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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2010 2
2011 2
2012 2
2013 1
2015 1
2016 2
2017 1
2018 1
2019 1
2020 5
2021 4
2022 2
2023 5
2024 1

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27 results

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Page 1
Elp3-mediated codon-dependent translation promotes mTORC2 activation and regulates macrophage polarization.
Chen D, Nemazanyy I, Peulen O, Shostak K, Xu X, Tang SC, Wathieu C, Turchetto S, Tielens S, Nguyen L, Close P, Desmet C, Klein S, Florin A, Büttner R, Petrellis G, Dewals B, Chariot A. Chen D, et al. EMBO J. 2022 Sep 15;41(18):e109353. doi: 10.15252/embj.2021109353. Epub 2022 Aug 3. EMBO J. 2022. PMID: 35920020 Free PMC article.
The metabolic reprogramming linked to M2 macrophage polarization relies on Elp3 and the translation of multiple candidates, including the mitochondrial ribosome large subunit proteins Mrpl3, Mrpl13, and Mrpl47. By promoting translation of its activator Ric8b in a codon-dep …
The metabolic reprogramming linked to M2 macrophage polarization relies on Elp3 and the translation of multiple candidates, including the mi …
CENPL, ISG20L2, LSM4, MRPL3 are four novel hub genes and may serve as diagnostic and prognostic markers in breast cancer.
Yin J, Lin C, Jiang M, Tang X, Xie D, Chen J, Ke R. Yin J, et al. Sci Rep. 2021 Aug 2;11(1):15610. doi: 10.1038/s41598-021-95068-6. Sci Rep. 2021. PMID: 34341433 Free PMC article.
EZH2 was recognized as a key gene by PPI network analysis. CENPL, ISG20L2, LSM4, MRPL3 were identified as four novel hub genes through the WGCNA analysis and literate search. Among these, many studies on EZH2 in breast cancer have been reported, but no studies are related …
EZH2 was recognized as a key gene by PPI network analysis. CENPL, ISG20L2, LSM4, MRPL3 were identified as four novel hub genes throug …
Structural Variant in Mitochondrial-Associated Gene (MRPL3) Induces Adult-Onset Neurodegeneration with Memory Impairment in the Mouse.
Cahill LS, Cameron JM, Winterburn J, Macos P, Hoggarth J, Dzamba M, Brudno M, Nutter LMJ, Sproule TJ, Burgess RW, Henkelman RM, Sled JG. Cahill LS, et al. J Neurosci. 2020 Jun 3;40(23):4576-4585. doi: 10.1523/JNEUROSCI.0013-20.2020. Epub 2020 Apr 27. J Neurosci. 2020. PMID: 32341096 Free PMC article.
Using structural variant analysis, we identified an intronic mutation in a mitochondrial-associated gene (Mrpl3) that is responsible for the decrepit phenotype. While the function of this gene is unknown, embryonic lethality in Mrpl3 knock-out mice suggests it is cr …
Using structural variant analysis, we identified an intronic mutation in a mitochondrial-associated gene (Mrpl3) that is responsible …
Exome sequencing identifies MRPL3 mutation in mitochondrial cardiomyopathy.
Galmiche L, Serre V, Beinat M, Assouline Z, Lebre AS, Chretien D, Nietschke P, Benes V, Boddaert N, Sidi D, Brunelle F, Rio M, Munnich A, Rötig A. Galmiche L, et al. Hum Mutat. 2011 Nov;32(11):1225-31. doi: 10.1002/humu.21562. Epub 2011 Sep 14. Hum Mutat. 2011. PMID: 21786366
By combining exome sequencing in conjunction with genetic mapping, we have identified the first mutation in large mitochondrial ribosomal protein MRPL3 in a family of four sibs with hypertrophic cardiomyopathy, psychomotor retardation, and multiple respiratory chain defici …
By combining exome sequencing in conjunction with genetic mapping, we have identified the first mutation in large mitochondrial ribosomal pr …
Analysis of the MRPL3, DNAJC13 and OFCC1 variants in Chinese Han patients with TS-CTD.
