168 related articles for article (PubMed ID: 31056746)
21. Matrin 3 variants are frequent in Italian ALS patients.
Marangi G; Lattante S; Doronzio PN; Conte A; Tasca G; Monforte M; Patanella AK; Bisogni G; Meleo E; La Spada S; Zollino M; Sabatelli M
Neurobiol Aging; 2017 Jan; 49():218.e1-218.e7. PubMed ID: 28029397
[TBL] [Abstract][Full Text] [Related]
22. Genetic analysis of matrin 3 gene in French amyotrophic lateral sclerosis patients and frontotemporal lobar degeneration with amyotrophic lateral sclerosis patients.
Millecamps S; De Septenville A; Teyssou E; Daniau M; Camuzat A; Albert M; LeGuern E; Galimberti D; ; Brice A; Marie Y; Le Ber I
Neurobiol Aging; 2014 Dec; 35(12):2882.e13-2882.e15. PubMed ID: 25158920
[TBL] [Abstract][Full Text] [Related]
23. First Family of
Cavalli M; Cardani R; Renna LV; Toffetti M; Villa L; Meola G
Front Neurol; 2021; 12():715386. PubMed ID: 34659085
[TBL] [Abstract][Full Text] [Related]
24. Multisystem proteinopathy: Where myopathy and motor neuron disease converge.
Korb MK; Kimonis VE; Mozaffar T
Muscle Nerve; 2021 Apr; 63(4):442-454. PubMed ID: 33145792
[TBL] [Abstract][Full Text] [Related]
25. Expanding the Phenotypic Spectrum of Vocal Cord and Pharyngeal Weakness With Distal Myopathy due to the p.S85C MATR3 Mutation.
Manini A; Velardo D; Ciscato P; Cinnante C; Moggio M; Comi G; Corti S; Ronchi D
Neurol Genet; 2022 Aug; 8(4):e200006. PubMed ID: 35812165
[TBL] [Abstract][Full Text] [Related]
26. Selective Loss of MATR3 in Spinal Interneurons, Upper Motor Neurons and Hippocampal CA1 Neurons in a MATR3 S85C Knock-In Mouse Model of Amyotrophic Lateral Sclerosis.
You J; Maksimovic K; Lee J; Khan M; Masuda R; Park J
Biology (Basel); 2022 Feb; 11(2):. PubMed ID: 35205163
[TBL] [Abstract][Full Text] [Related]
27. Mutational analysis of MATR3 in Taiwanese patients with amyotrophic lateral sclerosis.
Lin KP; Tsai PC; Liao YC; Chen WT; Tsai CP; Soong BW; Lee YC
Neurobiol Aging; 2015 May; 36(5):2005.e1-4. PubMed ID: 25771394
[TBL] [Abstract][Full Text] [Related]
28. Nuclear poly(A) binding protein 1 (PABPN1) and Matrin3 interact in muscle cells and regulate RNA processing.
Banerjee A; Vest KE; Pavlath GK; Corbett AH
Nucleic Acids Res; 2017 Oct; 45(18):10706-10725. PubMed ID: 28977530
[TBL] [Abstract][Full Text] [Related]
29. MATR3 pathogenic variants differentially impair its cryptic splicing repression function.
Khan M; Chen XXL; Dias M; Santos JR; Kour S; You J; van Bruggen R; Youssef MMM; Wan YW; Liu Z; Rosenfeld JA; Tan Q; Pandey UB; Yalamanchili HK; Park J
FEBS Lett; 2024 Feb; 598(4):415-436. PubMed ID: 38320753
[TBL] [Abstract][Full Text] [Related]
30. MATR3's Role beyond the Nuclear Matrix: From Gene Regulation to Its Implications in Amyotrophic Lateral Sclerosis and Other Diseases.
