These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
1593 related articles for article (PubMed ID: 23455423)
1. Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS. Kim HJ; Kim NC; Wang YD; Scarborough EA; Moore J; Diaz Z; MacLea KS; Freibaum B; Li S; Molliex A; Kanagaraj AP; Carter R; Boylan KB; Wojtas AM; Rademakers R; Pinkus JL; Greenberg SA; Trojanowski JQ; Traynor BJ; Smith BN; Topp S; Gkazi AS; Miller J; Shaw CE; Kottlors M; Kirschner J; Pestronk A; Li YR; Ford AF; Gitler AD; Benatar M; King OD; Kimonis VE; Ross ED; Weihl CC; Shorter J; Taylor JP Nature; 2013 Mar; 495(7442):467-73. PubMed ID: 23455423 [TBL] [Abstract][Full Text] [Related]
2. Motor neuron involvement in multisystem proteinopathy: implications for ALS. Benatar M; Wuu J; Fernandez C; Weihl CC; Katzen H; Steele J; Oskarsson B; Taylor JP Neurology; 2013 May; 80(20):1874-80. PubMed ID: 23635965 [TBL] [Abstract][Full Text] [Related]
3. No mutations in hnRNPA1 and hnRNPA2B1 in Dutch patients with amyotrophic lateral sclerosis, frontotemporal dementia, and inclusion body myopathy. Seelen M; Visser AE; Overste DJ; Kim HJ; Palud A; Wong TH; van Swieten JC; Scheltens P; Voermans NC; Baas F; de Jong JM; van der Kooi AJ; de Visser M; Veldink JH; Taylor JP; Van Es MA; van den Berg LH Neurobiol Aging; 2014 Aug; 35(8):1956.e9-1956.e11. PubMed ID: 24612671 [TBL] [Abstract][Full Text] [Related]
4. The heterozygous R155C VCP mutation: Toxic in humans! Harmless in mice? Clemen CS; Winter L; Strucksberg KH; Berwanger C; Türk M; Kornblum C; Florin A; Aguilar-Pimentel JA; Amarie OV; Becker L; Garrett L; Hans W; Moreth K; Neff F; Pingen L; Rathkolb B; Rácz I; Rozman J; Treise I; Fuchs H; Gailus-Durner V; de Angelis MH; Vorgerd M; Eichinger L; Schröder R Biochem Biophys Res Commun; 2018 Sep; 503(4):2770-2777. PubMed ID: 30100055 [TBL] [Abstract][Full Text] [Related]
5. RNA-binding proteins with prion-like domains in health and disease. Harrison AF; Shorter J Biochem J; 2017 Apr; 474(8):1417-1438. PubMed ID: 28389532 [TBL] [Abstract][Full Text] [Related]
6. Genetic interaction of hnRNPA2B1 and DNAJB6 in a Drosophila model of multisystem proteinopathy. Li S; Zhang P; Freibaum BD; Kim NC; Kolaitis RM; Molliex A; Kanagaraj AP; Yabe I; Tanino M; Tanaka S; Sasaki H; Ross ED; Taylor JP; Kim HJ Hum Mol Genet; 2016 Mar; 25(5):936-50. PubMed ID: 26744327 [TBL] [Abstract][Full Text] [Related]
7. Mutations in human prion-like domains: pathogenic but not always amyloidogenic. Bartolomé-Nafría A; García-Pardo J; Ventura S Prion; 2024 Dec; 18(1):28-39. PubMed ID: 38512820 [TBL] [Abstract][Full Text] [Related]
8. hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypes. Le Ber I; Van Bortel I; Nicolas G; Bouya-Ahmed K; Camuzat A; Wallon D; De Septenville A; Latouche M; Lattante S; Kabashi E; Jornea L; Hannequin D; Brice A; Neurobiol Aging; 2014 Apr; 35(4):934.e5-6. PubMed ID: 24119545 [TBL] [Abstract][Full Text] [Related]
