BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

101 related articles for article (PubMed ID: 24881576)

  • 21. Severe Zellweger spectrum disorder due to a novel missense variant in the PEX13 gene: A case report and the literature review.
    Su L; Peng MZ; Chen XD; Wu S; Liu L
    Mol Genet Genomic Med; 2024 Jan; 12(1):e2315. PubMed ID: 37962062
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A mouse model for Zellweger syndrome.
    Baes M; Gressens P; Baumgart E; Carmeliet P; Casteels M; Fransen M; Evrard P; Fahimi D; Declercq PE; Collen D; van Veldhoven PP; Mannaerts GP
    Nat Genet; 1997 Sep; 17(1):49-57. PubMed ID: 9288097
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Pex13, the mouse ortholog of the human peroxisome biogenesis disorder PEX13 gene: gene structure, tissue expression, and localization of the protein to peroxisomes.
    Björkman J; Gould SJ; Crane DI
    Genomics; 2002 Feb; 79(2):162-8. PubMed ID: 11829486
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Targeted deletion of the PEX2 peroxisome assembly gene in mice provides a model for Zellweger syndrome, a human neuronal migration disorder.
    Faust PL; Hatten ME
    J Cell Biol; 1997 Dec; 139(5):1293-305. PubMed ID: 9382874
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Structural basis for serotonergic regulation of neural circuits in the mouse olfactory bulb.
    Suzuki Y; Kiyokage E; Sohn J; Hioki H; Toida K
    J Comp Neurol; 2015 Feb; 523(2):262-80. PubMed ID: 25234191
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Zellweger syndrome knockout mouse models challenge putative peroxisomal beta-oxidation involvement in docosahexaenoic acid (22:6n-3) biosynthesis.
    Infante JP; Huszagh VA
    Mol Genet Metab; 2001 Jan; 72(1):1-7. PubMed ID: 11161822
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Recognition of Zellweger syndrome in infancy.
    Grayer J
    Adv Neonatal Care; 2005 Feb; 5(1):5-13. PubMed ID: 15685158
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Peroxisome biogenesis disorders: the role of peroxisomes and metabolic dysfunction in developing brain.
    Faust PL; Banka D; Siriratsivawong R; Ng VG; Wikander TM
    J Inherit Metab Dis; 2005; 28(3):369-83. PubMed ID: 15868469
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Pex3p-dependent peroxisomal biogenesis initiates in the endoplasmic reticulum of human fibroblasts.
    Toro AA; Araya CA; Córdova GJ; Arredondo CA; Cárdenas HG; Moreno RE; Venegas A; Koenig CS; Cancino J; Gonzalez A; Santos MJ
    J Cell Biochem; 2009 Aug; 107(6):1083-96. PubMed ID: 19479899
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mass spectrometric analysis of ceramide perturbations in brain and fibroblasts of mice and human patients with peroxisomal disorders.
    Pettus BJ; Baes M; Busman M; Hannun YA; Van Veldhoven PP
    Rapid Commun Mass Spectrom; 2004; 18(14):1569-74. PubMed ID: 15282781
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The Arabidopsis pex12 and pex13 mutants are defective in both PTS1- and PTS2-dependent protein transport to peroxisomes.
    Mano S; Nakamori C; Nito K; Kondo M; Nishimura M
    Plant J; 2006 Aug; 47(4):604-18. PubMed ID: 16813573
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Peroxisomes: the neuropathological consequences of peroxisomal dysfunction in the developing brain.
    Barry DS; O'Keeffe GW
    Int J Biochem Cell Biol; 2013 Sep; 45(9):2012-5. PubMed ID: 23830890
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Effect of sex steroid hormones on the number of serotonergic neurons in rat dorsal raphe nucleus.
    Kunimura Y; Iwata K; Iijima N; Kobayashi M; Ozawa H
    Neurosci Lett; 2015 May; 594():127-32. PubMed ID: 25827489
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Zellweger syndrome and associated brain malformations: report of a novel Peroxin1 (PEX1) mutation in a Native American infant.
    Mohebbi MR; Rush ET; Rizzo WB; Banagale RC
    J Child Neurol; 2012 Dec; 27(12):1589-92. PubMed ID: 22378672
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Neocortical and cerebellar developmental abnormalities in conditions of selective elimination of peroxisomes from brain or from liver.
    Krysko O; Hulshagen L; Janssen A; Schütz G; Klein R; De Bruycker M; Espeel M; Gressens P; Baes M
    J Neurosci Res; 2007 Jan; 85(1):58-72. PubMed ID: 17075904
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Brain-specific conditional and time-specific inducible Tph2 knockout mice possess normal serotonergic gene expression in the absence of serotonin during adult life.
    Kriegebaum C; Song NN; Gutknecht L; Huang Y; Schmitt A; Reif A; Ding YQ; Lesch KP
    Neurochem Int; 2010 Nov; 57(5):512-7. PubMed ID: 20599453
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Overwhelming sepsis in a neonate affected by Zellweger syndrome due to a compound heterozygosis in PEX 6 gene: a case report.
    Lucaccioni L; Righi B; Cingolani GM; Lugli L; Della Casa E; Torcetta F; Iughetti L; Berardi A
    BMC Med Genet; 2020 Nov; 21(1):229. PubMed ID: 33213396
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Presence of peroxisomal membrane proteins in liver and fibroblasts from patients with the Zellweger syndrome and related disorders: evidence for the existence of peroxisomal ghosts.
    Wiemer EA; Brul S; Just WW; Van Driel R; Brouwer-Kelder E; Van Den Berg M; Weijers PJ; Schutgens RB; Van Den Bosch H; Schram A
    Eur J Cell Biol; 1989 Dec; 50(2):407-17. PubMed ID: 2697558
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Identification of a novel PEX14 mutation in Zellweger syndrome.
    Huybrechts SJ; Van Veldhoven PP; Hoffman I; Zeevaert R; de Vos R; Demaerel P; Brams M; Jaeken J; Fransen M; Cassiman D
    J Med Genet; 2008 Jun; 45(6):376-83. PubMed ID: 18285423
    [TBL] [Abstract][Full Text] [Related]  

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