Zobrazeno 1 - 10
of 2 513
pro vyhledávání: '"KMT2B"'
Autor:
Zhang, Liying1,2 (AUTHOR), Luo, Luqiao2 (AUTHOR), Liu, Chao2 (AUTHOR), Li, Zhi2 (AUTHOR) lizhi20203939@163.com
Publikováno v:
Diagnostic Pathology. 2/12/2024, Vol. 19 Issue 1, p1-7. 7p.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Ramón-Gómez JL; Instituto Roosevelt, Bogotá DC, Colombia., Bernal-Pacheco O; Instituto Roosevelt, Bogotá DC, Colombia., Zarante-Bahamón AM; Hospital Universitario San Ignacio, Bogotá DC, Colombia.; Instituto Roosevelt, Bogotá DC, Colombia., Martínez-Córdoba N; Universidad Militar Nueva Granada, Bogotá, Colombia., Lince-Rivera I; Universidad Militar Nueva Granada, Bogotá, Colombia.
Publikováno v:
Revista de neurologia [Rev Neurol] 2024 May 16; Vol. 78 (10), pp. 285-291.
Publikováno v:
Diagnostic Pathology, Vol 19, Iss 1, Pp 1-7 (2024)
Abstract Background Low-grade Fibromyxoid Sarcoma(LGFM)is a rare fibrosarcoma, which mainly occurs in young people and is mostly seen in the trunk and limbs. The tumor is usually FUS-CREB3L2 fusion caused by t(7;16)(q32-34;p11)chromosome translocatio
Externí odkaz:
https://doaj.org/article/b13335f67517405fb03419837077f7c4
Autor:
Andrea Rangel, Yully1, Espinosa, Eugenia1
Publikováno v:
Revista Biomedica. sep2022, Vol. 42 Issue 3, p429-434. 6p.
Autor:
Grosz, Bianca R.1 (AUTHOR) bgro4046@uni.sydney.edu.au, Tisch, Stephen2,3 (AUTHOR), Tchan, Michel C.4,5,6 (AUTHOR), Fung, Victor S. C.6,7 (AUTHOR), Darveniza, Paul2 (AUTHOR), Fellner, Avi8,9,10 (AUTHOR), Kurian, Manju A.11 (AUTHOR), McLean, Alison4 (AUTHOR), Tomlinson, Susan E.2,6 (AUTHOR), Smyth, Renee4 (AUTHOR), Devery, Sophie4 (AUTHOR), Wu, Kathy H. C.3,4,6,12 (AUTHOR), Kennerson, Marina L.1,6,13 (AUTHOR), Kumar, Kishore R.6,8,13,14 (AUTHOR) kkum4618@uni.sydney.edu.au
Publikováno v:
Molecular Genetics & Genomic Medicine. May2022, Vol. 10 Issue 5, p1-6. 6p.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
The clinical spectrum and pathogenesis associated with KMT2B variants in Chinese pediatric patients.
Autor:
Ding S; Institute of Molecular Medicine, College of Future Technology, Peking University, Beijing, China., Xie G; Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China., Han Z; Institute of Molecular Medicine, College of Future Technology, Peking University, Beijing, China., Wang Y; Institute of Molecular Medicine, College of Future Technology, Peking University, Beijing, China., Shi M; Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China., Zhai F; Department of Functional Neurosurgery, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China; Laboratory for Clinical Medicine, Capital Medical University, China., Liu T; Department of Functional Neurosurgery, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China; Laboratory for Clinical Medicine, Capital Medical University, China., Xie Z; Department of Functional Neurosurgery, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China; Laboratory for Clinical Medicine, Capital Medical University, China., Zhang W; Department of Neurology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China; Laboratory for Clinical Medicine, Capital Medical University, China., Wu Y; Department of Neurology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China; Laboratory for Clinical Medicine, Capital Medical University, China., Yang X; Department of Neurology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China; Laboratory for Clinical Medicine, Capital Medical University, China., Zhou A; Department of Neurology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China; Laboratory for Clinical Medicine, Capital Medical University, China., Fang F; Department of Neurology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China; Laboratory for Clinical Medicine, Capital Medical University, China., Ren S; Department of Neurology, Baoding Children's Hospital, China., Liang S; Department of Functional Neurosurgery, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China; Laboratory for Clinical Medicine, Capital Medical University, China., Cao H; Institute of Molecular Medicine, College of Future Technology, Peking University, Beijing, China., Xiong H; Department of Neurology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China; Laboratory for Clinical Medicine, Capital Medical University, China. Electronic address: xh_bjbj@163.com., Ding C; Department of Neurology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China; Laboratory for Clinical Medicine, Capital Medical University, China; Department of Neurology, Baoding Children's Hospital, China. Electronic address: chding2018@126.com., Dai L; Department of Neurology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China; Laboratory for Clinical Medicine, Capital Medical University, China. Electronic address: dailifang1111@126.com.
Publikováno v:
Parkinsonism & related disorders [Parkinsonism Relat Disord] 2024 Dec; Vol. 129, pp. 107172. Date of Electronic Publication: 2024 Oct 16.
Publikováno v:
Translational Oncology, Vol 37, Iss , Pp 101778- (2023)
Background and aims: Wnt signaling is essential for the maintenance of cancer stem cells (CSCs), but mutations in the β-catenin and APC genes are less common in non-small cell lung carcinoma (NSCLC). Thus, the mechanism underlying the constitutive a
Externí odkaz:
https://doaj.org/article/a03dc3c6dd16454bac0acf0feb789a78