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Journal Abstract Search

263 related items for PubMed ID: 22659211

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  • 5. Peripheral nervous system plasmalogens regulate Schwann cell differentiation and myelination.
    da Silva TF, Eira J, Lopes AT, Malheiro AR, Sousa V, Luoma A, Avila RL, Wanders RJ, Just WW, Kirschner DA, Sousa MM, Brites P.
    J Clin Invest; 2014 Jun; 124(6):2560-70. PubMed ID: 24762439
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  • 8. Oral administration of a synthetic vinyl-ether plasmalogen normalizes open field activity in a mouse model of rhizomelic chondrodysplasia punctata.
    Fallatah W, Smith T, Cui W, Jayasinghe D, Di Pietro E, Ritchie SA, Braverman N.
    Dis Model Mech; 2020 Jan 24; 13(1):. PubMed ID: 31862688
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  • 14. Rhizomelic chondrodysplasia punctata and cardiac pathology.
    Huffnagel IC, Clur SA, Bams-Mengerink AM, Blom NA, Wanders RJ, Waterham HR, Poll-The BT.
    J Med Genet; 2013 Jul 24; 50(7):419-24. PubMed ID: 23572185
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  • 16. Alkyl-glycerol rescues plasmalogen levels and pathology of ether-phospholipid deficient mice.
    Brites P, Ferreira AS, da Silva TF, Sousa VF, Malheiro AR, Duran M, Waterham HR, Baes M, Wanders RJ.
    PLoS One; 2011 Jul 24; 6(12):e28539. PubMed ID: 22163031
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  • 17. Expanding the genotypic and phenotypic landscapes of rhizomelic chondrodysplasia punctata type 3 (RCDP3) with two novel families, and a review of the literature.
    İli EG, Gezdirici A, Di Pietro E, Yergeau C, Braverman N.
    Am J Med Genet A; 2022 Nov 24; 188(11):3229-3235. PubMed ID: 35986576
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  • 18. Defective lipid remodeling of GPI anchors in peroxisomal disorders, Zellweger syndrome, and rhizomelic chondrodysplasia punctata.
    Kanzawa N, Shimozawa N, Wanders RJ, Ikeda K, Murakami Y, Waterham HR, Mukai S, Fujita M, Maeda Y, Taguchi R, Fujiki Y, Kinoshita T.
    J Lipid Res; 2012 Apr 24; 53(4):653-63. PubMed ID: 22253471
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  • 19. Peroxisome biogenesis disorders.
    Steinberg SJ, Dodt G, Raymond GV, Braverman NE, Moser AB, Moser HW.
    Biochim Biophys Acta; 2006 Dec 24; 1763(12):1733-48. PubMed ID: 17055079
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  • 20. Rhizomelic chondrodysplasia punctata, a peroxisomal biogenesis disorder caused by defects in Pex7p, a peroxisomal protein import receptor: a minireview.
    Purdue PE, Skoneczny M, Yang X, Zhang JW, Lazarow PB.
    Neurochem Res; 1999 Apr 24; 24(4):581-6. PubMed ID: 10227689
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