Deubiquitinase USP19 extends the residual enzymatic activity of phenylalanine hydroxylase variants
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2045-2322
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Anmerkungen
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online resource.
- Erschienen in
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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
- Urheber
-
Sarodaya, Neha
Tyagi, Apoorvi
Kim, Hyun-Jin
Kang, Ju-Seop
Singh, Vijai
Hong, Seok-Ho
Kim, Woo Jin
Kim, Kye-Seong
Ramakrishna, Suresh
- Beteiligte Personen und Organisationen
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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
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:21 MESZ
Datenpartner
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Beteiligte
- 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
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Typed Ember extends Confidence
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Analysis of the cryptic biosynthetic gene cluster encoding the RiPP curacozole reveals a phenylalanine-specific peptide hydroxylase
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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
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The spectrum of phenylalanine hydroxylase variants and genotype–phenotype correlation in phenylketonuria patients in Gansu, China
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Suspected pterin-4a-carbinolamine dehydratase deficiency : hyperphenylalaninaemia due to inhibition of phenylalanine hydroxylase by tetrahydro-7-biopterin
Typed Ember extends Confidence
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