BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

320 related articles for article (PubMed ID: 22448145)

  • 1. Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans.
    Bayat V; Thiffault I; Jaiswal M; Tétreault M; Donti T; Sasarman F; Bernard G; Demers-Lamarche J; Dicaire MJ; Mathieu J; Vanasse M; Bouchard JP; Rioux MF; Lourenco CM; Li Z; Haueter C; Shoubridge EA; Graham BH; Brais B; Bellen HJ
    PLoS Biol; 2012; 10(3):e1001288. PubMed ID: 22448145
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Novel, compound heterozygous, single-nucleotide variants in MARS2 associated with developmental delay, poor growth, and sensorineural hearing loss.
    Webb BD; Wheeler PG; Hagen JJ; Cohen N; Linderman MD; Diaz GA; Naidich TP; Rodenburg RJ; Houten SM; Schadt EE
    Hum Mutat; 2015 Jun; 36(6):587-92. PubMed ID: 25754315
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Impaired Mitochondrial Energy Production Causes Light-Induced Photoreceptor Degeneration Independent of Oxidative Stress.
    Jaiswal M; Haelterman NA; Sandoval H; Xiong B; Donti T; Kalsotra A; Yamamoto S; Cooper TA; Graham BH; Bellen HJ
    PLoS Biol; 2015 Jul; 13(7):e1002197. PubMed ID: 26176594
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Methionyl-tRNA Synthetase Regulates Lifespan in
    Suh YS; Yeom E; Nam JW; Min KJ; Lee J; Yu K
    Mol Cells; 2020 Mar; 43(3):304-311. PubMed ID: 31940717
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mito-Nuclear Interactions Affecting Lifespan and Neurodegeneration in a
    Loewen CA; Ganetzky B
    Genetics; 2018 Apr; 208(4):1535-1552. PubMed ID: 29496745
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Loss of the Drosophila m-AAA mitochondrial protease paraplegin results in mitochondrial dysfunction, shortened lifespan, and neuronal and muscular degeneration.
    Pareek G; Thomas RE; Pallanck LJ
    Cell Death Dis; 2018 Feb; 9(3):304. PubMed ID: 29467464
    [TBL] [Abstract][Full Text] [Related]  

