343 related articles for article (PubMed ID: 33236345)
1. Aminoacyl-tRNA synthetases in Charcot-Marie-Tooth disease: A gain or a loss?
Zhang H; Zhou ZW; Sun L
J Neurochem; 2021 May; 157(3):351-369. PubMed ID: 33236345
[TBL] [Abstract][Full Text] [Related]
2. Neurodegenerative Charcot-Marie-Tooth disease as a case study to decipher novel functions of aminoacyl-tRNA synthetases.
Wei N; Zhang Q; Yang XL
J Biol Chem; 2019 Apr; 294(14):5321-5339. PubMed ID: 30643024
[TBL] [Abstract][Full Text] [Related]
3. Peripheral neuropathy via mutant tRNA synthetases: Inhibition of protein translation provides a possible explanation.
Storkebaum E
Bioessays; 2016 Sep; 38(9):818-29. PubMed ID: 27352040
[TBL] [Abstract][Full Text] [Related]
4.
Morant L; Erfurth ML; Jordanova A
Genes (Basel); 2021 Sep; 12(10):. PubMed ID: 34680913
[TBL] [Abstract][Full Text] [Related]
5. CMT disease severity correlates with mutation-induced open conformation of histidyl-tRNA synthetase, not aminoacylation loss, in patient cells.
Blocquel D; Sun L; Matuszek Z; Li S; Weber T; Kuhle B; Kooi G; Wei N; Baets J; Pan T; Schimmel P; Yang XL
Proc Natl Acad Sci U S A; 2019 Sep; 116(39):19440-19448. PubMed ID: 31501329
[TBL] [Abstract][Full Text] [Related]
6. Human diseases linked to cytoplasmic aminoacyl-tRNA synthetases.
Jiang L; Jones J; Yang XL
Enzymes; 2020; 48():277-319. PubMed ID: 33837707
[TBL] [Abstract][Full Text] [Related]
7. The role of tRNA synthetases in neurological and neuromuscular disorders.
Boczonadi V; Jennings MJ; Horvath R
FEBS Lett; 2018 Mar; 592(5):703-717. PubMed ID: 29288497
[TBL] [Abstract][Full Text] [Related]
8. CMT-associated mutations in glycyl- and tyrosyl-tRNA synthetases exhibit similar pattern of toxicity and share common genetic modifiers in Drosophila.
Ermanoska B; Motley WW; Leitão-Gonçalves R; Asselbergh B; Lee LH; De Rijk P; Sleegers K; Ooms T; Godenschwege TA; Timmerman V; Fischbeck KH; Jordanova A
Neurobiol Dis; 2014 Aug; 68():180-9. PubMed ID: 24807208
[TBL] [Abstract][Full Text] [Related]
9. [Searching for non-canonical functions of aminoacyl-tRNA synthases based on mutations carried by Charcot-Marie-Tooth patients].
Misiorek JO
Postepy Biochem; 2023 Mar; 69(1):42-46. PubMed ID: 37493554
[TBL] [Abstract][Full Text] [Related]
10. Recent Advances in
Kitani-Morii F; Noto YI
Int J Mol Sci; 2020 Oct; 21(19):. PubMed ID: 33049996
[TBL] [Abstract][Full Text] [Related]
11. Transcriptional dysregulation by a nucleus-localized aminoacyl-tRNA synthetase associated with Charcot-Marie-Tooth neuropathy.
Bervoets S; Wei N; Erfurth ML; Yusein-Myashkova S; Ermanoska B; Mateiu L; Asselbergh B; Blocquel D; Kakad P; Penserga T; Thomas FP; Guergueltcheva V; Tournev I; Godenschwege T; Jordanova A; Yang XL
Nat Commun; 2019 Nov; 10(1):5045. PubMed ID: 31695036
[TBL] [Abstract][Full Text] [Related]
12. A recurrent loss-of-function alanyl-tRNA synthetase (AARS) mutation in patients with Charcot-Marie-Tooth disease type 2N (CMT2N).
McLaughlin HM; Sakaguchi R; Giblin W; ; Wilson TE; Biesecker L; Lupski JR; Talbot K; Vance JM; Züchner S; Lee YC; Kennerson M; Hou YM; Nicholson G; Antonellis A
Hum Mutat; 2012 Jan; 33(1):244-53. PubMed ID: 22009580
[TBL] [Abstract][Full Text] [Related]
13. Associations between Neurological Diseases and Mutations in the Human Glycyl-tRNA Synthetase.
Vinogradova ES; Nikonov OS; Nikonova EY
Biochemistry (Mosc); 2021 Jan; 86(Suppl 1):S12-S23. PubMed ID: 33827397
[TBL] [Abstract][Full Text] [Related]
14. Aminoacyl-tRNA synthetases in human health and disease.
Turvey AK; Horvath GA; Cavalcanti ARO
Front Physiol; 2022; 13():1029218. PubMed ID: 36330207
[TBL] [Abstract][Full Text] [Related]
15. An assessment of mechanisms underlying peripheral axonal degeneration caused by aminoacyl-tRNA synthetase mutations.
Stum M; McLaughlin HM; Kleinbrink EL; Miers KE; Ackerman SL; Seburn KL; Antonellis A; Burgess RW
Mol Cell Neurosci; 2011 Feb; 46(2):432-43. PubMed ID: 21115117
[TBL] [Abstract][Full Text] [Related]
16. Aminoacyl-tRNA synthetases and tRNAs in human disease: an introduction to the JBC Reviews thematic series.
Musier-Forsyth K
J Biol Chem; 2019 Apr; 294(14):5292-5293. PubMed ID: 30799306
[TBL] [Abstract][Full Text] [Related]
17. Impaired protein translation in Drosophila models for Charcot-Marie-Tooth neuropathy caused by mutant tRNA synthetases.
Niehues S; Bussmann J; Steffes G; Erdmann I; Köhrer C; Sun L; Wagner M; Schäfer K; Wang G; Koerdt SN; Stum M; Jaiswal S; RajBhandary UL; Thomas U; Aberle H; Burgess RW; Yang XL; Dieterich D; Storkebaum E
Nat Commun; 2015 Jul; 6():7520. PubMed ID: 26138142
[TBL] [Abstract][Full Text] [Related]
18. Hypermorphic and hypomorphic AARS alleles in patients with CMT2N expand clinical and molecular heterogeneities.
Weterman MAJ; Kuo M; Kenter SB; Gordillo S; Karjosukarso DW; Takase R; Bronk M; Oprescu S; van Ruissen F; Witteveen RJW; Bienfait HME; Breuning M; Verhamme C; Hou YM; de Visser M; Antonellis A; Baas F
Hum Mol Genet; 2018 Dec; 27(23):4036-4050. PubMed ID: 30124830
[TBL] [Abstract][Full Text] [Related]
19. Aminoacyl-tRNA synthetases in medicine and disease.
Yao P; Fox PL
EMBO Mol Med; 2013 Mar; 5(3):332-43. PubMed ID: 23427196
[TBL] [Abstract][Full Text] [Related]
20. Four pedigrees with aminoacyl-tRNA synthetase abnormalities.
Okamoto N; Miya F; Tsunoda T; Kanemura Y; Saitoh S; Kato M; Yanagi K; Kaname T; Kosaki K
Neurol Sci; 2022 Apr; 43(4):2765-2774. PubMed ID: 34585293
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
