Zobrazeno 1 - 10
of 107
pro vyhledávání: '"Minako, MORI"'
Autor:
Yasuo Kubota, Xiaorong Gu, Laila Terkawi, Juraj Bodo, Bartlomiej P. Przychodzen, Hussein Awada, Nakisha Williams, Carmelo Gurnari, Naomi Kawashima, Mai Aly, Arda Durmaz, Minako Mori, Ben Ponvilawan, Tariq Kewan, Waled Bahaj, Manja Meggendorfer, Babal K. Jha, Valeria Visconte, Heesun J. Rogers, Torsten Haferlach, Jaroslaw P. Maciejewski
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-12 (2024)
Abstract PHF6 mutations (PHF6 MT) are identified in various myeloid neoplasms (MN). However, little is known about the precise function and consequences of PHF6 in MN. Here we show three main findings in our comprehensive genomic and proteomic study.
Externí odkaz:
https://doaj.org/article/a86ae8fe55bc46c2af1a9650289584f9
Autor:
Waled Bahaj, Tariq Kewan, Carmelo Gurnari, Arda Durmaz, Ben Ponvilawan, Ishani Pandit, Yasuo Kubota, Olisaemeka D. Ogbue, Misam Zawit, Yazan Madanat, Taha Bat, Suresh K. Balasubramanian, Hussein Awada, Ramsha Ahmed, Minako Mori, Manja Meggendorfer, Torsten Haferlach, Valeria Visconte, Jaroslaw P. Maciejewski
Publikováno v:
Journal of Hematology & Oncology, Vol 16, Iss 1, Pp 1-12 (2023)
Abstract Background TP53 mutations (TP53 MT ) occur in diverse genomic configurations. Particularly, biallelic inactivation is associated with poor overall survival in cancer. Lesions affecting only one allele might not be directly leukemogenic, ques
Externí odkaz:
https://doaj.org/article/be24204f0e834aaeb1aa9535926fa7e7
Autor:
Tariq Kewan, Arda Durmaz, Waled Bahaj, Carmelo Gurnari, Laila Terkawi, Hussein Awada, Olisaemeka D. Ogbue, Ramsha Ahmed, Simona Pagliuca, Hassan Awada, Yasuo Kubota, Minako Mori, Ben Ponvilawan, Bayan Al-Share, Bhumika J. Patel, Hetty E. Carraway, Jacob Scott, Suresh K. Balasubramanian, Taha Bat, Yazan Madanat, Mikkael A. Sekeres, Torsten Haferlach, Valeria Visconte, Jaroslaw P. Maciejewski
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-10 (2023)
Abstract Genomic mutations drive the pathogenesis of myelodysplastic syndromes and acute myeloid leukemia. While morphological and clinical features have dominated the classical criteria for diagnosis and classification, incorporation of molecular da
Externí odkaz:
https://doaj.org/article/6c02bbbd75f840c28ae20ecd4c63c506
Autor:
Issei Oi, Zentaro Saito, Takanori Ito, Takuma Imakita, Osamu Kanai, Kohei Fujita, Hiromasa Tachibana, Minako Mori, Koki Moriyoshi, Tadashi Mio
Publikováno v:
Respirology Case Reports, Vol 11, Iss 7, Pp n/a-n/a (2023)
Abstract This report describes the case of a 79‐year‐old Japanese man diagnosed with orbital extranodal marginal zone lymphoma (EMZL) and stage IIIA lung cancer. The patient received concurrent chemoradiation for lung cancer with carboplatin/pacl
Externí odkaz:
https://doaj.org/article/e1a4d9138a9840deb9bfd191409971ae
Autor:
Tariq Kewan, Arda Durmaz, Waled Bahaj, Carmelo Gurnari, Laila Terkawi, Hussein Awada, Olisaemeka D. Ogbue, Ramsha Ahmed, Simona Pagliuca, Hassan Awada, Yasuo Kubota, Minako Mori, Ben Ponvilawan, Bayan Al-Share, Bhumika J. Patel, Hetty E. Carraway, Jacob Scott, Suresh K. Balasubramanian, Taha Bat, Yazan Madanat, Mikkael A. Sekeres, Torsten Haferlach, Valeria Visconte, Jaroslaw P. Maciejewski
