Baes M - Search Results

1

Neuronal migration disorder in Zellweger mice is secondary to glutamate receptor dysfunction.

Gressens P, Baes M, Leroux P, Lombet A, Van Veldhoven P, Janssen A, Vamecq J, Marret S, Evrard P. Gressens P, et al. Among authors: baes m. Ann Neurol. 2000 Sep;48(3):336-43. Ann Neurol. 2000. PMID: 10976640

2

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. Baes M, et al. Nat Genet. 1997 Sep;17(1):49-57. doi: 10.1038/ng0997-49. Nat Genet. 1997. PMID: 9288097

3

Docosahexaenoic acid deficit is not a major pathogenic factor in peroxisome-deficient mice.

Janssen A, Baes M, Gressens P, Mannaerts GP, Declercq P, Van Veldhoven PP. Janssen A, et al. Among authors: baes m. Lab Invest. 2000 Jan;80(1):31-5. doi: 10.1038/labinvest.3780005. Lab Invest. 2000. PMID: 10653000 Free article.

4

Do sphingoid bases interact with the peroxisome proliferator activated receptor alpha (PPAR-alpha)?

Van Veldhoven PP, Mannaerts GP, Declercq P, Baes M. Van Veldhoven PP, et al. Among authors: baes m. Cell Signal. 2000 Jul;12(7):475-9. doi: 10.1016/s0898-6568(00)00092-9. Cell Signal. 2000. PMID: 10989283

5

Prenatal and postnatal development of peroxisomal lipid-metabolizing pathways in the mouse.

Huyghe S, Casteels M, Janssen A, Meulders L, Mannaerts GP, Declercq PE, Van Veldhoven PP, Baes M. Huyghe S, et al. Among authors: baes m. Biochem J. 2001 Feb 1;353(Pt 3):673-80. doi: 10.1042/0264-6021:3530673. Biochem J. 2001. PMID: 11171065 Free PMC article.

6

Further insights into peroxisomal lipid breakdown via alpha- and beta-oxidation.

Van Veldhoven PP, Casteels M, Mannaerts GP, Baes M. Van Veldhoven PP, et al. Among authors: baes m. Biochem Soc Trans. 2001 May;29(Pt 2):292-8. doi: 10.1042/0300-5127:0290292. Biochem Soc Trans. 2001. PMID: 11356170

7

The neuronal migration defect in mice with Zellweger syndrome (Pex5 knockout) is not caused by the inactivity of peroxisomal beta-oxidation.

Baes M, Gressens P, Huyghe S, De NK, Qi C, Jia Y, Mannaerts GP, Evrard P, Van VP, Declercq PE, Reddy JK. Baes M, et al. J Neuropathol Exp Neurol. 2002 Apr;61(4):368-74. doi: 10.1093/jnen/61.4.368. J Neuropathol Exp Neurol. 2002. PMID: 11939592

8

Impaired neuronal migration and endochondral ossification in Pex7 knockout mice: a model for rhizomelic chondrodysplasia punctata.

Brites P, Motley AM, Gressens P, Mooyer PA, Ploegaert I, Everts V, Evrard P, Carmeliet P, Dewerchin M, Schoonjans L, Duran M, Waterham HR, Wanders RJ, Baes M. Brites P, et al. Among authors: baes m. Hum Mol Genet. 2003 Sep 15;12(18):2255-67. doi: 10.1093/hmg/ddg236. Epub 2003 Jul 15. Hum Mol Genet. 2003. PMID: 12915479

9

Neuronal migration depends on intact peroxisomal function in brain and in extraneuronal tissues.

Janssen A, Gressens P, Grabenbauer M, Baumgart E, Schad A, Vanhorebeek I, Brouwers A, Declercq PE, Fahimi D, Evrard P, Schoonjans L, Collen D, Carmeliet P, Mannaerts G, Van Veldhoven P, Baes M. Janssen A, et al. Among authors: baes m. J Neurosci. 2003 Oct 29;23(30):9732-41. doi: 10.1523/JNEUROSCI.23-30-09732.2003. J Neurosci. 2003. PMID: 14586000 Free PMC article.

10

Lessons from knockout mice. I: Phenotypes of mice with peroxisome biogenesis disorders.

Baes M, Van Veldhoven PP. Baes M, et al. Adv Exp Med Biol. 2003;544:113-22. doi: 10.1007/978-1-4419-9072-3_16. Adv Exp Med Biol. 2003. PMID: 14713222 Review. No abstract available.

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