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 *

118 related articles for article (PubMed ID: 32931159)

  • 21. Impaired function of p53R2 in Rrm2b-null mice causes severe renal failure through attenuation of dNTP pools.
    Kimura T; Takeda S; Sagiya Y; Gotoh M; Nakamura Y; Arakawa H
    Nat Genet; 2003 Aug; 34(4):440-5. PubMed ID: 12858174
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A novel mutation of the RRM2B gene in an infant with early fatal encephalomyopathy, central hypomyelination, and tubulopathy.
    Acham-Roschitz B; Plecko B; Lindbichler F; Bittner R; Mache CJ; Sperl W; Mayr JA
    Mol Genet Metab; 2009 Nov; 98(3):300-4. PubMed ID: 19616983
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Rapid development of glomerular injury and renal failure in mice lacking p53R2.
    Powell DR; Desai U; Sparks MJ; Hansen G; Gay J; Schrick J; Shi ZZ; Hicks J; Vogel P
    Pediatr Nephrol; 2005 Mar; 20(3):432-40. PubMed ID: 15723268
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Diagnosing mitochondrial, neurogastrointestinal leukoencephalopathy requires mutations in TYMP1, POLG1, LIG1, or RRM2B.
    Finsterer J
    J Med Case Rep; 2023 Apr; 17(1):162. PubMed ID: 37055871
    [No Abstract]   [Full Text] [Related]  

  • 25. Rrm2b deletion causes mitochondrial metabolic defects in renal tubules.
    Chen YF; Lin IH; Guo YR; Chiu WJ; Wu MS; Jia W; Yen Y
    Sci Rep; 2019 Sep; 9(1):13238. PubMed ID: 31519977
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Ribonucleotide reductase M2B inhibits cell migration and spreading by early growth response protein 1-mediated phosphatase and tensin homolog/Akt1 pathway in hepatocellular carcinoma.
    Tian H; Ge C; Li H; Zhao F; Hou H; Chen T; Jiang G; Xie H; Cui Y; Yao M; Li J
    Hepatology; 2014 Apr; 59(4):1459-70. PubMed ID: 24214128
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Troponin T3 associates with DNA consensus sequence that overlaps with p53 binding motifs.
    Nunez Lopez YO; Messi ML; Pratley RE; Zhang T; Delbono O
    Exp Gerontol; 2018 Jul; 108():35-40. PubMed ID: 29596868
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Mitochondrial DNA maintenance defects.
    El-Hattab AW; Craigen WJ; Scaglia F
    Biochim Biophys Acta Mol Basis Dis; 2017 Jun; 1863(6):1539-1555. PubMed ID: 28215579
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genomic landscape of DNA repair genes in cancer.
    Chae YK; Anker JF; Carneiro BA; Chandra S; Kaplan J; Kalyan A; Santa-Maria CA; Platanias LC; Giles FJ
    Oncotarget; 2016 Apr; 7(17):23312-21. PubMed ID: 27004405
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Whole-exome sequencing of Finnish hereditary breast cancer families.
    Määttä K; Rantapero T; Lindström A; Nykter M; Kankuri-Tammilehto M; Laasanen SL; Schleutker J
    Eur J Hum Genet; 2016 Jan; 25(1):85-93. PubMed ID: 27782108
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Ribonucleotide reductase and mitochondrial DNA synthesis.
    Thelander L
    Nat Genet; 2007 Jun; 39(6):703-4. PubMed ID: 17534360
    [No Abstract]   [Full Text] [Related]  

  • 32. Differential involvement of the related DNA helicases Pif1p and Rrm3p in mtDNA point mutagenesis and stability.
    O'Rourke TW; Doudican NA; Zhang H; Eaton JS; Doetsch PW; Shadel GS
    Gene; 2005 Jul; 354():86-92. PubMed ID: 15907372
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Novel biallelic variants in
    Schultz-Rogers L; Ferrer A; Dsouza NR; Zimmermann MT; Smith BE; Klee EW; Dhamija R
    Cold Spring Harb Mol Case Stud; 2019 Dec; 5(6):. PubMed ID: 31604776
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Case Report: A novel
    Wang Y; Hang L; Shou W; Li C; Dong F; Feng X; Jin R; Li B; Xiao S
    Front Pediatr; 2024; 12():1363728. PubMed ID: 38737634
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Knockdown of poc1b causes abnormal photoreceptor sensory cilium and vision impairment in zebrafish.
    Zhang C; Zhang Q; Wang F; Liu Q
    Biochem Biophys Res Commun; 2015 Oct; 465(4):651-7. PubMed ID: 26188096
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Regulation of p53R2 and its role as potential target for cancer therapy.
    Wang X; Zhenchuk A; Wiman KG; Albertioni F
    Cancer Lett; 2009 Apr; 276(1):1-7. PubMed ID: 18760875
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mouse models of oxidative phosphorylation dysfunction and disease.
    Vempati UD; Torraco A; Moraes CT
    Methods; 2008 Dec; 46(4):241-7. PubMed ID: 18848991
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A novel mutation in
    Diquigiovanni C; Bergamini C; Diaz R; Liparulo I; Bianco F; Masin L; Baldassarro VA; Rizzardi N; Tranchina A; Buscherini F; Wischmeijer A; Pippucci T; Scarano E; Cordelli DM; Fato R; Seri M; Paracchini S; Bonora E
    FASEB J; 2019 Oct; 33(10):11284-11302. PubMed ID: 31314595
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Right Brain: Withholding treatment from a child with an epileptic encephalomyopathy.
    Rothstein A; Lewis A
    Neurology; 2018 May; 90(18):857-859. PubMed ID: 29712807
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Whole-Genome Linkage Analysis with Whole-Exome Sequencing Identifies a Novel Frameshift Variant in NEFH in a Chinese Family with Charcot-Marie-Tooth 2: A Novel Variant in NEFH for Charcot-Marie-Tooth 2.
    Bian X; Lin P; Li J; Long F; Duan R; Yuan Q; Li Y; Gao F; Gao S; Wei S; Li X; Sun W; Gong Y; Yan C; Liu Q
    Neurodegener Dis; 2018; 18(2-3):74-83. PubMed ID: 29587262
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.