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Chorein deficiency promotes ferroptosis.
Nishizawa Y, Sakimoto H, Nagata O, Sasaki N, Urata Y, Arai K, Hiwatashi H, Yokoyama I, Kishida S, Sano A, Nakamura M. Nishizawa Y, et al. Among authors: sasaki n. FEBS Open Bio. 2024 Nov 8. doi: 10.1002/2211-5463.13870. Online ahead of print. FEBS Open Bio. 2024. PMID: 39514409 Free article.
The Role of Chorein Deficiency in Late Spermatogenesis.
Arai K, Nishizawa Y, Nagata O, Sakimoto H, Sasaki N, Sano A, Nakamura M. Arai K, et al. Among authors: sasaki n. Biomedicines. 2024 Jan 22;12(1):240. doi: 10.3390/biomedicines12010240. Biomedicines. 2024. PMID: 38275411 Free PMC article.
Chorein interacts with α-tubulin and histone deacetylase 6, and overexpression preserves cell viability during nutrient deprivation in human embryonic kidney 293 cells.
Sasaki N, Nakamura M, Kodama A, Urata Y, Shiokawa N, Hayashi T, Sano A. Sasaki N, et al. FASEB J. 2016 Nov;30(11):3726-3732. doi: 10.1096/fj.201500191RR. Epub 2016 Jul 28. FASEB J. 2016. PMID: 27468757
These results suggest that chorein/histone deacetylase 6/alpha-tubulin interactions may play an important role in starvation-induced cell stress, and their disruption may be one of the molecular pathogenic mechanisms of chorea-acanthocytosis.-Sasaki, N., Nakamura, M …
These results suggest that chorein/histone deacetylase 6/alpha-tubulin interactions may play an important role in starvation-induced cell st …
Mouse model of chorea-acanthocytosis exhibits male infertility caused by impaired sperm motility as a result of ultrastructural morphological abnormalities in the mitochondrial sheath in the sperm midpiece.
Nagata O, Nakamura M, Sakimoto H, Urata Y, Sasaki N, Shiokawa N, Sano A. Nagata O, et al. Among authors: sasaki n. Biochem Biophys Res Commun. 2018 Sep 5;503(2):915-920. doi: 10.1016/j.bbrc.2018.06.096. Epub 2018 Jun 21. Biochem Biophys Res Commun. 2018. PMID: 29928881
Novel pathogenic XK mutations in McLeod syndrome and interaction between XK protein and chorein.
Urata Y, Nakamura M, Sasaki N, Shiokawa N, Nishida Y, Arai K, Hiwatashi H, Yokoyama I, Narumi S, Terayama Y, Murakami T, Ugawa Y, Sakamoto H, Kaneko S, Nakazawa Y, Yamasaki R, Sadashima S, Sakai T, Arai H, Sano A. Urata Y, et al. Among authors: sasaki n. Neurol Genet. 2019 Apr 22;5(3):e328. doi: 10.1212/NXG.0000000000000328. eCollection 2019 Jun. Neurol Genet. 2019. PMID: 31086825 Free PMC article.
Positional cloning and comprehensive mutation analysis identified a novel KDM2B mutation in a Japanese family with minor malformations, intellectual disability, and schizophrenia.
Yokotsuka-Ishida S, Nakamura M, Tomiyasu Y, Nagai M, Kato Y, Tomiyasu A, Umehara H, Hayashi T, Sasaki N, Ueno SI, Sano A. Yokotsuka-Ishida S, et al. Among authors: sasaki n. J Hum Genet. 2021 Jun;66(6):597-606. doi: 10.1038/s10038-020-00889-4. Epub 2021 Jan 6. J Hum Genet. 2021. PMID: 33402700
Guided Internet-Based Cognitive Behavioral Therapy for Women With Bulimia Nervosa: Protocol for a Multicenter Randomized Controlled Trial.
Hamatani S, Matsumoto K, Andersson G, Tomioka Y, Numata S, Kamashita R, Sekiguchi A, Sato Y, Fukudo S, Sasaki N, Nakamura M, Otani R, Sakuta R, Hirano Y, Kosaka H, Mizuno Y. Hamatani S, et al. Among authors: sasaki n. JMIR Res Protoc. 2023 Sep 19;12:e49828. doi: 10.2196/49828. JMIR Res Protoc. 2023. PMID: 37725414 Free PMC article.
2,475 results