Deubiquitinase USP19 extends the residual enzymatic activity of phenylalanine hydroxylase variants
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2045-2322
- 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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Deubiquitinase USP19 extends the residual enzymatic activity of phenylalanine hydroxylase variants ; volume:12 ; number:1 ; day:20 ; month:8 ; year:2022 ; pages:1-13 ; date:12.2022
Scientific reports ; 12, Heft 1 (20.8.2022), 1-13, 12.2022
- Creator
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Sarodaya, Neha
Tyagi, Apoorvi
Kim, Hyun-Jin
Kang, Ju-Seop
Singh, Vijai
Hong, Seok-Ho
Kim, Woo Jin
Kim, Kye-Seong
Ramakrishna, Suresh
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41598-022-18656-0
- URN
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urn:nbn:de:101:1-2022110921062246320532
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:21 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Sarodaya, Neha
- Tyagi, Apoorvi
- Kim, Hyun-Jin
- Kang, Ju-Seop
- Singh, Vijai
- Hong, Seok-Ho
- Kim, Woo Jin
- Kim, Kye-Seong
- Ramakrishna, Suresh
- SpringerLink (Online service)
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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
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
Gold nanoparticle formation as an indicator of enzymatic methods: colorimetric l-phenylalanine determination
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
Suspected pterin-4a-carbinolamine dehydratase deficiency : hyperphenylalaninaemia due to inhibition of phenylalanine hydroxylase by tetrahydro-7-biopterin
Typed Ember extends Confidence
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
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
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
Gold nanoparticle formation as an indicator of enzymatic methods: colorimetric l-phenylalanine determination
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
Suspected pterin-4a-carbinolamine dehydratase deficiency : hyperphenylalaninaemia due to inhibition of phenylalanine hydroxylase by tetrahydro-7-biopterin
Typed Ember extends Confidence
Nutritional management of phenylalanine hydroxylase (PAH) deficiency in pediatric patients in Canada: a survey of dietitians’ current practices