Possible association between common variants of the phenylalanine hydroxylase (PAH) gene and memory performance in healthy adults
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1744-9081
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Possible association between common variants of the phenylalanine hydroxylase (PAH) gene and memory performance in healthy adults ; volume:9 ; number:1 ; day:30 ; month:7 ; year:2013 ; pages:1-6 ; date:12.2013
Behavioral and brain functions ; 9, Heft 1 (30.7.2013), 1-6, 12.2013
- Creator
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Teraishi, Toshiya
Sasayama, Daimei
Hori, Hiroaki
Yamamoto, Noriko
Fujii, Takashi
Matsuo, Junko
Nagashima, Anna
Kinoshita, Yukiko
Hattori, Kotaro
Ota, Miho
Fujii, Sayaka
Kunugi, Hiroshi
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/1744-9081-9-30
- URN
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urn:nbn:de:101:1-2021082808063079117034
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:48 AM CEST
Data provider
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Teraishi, Toshiya
- Sasayama, Daimei
- Hori, Hiroaki
- Yamamoto, Noriko
- Fujii, Takashi
- Matsuo, Junko
- Nagashima, Anna
- Kinoshita, Yukiko
- Hattori, Kotaro
- Ota, Miho
- Fujii, Sayaka
- Kunugi, Hiroshi
- SpringerLink (Online service)
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PAH
Deubiquitinase USP19 extends the residual enzymatic activity of phenylalanine hydroxylase variants
Characterization of phenylalanine hydroxylase gene variants and analysis of genotype–phenotype correlation in patients with phenylalanine hydroxylase deficiency from Fujian Province, Southeastern China
Nutritional management of phenylalanine hydroxylase (PAH) deficiency in pediatric patients in Canada: a survey of dietitians’ current practices
The spectrum of phenylalanine hydroxylase variants and genotype–phenotype correlation in phenylketonuria patients in Gansu, China
Engineered Escherichia coli platforms for tyrosine-derivative production from phenylalanine using phenylalanine hydroxylase and tetrahydrobiopterin-regeneration system
Mutational and phenotypic spectrum of phenylalanine hydroxylase deficiency in Zhejiang Province, China
Birth prevalence of phenylalanine hydroxylase deficiency: a systematic literature review and meta-analysis
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
Molecular mechanisms of PAH function in response to phenylalanine and tetrahydrobiopterin binding : implications for clinical management
Steroid 21-hydroxylase gene variants and late-life depression
Suspected pterin-4a-carbinolamine dehydratase deficiency : hyperphenylalaninaemia due to inhibition of phenylalanine hydroxylase by tetrahydro-7-biopterin
PAH
Deubiquitinase USP19 extends the residual enzymatic activity of phenylalanine hydroxylase variants
Characterization of phenylalanine hydroxylase gene variants and analysis of genotype–phenotype correlation in patients with phenylalanine hydroxylase deficiency from Fujian Province, Southeastern China
Nutritional management of phenylalanine hydroxylase (PAH) deficiency in pediatric patients in Canada: a survey of dietitians’ current practices
The spectrum of phenylalanine hydroxylase variants and genotype–phenotype correlation in phenylketonuria patients in Gansu, China
Engineered Escherichia coli platforms for tyrosine-derivative production from phenylalanine using phenylalanine hydroxylase and tetrahydrobiopterin-regeneration system
Mutational and phenotypic spectrum of phenylalanine hydroxylase deficiency in Zhejiang Province, China
Birth prevalence of phenylalanine hydroxylase deficiency: a systematic literature review and meta-analysis
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
Molecular mechanisms of PAH function in response to phenylalanine and tetrahydrobiopterin binding : implications for clinical management
Steroid 21-hydroxylase gene variants and late-life depression
Suspected pterin-4a-carbinolamine dehydratase deficiency : hyperphenylalaninaemia due to inhibition of phenylalanine hydroxylase by tetrahydro-7-biopterin