Santos JR; Park J
Cells; 2024 Jun; 13(11):. PubMed ID: 38891112
[TBL] [Abstract][Full Text] [Related]
31. Matrin 3-dependent neurotoxicity is modified by nucleic acid binding and nucleocytoplasmic localization.
Malik AM; Miguez RA; Li X; Ho YS; Feldman EL; Barmada SJ
Elife; 2018 Jul; 7():. PubMed ID: 30015619
[TBL] [Abstract][Full Text] [Related]
32. Heterogeneity of Matrin 3 in the developing and aging murine central nervous system.
Rayaprolu S; D'Alton S; Crosby K; Moloney C; Howard J; Duffy C; Cabrera M; Siemienski Z; Hernandez AR; Gallego-Iradi C; Borchelt DR; Lewis J
J Comp Neurol; 2016 Oct; 524(14):2740-52. PubMed ID: 26878116
[TBL] [Abstract][Full Text] [Related]
33. Neuronal activity regulates Matrin 3 abundance and function in a calcium-dependent manner through calpain-mediated cleavage and calmodulin binding.
Malik AM; Wu JJ; Gillies CA; Doctrove QA; Li X; Huang H; Tank EHM; Shakkottai VG; Barmada S
Proc Natl Acad Sci U S A; 2023 Apr; 120(15):e2206217120. PubMed ID: 37011198
[TBL] [Abstract][Full Text] [Related]
34. A robust TDP-43 knock-in mouse model of ALS.
Huang SL; Wu LS; Lee M; Chang CW; Cheng WC; Fang YS; Chen YR; Cheng PL; Shen CJ
Acta Neuropathol Commun; 2020 Jan; 8(1):3. PubMed ID: 31964415
[TBL] [Abstract][Full Text] [Related]
35. MATR3 mutation analysis in a Chinese cohort with sporadic amyotrophic lateral sclerosis.
Xu L; Li J; Tang L; Zhang N; Fan D
Neurobiol Aging; 2016 Feb; 38():218.e3-218.e4. PubMed ID: 26708275
[TBL] [Abstract][Full Text] [Related]
36. Differential effects of mutant SOD1 on protein structure of skeletal muscle and spinal cord of familial amyotrophic lateral sclerosis: role of chaperone network.
Wei R; Bhattacharya A; Hamilton RT; Jernigan AL; Chaudhuri AR
Biochem Biophys Res Commun; 2013 Aug; 438(1):218-23. PubMed ID: 23886956
[TBL] [Abstract][Full Text] [Related]
37. Impairment of respiratory function in late-onset distal myopathy due to MATR3 Mutation.
Kraya T; Schmidt B; Müller T; Hanisch F
Muscle Nerve; 2015 Jun; 51(6):916-8. PubMed ID: 25677933
[TBL] [Abstract][Full Text] [Related]
38. Generation and characterization of a human iPSC line from an ALS patient carrying the Q66K-MATR3 mutation.
Pollini D; Loffredo R; Cardano M; Conti L; Lattante S; Notarangelo A; Sabatelli M; Provenzani A
Stem Cell Res; 2018 Dec; 33():146-150. PubMed ID: 30366341
[TBL] [Abstract][Full Text] [Related]
39. TIA1 variant drives myodegeneration in multisystem proteinopathy with SQSTM1 mutations.
Lee Y; Jonson PH; Sarparanta J; Palmio J; Sarkar M; Vihola A; Evilä A; Suominen T; Penttilä S; Savarese M; Johari M; Minot MC; Hilton-Jones D; Maddison P; Chinnery P; Reimann J; Kornblum C; Kraya T; Zierz S; Sue C; Goebel H; Azfer A; Ralston SH; Hackman P; Bucelli RC; Taylor JP; Weihl CC; Udd B
J Clin Invest; 2018 Mar; 128(3):1164-1177. PubMed ID: 29457785
[TBL] [Abstract][Full Text] [Related]
40. A Gne knockout mouse expressing human GNE D176V mutation develops features similar to distal myopathy with rimmed vacuoles or hereditary inclusion body myopathy.
Malicdan MC; Noguchi S; Nonaka I; Hayashi YK; Nishino I
Hum Mol Genet; 2007 Nov; 16(22):2669-82. PubMed ID: 17704511
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
