Baas F - Search Results

1

Long-term survival and transmission of INI1-mutation via nonpenetrant males in a family with rhabdoid tumour predisposition syndrome.

Ammerlaan AC, Ararou A, Houben MP, Baas F, Tijssen CC, Teepen JL, Wesseling P, Hulsebos TJ. Ammerlaan AC, et al. Among authors: baas f. Br J Cancer. 2008 Jan 29;98(2):474-9. doi: 10.1038/sj.bjc.6604156. Epub 2007 Dec 18. Br J Cancer. 2008. PMID: 18087273 Free PMC article.

2

Germline mutation of INI1/SMARCB1 in familial schwannomatosis.

Hulsebos TJ, Plomp AS, Wolterman RA, Robanus-Maandag EC, Baas F, Wesseling P. Hulsebos TJ, et al. Among authors: baas f. Am J Hum Genet. 2007 Apr;80(4):805-10. doi: 10.1086/513207. Epub 2007 Feb 16. Am J Hum Genet. 2007. PMID: 17357086 Free PMC article.

3

SMARCB1/INI1 maternal germ line mosaicism in schwannomatosis.

Hulsebos TJ, Kenter SB, Jakobs ME, Baas F, Chong B, Delatycki MB. Hulsebos TJ, et al. Among authors: baas f. Clin Genet. 2010 Jan;77(1):86-91. doi: 10.1111/j.1399-0004.2009.01249.x. Epub 2009 Nov 3. Clin Genet. 2010. PMID: 19912265

4

Germline SMARCB1 mutation predisposes to multiple meningiomas and schwannomas with preferential location of cranial meningiomas at the falx cerebri.

van den Munckhof P, Christiaans I, Kenter SB, Baas F, Hulsebos TJ. van den Munckhof P, et al. Among authors: baas f. Neurogenetics. 2012 Feb;13(1):1-7. doi: 10.1007/s10048-011-0300-y. Epub 2011 Oct 26. Neurogenetics. 2012. PMID: 22038540

5

Premature termination of SMARCB1 translation may be followed by reinitiation in schwannomatosis-associated schwannomas, but results in absence of SMARCB1 expression in rhabdoid tumors.

Hulsebos TJ, Kenter S, Verhagen WI, Baas F, Flucke U, Wesseling P. Hulsebos TJ, et al. Among authors: baas f. Acta Neuropathol. 2014 Sep;128(3):439-48. doi: 10.1007/s00401-014-1281-3. Epub 2014 Apr 17. Acta Neuropathol. 2014. PMID: 24740647

6

Type 1 papillary renal cell carcinoma in a patient with schwannomatosis: Mosaic versus loss of SMARCB1 expression in respectively schwannoma and renal tumor cells.

Hulsebos TJ, Kenter S, Baas F, Nannenberg EA, Bleeker FE, van Minkelen R, van den Ouweland AM, Wesseling P, Flucke U. Hulsebos TJ, et al. Among authors: baas f. Genes Chromosomes Cancer. 2016 Apr;55(4):350-4. doi: 10.1002/gcc.22338. Epub 2016 Jan 22. Genes Chromosomes Cancer. 2016. PMID: 26799435

7

Distal myoclonus and late onset in a large Dutch family with myoclonus-dystonia.

Foncke EM, Gerrits MC, van Ruissen F, Baas F, Hedrich K, Tijssen CC, Klein C, Tijssen MA. Foncke EM, et al. Among authors: baas f. Neurology. 2006 Nov 14;67(9):1677-80. doi: 10.1212/01.wnl.0000242880.49051.1f. Neurology. 2006. PMID: 17101905

8

Germline SMARCB1 mutation and somatic NF2 mutations in familial multiple meningiomas.

Christiaans I, Kenter SB, Brink HC, van Os TA, Baas F, van den Munckhof P, Kidd AM, Hulsebos TJ. Christiaans I, et al. Among authors: baas f. J Med Genet. 2011 Feb;48(2):93-7. doi: 10.1136/jmg.2010.082420. Epub 2010 Oct 7. J Med Genet. 2011. PMID: 20930055

9

Identification of novel candidate oncogenes in chromosome region 17p11.2-p12 in human osteosarcoma.

Both J, Wu T, Bras J, Schaap GR, Baas F, Hulsebos TJ. Both J, et al. Among authors: baas f. PLoS One. 2012;7(1):e30907. doi: 10.1371/journal.pone.0030907. Epub 2012 Jan 26. PLoS One. 2012. PMID: 22292074 Free PMC article.

10

Oncogenic Properties of Candidate Oncogenes in Chromosome Region 17p11.2p12 in Human Osteosarcoma.

Both J, Wu T, Ten Asbroek AL, Baas F, Hulsebos TJ. Both J, et al. Among authors: baas f. Cytogenet Genome Res. 2016;150(1):52-59. doi: 10.1159/000451046. Epub 2016 Nov 16. Cytogenet Genome Res. 2016. PMID: 27846620

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