Takayuki Mito[Author] - Search Results

Year	Number of Results
2013	2
2014	2
2015	6
2018	2
2019	2
2022	1
2024	1

1

Mosaic dysfunction of mitophagy in mitochondrial muscle disease.

Mito T, Vincent AE, Faitg J, Taylor RW, Khan NA, McWilliams TG, Suomalainen A. Mito T, et al. Cell Metab. 2022 Feb 1;34(2):197-208.e5. doi: 10.1016/j.cmet.2021.12.017. Epub 2022 Jan 13. Cell Metab. 2022. PMID: 35030325 Free PMC article.

2

Ancestral allele of DNA polymerase gamma modifies antiviral tolerance.

Kang Y, Hepojoki J, Maldonado RS, Mito T, Terzioglu M, Manninen T, Kant R, Singh S, Othman A, Verma R, Uusimaa J, Wartiovaara K, Kareinen L, Zamboni N, Nyman TA, Paetau A, Kipar A, Vapalahti O, Suomalainen A. Kang Y, et al. Among authors: mito t. Nature. 2024 Apr 3. doi: 10.1038/s41586-024-07260-z. Online ahead of print. Nature. 2024. PMID: 38570685

3

Mito-mice∆ and mitochondrial DNA mutator mice as models of human osteoporosis caused not by aging but by hyperparathyroidism.

Mito T, Tani H, Suzuki M, Ishikawa K, Nakada K, Hayashi JI. Mito T, et al. Exp Anim. 2018 Nov 1;67(4):509-516. doi: 10.1538/expanim.18-0060. Epub 2018 Jul 4. Exp Anim. 2018. PMID: 29973435 Free PMC article.

4

Acquired Expression of Mutant Mitofusin 2 Causes Progressive Neurodegeneration and Abnormal Behavior.

Ishikawa K, Yamamoto S, Hattori S, Nishimura N, Tani H, Mito T, Matsumoto H, Miyakawa T, Nakada K. Ishikawa K, et al. Among authors: mito t. J Neurosci. 2019 Feb 27;39(9):1588-1604. doi: 10.1523/JNEUROSCI.2139-18.2018. Epub 2019 Jan 3. J Neurosci. 2019. PMID: 30606759 Free PMC article.

5

Disruption of the mouse Shmt2 gene confers embryonic anaemia via foetal liver-specific metabolomic disorders.

Tani H, Mito T, Velagapudi V, Ishikawa K, Umehara M, Nakada K, Suomalainen A, Hayashi JI. Tani H, et al. Among authors: mito t. Sci Rep. 2019 Nov 5;9(1):16054. doi: 10.1038/s41598-019-52372-6. Sci Rep. 2019. PMID: 31690790 Free PMC article.

6

Transmitochondrial mito-miceΔ and mtDNA mutator mice, but not aged mice, share the same spectrum of musculoskeletal disorders.

Mito T, Ishizaki H, Suzuki M, Morishima H, Ota A, Ishikawa K, Nakada K, Maeno A, Shiroishi T, Hayashi J. Mito T, et al. Biochem Biophys Res Commun. 2015 Jan 24;456(4):933-7. doi: 10.1016/j.bbrc.2014.12.009. Epub 2014 Dec 12. Biochem Biophys Res Commun. 2015. PMID: 25511702

7

Mice deficient in the Shmt2 gene have mitochondrial respiration defects and are embryonic lethal.

Tani H, Ohnishi S, Shitara H, Mito T, Yamaguchi M, Yonekawa H, Hashizume O, Ishikawa K, Nakada K, Hayashi JI. Tani H, et al. Among authors: mito t. Sci Rep. 2018 Jan 11;8(1):425. doi: 10.1038/s41598-017-18828-3. Sci Rep. 2018. PMID: 29323231 Free PMC article.

8

G7731A mutation in mouse mitochondrial tRNALys regulates late-onset disorders in transmitochondrial mice.

Shimizu A, Mito T, Hashizume O, Yonekawa H, Ishikawa K, Nakada K, Hayashi J. Shimizu A, et al. Among authors: mito t. Biochem Biophys Res Commun. 2015 Mar 27;459(1):66-70. doi: 10.1016/j.bbrc.2015.02.070. Epub 2015 Feb 23. Biochem Biophys Res Commun. 2015. PMID: 25721669

9

Mitochondrial DNA mutations in mutator mice confer respiration defects and B-cell lymphoma development.

Mito T, Kikkawa Y, Shimizu A, Hashizume O, Katada S, Imanishi H, Ota A, Kato Y, Nakada K, Hayashi J. Mito T, et al. PLoS One. 2013;8(2):e55789. doi: 10.1371/journal.pone.0055789. Epub 2013 Feb 13. PLoS One. 2013. PMID: 23418460 Free PMC article.

10

Epigenetic regulation of the nuclear-coded GCAT and SHMT2 genes confers human age-associated mitochondrial respiration defects.

Hashizume O, Ohnishi S, Mito T, Shimizu A, Ishikawa K, Nakada K, Soda M, Mano H, Togayachi S, Miyoshi H, Okita K, Hayashi J. Hashizume O, et al. Among authors: mito t. Sci Rep. 2015 May 22;5:10434. doi: 10.1038/srep10434. Sci Rep. 2015. PMID: 26000717 Free PMC article.

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