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Florence Coulet

Showing results (91-100 of 114) with videos related to

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Cancers|July 2, 2021
5' Region Large Genomic Rearrangements in the <i>BRCA1</i> Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent BreakpointsSandrine M Caputo, Dominique Telly, Adrien Briaux, et al.
JCO Precision Oncology|June 1, 2023
Mismatch Repair Deficiency and Lynch Syndrome Among Adult Patients With GliomaPatrick R Benusiglio, Fikret Elder, Mehdi Touat, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|May 3, 2011
Cross-validation study for epidermal growth factor receptor and KRAS mutation detection in 74 blinded non-small cell lung carcinoma samples: a total of 5550 exons sequenced by 15 molecular French laboratories (evaluation of the EGFR mutation status for the administration of EGFR-TKIs in non-small cell lung carcinoma [ERMETIC] project--part 1)Michèle Beau-Faller, Armelle Degeorges, Estelle Rolland, et al.
Genes, Chromosomes & Cancer|December 11, 2022
AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancerJulie Leclerc, Marie Beaumont, Roseline Vibert, et al.
Clinical Genetics|January 17, 2021
Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic ConsortiumFlavie Boulouard, Edwige Kasper, Marie-Pierre Buisine, et al.
Neuro-Oncology|September 11, 2019
Medulloblastomas associated with an APC germline pathogenic variant share the good prognosis of CTNNB1-mutated medulloblastomasAurore Surun, Pascale Varlet, Laurence Brugières, et al.
Journal of Medical Genetics|August 29, 2022
First estimates of diffuse gastric cancer risks for carriers of <i>CTNNA1</i> germline pathogenic variantsMarie Coudert, Youenn Drouet, Hélène Delhomelle, et al.
Human Mutation|January 24, 2006
Mutations of the TGF-beta type II receptor BMPR2 in pulmonary arterial hypertensionRajiv D Machado, Micheala A Aldred, Victoria James, et al.
Haematologica|June 6, 2024
Epstein-Barr virus and immune status imprint the immunogenomics of non-Hodgkin lymphomas occurring in immune-suppressed environmentsMarine Baron, Karim Labreche, Marianne Veyri, et al.
Nucleic Acids Research|May 12, 2018
Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effortRaphaël Leman, Pascaline Gaildrat, Gérald Le Gac, et al.
Pageof 12

Showing results (91-100 of 114) with videos related to

Sort By:
Pageof 12
Cancers|July 2, 2021
5' Region Large Genomic Rearrangements in the <i>BRCA1</i> Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent BreakpointsSandrine M Caputo, Dominique Telly, Adrien Briaux, et al.
JCO Precision Oncology|June 1, 2023
Mismatch Repair Deficiency and Lynch Syndrome Among Adult Patients With GliomaPatrick R Benusiglio, Fikret Elder, Mehdi Touat, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|May 3, 2011
Cross-validation study for epidermal growth factor receptor and KRAS mutation detection in 74 blinded non-small cell lung carcinoma samples: a total of 5550 exons sequenced by 15 molecular French laboratories (evaluation of the EGFR mutation status for the administration of EGFR-TKIs in non-small cell lung carcinoma [ERMETIC] project--part 1)Michèle Beau-Faller, Armelle Degeorges, Estelle Rolland, et al.
Genes, Chromosomes & Cancer|December 11, 2022
AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancerJulie Leclerc, Marie Beaumont, Roseline Vibert, et al.
Clinical Genetics|January 17, 2021
Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic ConsortiumFlavie Boulouard, Edwige Kasper, Marie-Pierre Buisine, et al.
Neuro-Oncology|September 11, 2019
Medulloblastomas associated with an APC germline pathogenic variant share the good prognosis of CTNNB1-mutated medulloblastomasAurore Surun, Pascale Varlet, Laurence Brugières, et al.
Journal of Medical Genetics|August 29, 2022
First estimates of diffuse gastric cancer risks for carriers of <i>CTNNA1</i> germline pathogenic variantsMarie Coudert, Youenn Drouet, Hélène Delhomelle, et al.
Human Mutation|January 24, 2006
Mutations of the TGF-beta type II receptor BMPR2 in pulmonary arterial hypertensionRajiv D Machado, Micheala A Aldred, Victoria James, et al.
Haematologica|June 6, 2024
Epstein-Barr virus and immune status imprint the immunogenomics of non-Hodgkin lymphomas occurring in immune-suppressed environmentsMarine Baron, Karim Labreche, Marianne Veyri, et al.
Nucleic Acids Research|May 12, 2018
Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effortRaphaël Leman, Pascaline Gaildrat, Gérald Le Gac, et al.
Pageof 12