Zobrazeno 1 - 10
of 2 312
pro vyhledávání: '"Atypical teratoid"'
Publikováno v:
International Journal of Nanomedicine, Vol Volume 19, Pp 5973-5993 (2024)
Sang-Soo Kim,1,2 Manish Moghe,1 Antonina Rait,1 Kathryn Donaldson,1 Joe B Harford,2 Esther H Chang1 1Department of Oncology, Lombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC, USA; 2SynerGene Therapeutics, Inc
Externí odkaz:
https://doaj.org/article/e876fde7562a40feaf75f4c875fa4249
Publikováno v:
Bioactive Materials, Vol 36, Iss , Pp 301-316 (2024)
Natural killer (NK) cells are cytotoxic immune cells that can eliminate target cells without prior stimulation. Human induced pluripotent stem cells (iPSCs) provide a robust source of NK cells for safe and effective cell-based immunotherapy against a
Externí odkaz:
https://doaj.org/article/60e23d6bd9644ea891c510a9c136de24
Autor:
Dennis S. Metselaar, Michaël H. Meel, Joshua R. Goulding, Aimeé du Chatinier, Leyla Rigamonti, Piotr Waranecki, Neal Geisemeyer, Mark C. de Gooijer, Marjolein Breur, Jan Koster, Sophie E.M. Veldhuijzen van Zanten, Marianna Bugiani, Niels E. Franke, Alyssa Reddy, Pieter Wesseling, Gertjan J.L. Kaspers, Esther Hulleman
Publikováno v:
Cell Reports Medicine, Vol 5, Iss 9, Pp 101700- (2024)
Summary: Atypical teratoid/rhabdoid tumors (ATRTs) are highly malignant embryonal tumors of the central nervous system with a dismal prognosis. Using a newly developed and validated patient-derived ATRT culture and xenograft model, alongside a panel
Externí odkaz:
https://doaj.org/article/dad8aa161f6e4aad834b1c8a6839ea6b
Publikováno v:
Xiehe Yixue Zazhi, Vol 15, Iss 3, Pp 655-660 (2024)
Atypical teratoid/rhabdoid tumor (AT/RT) is a rare malignancy located primarily in infratentorial or subcortical areas with a poor prognosis, and rarely in the lateral ventricle with a very poor prognosis. So far, only 6 cases of AT/RT in lateral ven
Externí odkaz:
https://doaj.org/article/95e4a55f3579421c983d54aa8175a159
Autor:
Kolcheva Maria Andreevna, Kumirova Ella Vyacheslavovna, Gorbatykh Svetlana Valeryevna, Makhmudova Gunai Nariman, Livshits Matvey Igorevich, Chmutin Gennadiy Yegorovich, Kislyakov Alexey Nikolaevich, Umerenkov Viktor Nikolaevich, Manuel de Jesus Encarnacion Ramirez, Nicola Montemurro
Publikováno v:
Surgeries, Vol 5, Iss 2, Pp 184-193 (2024)
Atypical teratoid-rhabdoid tumor (AT/RT) is a rare but one of the most aggressive embryonal tumors of the central nervous system (CNS), most often occurring in children under 3 years of age. AT/RT accounts for about 1–2% of all CNS neoplasms and ha
Externí odkaz:
https://doaj.org/article/e9b1dcd238d24005a18bdb3880a9470e
Akademický článek
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Publikováno v:
Bioactive Materials, Vol 31, Iss , Pp 136-150 (2024)
Atypical teratoid/rhabdoid tumor (ATRT) is a rare childhood malignancy that originates in the central nervous system. Over ninety-five percent of ATRT patients have biallelic inactivation of the tumor suppressor gene SMARCB1. ATRT has no standard tre
Externí odkaz:
https://doaj.org/article/981b6c5fed0d4886baa275cc660f7cf4
Publikováno v:
Cancer Management and Research, Vol Volume 15, Pp 1369-1393 (2023)
Katharina Gastberger,1,2 Victoria E Fincke,1,2 Marlena Mucha,1,2 Reiner Siebert,3 Martin Hasselblatt,4 Michael C Frühwald1,2 1Pediatrics and Adolescent Medicine, Swabian Children’s Cancer Center, University Medical Center Augsburg, Augsburg, Germa
Externí odkaz:
https://doaj.org/article/514aac6500bd46f184152c3b4d87f50a
Autor:
Run Yu, MD, PhD
Publikováno v:
AACE Clinical Case Reports, Vol 9, Iss 6, Pp 197-200 (2023)
Background/Objective: Clinical diagnosis of rare aggressive sellar malignancies requires a high index of suspicion. The objective was to report 2 patients with primary sellar atypical teratoid (AT)/rhabdoid tumor (RT) who presented with acute-onset h
Externí odkaz:
https://doaj.org/article/eff5e9b22ff84f2da06157cac7dfbbe7
Akademický článek
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