BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

215 related articles for article (PubMed ID: 33545634)

  • 21. A newly identified mutation in the
    Tanaka AJ; Okumoto K; Tamura S; Abe Y; Hirsch Y; Deng L; Ekstein J; Chung WK; Fujiki Y
    Cold Spring Harb Mol Case Stud; 2019 Feb; 5(1):. PubMed ID: 30446579
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Knockdown of PEX16 Induces Autophagic Degradation of Peroxisomes.
    Wei X; Maharjan Y; Dorotea D; Dutta RK; Kim D; Kim H; Mu Y; Park C; Park R
    Int J Mol Sci; 2021 Jul; 22(15):. PubMed ID: 34360754
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Structural Mapping of Missense Mutations in the Pex1/Pex6 Complex.
    Schieferdecker A; Wendler P
    Int J Mol Sci; 2019 Aug; 20(15):. PubMed ID: 31374812
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders.
    Yik WY; Steinberg SJ; Moser AB; Moser HW; Hacia JG
    Hum Mutat; 2009 Mar; 30(3):E467-80. PubMed ID: 19105186
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Heterogeneous nuclear ribonucleoprotein A1 promotes the expression of autophagy-related protein 6 in human colorectal cancer.
    Ji E; Lee H; Ahn S; Jung M; Lee SH; Lee JH; Lee EK
    Biochem Biophys Res Commun; 2019 May; 513(1):255-260. PubMed ID: 30954215
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Functional analysis of PEX13 mutation in a Zellweger syndrome spectrum patient reveals novel homooligomerization of PEX13 and its role in human peroxisome biogenesis.
    Krause C; Rosewich H; Woehler A; Gärtner J
    Hum Mol Genet; 2013 Oct; 22(19):3844-57. PubMed ID: 23716570
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Deficiency of the exportomer components Pex1, Pex6, and Pex15 causes enhanced pexophagy in Saccharomyces cerevisiae.
    Nuttall JM; Motley AM; Hettema EH
    Autophagy; 2014 May; 10(5):835-45. PubMed ID: 24657987
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Arginine improves peroxisome functioning in cells from patients with a mild peroxisome biogenesis disorder.
    Berendse K; Ebberink MS; Ijlst L; Poll-The BT; Wanders RJ; Waterham HR
    Orphanet J Rare Dis; 2013 Sep; 8():138. PubMed ID: 24016303
    [TBL] [Abstract][Full Text] [Related]  

  • 29. PEX1 mutations in the Zellweger spectrum of the peroxisome biogenesis disorders.
    Crane DI; Maxwell MA; Paton BC
    Hum Mutat; 2005 Sep; 26(3):167-75. PubMed ID: 16086329
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G.
    Muntau AC; Mayerhofer PU; Paton BC; Kammerer S; Roscher AA
    Am J Hum Genet; 2000 Oct; 67(4):967-75. PubMed ID: 10958759
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Novel PEX1 mutations and genotype-phenotype correlations in Australasian peroxisome biogenesis disorder patients.
    Maxwell MA; Allen T; Solly PB; Svingen T; Paton BC; Crane DI
    Hum Mutat; 2002 Nov; 20(5):342-51. PubMed ID: 12402331
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Liver disease predominates in a mouse model for mild human Zellweger spectrum disorder.
    Berendse K; Boek M; Gijbels M; Van der Wel NN; Klouwer FC; van den Bergh-Weerman MA; Shinde AB; Ofman R; Poll-The BT; Houten SM; Baes M; Wanders RJA; Waterham HR
    Biochim Biophys Acta Mol Basis Dis; 2019 Oct; 1865(10):2774-2787. PubMed ID: 31207289
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Longitudinal study of Pex1-G844D NMRI mouse model: A robust pre-clinical model for mild Zellweger spectrum disorder.
    Demaret T; Roumain M; Ambroise J; Evraerts J; Ravau J; Bouzin C; Bearzatto B; Gala JL; Stepman H; Marie S; Vincent MF; Muccioli GG; Najimi M; Sokal EM
    Biochim Biophys Acta Mol Basis Dis; 2020 Nov; 1866(11):165900. PubMed ID: 32693164
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Inhibition of BRD4 Promotes Pexophagy by Increasing ROS and ATM Activation.
    Kim YH; Jo DS; Park NY; Bae JE; Kim JB; Lee HJ; Kim SH; Kim SH; Lee S; Son M; Park K; Jeong K; Yeom E; Cho DH
    Cells; 2022 Sep; 11(18):. PubMed ID: 36139416
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Silencing PEX26 as an unconventional mode to kill drug-resistant cancer cells and forestall drug resistance.
    Dahabieh MS; Huang F; Goncalves C; Flores González RE; Prabhu S; Bolt A; Di Pietro E; Khoury E; Heath J; Xu ZY; Rémy-Sarrazin J; Mann KK; Orthwein A; Boisvert FM; Braverman N; Miller WH; Del Rincón SV
    Autophagy; 2022 Mar; 18(3):540-558. PubMed ID: 34074205
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Isoform-specific domain organization determines conformation and function of the peroxisomal biogenesis factor PEX26.
    Guder P; Lotz-Havla AS; Woidy M; Reiß DD; Danecka MK; Schatz UA; Becker M; Ensenauer R; Pagel P; Büttner L; Muntau AC; Gersting SW
    Biochim Biophys Acta Mol Cell Res; 2019 Mar; 1866(3):518-531. PubMed ID: 30366024
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Catalase inhibition induces pexophagy through ROS accumulation.
    Lee JN; Dutta RK; Maharjan Y; Liu ZQ; Lim JY; Kim SJ; Cho DH; So HS; Choe SK; Park R
    Biochem Biophys Res Commun; 2018 Jun; 501(3):696-702. PubMed ID: 29753736
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A facile forward-genetic screen for Arabidopsis autophagy mutants reveals twenty-one loss-of-function mutations disrupting six ATG genes.
    Young PG; Passalacqua MJ; Chappell K; Llinas RJ; Bartel B
    Autophagy; 2019 Jun; 15(6):941-959. PubMed ID: 30734619
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.
    Tamura S; Matsumoto N; Imamura A; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
    Biochem J; 2001 Jul; 357(Pt 2):417-26. PubMed ID: 11439091
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Yeast pex1 cells contain peroxisomal ghosts that import matrix proteins upon reintroduction of Pex1.
    Knoops K; de Boer R; Kram A; van der Klei IJ
    J Cell Biol; 2015 Dec; 211(5):955-62. PubMed ID: 26644511
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.