M. Husson

发表

Absence of correlation between radiation-induced CD8 T-lymphocyte apoptosis and sequelae in patients with prostate cancer accidentally overexposed to radiation

A. Rousseau, J. Merlin, D. Peiffert, 2018, Oncotarget.

Accelerated BRAF mutation analysis using a fully automated PCR platform improves the management of patients with metastatic melanoma

A. Leroux, J. Salleron, J. Merlin, 2018, Oncotarget.

Optimization of routine KRAS mutation PCR-based testing procedure for rational individualized first-line-targeted therapy selection in metastatic colorectal cancer

A. Leroux, J. Merlin, A. Chretien, 2013, Cancer medicine.

Epileptic patients with de novo STXBP1 mutations: Key clinical features based on 24 cases

A. Afenjar, N. Philip, D. Ville, 2015, Epilepsia.

Caspase-mediated cleavage, IAP binding, and ubiquitination: linking three mechanisms crucial for Drosophila NF-kappaB signaling.

J. Reichhart, P. Meier, N. Silverman, 2010, Molecular cell.

A sensitive assay for measuring SMN mRNA levels in peripheral blood and in muscle samples of patients affected with spinal muscular atrophy

J. Melki, A. Toutain, T. Frebourg, 2007, European Journal of Human Genetics.

DDB2 represses epithelial-to-mesenchymal transition and sensitizes pancreatic ductal adenocarcinoma cells to chemotherapy

J. Merlin, P. Gilson, S. Grandemange, 2022, Frontiers in Oncology.

Clinical and molecular phenotype of Aicardi-Goutieres syndrome.

A. Green, D. Bonthron, E. Bertini, 2007, American journal of human genetics.

Analysis of PIK3CA exon 9 and 20 mutations in breast cancers using PCR-HRM and PCR-ARMS: correlation with clinicopathological criteria.

J. Merlin, A. Harlé, P. Génin, 2013, Oncology reports.

A patient with hydranencephaly and PEHO-like dysmorphic features.

D. Lacombe, J. Pedespan, C. Goizet, 2003, Annales de genetique.

Evaluation of KRAS, NRAS and BRAF hotspot mutations detection for patients with metastatic colorectal cancer using direct DNA pipetting in a fully-automated platform and Next-Generation Sequencing for laboratory workflow optimisation

A. Leroux, J. Merlin, P. Gilson, 2019, PloS one.

Integrated routine workflow using next-generation sequencing and a fully-automated platform for the detection of KRAS, NRAS and BRAF mutations in formalin-fixed paraffin embedded samples with poor DNA quality in patients with colorectal carcinoma

A. Leroux, J. Merlin, P. Gilson, 2019, PloS one.

Rare RAS Mutations in Metastatic Colorectal Cancer Detected During Routine RAS Genotyping Using Next Generation Sequencing

A. Leroux, R. Boidot, J. Merlin, 2016, Targeted Oncology.

Evaluation of the Idylla ctEGFR mutation assay to detect EGFR mutations in plasma from patients with non-small cell lung cancers

J. Salleron, J. Merlin, P. Gilson, 2021, Scientific Reports.

LPIN1 gene mutations: a major cause of severe rhabdomyolysis in early childhood

Wolfgang Müller-Felber, Arnold Munnich, Laurence Hubert, 2010, Human mutation.

Evaluation of KRAS, NRAS and BRAF mutations detection in plasma using an automated system for patients with metastatic colorectal cancer

J. Merlin, P. Gilson, C. Gavoille, 2020, PloS one.

Xq28 copy number gain causing moyamoya disease and a novel moyamoya syndrome

C. Aloui, O. Quenez, D. Hervé, 2020, Journal of Medical Genetics.

Evaluation of 3 molecular-based assays for microsatellite instability detection in formalin-fixed tissues of patients with endometrial and colorectal cancers

A. Leroux, J. Salleron, J. Merlin, 2020, Scientific Reports.

Refractory Occipital Lobe Epilepsy Treated by Surgery in a Child with Chronic Encephalitis

A. Rougier, J. Pedespan, A. Vital, 2007, Pediatric Neurosurgery.

A mutation can hide another one: Think Structural Variants!

F. Sturtz, P. Derouault, A. Lia, 2020, Computational and structural biotechnology journal.

Uncommon mutational profiles of metastatic colorectal cancer detected during routine genotyping using next generation sequencing

A. Leroux, J. Merlin, P. Gilson, 2019, Scientific Reports.

Colorectal cancer screening programme: is the French faecal immunological test (FIT) threshold optimal?

R. Benamouzig, R. Coriat, S. Chaussade, 2021, Therapeutic advances in gastroenterology.

[Vaccinal status in children with seizures: a retrospective study conducted in the Bordeaux child hospital].

J. Pedespan, C. Gitiaux, P. Pillet, 2006, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Expanding the Spectrum of Neurological Manifestations in Cutis Laxa, Autosomal Recessive, Type IIIA

J. Pedespan, C. Goizet, M. Thibaud, 2020, Neuropediatrics.

cfDNA for accurate determination of RAS and BRAF mutations using OncoBEAM liquid biopsy in metastatic colorectal cancer patients: Results of the real-world multicentric ColoBEAM study.

D. Spaeth, J. Salleron, J. Merlin, 2019, Journal of Clinical Oncology.

Benign nocturnal alternating hemiplegia of childhood: Two cases with positive evolution

F. Picard, J. Pedespan, F. Villéga, 2011, Brain and Development.

Uncommon mutational profiles of metastatic colorectal cancer detected during routine genotyping using next generation sequencing

Shaun M. Kandathil, A. Leroux, J. Merlin, 2019, Scientific Reports.

Epileptic patients with de novo STXBP1 mutations: Key clinical features based on 24 cases

A. Afenjar, N. Philip, D. Ville, 2015, Epilepsia.

Caspase-mediated cleavage, IAP binding, and ubiquitination: linking three mechanisms crucial for Drosophila NF-kappaB signaling.

J. Reichhart, P. Meier, N. Silverman, 2010, Molecular cell.

CRISPR/Cas9-mediated knock-in of BRCA1/2 mutations restores response to olaparib in pancreatic cancer cell lines

P. Gilson, A. Harlé, M. Husson, 2023, Scientific reports.

Integrated Molecular Characterization of HER2-Low Breast Cancer Using Next Generation Sequencing (NGS)

P. Gilson, A. Harlé, M. Husson, 2023, Biomedicines.