Jean-pascal Meneboo

Lille, France

Last Updated: 09/26/2026

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Found 18 publications

Resolving non‑coding splice‑altering variants using an integrative genomic and transcriptomic workflow: application to FOXP1.

Resolving non‑coding splice‑altering variants using an integrative genomic and transcriptomic workflow: application to FOXP1.

Journal: Human genomics
Published: January 23, 2026

Author Correction: Full-length RNA-Seq of the RHOH gene in human B cells reveals new exons and splicing patterns.

Author Correction: Full-length RNA-Seq of the RHOH gene in human B cells reveals new exons and splicing patterns.

Journal: Scientific reports
Published: April 28, 2025

RPGRorf15 nanopore long-read sequencing improves retinitis pigmentosa molecular diagnosis for men and women.

RPGRorf15 nanopore long-read sequencing improves retinitis pigmentosa molecular diagnosis for men and women.

Journal: Human genetics
Published: April 23, 2025

Long-term patient-derived ovarian cancer organoids closely recapitulate tumor of origin and clinical response.

Long-term patient-derived ovarian cancer organoids closely recapitulate tumor of origin and clinical response.

Journal: Journal of experimental & clinical cancer research : CR
Published: April 01, 2025

LncRNA MYO16-AS1 and MICAL2 axis sustains proliferation and migration in ovarian cancer cells and unveils a therapeutic vulnerability in patient-derived tumor organoids.

LncRNA MYO16-AS1 and MICAL2 axis sustains proliferation and migration in ovarian cancer cells and unveils a therapeutic vulnerability in patient-derived tumor organoids.

Journal: Non-coding RNA research
Published: March 10, 2025

Early growth restriction disrupts mice intestinal clock and homeostasis without being prevented by lactoferrin.

Early growth restriction disrupts mice intestinal clock and homeostasis without being prevented by lactoferrin.

Journal: Pediatric research
Published: February 27, 2025

Combining long-read DNA and RNA sequencing to enhance molecular understanding of structural variations leading to copy gains.

Combining long-read DNA and RNA sequencing to enhance molecular understanding of structural variations leading to copy gains.

Journal: Computational and structural biotechnology journal
Published: February 26, 2025

Long-read sequencing of recurrent FGF12 duplications in epilepsy: Insights into structural mechanisms and aberrant isoforms.

Long-read sequencing of recurrent FGF12 duplications in epilepsy: Insights into structural mechanisms and aberrant isoforms.

Journal: Epilepsia
Published: February 25, 2025

Long non-coding RNA UCA1 modulates SMARCA2-containing SWI/SNF chromatin remodeling complexes in human colorectal cancer.

Long non-coding RNA UCA1 modulates SMARCA2-containing SWI/SNF chromatin remodeling complexes in human colorectal cancer.

Journal: iScience
Published: November 11, 2024

Comprehensive map of the regulatory network triggered by MET exon 14 skipping reveals important involvement of the RAS-ERK signaling pathway.

Comprehensive map of the regulatory network triggered by MET exon 14 skipping reveals important involvement of the RAS-ERK signaling pathway.

Journal: Cell death & disease
Published: October 28, 2024

Full-length RNA-Seq of the RHOH gene in human B cells reveals new exons and splicing patterns.

Full-length RNA-Seq of the RHOH gene in human B cells reveals new exons and splicing patterns.

Journal: Scientific reports
Published: March 19, 2024

MET variants with activating N-lobe mutations identified in hereditary papillary renal cell carcinomas still require ligand stimulation.

MET variants with activating N-lobe mutations identified in hereditary papillary renal cell carcinomas still require ligand stimulation.

Journal: Molecular oncology
Published: March 14, 2024
Showing 1-12 of 18

Last Updated: 09/26/2026