Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Anissa Djedid"'
Autor:
Shirin Lak, Valérie Janelle, Anissa Djedid, Gabrielle Boudreau, Ann Brasey, Véronique Lisi, Ali Smaani, Cédric Carli, Lambert Busque, Vincent-Philippe Lavallée, Jean-Sébastien Delisle
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 27, Iss , Pp 230-245 (2022)
Antigen-specific T cell expansion ex vivo followed by adoptive transfer enables targeting of a multitude of microbial and cancer antigens. However, clinical-scale T cell expansion from rare precursors requires repeated stimulation, which may lead to
Externí odkaz:
https://doaj.org/article/69663426dd644361ad6f2f2b985cbce2
Autor:
Marie-Claude Beauchamp, Anissa Djedid, Kevin Daupin, Kayla Clokie, Shruti Kumar, Jacek Majewski, Loydie Anne Jerome-Majewska
Publikováno v:
PLoS ONE, Vol 14, Iss 7, p e0219280 (2019)
Mutations in EFTUD2 are responsible for the autosomal dominant syndrome named MFDM (mandibulofacial dysostosis with microcephaly). However, it is not clear how reduced levels of EFTUD2 cause abnormalities associated with this syndrome. To determine i
Externí odkaz:
https://doaj.org/article/412905e3589f4083b86131b0c47d5a1e
Autor:
Benjamin A. Garcia, Jacek Majewski, Amanda Lisby, Anissa Djedid, Simone Sidoli, Dylan M. Marchione, John B. Wojcik
Tabbed excel spreadsheet with each tab representing a single supplementary table. The first cell of each tab contains a description of the contents. Supplemental Table 1: Log2 normalized protein abundances of proteins identified in FFPE MPNST samples
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c9429dd576b702b266af587d9817e39
https://doi.org/10.1158/0008-5472.22421621.v1
https://doi.org/10.1158/0008-5472.22421621.v1
Autor:
Benjamin A. Garcia, Jacek Majewski, Amanda Lisby, Anissa Djedid, Simone Sidoli, Dylan M. Marchione, John B. Wojcik
Merged pdf file containing supplementary figures 1-4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a04b314af2e02b66a7cb4f96894038c
https://doi.org/10.1158/0008-5472.22421624
https://doi.org/10.1158/0008-5472.22421624
Autor:
Benjamin A. Garcia, Jacek Majewski, Amanda Lisby, Anissa Djedid, Simone Sidoli, Dylan M. Marchione, John B. Wojcik
Word file containing legends for supplemental figures S1-S4 and Supplemental tables 1-5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c06051235dbeda9f51dc8fa26d3f99c
https://doi.org/10.1158/0008-5472.22421627
https://doi.org/10.1158/0008-5472.22421627
Autor:
Benjamin A. Garcia, Jacek Majewski, Amanda Lisby, Anissa Djedid, Simone Sidoli, Dylan M. Marchione, John B. Wojcik
Malignant peripheral nerve sheath tumor (MPNST) is an aggressive sarcoma with recurrent loss-of-function alterations in polycomb-repressive complex 2 (PRC2), a histone-modifying complex involved in transcriptional silencing. To understand the role of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ae3041ed34aee9a0435889c9c96d34e
https://doi.org/10.1158/0008-5472.c.6510974.v1
https://doi.org/10.1158/0008-5472.c.6510974.v1
Autor:
Jennifer L. Fish, Kym M. Boycott, Fjodor Merkuri, Peter C. Stirling, Rachel Aber, Matthew A. Lines, Eric Bareke, Marie-Claude Beauchamp, Anissa Djedid, Loydie A. Jerome-Majewska, Annie S. Tam, Jacek Majewski
Publikováno v:
Hum Mol Genet
EFTUD2 is mutated in patients with mandibulofacial dysostosis with microcephaly (MFDM). We generated a mutant mouse line with conditional mutation in Eftud2 and used Wnt1-Cre2 to delete it in neural crest cells. Homozygous deletion of Eftud2 causes b
Autor:
Shirin, Lak, Valérie, Janelle, Anissa, Djedid, Gabrielle, Boudreau, Ann, Brasey, Véronique, Lisi, Ali, Smaani, Cédric, Carli, Lambert, Busque, Vincent-Philippe, Lavallée, Jean-Sébastien, Delisle
Publikováno v:
Molecular therapy. Methodsclinical development. 27
Antigen-specific T cell expansion
Autor:
Anissa Djedid, Lambert Busque, Véronique Lisi, Jean-Sébastien Delisle, Valérie Janelle, Ann Brasey, Vincent-Philippe Lavallée, Shirin Lak, Gabrielle Boudreau, Cédric Carli
BackgroundThe stimulation and expansion of antigen-specific T cells ex vivo enables the targeting of a multitude of cancer antigens. However, clinical scale T-cell expansion from rare precursors requires repeated stimulations ex vivo leading to T-cel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69f5207fdd31befbebaed580b0e1c1c7
https://doi.org/10.1101/2021.08.30.21262835
https://doi.org/10.1101/2021.08.30.21262835
Autor:
Marcus A. Cheek, Michael-Christopher Keogh, John T. McGuire, Matthew R. Marunde, Daniel N. Weinberg, Simon Papillon-Cavanagh, Kartik N. Rajagopalan, Chao Lu, Haitao Li, Nada Jabado, Jacek Majewski, Yuan Yue, Anissa Djedid, Eric Bareke, Xinjing Xu, Ashot S. Harutyunyan, Xiao Chen, Agata E. Lemiesz, Cynthia Horth, Hamid Nikbakht, Matthew J. Meiners, Haifen Chen, Dylan M. Marchione, Benjamin A. Garcia, C. David Allis
Publikováno v:
Nature
Enzymes that catalyse CpG methylation in DNA, including the DNA methyltransferases 1 (DNMT1), 3A (DNMT3A) and 3B (DNMT3B), are indispensable for mammalian tissue development and homeostasis1–4. They are also implicated in human developmental disord