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199 results

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NUP98-BPTF gene fusion identified in primary refractory acute megakaryoblastic leukemia of infancy.
Roussy M, Bilodeau M, Jouan L, Tibout P, Laramée L, Lemyre E, Léveillé F, Tihy F, Cardin S, Sauvageau C, Couture F, Louis I, Choblet A, Patey N, Gendron P, Duval M, Teira P, Hébert J, Wilhelm BT, Choi JK, Gruber TA, Bittencourt H, Cellot S. Roussy M, et al. Among authors: couture f. Genes Chromosomes Cancer. 2018 Jun;57(6):311-319. doi: 10.1002/gcc.22532. Epub 2018 Mar 28. Genes Chromosomes Cancer. 2018. PMID: 29427526
Human models of NUP98-KDM5A megakaryocytic leukemia in mice contribute to uncovering new biomarkers and therapeutic vulnerabilities.
Cardin S, Bilodeau M, Roussy M, Aubert L, Milan T, Jouan L, Rouette A, Laramée L, Gendron P, Duchaine J, Decaluwe H, Spinella JF, Mourad S, Couture F, Sinnett D, Haddad É, Landry JR, Ma J, Humphries RK, Roux PP, Hébert J, Gruber TA, Wilhelm BT, Cellot S. Cardin S, et al. Among authors: couture f. Blood Adv. 2019 Nov 12;3(21):3307-3321. doi: 10.1182/bloodadvances.2019030981. Blood Adv. 2019. PMID: 31698461 Free PMC article.
Intensive monitoring of minimal residual disease and chimerism after allogeneic hematopoietic stem cell transplantation for acute leukemia in children.
Pincez T, Santiago R, Bittencourt H, Louis I, Bilodeau M, Rouette A, Jouan L, Landry JR, Couture F, Richer J, Teira P, Duval M, Cellot S. Pincez T, et al. Among authors: couture f. Bone Marrow Transplant. 2021 Dec;56(12):2981-2989. doi: 10.1038/s41409-021-01408-5. Epub 2021 Sep 2. Bone Marrow Transplant. 2021. PMID: 34475524
Novel PDE10A-BRAF Fusion With Concomitant NF1 Mutation Identified in an Undifferentiated Sarcoma of Infancy With Sustained Response to Trametinib.
Vairy S, Jouan L, Bilodeau M, Dormoy-Raclet V, Gendron P, Couture F, Léveillé F, Tihy F, Lemyre E, Bouron-Dal Soglio D, Jabado N, Kleinman CL, Marzouki M, Cellot S. Vairy S, et al. Among authors: couture f. JCO Precis Oncol. 2018 Nov;2:1-13. doi: 10.1200/PO.18.00007. JCO Precis Oncol. 2018. PMID: 35135143 No abstract available.
The diagnosis of a haemophilia A carrier over 2 decades.
Dubé E, Gauthier J, Merlen C, Bonnefoy A, Couture F, Lillicrap D, Rivard GE. Dubé E, et al. Among authors: couture f. Haemophilia. 2021 Jan;27(1):e133-e136. doi: 10.1111/hae.14073. Epub 2020 Jun 11. Haemophilia. 2021. PMID: 32526814 No abstract available.
A homozygous loss-of-function variant in MYH11 in a case with megacystis-microcolon-intestinal hypoperistalsis syndrome.
Gauthier J, Ouled Amar Bencheikh B, Hamdan FF, Harrison SM, Baker LA, Couture F, Thiffault I, Ouazzani R, Samuels ME, Mitchell GA, Rouleau GA, Michaud JL, Soucy JF. Gauthier J, et al. Among authors: couture f. Eur J Hum Genet. 2015 Sep;23(9):1266-8. doi: 10.1038/ejhg.2014.256. Epub 2014 Nov 19. Eur J Hum Genet. 2015. PMID: 25407000 Free PMC article.
New adenovirus vectors for protein production and gene transfer.
Massie B, Mosser DD, Koutroumanis M, Vitté-Mony I, Lamoureux L, Couture F, Paquet L, Guilbault C, Dionne J, Chahla D, Jolicoeur P, Langelier Y. Massie B, et al. Among authors: couture f. Cytotechnology. 1998 Nov;28(1-3):53-64. doi: 10.1023/A:1008013211222. Cytotechnology. 1998. PMID: 19003407 Free PMC article.
199 results