Genevieve Morrow
1030 Avenue De La Médecine
Quebec, QC G1V0A6, Canada
Quebec, QC G1V0A6, Canada
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 19 publications
Presence of three mutations in the fumarylacetoacetate hydrolase gene in a patient with atypical symptoms of hereditary tyrosinemia type I.
Journal: Molecular genetics and metabolism
Published: October 19, 2018
Age Dependent Dysfunction of Mitochondrial and ROS Metabolism Induced by Mitonuclear Mismatch.
Journal: Frontiers in genetics
Published: June 29, 2018
Identification of proteins interacting with the mitochondrial small heat shock protein Hsp22 of Drosophila melanogaster: Implication in mitochondrial homeostasis.
Journal: PloS one
Published: November 24, 2017
Biochemical and Clinical Aspects of Hereditary Tyrosinemia Type 1.
Journal: Advances in experimental medicine and biology
Published: July 30, 2017
Molecular Aspects of the FAH Mutations Involved in HT1 Disease.
Journal: Advances in experimental medicine and biology
Published: July 30, 2017
Effect of N-terminal region of nuclear Drosophila melanogaster small heat shock protein DmHsp27 on function and quaternary structure.
Journal: PloS one
Published: January 27, 2017
Oligomeric structure and chaperone-like activity of Drosophila melanogaster mitochondrial small heat shock protein Hsp22 and arginine mutants in the alpha-crystallin domain.
Journal: Cell stress & chaperones
Published: January 25, 2017
Oligomerization and chaperone-like activity of Drosophila melanogaster small heat shock protein DmHsp27 and three arginine mutants in the alpha-crystallin domain.
Journal: Cell stress & chaperones
Published: September 08, 2016
In Vitro Structural and Functional Characterization of the Small Heat Shock Proteins (sHSP) of the Cyanophage S-ShM2 and Its Host, Synechococcus sp. WH7803.
Journal: PloS one
Published: June 21, 2016
Changes in Drosophila mitochondrial proteins following chaperone-mediated lifespan extension confirm a role of Hsp22 in mitochondrial UPR and reveal a mitochondrial localization for cathepsin D.
Journal: Mechanisms of ageing and development
Published: December 11, 2015
Identification of circulating microRNAs during the liver neoplastic process in a murine model of hereditary tyrosinemia type 1.
Journal: Scientific reports
Published: November 15, 2015
Molecular changes associated with chronic liver damage and neoplastic lesions in a murine model of hereditary tyrosinemia type 1.
Journal: Biochimica et biophysica acta
Published: March 15, 2015
Last Updated: 09/26/2026