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Oncotarget|September 30, 2024
<i>UBA1</i> dysfunction in VEXAS and cancerMaki Sakuma, Torsten Haferlach, Wencke WalterBMC Molecular Biology|September 25, 2015
Deciphering targeting rules of splicing modulator compounds: case of TG003Maki Sakuma, Kei Iida, Masatoshi HagiwaraInternal Medicine (Tokyo, Japan)|July 31, 2022
Hereditary Hemorrhagic Telangiectasia Presenting with Asymptomatic Liver Lesions and a History of Early-onset Myocardial Infarction and Multiple Intracranial AneurysmsMaki Sakuma, Takeshi Inagaki, Reiko Arakawa, et al.Leukemia|February 24, 2023
Novel causative variants of VEXAS in UBA1 detected through whole genome transcriptome sequencing in a large cohort of hematological malignanciesMaki Sakuma, Piers Blombery, Manja Meggendorfer, et al.Leukemia|October 9, 2025
Distinct characteristics of VEXAS-causative UBA1 M41 and recurrent functional non-M41 mutationsMaki Sakuma, Amy K Wang, Samuel J Magaziner, et al.RNA (New York, N.Y.)|June 9, 2017
RBM24 promotes U1 snRNP recognition of the mutated 5' splice site in the <i>IKBKAP</i> gene of familial dysautonomiaKenji Ohe, Mayumi Yoshida, Akiko Nakano-Kobayashi, et al.Pageof 1