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Results: 1 to 20 of 169

1.

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. doi: 10.1016/j.biocel.2013.06.019. Epub 2013 Jul 2. Review.

PMID:
23830890
[PubMed - indexed for MEDLINE]
2.

Peroxisome biogenesis disorders: Biological, clinical and pathophysiological perspectives.

Braverman NE, D'Agostino MD, Maclean GE.

Dev Disabil Res Rev. 2013 Jun;17(3):187-96. doi: 10.1002/ddrr.1113. Review.

PMID:
23798008
[PubMed - indexed for MEDLINE]
3.

Child neurology: Zellweger syndrome.

Lee PR, Raymond GV.

Neurology. 2013 May 14;80(20):e207-10. doi: 10.1212/WNL.0b013e3182929f8e. Review.

PMID:
23671347
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Peroxisomal disorders.

Aubourg P, Wanders R.

Handb Clin Neurol. 2013;113:1593-609. doi: 10.1016/B978-0-444-59565-2.00028-9. Review.

PMID:
23622381
[PubMed - indexed for MEDLINE]
5.

Neonatal adrenoleukodystrophy: a clinical, pathologic, and biochemical study.

Farrell DF.

Pediatr Neurol. 2012 Nov;47(5):330-6. doi: 10.1016/j.pediatrneurol.2012.07.006. Review.

PMID:
23044013
[PubMed - indexed for MEDLINE]
6.

Genetics and molecular basis of human peroxisome biogenesis disorders.

Waterham HR, Ebberink MS.

Biochim Biophys Acta. 2012 Sep;1822(9):1430-41. doi: 10.1016/j.bbadis.2012.04.006. Epub 2012 Apr 25. Review.

PMID:
22871920
[PubMed - indexed for MEDLINE]
Free Article
7.

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. doi: 10.1016/j.bbadis.2012.06.004. Epub 2012 Jun 13. Review.

PMID:
22705440
[PubMed - indexed for MEDLINE]
Free Article
8.

Peroxisomal leukoencephalopathy.

Poll-The BT, Engelen M.

Semin Neurol. 2012 Feb;32(1):42-50. doi: 10.1055/s-0032-1306385. Epub 2012 Mar 15. Review.

PMID:
22422205
[PubMed - indexed for MEDLINE]
9.

New insights into dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p in shuttling of PTS1-receptor Pex5p during peroxisome biogenesis.

Fujiki Y, Nashiro C, Miyata N, Tamura S, Okumoto K.

Biochim Biophys Acta. 2012 Jan;1823(1):145-9. doi: 10.1016/j.bbamcr.2011.10.012. Epub 2011 Nov 4. Review.

PMID:
22079764
[PubMed - indexed for MEDLINE]
Free Article
10.

[Why do not all smokers stop smoking?].

Zellweger JP.

Ther Umsch. 2010 Aug;67(8):399-402. doi: 10.1024/0040-5930/a000070. Review. German.

PMID:
20687041
[PubMed - indexed for MEDLINE]
11.

Zellweger syndrome with unusual findings: non-immune hydrops fetalis, dermal erythropoiesis and hypoplastic toe nails.

Dursun A, Gucer S, Ebberink MS, Yigit S, Wanders RJ, Waterham HR.

J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S345-8. doi: 10.1007/s10545-009-9010-0. Epub 2009 Dec 23. Review.

PMID:
20033294
[PubMed - indexed for MEDLINE]
12.

Lipid oxidation and peroxidation in CNS health and disease: from molecular mechanisms to therapeutic opportunities.

Adibhatla RM, Hatcher JF.

Antioxid Redox Signal. 2010 Jan;12(1):125-69. doi: 10.1089/ARS.2009.2668. Review. Erratum in: Antioxid Redox Signal. 2010 Feb;12(2):321. Khanna, Savita [removed];Kulkarni, Shrinivas K [removed]; Maher, Pamela [removed]; Mancuso, Cesare [removed]; Rapoport, Stanley I [removed]; Smith, Mark [removed]; Thomas, Bobby [removed]; Yagami, Tatsurou [removed].

PMID:
19624272
[PubMed - indexed for MEDLINE]
13.

[Outpatient diagnosis of coronary artery disease].

Abbuehl H, Zellweger MJ, Hoffmann A.

Ther Umsch. 2009 Apr;66(4):231-40. doi: 10.1024/0040-5930.66.4.231. Review. German.

PMID:
19358134
[PubMed - indexed for MEDLINE]
14.

Mechanisms of disease: Inborn errors of bile acid synthesis.

Sundaram SS, Bove KE, Lovell MA, Sokol RJ.

Nat Clin Pract Gastroenterol Hepatol. 2008 Aug;5(8):456-68. doi: 10.1038/ncpgasthep1179. Epub 2008 Jun 24. Review.

PMID:
18577977
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p involved in shuttling of the PTS1 receptor Pex5p in peroxisome biogenesis.

Fujiki Y, Miyata N, Matsumoto N, Tamura S.

Biochem Soc Trans. 2008 Feb;36(Pt 1):109-13. doi: 10.1042/BST0360109. Review.

PMID:
18208396
[PubMed - indexed for MEDLINE]
16.

Drug delivery to peroxisomes: employing unique trafficking mechanisms to target protein therapeutics.

Terlecky SR, Koepke JI.

Adv Drug Deliv Rev. 2007 Aug 10;59(8):739-47. Epub 2007 Jun 28. Review.

PMID:
17659806
[PubMed - indexed for MEDLINE]
17.

[Pathogenic gene in an inherited peroxisome disorder and its cellular dysfunction].

Tamura S.

Seikagaku. 2007 Apr;79(4):329-39. Review. Japanese. No abstract available.

PMID:
17511251
[PubMed - indexed for MEDLINE]
18.

Peroxisome biogenesis disorders.

Steinberg SJ, Dodt G, Raymond GV, Braverman NE, Moser AB, Moser HW.

Biochim Biophys Acta. 2006 Dec;1763(12):1733-48. Epub 2006 Sep 14. Review.

PMID:
17055079
[PubMed - indexed for MEDLINE]
Free Article
19.

Generalised and conditional inactivation of Pex genes in mice.

Baes M, Van Veldhoven PP.

Biochim Biophys Acta. 2006 Dec;1763(12):1785-93. Epub 2006 Aug 25. Review.

PMID:
17007945
[PubMed - indexed for MEDLINE]
Free Article
20.

Identification of diffuse and focal brain lesions by clinical magnetic resonance spectroscopy.

Kingsley PB, Shah TC, Woldenberg R.

NMR Biomed. 2006 Jun;19(4):435-62. Review.

PMID:
16763970
[PubMed - indexed for MEDLINE]

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