Jessica Ohana

Paris, 75013, France

Last Updated: 09/26/2026

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Found 14 publications

Comprehensive transcriptomic profiling reveals impaired polyamine metabolism as a contributor to age-related muscle decline.

Comprehensive transcriptomic profiling reveals impaired polyamine metabolism as a contributor to age-related muscle decline.

Journal: iScience
Published: February 27, 2026

EMILIN1 emerges as a TGFβ/SETDB1-regulated secreted biomarker in Duchenne muscular dystrophy.

EMILIN1 emerges as a TGFβ/SETDB1-regulated secreted biomarker in Duchenne muscular dystrophy.

Journal: Cell death & disease
Published: November 20, 2025

MicroAge mission: experimental design and hardware for a bespoke culture system supporting tissue-engineered skeletal muscle.

MicroAge mission: experimental design and hardware for a bespoke culture system supporting tissue-engineered skeletal muscle.

Journal: NPJ microgravity
Published: July 03, 2025

Best reference genes for unbiased normalized transcript expression in normal and dystrophic human cell models of myogenesis.

Best reference genes for unbiased normalized transcript expression in normal and dystrophic human cell models of myogenesis.

Journal: PloS one
Published: June 05, 2025

A comparison of human skeletal muscle cell maturation in 2D versus 3D culture: A quantitative proteomic study.

A comparison of human skeletal muscle cell maturation in 2D versus 3D culture: A quantitative proteomic study.

Journal: Physiological reports
Published: April 18, 2025

Patient-Oriented In Vitro Studies in Duchenne Muscular Dystrophy: Validation of a 3D Skeletal Muscle Organoid Platform.

Patient-Oriented In Vitro Studies in Duchenne Muscular Dystrophy: Validation of a 3D Skeletal Muscle Organoid Platform.

Journal: Biomedicines
Published: March 26, 2025

HDAC11 deficiency improves muscle phenotype in a Duchenne muscular dystrophy murine model by reducing inflammation and fibrosis.

HDAC11 deficiency improves muscle phenotype in a Duchenne muscular dystrophy murine model by reducing inflammation and fibrosis.

Journal: Life sciences
Published: January 22, 2025

The Emerging TNNT3 Spectrum: From Distal Arthrogryposis to Congenital Myopathy.

The Emerging TNNT3 Spectrum: From Distal Arthrogryposis to Congenital Myopathy.

Journal: Human mutation
Published: November 21, 2024

miR-107 represses DMPK and is sequestered by CUG repeats triggering the MSI2/miR-7 pathogenesis axis in myotonic dystrophy.

miR-107 represses DMPK and is sequestered by CUG repeats triggering the MSI2/miR-7 pathogenesis axis in myotonic dystrophy.

Journal: Molecular therapy. Nucleic acids
Published: May 20, 2024

Deletion of exons 45 to 55 in the DMD gene: from the therapeutic perspective to the in vitro model.

Deletion of exons 45 to 55 in the DMD gene: from the therapeutic perspective to the in vitro model.

Journal: Skeletal muscle
Published: January 07, 2024

Cellular and Genomic Features of Muscle Differentiation from Isogenic Fibroblasts and Myoblasts.

Cellular and Genomic Features of Muscle Differentiation from Isogenic Fibroblasts and Myoblasts.

Journal: Cells
Published: June 30, 2023

Therapeutic potential of oleic acid supplementation in myotonic dystrophy muscle cell models.

Therapeutic potential of oleic acid supplementation in myotonic dystrophy muscle cell models.

Journal: Biological research
Published: June 14, 2023
Showing 1-12 of 14

Last Updated: 09/26/2026