Marie-france Champy

Illkirch-graffenstaden, France

Last Updated: 09/26/2026

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Found 22 publications

Loss of Sult1a1 reduces body weight and increases browning of white adipose tissue.

Loss of Sult1a1 reduces body weight and increases browning of white adipose tissue.

Journal: Frontiers in endocrinology

Published: June 12, 2024

Loss of low-molecular-weight protein tyrosine phosphatase shows limited improvement in glucose tolerance but causes mild cardiac hypertrophy in mice.

Loss of low-molecular-weight protein tyrosine phosphatase shows limited improvement in glucose tolerance but causes mild cardiac hypertrophy in mice.

Journal: American journal of physiology. Endocrinology and metabolism

Published: April 11, 2022

Microglia-specific knock-down of Bmal1 improves memory and protects mice from high fat diet-induced obesity.

Microglia-specific knock-down of Bmal1 improves memory and protects mice from high fat diet-induced obesity.

Journal: Molecular psychiatry

Published: December 24, 2020

SCA7 Mouse Cerebellar Pathology Reveals Preferential Downregulation of Key Purkinje Cell-Identity Genes and Shared Disease Signature with SCA1 and SCA2.

SCA7 Mouse Cerebellar Pathology Reveals Preferential Downregulation of Key Purkinje Cell-Identity Genes and Shared Disease Signature with SCA1 and SCA2.

Journal: The Journal of neuroscience : the official journal of the Society for Neuroscience

Published: July 15, 2020

Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.

Mouse mutant phenotyping at scale reveals novel genes controlling bone mineral density.

Journal: PLoS genetics

Published: March 25, 2020

High-throughput discovery of genetic determinants of circadian misalignment.

High-throughput discovery of genetic determinants of circadian misalignment.

Journal: PLoS genetics

Published: July 15, 2019

Soft windowing application to improve analysis of high-throughput phenotyping data.

Soft windowing application to improve analysis of high-throughput phenotyping data.

Journal: Bioinformatics (Oxford, England)

Published: May 09, 2019

Identification of genetic elements in metabolism by high-throughput mouse phenotyping.

Identification of genetic elements in metabolism by high-throughput mouse phenotyping.

Journal: Nature communications

Published: November 24, 2016

Nox4 genetic inhibition in experimental hypertension and metabolic syndrome.

Nox4 genetic inhibition in experimental hypertension and metabolic syndrome.

Journal: Archives of cardiovascular diseases

Published: October 13, 2016

Atp6ap2 ablation in adult mice impairs viability through multiple organ deficiencies.

Atp6ap2 ablation in adult mice impairs viability through multiple organ deficiencies.

Journal: Scientific reports

Published: June 28, 2016

Physiological Expression of AMPKγ2RG Mutation Causes Wolff-Parkinson-White Syndrome and Induces Kidney Injury in Mice.

Physiological Expression of AMPKγ2RG Mutation Causes Wolff-Parkinson-White Syndrome and Induces Kidney Injury in Mice.

Journal: The Journal of biological chemistry

Published: May 17, 2016

Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome.

Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome.

Journal: Neuron

Published: March 24, 2016

Showing 1-12 of 22

Last Updated: 09/26/2026