286 related articles for article (PubMed ID: 31043593)
1. Structural basis for reversible amyloids of hnRNPA1 elucidates their role in stress granule assembly.
Gui X; Luo F; Li Y; Zhou H; Qin Z; Liu Z; Gu J; Xie M; Zhao K; Dai B; Shin WS; He J; He L; Jiang L; Zhao M; Sun B; Li X; Liu C; Li D
Nat Commun; 2019 May; 10(1):2006. PubMed ID: 31043593
[TBL] [Abstract][Full Text] [Related]
2. The nuclear localization sequence mediates hnRNPA1 amyloid fibril formation revealed by cryoEM structure.
Sun Y; Zhao K; Xia W; Feng G; Gu J; Ma Y; Gui X; Zhang X; Fang Y; Sun B; Wang R; Liu C; Li D
Nat Commun; 2020 Dec; 11(1):6349. PubMed ID: 33311513
[TBL] [Abstract][Full Text] [Related]
3. Phase separation by low complexity domains promotes stress granule assembly and drives pathological fibrillization.
Molliex A; Temirov J; Lee J; Coughlin M; Kanagaraj AP; Kim HJ; Mittag T; Taylor JP
Cell; 2015 Sep; 163(1):123-33. PubMed ID: 26406374
[TBL] [Abstract][Full Text] [Related]
4. Characterization of HNRNPA1 mutations defines diversity in pathogenic mechanisms and clinical presentation.
Beijer D; Kim HJ; Guo L; O'Donovan K; Mademan I; Deconinck T; Van Schil K; Fare CM; Drake LE; Ford AF; Kochański A; Kabzińska D; Dubuisson N; Van den Bergh P; Voermans NC; Lemmers RJ; van der Maarel SM; Bonner D; Sampson JB; Wheeler MT; Mehrabyan A; Palmer S; De Jonghe P; Shorter J; Taylor JP; Baets J
JCI Insight; 2021 Jul; 6(14):. PubMed ID: 34291734
[TBL] [Abstract][Full Text] [Related]
5. Multiple Sclerosis-Associated hnRNPA1 Mutations Alter hnRNPA1 Dynamics and Influence Stress Granule Formation.
Clarke JWE; Thibault PA; Salapa HE; Kim DE; Hutchinson C; Levin MC
Int J Mol Sci; 2021 Mar; 22(6):. PubMed ID: 33809384
[TBL] [Abstract][Full Text] [Related]
6. Formation and Maturation of Phase-Separated Liquid Droplets by RNA-Binding Proteins.
Lin Y; Protter DS; Rosen MK; Parker R
Mol Cell; 2015 Oct; 60(2):208-19. PubMed ID: 26412307
[TBL] [Abstract][Full Text] [Related]
7. Cryo-EM Structure of the Full-length hnRNPA1 Amyloid Fibril.
Sharma K; Banerjee S; Savran D; Rajes C; Wiese S; Girdhar A; Schwierz N; Lee C; Shorter J; Schmidt M; Guo L; Fändrich M
J Mol Biol; 2023 Sep; 435(18):168211. PubMed ID: 37481159
[TBL] [Abstract][Full Text] [Related]
8. Molecular epidemiological study of familial amyotrophic lateral sclerosis in Japanese population by whole-exome sequencing and identification of novel HNRNPA1 mutation.
Naruse H; Ishiura H; Mitsui J; Date H; Takahashi Y; Matsukawa T; Tanaka M; Ishii A; Tamaoka A; Hokkoku K; Sonoo M; Segawa M; Ugawa Y; Doi K; Yoshimura J; Morishita S; Goto J; Tsuji S
Neurobiol Aging; 2018 Jan; 61():255.e9-255.e16. PubMed ID: 29033165
[TBL] [Abstract][Full Text] [Related]
