Oudejans CB - Search Results

1

Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matter.

van der Knaap MS, Leegwater PA, Könst AA, Visser A, Naidu S, Oudejans CB, Schutgens RB, Pronk JC. van der Knaap MS, et al. Among authors: oudejans cb. Ann Neurol. 2002 Feb;51(2):264-70. doi: 10.1002/ana.10112. Ann Neurol. 2002. PMID: 11835386

2

Identification of novel mutations in MLC1 responsible for megalencephalic leukoencephalopathy with subcortical cysts.

Leegwater PA, Boor PK, Yuan BQ, van der Steen J, Visser A, Könst AA, Oudejans CB, Schutgens RB, Pronk JC, van der Knaap MS. Leegwater PA, et al. Among authors: oudejans cb. Hum Genet. 2002 Mar;110(3):279-83. doi: 10.1007/s00439-002-0682-x. Epub 2002 Feb 8. Hum Genet. 2002. PMID: 11935341

3

Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter.

Leegwater PA, Vermeulen G, Könst AA, Naidu S, Mulders J, Visser A, Kersbergen P, Mobach D, Fonds D, van Berkel CG, Lemmers RJ, Frants RR, Oudejans CB, Schutgens RB, Pronk JC, van der Knaap MS. Leegwater PA, et al. Among authors: oudejans cb. Nat Genet. 2001 Dec;29(4):383-8. doi: 10.1038/ng764. Nat Genet. 2001. PMID: 11704758

4

The gene for leukoencephalopathy with vanishing white matter is located on chromosome 3q27.

Leegwater PA, Könst AA, Kuyt B, Sandkuijl LA, Naidu S, Oudejans CB, Schutgens RB, Pronk JC, van der Knaap MS. Leegwater PA, et al. Among authors: oudejans cb. Am J Hum Genet. 1999 Sep;65(3):728-34. doi: 10.1086/302548. Am J Hum Genet. 1999. PMID: 10441579 Free PMC article.

5

Mutations of MLC1 (KIAA0027), encoding a putative membrane protein, cause megalencephalic leukoencephalopathy with subcortical cysts.

Leegwater PA, Yuan BQ, van der Steen J, Mulders J, Könst AA, Boor PK, Mejaski-Bosnjak V, van der Maarel SM, Frants RR, Oudejans CB, Schutgens RB, Pronk JC, van der Knaap MS. Leegwater PA, et al. Among authors: oudejans cb. Am J Hum Genet. 2001 Apr;68(4):831-8. doi: 10.1086/319519. Epub 2001 Mar 6. Am J Hum Genet. 2001. PMID: 11254442 Free PMC article.

6

MLC1: a novel protein in distal astroglial processes.

Boor PK, de Groot K, Waisfisz Q, Kamphorst W, Oudejans CB, Powers JM, Pronk JC, Scheper GC, van der Knaap MS. Boor PK, et al. Among authors: oudejans cb. J Neuropathol Exp Neurol. 2005 May;64(5):412-9. doi: 10.1093/jnen/64.5.412. J Neuropathol Exp Neurol. 2005. PMID: 15892299

7

Spontaneous MxA mRNA level predicts relapses in patients with recently diagnosed MS.

van der Voort LF, Vennegoor A, Visser A, Knol DL, Uitdehaag BM, Barkhof F, Oudejans CB, Polman CH, Killestein J. van der Voort LF, et al. Among authors: oudejans cb. Neurology. 2010 Oct 5;75(14):1228-33. doi: 10.1212/WNL.0b013e3181f6c556. Neurology. 2010. PMID: 20921509

8

Lack of interferon-beta bioactivity is associated with the occurrence of relapses in multiple sclerosis.

van der Voort LF, Visser A, Knol DL, Oudejans CB, Polman CH, Killestein J. van der Voort LF, et al. Among authors: oudejans cb. Eur J Neurol. 2009 Sep;16(9):1049-52. doi: 10.1111/j.1468-1331.2009.02649.x. Epub 2009 May 22. Eur J Neurol. 2009. PMID: 19486142

9

The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with down-regulated expression in androgenetic placentas.

Oudejans CB, Mulders J, Lachmeijer AM, van Dijk M, Könst AA, Westerman BA, van Wijk IJ, Leegwater PA, Kato HD, Matsuda T, Wake N, Dekker GA, Pals G, ten Kate LP, Blankenstein MA. Oudejans CB, et al. Mol Hum Reprod. 2004 Aug;10(8):589-98. doi: 10.1093/molehr/gah080. Epub 2004 Jun 18. Mol Hum Reprod. 2004. PMID: 15208369

10

Maternal segregation of the Dutch preeclampsia locus at 10q22 with a new member of the winged helix gene family.

van Dijk M, Mulders J, Poutsma A, Könst AA, Lachmeijer AM, Dekker GA, Blankenstein MA, Oudejans CB. van Dijk M, et al. Among authors: oudejans cb. Nat Genet. 2005 May;37(5):514-9. doi: 10.1038/ng1541. Epub 2005 Apr 3. Nat Genet. 2005. PMID: 15806103

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