Similar articles for PMID: 30130494

Year	Number of Results
2001	1
2002	1
2004	3
2005	2
2006	4
2007	8
2008	4
2009	7
2010	5
2011	6
2012	6
2013	7
2014	6
2015	5
2016	8
2017	10
2018	11
2019	8
2020	3
2021	6
2022	4
2023	2
2024	0

1

Muscle-dominant wild-type TDP-43 expression induces myopathological changes featuring tubular aggregates and TDP-43-positive inclusions.

Tawara N, Yamashita S, Kawakami K, Kurashige T, Zhang Z, Tasaki M, Yamamoto Y, Nishikami T, Doki T, Zhang X, Matsuo Y, Kimura E, Tawara A, Maeda Y, Hauschka SD, Maruyama H, Ando Y. Tawara N, et al. Exp Neurol. 2018 Nov;309:169-180. doi: 10.1016/j.expneurol.2018.08.006. Epub 2018 Aug 18. Exp Neurol. 2018. PMID: 30130494

2

CYLD dysregulation in pathogenesis of sporadic inclusion body myositis.

Yamashita S, Matsuo Y, Tawara N, Hara K, Yamamoto M, Nishikami T, Kawakami K, Zhang X, Zhang Z, Doki T, Ando Y. Yamashita S, et al. Sci Rep. 2019 Aug 12;9(1):11606. doi: 10.1038/s41598-019-48115-2. Sci Rep. 2019. PMID: 31406156 Free PMC article.

3

Abnormal distribution of heterogeneous nuclear ribonucleoproteins in sporadic inclusion body myositis.

Pinkus JL, Amato AA, Taylor JP, Greenberg SA. Pinkus JL, et al. Neuromuscul Disord. 2014 Jul;24(7):611-6. doi: 10.1016/j.nmd.2014.04.012. Epub 2014 May 6. Neuromuscul Disord. 2014. PMID: 24857366

4

TAR DNA-Binding protein 43 accumulation in protein aggregate myopathies.

Olivé M, Janué A, Moreno D, Gámez J, Torrejón-Escribano B, Ferrer I. Olivé M, et al. J Neuropathol Exp Neurol. 2009 Mar;68(3):262-73. doi: 10.1097/NEN.0b013e3181996d8f. J Neuropathol Exp Neurol. 2009. PMID: 19225410

5

Sarcoplasmic redistribution of nuclear TDP-43 in inclusion body myositis.

Salajegheh M, Pinkus JL, Taylor JP, Amato AA, Nazareno R, Baloh RH, Greenberg SA. Salajegheh M, et al. Muscle Nerve. 2009 Jul;40(1):19-31. doi: 10.1002/mus.21386. Muscle Nerve. 2009. PMID: 19533646 Free PMC article.

6

Loss of TDP-43 function and rimmed vacuoles persist after T cell depletion in a xenograft model of sporadic inclusion body myositis.

Britson KA, Ling JP, Braunstein KE, Montagne JM, Kastenschmidt JM, Wilson A, Ikenaga C, Tsao W, Pinal-Fernandez I, Russell KA, Reed N, Mozaffar T, Wagner KR, Ostrow LW, Corse AM, Mammen AL, Villalta SA, Larman HB, Wong PC, Lloyd TE. Britson KA, et al. Sci Transl Med. 2022 Jan 19;14(628):eabi9196. doi: 10.1126/scitranslmed.abi9196. Epub 2022 Jan 19. Sci Transl Med. 2022. PMID: 35044790 Free PMC article.

7

Homocysteine-induced endoplasmic reticulum protein (Herp) is up-regulated in sporadic inclusion-body myositis and in endoplasmic reticulum stress-induced cultured human muscle fibers.

Nogalska A, Engel WK, McFerrin J, Kokame K, Komano H, Askanas V. Nogalska A, et al. J Neurochem. 2006 Mar;96(5):1491-9. doi: 10.1111/j.1471-4159.2006.03668.x. Epub 2006 Jan 25. J Neurochem. 2006. PMID: 16441512 Free article.

8

Pathomechanisms of anti-cytosolic 5'-nucleotidase 1A autoantibodies in sporadic inclusion body myositis.

Tawara N, Yamashita S, Zhang X, Korogi M, Zhang Z, Doki T, Matsuo Y, Nakane S, Maeda Y, Sugie K, Suzuki N, Aoki M, Ando Y. Tawara N, et al. Ann Neurol. 2017 Apr;81(4):512-525. doi: 10.1002/ana.24919. Epub 2017 Apr 3. Ann Neurol. 2017. PMID: 28318044

9

Primary over-expression of AβPP in muscle does not lead to the development of inclusion body myositis in a new lineage of the MCK-AβPP transgenic mouse.

Luo YB, Johnsen RD, Griffiths L, Needham M, Fabian VA, Fletcher S, Wilton SD, Mastaglia FL. Luo YB, et al. Int J Exp Pathol. 2013 Dec;94(6):418-25. doi: 10.1111/iep.12048. Epub 2013 Oct 31. Int J Exp Pathol. 2013. PMID: 24205796 Free PMC article.

10

TDP-43 accumulation in inclusion body myopathy muscle suggests a common pathogenic mechanism with frontotemporal dementia.

Weihl CC, Temiz P, Miller SE, Watts G, Smith C, Forman M, Hanson PI, Kimonis V, Pestronk A. Weihl CC, et al. J Neurol Neurosurg Psychiatry. 2008 Oct;79(10):1186-9. doi: 10.1136/jnnp.2007.131334. J Neurol Neurosurg Psychiatry. 2008. PMID: 18796596 Free PMC article.

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