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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

231 related articles for article (PubMed ID: 25008111)

  • 1. A human mitochondrial poly(A) polymerase mutation reveals the complexities of post-transcriptional mitochondrial gene expression.
    Wilson WC; Hornig-Do HT; Bruni F; Chang JH; Jourdain AA; Martinou JC; Falkenberg M; Spåhr H; Larsson NG; Lewis RJ; Hewitt L; Baslé A; Cross HE; Tong L; Lebel RR; Crosby AH; Chrzanowska-Lightowlers ZM; Lightowlers RN
    Hum Mol Genet; 2014 Dec; 23(23):6345-55. PubMed ID: 25008111
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Helicase SUV3, polynucleotide phosphorylase, and mitochondrial polyadenylation polymerase form a transient complex to modulate mitochondrial mRNA polyadenylated tail lengths in response to energetic changes.
    Wang DD; Guo XE; Modrek AS; Chen CF; Chen PL; Lee WH
    J Biol Chem; 2014 Jun; 289(24):16727-35. PubMed ID: 24770417
    [TBL] [Abstract][Full Text] [Related]  

  • 3. LRPPRC/SLIRP suppresses PNPase-mediated mRNA decay and promotes polyadenylation in human mitochondria.
    Chujo T; Ohira T; Sakaguchi Y; Goshima N; Nomura N; Nagao A; Suzuki T
    Nucleic Acids Res; 2012 Sep; 40(16):8033-47. PubMed ID: 22661577
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Biallelic Mutations in MTPAP Associated with a Lethal Encephalopathy.
    Van Eyck L; Bruni F; Ronan A; Briggs TA; Roscioli T; Rice GI; Vassallo G; Rodero MP; He L; Taylor RW; Livingston JH; Chrzanowska-Lightowlers ZMA; Crow YJ
    Neuropediatrics; 2020 Jun; 51(3):178-184. PubMed ID: 31779033
    [TBL] [Abstract][Full Text] [Related]  

  • 5. SLIRP Regulates the Rate of Mitochondrial Protein Synthesis and Protects LRPPRC from Degradation.
    Lagouge M; Mourier A; Lee HJ; Spåhr H; Wai T; Kukat C; Silva Ramos E; Motori E; Busch JD; Siira S; ; Kremmer E; Filipovska A; Larsson NG
    PLoS Genet; 2015 Aug; 11(8):e1005423. PubMed ID: 26247782
    [TBL] [Abstract][Full Text] [Related]  

  • 6. LRPPRC and SLIRP synergize to maintain sufficient and orderly mammalian mitochondrial translation.
    Rubalcava-Gracia D; Bubb K; Levander F; Burr SP; August AV; Chinnery PF; Koolmeister C; Larsson NG
    Nucleic Acids Res; 2024 Oct; 52(18):11266-11282. PubMed ID: 39087558
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Human mitochondrial mRNAs are stabilized with polyadenylation regulated by mitochondria-specific poly(A) polymerase and polynucleotide phosphorylase.
    Nagaike T; Suzuki T; Katoh T; Ueda T
    J Biol Chem; 2005 May; 280(20):19721-7. PubMed ID: 15769737
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Assembly of a processive messenger RNA polyadenylation complex.
    Bienroth S; Keller W; Wahle E
    EMBO J; 1993 Feb; 12(2):585-94. PubMed ID: 8440247
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 3' adenylation determines mRNA abundance and monitors completion of RNA editing in T. brucei mitochondria.
    Etheridge RD; Aphasizheva I; Gershon PD; Aphasizhev R
    EMBO J; 2008 Jun; 27(11):1596-608. PubMed ID: 18464794
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Defective mitochondrial mRNA maturation is associated with spastic ataxia.
    Crosby AH; Patel H; Chioza BA; Proukakis C; Gurtz K; Patton MA; Sharifi R; Harlalka G; Simpson MA; Dick K; Reed JA; Al-Memar A; Chrzanowska-Lightowlers ZM; Cross HE; Lightowlers RN
    Am J Hum Genet; 2010 Nov; 87(5):655-60. PubMed ID: 20970105
    [TBL] [Abstract][Full Text] [Related]  

  • 11. LRPPRC and SLIRP interact in a ribonucleoprotein complex that regulates posttranscriptional gene expression in mitochondria.
    Sasarman F; Brunel-Guitton C; Antonicka H; Wai T; Shoubridge EA;
    Mol Biol Cell; 2010 Apr; 21(8):1315-23. PubMed ID: 20200222
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Stable PNPase RNAi silencing: its effect on the processing and adenylation of human mitochondrial RNA.
    Slomovic S; Schuster G
    RNA; 2008 Feb; 14(2):310-23. PubMed ID: 18083837
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Ablation of Mto1 in zebrafish exhibited hypertrophic cardiomyopathy manifested by mitochondrion RNA maturation deficiency.
    Zhang Q; He X; Yao S; Lin T; Zhang L; Chen D; Chen C; Yang Q; Li F; Zhu YM; Guan MX
    Nucleic Acids Res; 2021 May; 49(8):4689-4704. PubMed ID: 33836087
    [TBL] [Abstract][Full Text] [Related]  

  • 14. LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population.
    Oláhová M; Hardy SA; Hall J; Yarham JW; Haack TB; Wilson WC; Alston CL; He L; Aznauryan E; Brown RM; Brown GK; Morris AA; Mundy H; Broomfield A; Barbosa IA; Simpson MA; Deshpande C; Moeslinger D; Koch J; Stettner GM; Bonnen PE; Prokisch H; Lightowlers RN; McFarland R; Chrzanowska-Lightowlers ZM; Taylor RW
    Brain; 2015 Dec; 138(Pt 12):3503-19. PubMed ID: 26510951
    [TBL] [Abstract][Full Text] [Related]  

  • 15. LRPPRC mutation suppresses cytochrome oxidase activity by altering mitochondrial RNA transcript stability in a mouse model.
    Xu F; Addis JB; Cameron JM; Robinson BH
    Biochem J; 2012 Jan; 441(1):275-83. PubMed ID: 21880015
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Polyadenylation is the key aspect of GLD-2 function in
    Nousch M; Minasaki R; Eckmann CR
    RNA; 2017 Aug; 23(8):1180-1187. PubMed ID: 28490506
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Poly (A) tail length of human mitochondrial mRNAs is tissue-specific and a mutation in LRPPRC results in transcript-specific patterns of deadenylation.
    Honarmand S; Shoubridge EA
    Mol Genet Metab Rep; 2020 Dec; 25():100687. PubMed ID: 33312877
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mitochondrial poly(A) polymerase and polyadenylation.
    Chang JH; Tong L
    Biochim Biophys Acta; 2012; 1819(9-10):992-7. PubMed ID: 22172994
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Structure of mitochondrial poly(A) RNA polymerase reveals the structural basis for dimerization, ATP selectivity and the SPAX4 disease phenotype.
    Lapkouski M; Hällberg BM
    Nucleic Acids Res; 2015 Oct; 43(18):9065-75. PubMed ID: 26319014
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Tissue-specific responses to the LRPPRC founder mutation in French Canadian Leigh Syndrome.
    Sasarman F; Nishimura T; Antonicka H; Weraarpachai W; Shoubridge EA;
    Hum Mol Genet; 2015 Jan; 24(2):480-91. PubMed ID: 25214534
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.