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

Detalles Bibliográficos
Autores principales: Haaike, Colemonts-Vroninks, Brendan, Norman P., Sven, Van Laere, Andrew, Davison S., Lionel, Marcélis, Georges, Casimir, Philippe, Goyens, Paul, Claes, Dimitri, De Bundel, Geert, Martens, Rao, Ranganath Lakshminarayan, Tamara, Vanhaecke, James A, Gallagher, Joery, De Kock
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chongqing Medical University 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10363636/
https://www.ncbi.nlm.nih.gov/pubmed/37492745
http://dx.doi.org/10.1016/j.gendis.2022.11.013
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author Haaike, Colemonts-Vroninks
Brendan, Norman P.
Sven, Van Laere
Andrew, Davison S.
Lionel, Marcélis
Georges, Casimir
Philippe, Goyens
Paul, Claes
Dimitri, De Bundel
Geert, Martens
Rao, Ranganath Lakshminarayan
Tamara, Vanhaecke
James A, Gallagher
Joery, De Kock
author_facet Haaike, Colemonts-Vroninks
Brendan, Norman P.
Sven, Van Laere
Andrew, Davison S.
Lionel, Marcélis
Georges, Casimir
Philippe, Goyens
Paul, Claes
Dimitri, De Bundel
Geert, Martens
Rao, Ranganath Lakshminarayan
Tamara, Vanhaecke
James A, Gallagher
Joery, De Kock
author_sort Haaike, Colemonts-Vroninks
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spelling pubmed-103636362023-07-25 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 P. Sven, Van Laere Andrew, Davison S. Lionel, Marcélis Georges, Casimir Philippe, Goyens Paul, Claes Dimitri, De Bundel Geert, Martens Rao, Ranganath Lakshminarayan Tamara, Vanhaecke James A, Gallagher Joery, De Kock Genes Dis Rapid Communication Chongqing Medical University 2022-12-26 /pmc/articles/PMC10363636/ /pubmed/37492745 http://dx.doi.org/10.1016/j.gendis.2022.11.013 Text en © 2022 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Rapid Communication
Haaike, Colemonts-Vroninks
Brendan, Norman P.
Sven, Van Laere
Andrew, Davison S.
Lionel, Marcélis
Georges, Casimir
Philippe, Goyens
Paul, Claes
Dimitri, De Bundel
Geert, Martens
Rao, Ranganath Lakshminarayan
Tamara, Vanhaecke
James A, Gallagher
Joery, De Kock
Short-term nitisinone discontinuation of hereditary tyrosinemia type 1 mice causes metabolic alterations in glutathione metabolism/biosynthesis and multiple amino acid degradation pathways
title Short-term nitisinone discontinuation of hereditary tyrosinemia type 1 mice causes metabolic alterations in glutathione metabolism/biosynthesis and multiple amino acid degradation pathways
title_full Short-term nitisinone discontinuation of hereditary tyrosinemia type 1 mice causes metabolic alterations in glutathione metabolism/biosynthesis and multiple amino acid degradation pathways
title_fullStr Short-term nitisinone discontinuation of hereditary tyrosinemia type 1 mice causes metabolic alterations in glutathione metabolism/biosynthesis and multiple amino acid degradation pathways
title_full_unstemmed Short-term nitisinone discontinuation of hereditary tyrosinemia type 1 mice causes metabolic alterations in glutathione metabolism/biosynthesis and multiple amino acid degradation pathways
title_short Short-term nitisinone discontinuation of hereditary tyrosinemia type 1 mice causes metabolic alterations in glutathione metabolism/biosynthesis and multiple amino acid degradation pathways
title_sort short-term nitisinone discontinuation of hereditary tyrosinemia type 1 mice causes metabolic alterations in glutathione metabolism/biosynthesis and multiple amino acid degradation pathways
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10363636/
https://www.ncbi.nlm.nih.gov/pubmed/37492745
http://dx.doi.org/10.1016/j.gendis.2022.11.013
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