  • 7. MARS2 drives metabolic switch of non-small-cell lung cancer cells via interaction with MCU.
    Son J; Jung O; Kim JH; Park KS; Kweon HS; Nguyen NT; Lee YJ; Cha H; Lee Y; Tran Q; Seo Y; Park J; Choi J; Cheong H; Lee SY
    Redox Biol; 2023 Apr; 60():102628. PubMed ID: 36774778
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutations in the mitochondrial tryptophanyl-tRNA synthetase cause growth retardation and progressive leukoencephalopathy.
    Maffezzini C; Laine I; Dallabona C; Clemente P; Calvo-Garrido J; Wibom R; Naess K; Barbaro M; Falk A; Donnini C; Freyer C; Wredenberg A; Wedell A
    Mol Genet Genomic Med; 2019 Jun; 7(6):e654. PubMed ID: 30920170
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation.
    Jiang P; Jin X; Peng Y; Wang M; Liu H; Liu X; Zhang Z; Ji Y; Zhang J; Liang M; Zhao F; Sun YH; Zhang M; Zhou X; Chen Y; Mo JQ; Huang T; Qu J; Guan MX
    Hum Mol Genet; 2016 Feb; 25(3):584-96. PubMed ID: 26647310
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Expression of the Ciona intestinalis alternative oxidase (AOX) in Drosophila complements defects in mitochondrial oxidative phosphorylation.
    Fernandez-Ayala DJ; Sanz A; Vartiainen S; Kemppainen KK; Babusiak M; Mustalahti E; Costa R; Tuomela T; Zeviani M; Chung J; O'Dell KM; Rustin P; Jacobs HT
    Cell Metab; 2009 May; 9(5):449-60. PubMed ID: 19416715
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Physiological and pathological roles of FATP-mediated lipid droplets in Drosophila and mice retina.
    Van Den Brink DM; Cubizolle A; Chatelain G; Davoust N; Girard V; Johansen S; Napoletano F; Dourlen P; Guillou L; Angebault-Prouteau C; Bernoud-Hubac N; Guichardant M; Brabet P; Mollereau B
    PLoS Genet; 2018 Sep; 14(9):e1007627. PubMed ID: 30199545
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Overexpressed PERK suppresses the neurodegenerative phenotypes in PINK1
    Cui Y; Wen X; Nan Y; Xiang G; Wei Z; Wei L; Xia Y; Li Q
    Neurochem Int; 2020 Nov; 140():104825. PubMed ID: 32898622
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy.
    Higuchi Y; Okunushi R; Hara T; Hashiguchi A; Yuan J; Yoshimura A; Murayama K; Ohtake A; Ando M; Hiramatsu Y; Ishihara S; Tanabe H; Okamoto Y; Matsuura E; Ueda T; Toda T; Yamashita S; Yamada K; Koide T; Yaguchi H; Mitsui J; Ishiura H; Yoshimura J; Doi K; Morishita S; Sato K; Nakagawa M; Yamaguchi M; Tsuji S; Takashima H
    Brain; 2018 Jun; 141(6):1622-1636. PubMed ID: 29718187
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Characterization of MSM1, the structural gene for yeast mitochondrial methionyl-tRNA synthetase.
    Tzagoloff A; Vambutas A; Akai A
    Eur J Biochem; 1989 Feb; 179(2):365-71. PubMed ID: 2645139
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Promiscuous methionyl-tRNA synthetase mediates adaptive mistranslation to protect cells against oxidative stress.
    Lee JY; Kim DG; Kim BG; Yang WS; Hong J; Kang T; Oh YS; Kim KR; Han BW; Hwang BJ; Kang BS; Kang MS; Kim MH; Kwon NH; Kim S
    J Cell Sci; 2014 Oct; 127(Pt 19):4234-45. PubMed ID: 25097229
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mitochondrial peptidase IMMP2L mutation causes early onset of age-associated disorders and impairs adult stem cell self-renewal.
    George SK; Jiao Y; Bishop CE; Lu B
    Aging Cell; 2011 Aug; 10(4):584-94. PubMed ID: 21332923
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Normal mitochondrial dynamics requires rhomboid-7 and affects Drosophila lifespan and neuronal function.
    McQuibban GA; Lee JR; Zheng L; Juusola M; Freeman M
    Curr Biol; 2006 May; 16(10):982-9. PubMed ID: 16713954
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Overexpression of mitochondrial histidyl-tRNA synthetase restores mitochondrial dysfunction caused by a deafness-associated tRNA
    Gong S; Wang X; Meng F; Cui L; Yi Q; Zhao Q; Cang X; Cai Z; Mo JQ; Liang Y; Guan MX
    J Biol Chem; 2020 Jan; 295(4):940-954. PubMed ID: 31819004
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Alanyl-tRNA Synthetase 2 (AARS2)-Related Ataxia Without Leukoencephalopathy.
    Kuo ME; Antonellis A; Shakkottai VG
    Cerebellum; 2020 Feb; 19(1):154-160. PubMed ID: 31705293
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation: clinical and genetic characterization and target for therapy.
    van Berge L; Hamilton EM; Linnankivi T; Uziel G; Steenweg ME; Isohanni P; Wolf NI; Krägeloh-Mann I; Brautaset NJ; Andrews PI; de Jong BA; al Ghamdi M; van Wieringen WN; Tannous BA; Hulleman E; Würdinger T; van Berkel CG; Polder E; Abbink TE; Struys EA; Scheper GC; van der Knaap MS;
    Brain; 2014 Apr; 137(Pt 4):1019-29. PubMed ID: 24566671
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.