Molecular changes associated with chronic liver damage and neoplastic lesions in a murine model of hereditary tyrosinemia type 1-Reference-Cited by-同舟云学术

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Molecular changes associated with chronic liver damage and neoplastic lesions in a murine model of hereditary tyrosinemia type 1

Published:2015-12 Issue:12 Volume:1852 Page:2603-2617
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Angileri Francesca,Roy Vincent,Morrow Geneviève,Scoazec Jean Yves,Gadot Nicolas,Orejuela Diana,Tanguay Robert M.

Funder

CIHR

Fondation du Grand Défi Pierre Lavoie

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference87 articles.

1. Tyrosine and its catabolites: from disease to cancer;Tanguay;Acta Biochim. Pol.,1996

2. Hypertyrosinemia;Mitchell,2001

3. Tyrosinemia: a review;Russo;Pediatr. Dev. Pathol.,2001

4. The pathophysiology and treatment of hereditary tyrosinemia type 1;Grompe;Semin. Liver Dis.,2001

5. Fumarylacetoacetate, the metabolite accumulating in hereditary tyrosinemia, activates the ERK pathway and induces mitotic abnormalities and genomic instability;Jorquera;Hum. Mol. Genet.,2001

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1. Hereditary Tyrosinemia Type 1 Mice under Continuous Nitisinone Treatment Display Remnants of an Uncorrected Liver Disease Phenotype;Genes;2023-03-11

2. The compound heterozygous mutations of c.607G>a and c.657delC in the FAH gene are associated with renal damage with hereditary tyrosinemia type 1 (HT1);Molecular Genetics & Genomic Medicine;2022-11-12

3. mRNA-Based Approaches to Treating Liver Diseases;Cells;2022-10-21

4. mRNA-based therapy proves superior to the standard of care for treating hereditary tyrosinemia 1 in a mouse model;Molecular Therapy - Methods & Clinical Development;2022-09

5. A versatile transposon-based technology to generate loss- and gain-of-function phenotypes in the mouse liver;BMC Biology;2022-04-01

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