Zobrazeno 1 - 10
of 93
pro vyhledávání: '"P. Shooshtarizadeh"'
Autor:
Anne Helness, Jennifer Fraszczak, Charles Joly-Beauparlant, Halil Bagci, Christian Trahan, Kaifee Arman, Peiman Shooshtarizadeh, Riyan Chen, Marina Ayoub, Jean-François Côté, Marlene Oeffinger, Arnaud Droit, Tarik Möröy
Publikováno v:
Communications Biology, Vol 4, Iss 1, Pp 1-16 (2021)
Helness et al. show that GFI1/CHD4 complexes critically regulate chromatin accessibility and histone modifications to regulate target genes affecting diverse cellular processes in neutrophils. Their results provide further insight into the molecular
Externí odkaz:
https://doaj.org/article/f4208fa66ce144baa1f83bed6e3a7a19
Publikováno v:
Journal of English Language Teaching and Learning, Vol 13, Iss 27, Pp 359-388 (2021)
Situated-learning translation training approach has been proven to be an efficacious translation training approach in cultivating translators' long-life learning, translation competence as well as translator competence. However, previous studies have
Externí odkaz:
https://doaj.org/article/88735ff10a1c466f95b5a2c50b60a8a2
Publikováno v:
Middle East Journal of Cancer, Vol 11, Iss 3, Pp 254-259 (2020)
Background: The main oncogenic action of CD99 and cyclin D1 biomarkers is referred to any mutation, amplification, and overexpression in cyclin D1 coding gene, altering cell cycle progression as the main mechanism observed in a variety of tumors.
Externí odkaz:
https://doaj.org/article/72a2c5745d994ea4bec29490afb1e6f6
Publikováno v:
Iranian Journal of Pathology, Vol 14, Iss 2, Pp 165-174 (2019)
The malignant transformation of conventional giant cell tumor of bone (GCTOB) is rare and usually occurs with irradiation. Here we report two neglected cases of conventional GCTOB with spontaneous malignant transformation at 11 and 16 years after ini
Externí odkaz:
https://doaj.org/article/b993160818b543c186dc63c372d26984
Autor:
Peiman Shooshtarizadeh, Anne Helness, Charles Vadnais, Nelleke Brouwer, Hugues Beauchemin, Riyan Chen, Halil Bagci, Frank J. T. Staal, Jean-François Coté, Tarik Möröy
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-16 (2019)
Gfi1b regulates cellularity of haematopoietic stem cells (HSCs) and megakaryocytes (MKs) as well as spreading of MKs on matrix. Here the authors show that Gfi1b regulates this behaviour by recruiting LSD1 and β-catenin to Wnt/β-catenin signalling t
Externí odkaz:
https://doaj.org/article/dc1d6a2a5faa46caa688da1feb30cd2a
Autor:
Anne Helness, Jennifer Fraszczak, Charles Joly-Beauparlant, Halil Bagci, Christian Trahan, Kaifee Arman, Peiman Shooshtarizadeh, Riyan Chen, Marina Ayoub, Jean-François Côté, Marlene Oeffinger, Arnaud Droit, Tarik Möröy
Publikováno v:
Communications Biology, Vol 5, Iss 1, Pp 1-1 (2022)
Externí odkaz:
https://doaj.org/article/0005a06cdadb487d9d99f9e5fdde562e
Publikováno v:
Journal of Nephropathology, Vol 7, Iss 3, Pp 166-170 (2018)
Background: Lupus nephritis (LN) is a serious complication of systemic lupus erythematosus (SLE). Activation of complement system which leads to the production of C4 and its ultimate product, C4d, plays an important role in the pathogenesis of LN. Ob
Externí odkaz:
https://doaj.org/article/afe67df6a98243b8af06dbc66f9525c9
Publikováno v:
Dental Research Journal, Vol 19, Iss 1, Pp 13-13 (2022)
Osteoblastoma (OSB) is an uncommon (3% of benign and 1% of all) primary bone neoplasm with extremely rare occurrence in head and neck, especially the maxillary bone region. OSB of the jaw mainly involves the mandible bone. We report a 10-month-old ma
Externí odkaz:
https://doaj.org/article/514deb12b04043318aa7fbbe28ce9c7c
Publikováno v:
Acta Medica Iranica, Vol 55, Iss 12 (2018)
Metachondromatosis which was first described in 1971 by Maroteaux is a rare genetic disease consisting of osteochondromas and enchondromas, caused by loss of function of the PTPN11 gene. It is distinct from other cartilaginous tumors such as multiple
Externí odkaz:
https://doaj.org/article/af631e7e07274278bbd1d22fc2d1be84
Gfi1b controls integrin signaling-dependent cytoskeleton dynamics and organization in megakaryocytes
Autor:
Hugues Beauchemin, Peiman Shooshtarizadeh, Charles Vadnais, Lothar Vassen, Yves D Pastore, Tarik Möröy
Publikováno v:
Haematologica, Vol 102, Iss 3 (2017)
Mutations in GFI1B are associated with inherited bleeding disorders called GFI1B-related thrombocytopenias. We show here that mice with a megakaryocyte-specific Gfi1b deletion exhibit a macrothrombocytopenic phenotype along a megakaryocytic dysplasia
Externí odkaz:
https://doaj.org/article/fb48704ea64e4b77976bdf071f107298