Sara Falcone

Oxford, ENG OX13PT, United Kingdom

Last Updated: 09/26/2026

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Found 11 publications

Transcriptomic analysis reveals a critical role for activating Gsα mutations in spontaneous feline hyperthyroidism.

Transcriptomic analysis reveals a critical role for activating Gsα mutations in spontaneous feline hyperthyroidism.

Journal: Scientific reports

Published: August 21, 2024

Whole genome sequencing identifies novel candidate genetic variants in canine stomatocytosis.

Whole genome sequencing identifies novel candidate genetic variants in canine stomatocytosis.

Journal: Gene

Published: May 11, 2024

Tissue Proteome of 2-Hydroxyacyl-CoA Lyase Deficient Mice Reveals Peroxisome Proliferation and Activation of ω-Oxidation.

Tissue Proteome of 2-Hydroxyacyl-CoA Lyase Deficient Mice Reveals Peroxisome Proliferation and Activation of ω-Oxidation.

Journal: International journal of molecular sciences

Published: December 16, 2021

Tissue-specific differences in the assembly of mitochondrial Complex I are revealed by a novel ENU mutation in ECSIT.

Tissue-specific differences in the assembly of mitochondrial Complex I are revealed by a novel ENU mutation in ECSIT.

Journal: Cardiovascular research

Published: November 21, 2021

A novel model of nephrotic syndrome results from a point mutation in Lama5 and is modified by genetic background.

A novel model of nephrotic syndrome results from a point mutation in Lama5 and is modified by genetic background.

Journal: Kidney international

Published: June 30, 2021

Chronically elevated branched chain amino acid levels are pro-arrhythmic.

Chronically elevated branched chain amino acid levels are pro-arrhythmic.

Journal: Cardiovascular research

Published: February 03, 2021

Identification of an Altered Matrix Signature in Kidney Aging and Disease.

Identification of an Altered Matrix Signature in Kidney Aging and Disease.

Journal: Journal of the American Society of Nephrology : JASN

Published: October 12, 2020

Generation and Identification of Mutations Resulting in Chronic and Age-Related Phenotypes in Mice.

Generation and Identification of Mutations Resulting in Chronic and Age-Related Phenotypes in Mice.

Journal: Current protocols in mouse biology

Published: June 22, 2018

Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis.

Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis.

Journal: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research

Published: April 20, 2018

Modification of an aggressive model of Alport Syndrome reveals early differences in disease pathogenesis due to genetic background.

Modification of an aggressive model of Alport Syndrome reveals early differences in disease pathogenesis due to genetic background.

Journal: Scientific reports

Published: August 31, 2017

Novel gene function revealed by mouse mutagenesis screens for models of age-related disease.

Novel gene function revealed by mouse mutagenesis screens for models of age-related disease.

Journal: Nature communications

Published: February 29, 2016

Showing 1-11 of 11

Last Updated: 09/26/2026