deficiency : hyperphenylalaninaemia due to inhibition of phenylalanine hydroxylase by tetrahydro-7-biopterin
The spectrum of phenylalanine hydroxylase variants and genotype–phenotype correlation in phenylketonuria patients in Gansu, China
Possible association between common variants of the phenylalanine hydroxylase (PAH) gene and memory performance in healthy adults
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Hemmung der adrenalen 17α-Hydroxylase, 16α-Hydroxylase, 11β-Hydroxylase und 18-Hydroxylase beim Menschen durch Ketoconazol
Phenylalanine hydroxylase-stimulating protein/pterin-4alpha-carbinolamine dehydratase from rat and human liver : purification, characterization, and complete amino acid sequence
Mutational and phenotypic spectrum of phenylalanine hydroxylase deficiency in Zhejiang Province, China
Characterization of phenylalanine hydroxylase gene variants and analysis of genotype–phenotype correlation in patients with phenylalanine hydroxylase deficiency from Fujian Province, Southeastern China
Engineered Escherichia coli platforms for tyrosine-derivative production from phenylalanine using phenylalanine hydroxylase and tetrahydrobiopterin-regeneration system
Deubiquitinase USP19 extends the residual enzymatic activity of phenylalanine hydroxylase variants
Birth prevalence of phenylalanine hydroxylase deficiency: a systematic literature review and meta-analysis
Suspected pterin-4a-carbinolamine dehydratase deficiency : hyperphenylalaninaemia due to inhibition of phenylalanine hydroxylase by tetrahydro-7-biopterin
The spectrum of phenylalanine hydroxylase variants and genotype–phenotype correlation in phenylketonuria patients in Gansu, China
Possible association between common variants of the phenylalanine hydroxylase (PAH) gene and memory performance in healthy adults
Nutritional management of phenylalanine hydroxylase (PAH) deficiency in pediatric patients in Canada: a survey of dietitians’ current practices
Analysis of the cryptic biosynthetic gene cluster encoding the RiPP curacozole reveals a phenylalanine-specific peptide hydroxylase
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