9. Atomic structures of FUS LC domain segments reveal bases for reversible amyloid fibril formation.
Luo F; Gui X; Zhou H; Gu J; Li Y; Liu X; Zhao M; Li D; Li X; Liu C
Nat Struct Mol Biol; 2018 Apr; 25(4):341-346. PubMed ID: 29610493
[TBL] [Abstract][Full Text] [Related]
10. Whole-exome sequencing identifies a missense mutation in hnRNPA1 in a family with flail arm ALS.
Liu Q; Shu S; Wang RR; Liu F; Cui B; Guo XN; Lu CX; Li XG; Liu MS; Peng B; Cui LY; Zhang X
Neurology; 2016 Oct; 87(17):1763-1769. PubMed ID: 27694260
[TBL] [Abstract][Full Text] [Related]
11. Electrostatic modulation of hnRNPA1 low-complexity domain liquid-liquid phase separation and aggregation.
Tsoi PS; Quan MD; Choi KJ; Dao KM; Ferreon JC; Ferreon ACM
Protein Sci; 2021 Jul; 30(7):1408-1417. PubMed ID: 33982369
[TBL] [Abstract][Full Text] [Related]
12. TDP-43 regulates the alternative splicing of hnRNP A1 to yield an aggregation-prone variant in amyotrophic lateral sclerosis.
Deshaies JE; Shkreta L; Moszczynski AJ; Sidibé H; Semmler S; Fouillen A; Bennett ER; Bekenstein U; Destroismaisons L; Toutant J; Delmotte Q; Volkening K; Stabile S; Aulas A; Khalfallah Y; Soreq H; Nanci A; Strong MJ; Chabot B; Vande Velde C
Brain; 2018 May; 141(5):1320-1333. PubMed ID: 29562314
[TBL] [Abstract][Full Text] [Related]
13. The interface of condensates of the hnRNPA1 low-complexity domain promotes formation of amyloid fibrils.
Linsenmeier M; Faltova L; Morelli C; Capasso Palmiero U; Seiffert C; Küffner AM; Pinotsi D; Zhou J; Mezzenga R; Arosio P
Nat Chem; 2023 Oct; 15(10):1340-1349. PubMed ID: 37749234
[TBL] [Abstract][Full Text] [Related]
14. ALS Mutations Disrupt Phase Separation Mediated by α-Helical Structure in the TDP-43 Low-Complexity C-Terminal Domain.
Conicella AE; Zerze GH; Mittal J; Fawzi NL
Structure; 2016 Sep; 24(9):1537-49. PubMed ID: 27545621
[TBL] [Abstract][Full Text] [Related]
15. ALS-linked mutations in ubiquilin-2 or hnRNPA1 reduce interaction between ubiquilin-2 and hnRNPA1.
Gilpin KM; Chang L; Monteiro MJ
Hum Mol Genet; 2015 May; 24(9):2565-77. PubMed ID: 25616961
[TBL] [Abstract][Full Text] [Related]
16. The roles of intrinsic disorder-based liquid-liquid phase transitions in the "Dr. Jekyll-Mr. Hyde" behavior of proteins involved in amyotrophic lateral sclerosis and frontotemporal lobar degeneration.
Uversky VN
Autophagy; 2017; 13(12):2115-2162. PubMed ID: 28980860
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Stress Induces Dynamic, Cytotoxicity-Antagonizing TDP-43 Nuclear Bodies via Paraspeckle LncRNA NEAT1-Mediated Liquid-Liquid Phase Separation.
Wang C; Duan Y; Duan G; Wang Q; Zhang K; Deng X; Qian B; Gu J; Ma Z; Zhang S; Guo L; Liu C; Fang Y
Mol Cell; 2020 Aug; 79(3):443-458.e7. PubMed ID: 32649883
[TBL] [Abstract][Full Text] [Related]
19. Proteomic analysis of FUS interacting proteins provides insights into FUS function and its role in ALS.
Kamelgarn M; Chen J; Kuang L; Arenas A; Zhai J; Zhu H; Gal J
Biochim Biophys Acta; 2016 Oct; 1862(10):2004-14. PubMed ID: 27460707
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