Guo Y, Deng X, Zhang J, Su L, Xu H, Luo Z, Deng H. Guo Y, et al. Neurosci Lett. 2012 May 23;517(1):18-20. doi: 10.1016/j.neulet.2012.03.097. Epub 2012 Apr 9. Neurosci Lett. 2012. PMID: 22507240
Tourette syndrome/chronic tic phenotype (TS-CTD) is a neurological disorder manifested particularly by motor and vocal tics and associated with a variety of behavioral abnormalities. Recently, the mitochondrial ribosomal protein L3 gene (MRPL3) S75N, the DnaJ (Hsp40) homol …
Tourette syndrome/chronic tic phenotype (TS-CTD) is a neurological disorder manifested particularly by motor and vocal tics and associated w …
COXPD9 in an individual from Puerto Rico and literature review.
Alsharhan H, Muraresku C, Ganetzky RD. Alsharhan H, et al. Am J Med Genet A. 2021 Aug;185(8):2519-2525. doi: 10.1002/ajmg.a.62344. Epub 2021 May 19. Am J Med Genet A. 2021. PMID: 34008913 Review.
We present here the sixth individual with combined oxidative phosphorylation deficiency-9 (COXPD9) secondary to a likely pathogenic homozygous MRPL3 variant c.571A > C; p.(Thr191Pro). MRPL3 encodes a large mitochondrial ribosome subunit protein, impairing the mit …
We present here the sixth individual with combined oxidative phosphorylation deficiency-9 (COXPD9) secondary to a likely pathogenic homozygo …
Transcriptomic profiles of multiple organ dysfunction syndrome phenotypes in pediatric critical influenza.
Novak T, Crawford JC, Hahn G, Hall MW, Thair SA, Newhams MM, Chou J, Mourani PM, Tarquinio KM, Markovitz B, Loftis LL, Weiss SL, Higgerson R, Schwarz AJ, Pinto NP, Thomas NJ, Gedeit RG, Sanders RC Jr, Mahapatra S, Coates BM, Cvijanovich NZ, Ackerman KG, Tellez DW, McQuillen P, Kurachek SC, Shein SL, Lange C, Thomas PG, Randolph AG. Novak T, et al. Front Immunol. 2023 Jul 18;14:1220028. doi: 10.3389/fimmu.2023.1220028. eCollection 2023. Front Immunol. 2023. PMID: 37533854 Free PMC article.
Instead, five genes involved in protein metabolism and/or adaptive immunity signaling pathways (RPL3, MRPL3, HLA-DMB, EEF1G, CD8A) were associated with MODS recovery within a week. ...
Instead, five genes involved in protein metabolism and/or adaptive immunity signaling pathways (RPL3, MRPL3, HLA-DMB, EEF1G, CD8A) we …
Nuclear-encoded mitochondrial ribosomal proteins are required to initiate gastrulation.
Cheong A, Archambault D, Degani R, Iverson E, Tremblay KD, Mager J. Cheong A, et al. Development. 2020 May 26;147(10):dev188714. doi: 10.1242/dev.188714. Development. 2020. PMID: 32376682 Free PMC article.
Presented here are the null phenotypes for 21 nuclear-encoded mitochondrial proteins and in-depth characterization of mouse embryos mutant for the Mrp genes Mrpl3, Mrpl22, Mrpl44, Mrps18c and Mrps22 Loss of each MRP results in successful implantation and egg-cylinder forma …
Presented here are the null phenotypes for 21 nuclear-encoded mitochondrial proteins and in-depth characterization of mouse embryos mutant f …
A Novel Cuproptosis-Associated Gene Signature to Predict Prognosis in Patients with Pancreatic Cancer.
Du Y, Jiang W, Hou S, Chen Z, Zhou W. Du Y, et al. Biomed Res Int. 2023 Jan 18;2023:3419401. doi: 10.1155/2023/3419401. eCollection 2023. Biomed Res Int. 2023. PMID: 36714025 Free PMC article.
CONCLUSIONS: We constructed a prognostic model containing eight cuproptosis-related genes (AKR1B10, KLHL29, PROM2, PIP5K1C, KIF18B, AMIGO2, MRPL3, and PI4KB) that can accurately predict the prognosis of PAAD patients. ...
CONCLUSIONS: We constructed a prognostic model containing eight cuproptosis-related genes (AKR1B10, KLHL29, PROM2, PIP5K1C, KIF18B, AMIGO2, …
27 results