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3. Analysis of spinal and muscle pathology in transgenic mice overexpressing wild-type and ALS-linked mutant MATR3. Moloney C; Rayaprolu S; Howard J; Fromholt S; Brown H; Collins M; Cabrera M; Duffy C; Siemienski Z; Miller D; Borchelt DR; Lewis J Acta Neuropathol Commun; 2018 Dec; 6(1):137. PubMed ID: 30563574 [TBL] [Abstract][Full Text] [Related]
4. Phenotype of matrin-3-related distal myopathy in 16 German patients. Müller TJ; Kraya T; Stoltenburg-Didinger G; Hanisch F; Kornhuber M; Stoevesandt D; Senderek J; Weis J; Baum P; Deschauer M; Zierz S Ann Neurol; 2014 Nov; 76(5):669-80. PubMed ID: 25154462 [TBL] [Abstract][Full Text] [Related]
5. Transgenic mice overexpressing the ALS-linked protein Matrin 3 develop a profound muscle phenotype. Moloney C; Rayaprolu S; Howard J; Fromholt S; Brown H; Collins M; Cabrera M; Duffy C; Siemienski Z; Miller D; Swanson MS; Notterpek L; Borchelt DR; Lewis J Acta Neuropathol Commun; 2016 Nov; 4(1):122. PubMed ID: 27863507 [TBL] [Abstract][Full Text] [Related]
6. Clinicopathological features of the first Asian family having vocal cord and pharyngeal weakness with distal myopathy due to a MATR3 mutation. Yamashita S; Mori A; Nishida Y; Kurisaki R; Tawara N; Nishikami T; Misumi Y; Ueyama H; Imamura S; Higuchi Y; Hashiguchi A; Higuchi I; Morishita S; Yoshimura J; Uchino M; Takashima H; Tsuji S; Ando Y Neuropathol Appl Neurobiol; 2015 Apr; 41(3):391-8. PubMed ID: 25185957 [No Abstract] [Full Text] [Related]
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9. Knockdown of genes involved in axonal transport enhances the toxicity of human neuromuscular disease-linked MATR3 mutations in Drosophila. Zhao M; Kao CS; Arndt C; Tran DD; Cho WI; Maksimovic K; Chen XXL; Khan M; Zhu H; Qiao J; Peng K; Hong J; Xu J; Kim D; Kim JR; Lee J; van Bruggen R; Yoon WH; Park J FEBS Lett; 2020 Sep; 594(17):2800-2818. PubMed ID: 32515490 [TBL] [Abstract][Full Text] [Related]
10. Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3. Senderek J; Garvey SM; Krieger M; Guergueltcheva V; Urtizberea A; Roos A; Elbracht M; Stendel C; Tournev I; Mihailova V; Feit H; Tramonte J; Hedera P; Crooks K; Bergmann C; Rudnik-Schöneborn S; Zerres K; Lochmüller H; Seboun E; Weis J; Beckmann JS; Hauser MA; Jackson CE Am J Hum Genet; 2009 Apr; 84(4):511-8. PubMed ID: 19344878 [TBL] [Abstract][Full Text] [Related]
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12. Mutation analysis of MATR3 in Australian familial amyotrophic lateral sclerosis. Fifita JA; Williams KL; McCann EP; O'Brien A; Bauer DC; Nicholson GA; Blair IP Neurobiol Aging; 2015 Mar; 36(3):1602.e1-2. PubMed ID: 25523636 [TBL] [Abstract][Full Text] [Related]
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14. Subcellular Localization of Matrin 3 Containing Mutations Associated with ALS and Distal Myopathy. Gallego-Iradi MC; Clare AM; Brown HH; Janus C; Lewis J; Borchelt DR PLoS One; 2015; 10(11):e0142144. PubMed ID: 26528920 [TBL] [Abstract][Full Text] [Related]
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17. Matrin 3 Is a Component of Neuronal Cytoplasmic Inclusions of Motor Neurons in Sporadic Amyotrophic Lateral Sclerosis. Tada M; Doi H; Koyano S; Kubota S; Fukai R; Hashiguchi S; Hayashi N; Kawamoto Y; Kunii M; Tanaka K; Takahashi K; Ogawa Y; Iwata R; Yamanaka S; Takeuchi H; Tanaka F Am J Pathol; 2018 Feb; 188(2):507-514. PubMed ID: 29128563 [TBL] [Abstract][Full Text] [Related]
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20. MATR3 F115C knock-in mice do not exhibit motor defects or neuropathological features of ALS. van Bruggen R; Maksimovic K; You J; Tran DD; Lee HJ; Khan M; Kao CS; Kim JR; Cho W; Chen XXL; Park J Biochem Biophys Res Commun; 2021 Sep; 568():48-54. PubMed ID: 34182213 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]