研究者

J-GLOBAL ID：201401082200134685 更新日: 2021年10月27日

秋本千鶴

Akimoto Chizuru

論文 (9件)：

Chizuru Akimoto, Alexander E. Volk, Marka van Blitterswijk, Marleen Van den Broeck, Claire S. Leblond, Serge Lumbroso, William Camu, Birgit Neitzel, Osamu Onodera, Wouter van Rheenen, et al. A blinded international study on the reliability of genetic testing for GGGGCC-repeat expansions in C9orf72 reveals marked differences in results among 14 laboratories. JOURNAL OF MEDICAL GENETICS. 2014. 51. 6. 419-424
Eschbach J, Schwalenstöcker B, Soyal SM, Bayer H, Wiesner D, Akimoto C, Nilsson AC, Birve A, Meyer T, Dupuis L, et al. PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis. Human molecular genetics. 2013. 22. 17. 3477-3484
Ingre C, Landers JE, Rizik N, Volk AE, Akimoto C, Birve A, Hübers A, Keagle PJ, Piotrowska K, Press R, et al. A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic, and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts. Neurobiology of aging. 2013. 34. 1708.e1-6
Akimoto C, Sakashita E, Kasashima K, Kuroiwa K, Tominaga K, Hamamoto T, Endo H. Translational repression of the McKusick-Kaufman syndrome transcript by unique upstream open reading frames encoding mitochondrial proteins with alternative polyadenylation sites. Biochimica et biophysica acta. 2013. 1830. 3. 2728-2738
Chizuru Akimoto, Lars Forsgren, Jan Linder, Anna Birve, Irene Backlund, Jorgen Andersson, Ann-Charloth Nilsson, Helena Alstermark, Peter M. Andersen. No GGGGCC-hexanucleotide repeat expansion in C9ORF72 in parkinsonism patients in Sweden. AMYOTROPHIC LATERAL SCLEROSIS AND FRONTOTEMPORAL DEGENERATION. 2013. 14. 1. 26-29

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