9. Genetic and Pathological Assessment of hnRNPA1, hnRNPA2/B1, and hnRNPA3 in Familial and Sporadic Amyotrophic Lateral Sclerosis. Fifita JA; Zhang KY; Galper J; Williams KL; McCann EP; Hogan AL; Saunders N; Bauer D; Tarr IS; Pamphlett R; Nicholson GA; Rowe D; Yang S; Blair IP Neurodegener Dis; 2017; 17(6):304-312. PubMed ID: 29131108 [TBL] [Abstract][Full Text] [Related]
10. Disease mutations in the prion-like domains of hnRNPA1 and hnRNPA2/B1 introduce potent steric zippers that drive excess RNP granule assembly. Shorter J; Taylor JP Rare Dis; 2013; 1():e25200. PubMed ID: 25002999 [TBL] [Abstract][Full Text] [Related]
11. De novo design of RNA-binding proteins with a prion-like domain related to ALS/FTD proteinopathies. Mitsuhashi K; Ito D; Mashima K; Oyama M; Takahashi S; Suzuki N Sci Rep; 2017 Dec; 7(1):16871. PubMed ID: 29203801 [TBL] [Abstract][Full Text] [Related]
12. SVIP is a molecular determinant of lysosomal dynamic stability, neurodegeneration and lifespan. Johnson AE; Orr BO; Fetter RD; Moughamian AJ; Primeaux LA; Geier EG; Yokoyama JS; Miller BL; Davis GW Nat Commun; 2021 Jan; 12(1):513. PubMed ID: 33479240 [TBL] [Abstract][Full Text] [Related]
13. Mechanistic View of hnRNPA2 Low-Complexity Domain Structure, Interactions, and Phase Separation Altered by Mutation and Arginine Methylation. Ryan VH; Dignon GL; Zerze GH; Chabata CV; Silva R; Conicella AE; Amaya J; Burke KA; Mittal J; Fawzi NL Mol Cell; 2018 Feb; 69(3):465-479.e7. PubMed ID: 29358076 [TBL] [Abstract][Full Text] [Related]
14. Abnormal distribution of heterogeneous nuclear ribonucleoproteins in sporadic inclusion body myositis. Pinkus JL; Amato AA; Taylor JP; Greenberg SA Neuromuscul Disord; 2014 Jul; 24(7):611-6. PubMed ID: 24857366 [TBL] [Abstract][Full Text] [Related]
16. Phenotypic variability in three families with valosin-containing protein mutation. Spina S; Van Laar AD; Murrell JR; Hamilton RL; Kofler JK; Epperson F; Farlow MR; Lopez OL; Quinlan J; DeKosky ST; Ghetti B Eur J Neurol; 2013 Feb; 20(2):251-8. PubMed ID: 22900631 [TBL] [Abstract][Full Text] [Related]
17. Effects of Mutations on the Aggregation Propensity of the Human Prion-Like Protein hnRNPA2B1. Paul KR; Molliex A; Cascarina S; Boncella AE; Taylor JP; Ross ED Mol Cell Biol; 2017 Apr; 37(8):. PubMed ID: 28137911 [TBL] [Abstract][Full Text] [Related]
19. The homozygote VCP(R¹⁵⁵H/R¹⁵⁵H) mouse model exhibits accelerated human VCP-associated disease pathology. Nalbandian A; Llewellyn KJ; Kitazawa M; Yin HZ; Badadani M; Khanlou N; Edwards R; Nguyen C; Mukherjee J; Mozaffar T; Watts G; Weiss J; Kimonis VE PLoS One; 2012; 7(9):e46308. PubMed ID: 23029473 [TBL] [Abstract][Full Text] [Related]
20. From Prions to Stress Granules: Defining the Compositional Features of Prion-Like Domains That Promote Different Types of Assemblies. Fomicheva A; Ross ED Int J Mol Sci; 2021 Jan; 22(3):. PubMed ID: 33513942 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]