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 *

165 related articles for article (PubMed ID: 30094183)

  • 1. Expanding the spectrum of
    Kumar KR; Wali G; Davis RL; Mallawaarachchi AC; Palmer EE; Gayevskiy V; Minoche AE; Veivers D; Dinger ME; Mackay-Sim A; Cowley MJ; Sue CM
    Mol Genet Metab Rep; 2018 Sep; 16():46-51. PubMed ID: 30094183
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical, neuroradiological, and molecular characterization of patients with atypical Zellweger spectrum disorder caused by PEX16 mutations: a case series.
    Cheung A; Argyriou C; Yergeau C; D'Souza Y; Riou É; Lévesque S; Raymond G; Daba M; Rtskhiladze I; Tkemaladze T; Adang L; La Piana R; Bernard G; Braverman N
    Neurogenetics; 2022 Apr; 23(2):115-127. PubMed ID: 35106698
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Drosophila carrying pex3 or pex16 mutations are models of Zellweger syndrome that reflect its symptoms associated with the absence of peroxisomes.
    Nakayama M; Sato H; Okuda T; Fujisawa N; Kono N; Arai H; Suzuki E; Umeda M; Ishikawa HO; Matsuno K
    PLoS One; 2011; 6(8):e22984. PubMed ID: 21826223
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Atypical PEX16 peroxisome biogenesis disorder with mild biochemical disruptions and long survival.
    Zaabi NA; Kendi A; Al-Jasmi F; Takashima S; Shimozawa N; Al-Dirbashi OY
    Brain Dev; 2019 Jan; 41(1):57-65. PubMed ID: 30078639
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of an unusual variant peroxisome biogenesis disorder caused by mutations in the PEX16 gene.
    Ebberink MS; Csanyi B; Chong WK; Denis S; Sharp P; Mooijer PA; Dekker CJ; Spooner C; Ngu LH; De Sousa C; Wanders RJ; Fietz MJ; Clayton PT; Waterham HR; Ferdinandusse S
    J Med Genet; 2010 Sep; 47(9):608-15. PubMed ID: 20647552
    [TBL] [Abstract][Full Text] [Related]  

  • 6. PEX16 contributions to peroxisome import and metabolism revealed by viable Arabidopsis pex16 mutants.
    Burkhart SE; Llinas RJ; Bartel B
    J Integr Plant Biol; 2019 Jul; 61(7):853-870. PubMed ID: 30761735
    [TBL] [Abstract][Full Text] [Related]  

  • 7. PEX16: a multifaceted regulator of peroxisome biogenesis.
    Kim PK; Mullen RT
    Front Physiol; 2013 Sep; 4():241. PubMed ID: 24027535
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Critical role of the peroxisomal protein PEX16 in white adipocyte development and lipid homeostasis.
    Hofer DC; Pessentheiner AR; Pelzmann HJ; Schlager S; Madreiter-Sokolowski CT; Kolb D; Eichmann TO; Rechberger G; Bilban M; Graier WF; Kratky D; Bogner-Strauss JG
    Biochim Biophys Acta Mol Cell Biol Lipids; 2017 Mar; 1862(3):358-368. PubMed ID: 28017862
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. De novo formation and maintenance of mammalian peroxisomes in cultured PEX16-knockout cells generated by CRISPR/Cas9.
    Yagita Y; Abe Y; Fujiki Y
    J Cell Sci; 2022 May; 135(9):. PubMed ID: 35437598
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Induced pluripotent stem cell models of Zellweger spectrum disorder show impaired peroxisome assembly and cell type-specific lipid abnormalities.
    Wang XM; Yik WY; Zhang P; Lu W; Huang N; Kim BR; Shibata D; Zitting M; Chow RH; Moser AB; Steinberg SJ; Hacia JG
    Stem Cell Res Ther; 2015 Aug; 6():158. PubMed ID: 26319495
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.
    Honsho M; Tamura S; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
    Am J Hum Genet; 1998 Dec; 63(6):1622-30. PubMed ID: 9837814
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Chinese patients with adrenoleukodystrophy and Zellweger spectrum disorder presenting with hereditary spastic paraplegia.
    Chen YJ; Wang MW; Dong EL; Lin XH; Wang N; Zhang ZQ; Lin X; Chen WJ
    Parkinsonism Relat Disord; 2019 Aug; 65():256-260. PubMed ID: 31227335
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mechanism of impaired microtubule-dependent peroxisome trafficking and oxidative stress in SPAST-mutated cells from patients with Hereditary Spastic Paraplegia.
    Wali G; Sutharsan R; Fan Y; Stewart R; Tello Velasquez J; Sue CM; Crane DI; Mackay-Sim A
    Sci Rep; 2016 May; 6():27004. PubMed ID: 27229699
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular insights into peroxisome homeostasis and peroxisome biogenesis disorders.
    Fujiki Y; Okumoto K; Honsho M; Abe Y
    Biochim Biophys Acta Mol Cell Res; 2022 Nov; 1869(11):119330. PubMed ID: 35917894
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cellular and molecular aspects of Zellweger syndrome and other peroxisome biogenesis disorders.
    Brosius U; Gärtner J
    Cell Mol Life Sci; 2002 Jun; 59(6):1058-69. PubMed ID: 12169017
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Functional classification of Arabidopsis peroxisome biogenesis factors proposed from analyses of knockdown mutants.
    Nito K; Kamigaki A; Kondo M; Hayashi M; Nishimura M
    Plant Cell Physiol; 2007 Jun; 48(6):763-74. PubMed ID: 17478547
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Peroxisome biogenesis disorders: molecular basis for impaired peroxisomal membrane assembly: in metabolic functions and biogenesis of peroxisomes in health and disease.
    Fujiki Y; Yagita Y; Matsuzaki T
    Biochim Biophys Acta; 2012 Sep; 1822(9):1337-42. PubMed ID: 22705440
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Expanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxia.
    Renaud M; Guissart C; Mallaret M; Ferdinandusse S; Cheillan D; Drouot N; Muller J; Claustres M; Tranchant C; Anheim M; Koenig M
    J Neurol; 2016 Aug; 263(8):1552-8. PubMed ID: 27230853
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Multiple Domains in PEX16 Mediate Its Trafficking and Recruitment of Peroxisomal Proteins to the ER.
    Hua R; Gidda SK; Aranovich A; Mullen RT; Kim PK
    Traffic; 2015 Aug; 16(8):832-52. PubMed ID: 25903784
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.