Jimmy Perrot
Lyon, France
Last Updated: 09/26/2026
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Found 14 publications
The Spatial Organization of cDC1 with CD8+ T Cells is Critical for the Response to Immune Checkpoint Inhibitors in Patients with Melanoma.
Journal: Cancer immunology research
Published: May 07, 2024
Characterization of a Molecularly Distinct Subset of Oncocytic Pleomorphic Adenomas/Myoepitheliomas Harboring Recurrent ZBTB47-AS1::PLAG1 Gene Fusion.
Journal: The American journal of surgical pathology
Published: March 18, 2024
Deep phenotyping of nodal T-cell lymphomas reveals immune alterations and therapeutic targets.
Journal: Haematologica
Published: October 16, 2023
Sudden-onset painful eruption of the hands: A cutaneous chimeric antigen receptor T-cell therapy reaction.
Journal: JAAD case reports
Published: September 29, 2023
Uncovering the WWTR1::NCOA2 Gene fusion in low-grade myoepithelial-rich neoplasm with HMGA2 expression: A case report.
Journal: Genes, chromosomes & cancer
Published: September 27, 2023
Molecular Analyses of Chorionic-Type Intermediate Trophoblastic Lesions: Atypical Placental Site Nodules are Closer to Placental Site Nodules Than Epithelioid Trophoblastic Tumors.
Journal: Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc
Published: August 19, 2022
Pre-habilitation before colorectal cancer surgery could improve postoperative gastrointestinal function recovery: a case-matched study.
Journal: Langenbeck's archives of surgery
Published: May 12, 2021
Sympathetic axonal sprouting induces changes in macrophage populations and protects against pancreatic cancer.
Journal: Nature communications
Published: April 15, 2020
Giant axonal neuropathy: a multicenter retrospective study with genotypic spectrum expansion.
Journal: Neurogenetics
Published: August 21, 2019
Tracking the sarcoplasmic reticulum membrane voltage in muscle with a FRET biosensor.
Journal: The Journal of general physiology
Published: March 02, 2018
WES homozygosity mapping in a recessive form of Charcot-Marie-Tooth neuropathy reveals intronic GDAP1 variant leading to a premature stop codon.
Journal: Neurogenetics
Published: November 12, 2017
Last Updated: 09/26/2026