Tiffany Migeon
Paris, 75012, France
Last Updated: 09/26/2026
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Found 12 publications
TRPA1 inhibition reduces ocular pain and corneal neurogenic inflammation in a mouse model of dry eye disease.
Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
Published: June 30, 2025
Knock-down of the long isoform of the WNK1 kinase mitigates the anti-glomerular basement membrane glomerulonephritis in mice.
Journal: Scientific reports
Published: February 18, 2025
Signaling through cAMP-Epac1 induces metabolic reprogramming to protect podocytes in glomerulonephritis.
Journal: Kidney international
Published: September 22, 2023
Protective Role of the Podocyte IL-15 / STAT5 Pathway in Focal Segmental Glomerulosclerosis.
Journal: Kidney international reports
Published: July 26, 2023
Pulmonary hypertension without heart failure causes cardiorenal syndrome in a porcine model.
Journal: Scientific reports
Published: February 16, 2023
Heterozygous expression of Cre recombinase in podocytes has no impact on the anti-glomerular basement membrane glomerulonephritis model in C57BL/6J mice.
Journal: Physiological reports
Published: July 30, 2022
Transient Receptor Potential Channels: Important Players in Ocular Pain and Dry Eye Disease.
Journal: Pharmaceutics
Published: July 05, 2022
Activation of Notch3 in Renal Tubular Cells Leads to Progressive Cystic Kidney Disease.
Journal: International journal of molecular sciences
Published: December 21, 2021
Anaesthesia-Induced Transcriptomic Changes in the Context of Renal Ischemia Uncovered by the Use of a Novel Clamping Device.
Journal: International journal of molecular sciences
Published: July 31, 2021
Mutation affecting the conserved acidic WNK1 motif causes inherited hyperkalemic hyperchloremic acidosis.
Journal: The Journal of clinical investigation
Published: June 08, 2018
HANAC Col4a1 Mutation in Mice Leads to Skeletal Muscle Alterations due to a Primary Vascular Defect.
HANAC Col4a1 Mutation in Mice Leads to Skeletal Muscle Alterations due to a Primary Vascular Defect.
Journal: The American journal of pathology
Published: March 14, 2016
HANAC Syndrome Col4a1 Mutation Causes Neonate Glomerular Hyperpermeability and Adult Glomerulocystic Kidney Disease.
Journal: Journal of the American Society of Nephrology : JASN
Published: December 12, 2014
Showing 1-12 of 12
Last Updated: 09/26/2026