Short-term nitisinone discontinuation of hereditary tyrosinemia type 1 mice causes metabolic alterations in glutathione metabolism/biosynthesis and multiple amino acid degradation pathways

Haaike Colemonts-Vroninks; Brendan Norman; Sven Van Laere; Andrew Davison; Lionel Marcélis; G. Casimir; Philippe Goyens; Paul Claes; Dimitri De Bundel; Geert A Martens; Lakshminarayan Rao Ranganath; Tamara Vanhaecke; James Gallagher; Joery De Kock

doi:10.1016/j.gendis.2022.11.013

Short-term nitisinone discontinuation of hereditary tyrosinemia type 1 mice causes metabolic alterations in glutathione metabolism/biosynthesis and multiple amino acid degradation pathways

Haaike Colemonts-Vroninks
, Brendan Norman
, Sven Van Laere
, Andrew Davison
, Lionel Marcélis
, G. Casimir
, Philippe Goyens
, Paul Claes
, Dimitri De Bundel
, Geert A Martens
, Lakshminarayan Rao Ranganath
, Tamara Vanhaecke
, James Gallagher
, Joery De Kock

Onderzoeksoutput: Article › peer review

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Originele taal-2	English
Pagina's (van-tot)	1759-1762
Aantal pagina's	4
Tijdschrift	Genes&Diseases
Volume	10
Nummer van het tijdschrift	5
DOI's	https://doi.org/10.1016/j.gendis.2022.11.013
Status	Published - sep. 2023

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Funding Information:
This research was funded by the Research Foundation – Flanders (FWO) (No. 1518619N and G041521N), the Research Council (OZR) of the Vrije Universiteit Brussel (VUB), the Hercules Foundation, Wetenschappelijk Fonds Willy Gepts (WFWG) from the UZ Brussel and a Medical Grant from Swedish Orphan Biovitrum (SOBI) (No. AIIFUND37).

Copyright:
Copyright 2023 Elsevier B.V., All rights reserved.

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10.1016/j.gendis.2022.11.013Licentie: CC BY-NC-ND

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FWOAL1003: TALENT: Ontwikkelen van tyrosine ammonia lyase (TAL) enzymen van de mens ter behandeling van aangeboren stofwisselingsziektes van het tyrosine metabolisme
De Kock, J. (Administrative Promotor) & Colemonts-Vroninks, H. (Medewerker)
1/01/21 → 31/12/24
Project: Fundamenteel

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Colemonts-Vroninks, H., Norman, B., Van Laere, S., Davison, A., Marcélis, L., Casimir, G., Goyens, P., Claes, P., De Bundel, D., Martens, G. A., Ranganath, L. R., Vanhaecke, T., Gallagher, J., & De Kock, J. (2023). Short-term nitisinone discontinuation of hereditary tyrosinemia type 1 mice causes metabolic alterations in glutathione metabolism/biosynthesis and multiple amino acid degradation pathways. Genes&Diseases, 10(5), 1759-1762. https://doi.org/10.1016/j.gendis.2022.11.013

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title = "Short-term nitisinone discontinuation of hereditary tyrosinemia type 1 mice causes metabolic alterations in glutathione metabolism/biosynthesis and multiple amino acid degradation pathways",

abstract = "NA",

author = "Haaike Colemonts-Vroninks and Brendan Norman and \{Van Laere\}, Sven and Andrew Davison and Lionel Marc{\'e}lis and G. Casimir and Philippe Goyens and Paul Claes and \{De Bundel\}, Dimitri and Martens, \{Geert A\} and Ranganath, \{Lakshminarayan Rao\} and Tamara Vanhaecke and James Gallagher and \{De Kock\}, Joery",

note = "Funding Information: This research was funded by the Research Foundation – Flanders (FWO) (No. 1518619N and G041521N), the Research Council (OZR) of the Vrije Universiteit Brussel (VUB), the Hercules Foundation, Wetenschappelijk Fonds Willy Gepts (WFWG) from the UZ Brussel and a Medical Grant from Swedish Orphan Biovitrum (SOBI) (No. AIIFUND37). Copyright: Copyright 2023 Elsevier B.V., All rights reserved.",

year = "2023",

month = sep,

doi = "10.1016/j.gendis.2022.11.013",

language = "English",

volume = "10",

pages = "1759--1762",

journal = "Genes\&Diseases",

issn = "2352-3042",

number = "5",

}

Colemonts-Vroninks, H, Norman, B, Van Laere, S, Davison, A, Marcélis, L, Casimir, G, Goyens, P, Claes, P , De Bundel, D, Martens, GA, Ranganath, LR, Vanhaecke, T, Gallagher, J & De Kock, J 2023, 'Short-term nitisinone discontinuation of hereditary tyrosinemia type 1 mice causes metabolic alterations in glutathione metabolism/biosynthesis and multiple amino acid degradation pathways', Genes&Diseases, vol. 10, nr. 5, blz. 1759-1762. https://doi.org/10.1016/j.gendis.2022.11.013

TY - JOUR

T1 - Short-term nitisinone discontinuation of hereditary tyrosinemia type 1 mice causes metabolic alterations in glutathione metabolism/biosynthesis and multiple amino acid degradation pathways

AU - Colemonts-Vroninks, Haaike

AU - Norman, Brendan

AU - Van Laere, Sven

AU - Davison, Andrew

AU - Marcélis, Lionel

AU - Casimir, G.

AU - Goyens, Philippe

AU - Claes, Paul

AU - De Bundel, Dimitri

AU - Martens, Geert A

AU - Ranganath, Lakshminarayan Rao

AU - Vanhaecke, Tamara

AU - Gallagher, James

AU - De Kock, Joery

N1 - Funding Information: This research was funded by the Research Foundation – Flanders (FWO) (No. 1518619N and G041521N), the Research Council (OZR) of the Vrije Universiteit Brussel (VUB), the Hercules Foundation, Wetenschappelijk Fonds Willy Gepts (WFWG) from the UZ Brussel and a Medical Grant from Swedish Orphan Biovitrum (SOBI) (No. AIIFUND37). Copyright: Copyright 2023 Elsevier B.V., All rights reserved.

PY - 2023/9

Y1 - 2023/9

N2 - NA

AB - NA

UR - https://www.scopus.com/pages/publications/85146328175

U2 - 10.1016/j.gendis.2022.11.013

DO - 10.1016/j.gendis.2022.11.013

M3 - Article

SN - 2352-3042

VL - 10

SP - 1759

EP - 1762

JO - Genes&Diseases

JF - Genes&Diseases

IS - 5

ER -

Short-term nitisinone discontinuation of hereditary tyrosinemia type 1 mice causes metabolic alterations in glutathione metabolism/biosynthesis and multiple amino acid degradation pathways

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FWOAL1003: TALENT: Ontwikkelen van tyrosine ammonia lyase (TAL) enzymen van de mens ter behandeling van aangeboren stofwisselingsziektes van het tyrosine metabolisme

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