Devilee P - Search Results

1

Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.

Baysal BE, Ferrell RE, Willett-Brozick JE, Lawrence EC, Myssiorek D, Bosch A, van der Mey A, Taschner PE, Rubinstein WS, Myers EN, Richard CW 3rd, Cornelisse CJ, Devilee P, Devlin B. Baysal BE, et al. Among authors: devilee p. Science. 2000 Feb 4;287(5454):848-51. doi: 10.1126/science.287.5454.848. Science. 2000. PMID: 10657297

2

Repositioning the hereditary paraganglioma critical region on chromosome band 11q23.

Baysal BE, van Schothorst EM, Farr JE, Grashof P, Myssiorek D, Rubinstein WS, Taschner P, Cornelisse CJ, Devlin B, Devilee P, Richard CW 3rd. Baysal BE, et al. Among authors: devilee p. Hum Genet. 1999 Mar;104(3):219-25. doi: 10.1007/s004390050939. Hum Genet. 1999. PMID: 10323245

3

A high-resolution integrated map spanning the SDHD gene at 11q23: a 1.1-Mb BAC contig, a partial transcript map and 15 new repeat polymorphisms in a tumour-suppressor region.

Baysal BE, Willett-Brozick JE, Taschner PE, Dauwerse JG, Devilee P, Devlin B. Baysal BE, et al. Among authors: devilee p. Eur J Hum Genet. 2001 Feb;9(2):121-9. doi: 10.1038/sj.ejhg.5200585. Eur J Hum Genet. 2001. PMID: 11313745

4

Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families.

Hensen EF, Jordanova ES, van Minderhout IJ, Hogendoorn PC, Taschner PE, van der Mey AG, Devilee P, Cornelisse CJ. Hensen EF, et al. Among authors: devilee p. Oncogene. 2004 May 20;23(23):4076-83. doi: 10.1038/sj.onc.1207591. Oncogene. 2004. PMID: 15064708

5

A high-resolution STS, EST, and gene-based physical map of the hereditary paraganglioma region on chromosome 11q23.

Baysal BE, van Schothorst EM, Farr JE, James MR, Devilee P, Richard CW 3rd. Baysal BE, et al. Among authors: devilee p. Genomics. 1997 Sep 1;44(2):214-21. doi: 10.1006/geno.1997.4880. Genomics. 1997. PMID: 9299238

6

Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene.

Taschner PE, Jansen JC, Baysal BE, Bosch A, Rosenberg EH, Bröcker-Vriends AH, van Der Mey AG, van Ommen GJ, Cornelisse CJ, Devilee P. Taschner PE, et al. Among authors: devilee p. Genes Chromosomes Cancer. 2001 Jul;31(3):274-81. doi: 10.1002/gcc.1144. Genes Chromosomes Cancer. 2001. PMID: 11391798

7

The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency.

Bayley JP, Devilee P, Taschner PE. Bayley JP, et al. Among authors: devilee p. BMC Med Genet. 2005 Nov 16;6:39. doi: 10.1186/1471-2350-6-39. BMC Med Genet. 2005. PMID: 16288654 Free PMC article.

8

Mutations in SDHD are the major determinants of the clinical characteristics of Dutch head and neck paraganglioma patients.

Hensen EF, Siemers MD, Jansen JC, Corssmit EP, Romijn JA, Tops CM, van der Mey AG, Devilee P, Cornelisse CJ, Bayley JP, Vriends AH. Hensen EF, et al. Among authors: devilee p. Clin Endocrinol (Oxf). 2011 Nov;75(5):650-5. doi: 10.1111/j.1365-2265.2011.04097.x. Clin Endocrinol (Oxf). 2011. PMID: 21561462

9

Sdhd and SDHD/H19 knockout mice do not develop paraganglioma or pheochromocytoma.

Bayley JP, van Minderhout I, Hogendoorn PC, Cornelisse CJ, van der Wal A, Prins FA, Teppema L, Dahan A, Devilee P, Taschner PE. Bayley JP, et al. Among authors: devilee p. PLoS One. 2009 Nov 24;4(11):e7987. doi: 10.1371/journal.pone.0007987. PLoS One. 2009. PMID: 19956719 Free PMC article.

10

Confinement of PGL, an imprinted gene causing hereditary paragangliomas, to a 2-cM interval on 11q22-q23 and exclusion of DRD2 and NCAM as candidate genes.

van Schothorst EM, Jansen JC, Bardoel AF, van der Mey AG, James MJ, Sobol H, Weissenbach J, van Ommen GJ, Cornelisse CJ, Devilee P. van Schothorst EM, et al. Among authors: devilee p. Eur J Hum Genet. 1996;4(5):267-73. doi: 10.1159/000472213. Eur J Hum Genet. 1996. PMID: 8946172

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