Kolexia
Leclerc Julie
Pharmacien
Centre de Biologie - Pathologie
Lille, France
31 Activités
0 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Prédisposition génétique à une maladie Tumeurs colorectales héréditaires sans polypose Instabilité des microsatellites Tumeurs colorectales Tumeurs du côlon Tumeurs du poumon Carcinome épidermoïde Polypose adénomateuse colique Carcinome pulmonaire non à petites cellules

Industries

Roche
1 collaboration(s)
Dernière en 2016
{{person.topindus2.name}}
{{person.topindus2.tot}} collaboration(s)
Dernière en {{person.topindus2.last}}
{{person.topindus3.name}}
{{person.topindus3.tot}} collaboration(s)
Dernière en {{person.topindus3.last}}
{{person.topindus4.name}}
{{person.topindus4.tot}} collaboration(s)
Dernière en {{person.topindus4.last}}

Dernières activités

AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer.
Genes, chromosomes & cancer   21 décembre 2022
Genetic predisposition to neural crest-derived tumors: revisiting the role of KIF1B.
Endocrine connections   17 avril 2022
Diagnosis of Lynch Syndrome and Strategies to Distinguish Lynch-Related Tumors from Sporadic MSI/dMMR Tumors.
Cancers   26 janvier 2021
Colon cancer stemness as a reversible epigenetic state: Implications for anticancer therapies.
World journal of stem cells   28 septembre 2020
Hip survival after plain core decompression alone versus bone morphogenetic protein and/or bone marrow reinjection with core decompression for avascular osteonecrosis of the femoral head: a retrospective case control study in ninety two patients.
International orthopaedics   21 juillet 2020
Alu element insertion in the MLH1 exon 6 coding sequence as a mutation predisposing to Lynch syndrome.
Human mutation   30 mars 2020
Characterisation of heterozygous variants in French patients with Lynch syndrome.
Journal of medical genetics   28 janvier 2020
MSH2 c.1022T>C, p.Leu341Pro is a founder pathogenic variation and a major cause of Lynch syndrome in the North of France.
Genes, chromosomes & cancer   03 septembre 2019
of a SMAD4 retroduplication event using NGS targeted gene panel
Abstracts from the 50th European Society of Human Genetics Conference   01 juillet 2019
Lynch syndrome families with heritable constitutional epimutation reveal the diversity of genetic events associated with methylation of MLH1 promoter
Abstracts from the 51st European Society of Human Genetics (ESHG) Conference, in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG)   01 juillet 2019