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-1 (2024)
Externí odkaz:
https://doaj.org/article/01960e5d4a034cfc8740c0ade2b48edf
Autor:
Arda Durmaz, Carmelo Gurnari, Courtney E. Hershberger, Simona Pagliuca, Noah Daniels, Hassan Awada, Hussein Awada, Vera Adema, Minako Mori, Ben Ponvilawan, Yasuo Kubota, Tariq Kewan, Waled S. Bahaj, John Barnard, Jacob Scott, Richard A. Padgett, Torsten Haferlach, Jaroslaw P. Maciejewski, Valeria Visconte
Publikováno v:
iScience, Vol 26, Iss 3, Pp 106238- (2023)
Summary: RNA splicing dysfunctions are more widespread than what is believed by only estimating the effects resulting by splicing factor mutations (SFMT) in myeloid neoplasia (MN). The genetic complexity of MN is amenable to machine learning (ML) str
Externí odkaz:
https://doaj.org/article/d7344695913646679785ec82bb7788b6
Autor:
Carmelo Gurnari, Simona Pagliuca, Tariq Kewan, Waled Bahaj, Minako Mori, Bhumika J. Patel, Valeria Visconte, Jaroslaw P. Maciejewski
Publikováno v:
Blood Cancer Journal, Vol 11, Iss 11, Pp 1-3 (2021)
Externí odkaz:
https://doaj.org/article/ea6d5525e6a948c2b3309ca6928576df
Autor:
Minako Mori, Asuka Hira, Kenichi Yoshida, Hideki Muramatsu, Yusuke Okuno, Yuichi Shiraishi, Michiko Anmae, Jun Yasuda, Shu Tadaka, Kengo Kinoshita, Tomoo Osumi, Yasushi Noguchi, Souichi Adachi, Ryoji Kobayashi, Hiroshi Kawabata, Kohsuke Imai, Tomohiro Morio, Kazuo Tamura, Akifumi Takaori-Kondo, Masayuki Yamamoto, Satoru Miyano, Seiji Kojima, Etsuro Ito, Seishi Ogawa, Keitaro Matsuo, Hiromasa Yabe, Miharu Yabe, Minoru Takata
Publikováno v:
Haematologica, Vol 105, Iss 4 (2020)
Externí odkaz:
https://doaj.org/article/1e27fb0a8ca04310ab6bda480ec5592e
Autor:
Sadayoshi Watanabe, Shoji Matsumoto, Ichiro Nakahara, Akira Ishii, Taketo Hatano, Minako Mori, Eriko Morishita, Izumi Nagata
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Objective: A rare case of thromboembolic cerebral infarction due to carotid web in a patient with congenital protein C deficiency is reported.Case Presentation: A patient in her 40's with left-side hemiparesis was transferred to our hospital under co
Externí odkaz:
https://doaj.org/article/6d5bd33fd3284c6db9f529590606ec8d
Autor:
Yasuo Kubota, Misam Zawit, Jibran Durrani, Wenyi Shen, Waled Bahaj, Tariq Kewan, Ben Ponvilawan, Minako Mori, Manja Meggendorfer, Carmelo Gurnari, Thomas LaFramboise, Simone Feurstein, Mikkael A. Sekeres, Valeria Visconte, Lucy A. Godley, Torsten Haferlach, Jaroslaw P. Maciejewski
Publikováno v:
Leukemia. 36:2827-2834
Broader genetic screening has led to the growing recognition of the role of germline variants associated with adult bone marrow failure (BMF) and myeloid neoplasia (MN) not exclusively in children and young adults. In this study, we applied a germlin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81115f2e65cc62a19f034dfa59e6fc0c
https://doi.org/10.1038/s41375-022-01729-4
https://doi.org/10.1038/s41375-022-01729-4