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pro vyhledávání: '"T-15"'
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Autor:
Jingqiao Qiao, Caixia Han, Li Yu, Hong Wang, Ruiqi Wang, Xiangyu Meng, Shujiao He, Yonghui Li, Xuefeng Gao
Publikováno v:
Journal of Translational Medicine, Vol 19, Iss 1, Pp 1-13 (2021)
Journal of Translational Medicine
Journal of Translational Medicine
Background Rho GTPase activating protein 9 (ARHGAP9) is expressed in various types of cancers and can inactivate Rho GTPases that mainly regulate cytoskeletal dynamics. However, the exact role of ARHGAP9 in acute myeloid leukemia (AML) has yet to be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90c8c74b999b9f575b93991cbab51f12
https://doaj.org/article/147c961079de478cbc1ce7331aaa6897
https://doaj.org/article/147c961079de478cbc1ce7331aaa6897
Publikováno v:
Bosnian Journal of Basic Medical Sciences
Bosnian Journal of Basic Medical Sciences (2020)
Bosnian Journal of Basic Medical Sciences (2020)
Most acute promyelocytic leukemias (APL) are characterized by reciprocal translocations t(15;17)(q22;21), which results in the fusion of the promyelocytic leukemia protein (PML) gene at 15q22 with retinoic acid receptor a (RARα) gene at 17q21. Howev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0859a0cf88f81c3a47a84444c6317e09
http://europepmc.org/articles/PMC7982059
http://europepmc.org/articles/PMC7982059
Autor:
Jun Lee, Young Eun Kim
Publikováno v:
Laboratory Medicine Online. 11:211-213
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::973325633dc80bdcb2ba9eea2fb5b409
https://doi.org/10.47429/lmo.2021.11.3.211
https://doi.org/10.47429/lmo.2021.11.3.211
Autor:
Hossein Ayatollahi, Omolbanin Sargazi-Aval, Ali Fani, Payam Siyadat, Maryam Sheikhi, Mohammad Hadi Sadeghian, Ali Bazi
Publikováno v:
Iranian Journal of Pathology
Background & Objective: Acute promyelocytic leukemia (APL) with t(15;17)(q22;q12) is a relatively common subtype of acute myeloid leukemia (AML). Here, our objective was to ascertain the survival of patients with this leukemia in north-east of Iran.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78622da7e7cb554be47ce3725077b9d7
https://doi.org/10.30699/ijp.2020.101417.2007
https://doi.org/10.30699/ijp.2020.101417.2007
Autor:
Junqing Xu, Yanhong Zhang, Limei Yu, Riming Liu, Yongming Liu, Lina Chu, Weihua Wang, Yangyang Zhang, Li Ma, Yimin Xu
Publikováno v:
Molecular Cytogenetics, Vol 13, Iss 1, Pp 1-5 (2020)
Molecular Cytogenetics
Molecular Cytogenetics
Background Chromosomal rearrangements in addition to t(15;17) have been reported in 25-40% of APL patients, with a large predominance of trisomy 8. Other abnormalities are far less frequent, particularly as ider(17), and the prognostic significance i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d294faf1bdbf14c0798117c791b9562c
http://link.springer.com/article/10.1186/s13039-020-00479-1
http://link.springer.com/article/10.1186/s13039-020-00479-1
Publikováno v:
Pathology. 52:273-276
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eefa2db87fc9d7df864945c4c7931c3d
https://doi.org/10.1016/j.pathol.2019.10.013
https://doi.org/10.1016/j.pathol.2019.10.013
Publikováno v:
Cancer Biol Ther
Acute promyelocytic leukemia (APL) is characterized by the presence of promyelocytic leukemia-retinoic acid receptor α (PML-RARα) fusion gene, which is formed following the specific chromosomal translocation t(15;17)(q22;q21). However, cases with P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac03817b6b3b4e5526d6a90344c9bfbc
https://doi.org/10.1080/15384047.2019.1702398
https://doi.org/10.1080/15384047.2019.1702398
Publikováno v:
Intractable Rare Dis Res
Acute promyelocytic leukemia (APL) is characterized by the translocation t (15 ; 17) (q22 ; q21) cytogenetic abnormality in the majority of cases. In most of the cases the cells of APL have normal, diploid karyotype. There are very few cases presente
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cbee9207a61eb555b8850b15de50343
https://www.bib.irb.hr/1114541
https://www.bib.irb.hr/1114541
Autor:
Depei Wu, Xiaoyu Xu, Lijun Wen, Jinlan Pan, Zhao Zeng, Changgeng Ruan, Dewan Zhao, Zheng Wang, Li Yao, Man Wang, Jingzhi Shen, Jia Zhilin, Guangquan Mo, Xiaoqian Chen, Cai Wei, Yi Xu, Suning Chen, Ling Zhang, Wang Yao, Xiaomeng Chi, Zhen Shen
Publikováno v:
Molecular carcinogenesisREFERENCES. 60(2)
Acute promyelocytic leukemia (APL) is a unique disease entity in acute myeloid leukemia, characterized by PML-RARA fusion gene, which is generated by chromosomal translocation t(15;17)(q24;q21). We identified TNRC18-RARA as novel RARA fusion in resem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf7382b5de5077d8551462a6d1c97fb4
https://pubmed.ncbi.nlm.nih.gov/33428799
https://pubmed.ncbi.nlm.nih.gov/33428799