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Page 1
Functional evaluation of novel variants of B4GALNT1 in a patient with hereditary spastic paraplegia and the general population.
Inamori KI, Nakamura K, Shishido F, Hsu JC, Nagafuku M, Nitta T, Ikeda J, Yoshimura H, Kodaira M, Tsuchida N, Matsumoto N, Uemura S, Ohno S, Manabe N, Yamaguchi Y, Togayachi A, Aoki-Kinoshita KF, Nishihara S, Furukawa JI, Kaname T, Nakamura M, Shimohata T, Tadaka S, Shirota M, Kinoshita K, Nakamura Y, Ohno I, Sekijima Y, Inokuchi JI. Inamori KI, et al. Front Neurosci. 2024 Jul 31;18:1437668. doi: 10.3389/fnins.2024.1437668. eCollection 2024. Front Neurosci. 2024. PMID: 39145292 Free PMC article.
Neurological insights on two siblings with GM3 synthase deficiency due to novel compound heterozygous ST3GAL5 variants.
Watanabe S, Lei M, Nakagawa E, Takeshita E, Inamori KI, Shishido F, Sasaki M, Mitsuhashi S, Matsumoto N, Kimura Y, Iwasaki M, Takahashi Y, Mizusawa H, Migita O, Ohno I, Inokuchi JI. Watanabe S, et al. Among authors: inamori ki. Brain Dev. 2023 May;45(5):270-277. doi: 10.1016/j.braindev.2023.01.002. Epub 2023 Jan 21. Brain Dev. 2023. PMID: 36690566
Mass Spectrometry of Neutral Glycosphingolipids.
Suzuki A, Silsirivanit A, Watanabe T, Matsuda J, Inamori KI, Inokuchi JI. Suzuki A, et al. Among authors: inamori ki. Methods Mol Biol. 2023;2613:127-144. doi: 10.1007/978-1-0716-2910-9_11. Methods Mol Biol. 2023. PMID: 36587076
GM3 synthase deficiency increases brain glucose metabolism in mice.
Bharathi SS, Zhang BB, Paul E, Zhang Y, Schmidt AV, Fowler B, Wu Y, Tiemeyer M, Inamori KI, Inokuchi JI, Goetzman ES. Bharathi SS, et al. Among authors: inamori ki. Mol Genet Metab. 2022 Dec;137(4):342-348. doi: 10.1016/j.ymgme.2022.10.006. Epub 2022 Oct 28. Mol Genet Metab. 2022. PMID: 36335793 Free PMC article.
Cell density-dependent membrane distribution of ganglioside GM3 in melanoma cells.
Murate M, Yokoyama N, Tomishige N, Richert L, Humbert N, Pollet B, Makino A, Kono N, Mauri L, Aoki J, Sako Y, Sonnino S, Komura N, Ando H, Kaneko MK, Kato Y, Inamori KI, Inokuchi JI, Mély Y, Iwabuchi K, Kobayashi T. Murate M, et al. Among authors: inamori ki. Cell Mol Life Sci. 2023 May 30;80(6):167. doi: 10.1007/s00018-023-04813-9. Cell Mol Life Sci. 2023. PMID: 37249637 Free PMC article.
Chronic encephalomyelitis virus exhibits cellular tropism and evades pDCs by binding to sialylated integrins as the cell surface receptors.
Takeda K, Kaifu T, Michihata R, Kinugawa N, Fujioka A, Tateno A, Toshima K, Kanoh H, Inamori KI, Kamijo K, Himeda T, Ohara Y, Inokuchi JI, Nakamura A. Takeda K, et al. Among authors: inamori ki. Eur J Immunol. 2023 Oct;53(10):e2350452. doi: 10.1002/eji.202350452. Epub 2023 Sep 6. Eur J Immunol. 2023. PMID: 37565654 Free article.
Functional validation of novel variants in B4GALNT1 associated with early-onset complex hereditary spastic paraplegia with impaired ganglioside synthesis.
Alecu JE, Ohmi Y, Bhuiyan RH, Inamori KI, Nitta T, Saffari A, Jumo H, Ziegler M, de Gusmao CM, Sharma N, Ohno S, Manabe N, Yamaguchi Y, Kambe M, Furukawa K, Sahin M, Inokuchi JI, Furakawa K, Ebrahimi-Fakhari D. Alecu JE, et al. Among authors: inamori ki. Am J Med Genet A. 2022 Sep;188(9):2590-2598. doi: 10.1002/ajmg.a.62880. Epub 2022 Jul 1. Am J Med Genet A. 2022. PMID: 35775650 Free PMC article.
26 results