Buys CH - Search Results

1

Localization of the nucleotide excision repair gene ERCC6 to human chromosome 10q11-q21.

Troelstra C, Landsvater RM, Wiegant J, van der Ploeg M, Viel G, Buys CH, Hoeijmakers JH. Troelstra C, et al. Among authors: buys ch. Genomics. 1992 Apr;12(4):745-9. doi: 10.1016/0888-7543(92)90304-b. Genomics. 1992. PMID: 1349298

2

Development of multiple endocrine neoplasia type 2A does not involve substantial deletions of chromosome 10.

Landsvater RM, Mathew CG, Smith BA, Marcus EM, te Meerman GJ, Lips CJ, Geerdink RA, Nakamura Y, Ponder BA, Buys CH. Landsvater RM, et al. Among authors: buys ch. Genomics. 1989 Apr;4(3):246-50. doi: 10.1016/0888-7543(89)90327-3. Genomics. 1989. PMID: 2565874

3

BclI RFLP for the human vimentin gene.

Marcus EM, Smith BA, Telenius H, Landsvater RM, Buys CH, Ferrari S, Ponder BA, Mathew CG. Marcus EM, et al. Among authors: buys ch. Nucleic Acids Res. 1988 Sep 26;16(18):9068. doi: 10.1093/nar/16.18.9068. Nucleic Acids Res. 1988. PMID: 2902569 Free PMC article. No abstract available.

4

Mutation analysis of the RET proto-oncogene in Dutch families with MEN 2A, MEN 2B and FMTC: two novel mutations and one de novo mutation for MEN 2A.

Landsvater RM, Jansen RP, Hofstra RM, Buys CH, Lips CJ, Ploos van Amstel HK. Landsvater RM, et al. Among authors: buys ch. Hum Genet. 1996 Jan;97(1):11-4. doi: 10.1007/BF00218825. Hum Genet. 1996. PMID: 8557249

5

Extensive mutation scanning of RET in sporadic medullary thyroid carcinoma and of RET and VHL in sporadic pheochromocytoma reveals involvement of these genes in only a minority of cases.

Hofstra RM, Stelwagen T, Stulp RP, de Jong D, Hulsbeek M, Kamsteeg EJ, van den Berg A, Landsvater RM, Vermey A, Molenaar WM, Lips CJ, Buys CH. Hofstra RM, et al. Among authors: buys ch. J Clin Endocrinol Metab. 1996 Aug;81(8):2881-4. doi: 10.1210/jcem.81.8.8768845. J Clin Endocrinol Metab. 1996. PMID: 8768845

6

The clinical implications of a positive calcitonin test for C-cell hyperplasia in genetically unaffected members of an MEN2A kindred.

Landsvater RM, Rombouts AG, te Meerman GJ, Schillhorn-van Veen JM, Berends MJ, Geerdink RA, Struyvenberg A, Buys CH, Lips CJ. Landsvater RM, et al. Among authors: buys ch. Am J Hum Genet. 1993 Feb;52(2):335-42. Am J Hum Genet. 1993. PMID: 8094268 Free PMC article.

7

Identification of key recombinants in multiplex SMA families.

van der Steege G, Cobben JM, Brahe C, Osinga J, Zappata S, Scheffer H, Neri G, van Ommen GJ, ten Kate LP, Buys CH. van der Steege G, et al. Among authors: buys ch. Genomics. 1994 Jul 1;22(1):219-22. doi: 10.1006/geno.1994.1367. Genomics. 1994. PMID: 7959774

8

Somatic mutations of the RET proto-oncogene are not required for tumor development in multiple endocrine neoplasia type 2 (MEN 2) gene carriers.

Landsvater RM, de Wit MJ, Zewald RA, Hofstra RM, Buys CH, Ploos van Amstel HK, Höppener JW, Lips CJ. Landsvater RM, et al. Among authors: buys ch. Cancer Res. 1996 Nov 1;56(21):4853-5. Cancer Res. 1996. PMID: 8895732

9

The region of common allelic losses in sporadic renal cell carcinoma is bordered by the loci D3S2 and THRB.

van der Hout AH, van der Vlies P, Wijmenga C, Li FP, Oosterhuis JW, Buys CH. van der Hout AH, et al. Among authors: buys ch. Genomics. 1991 Nov;11(3):537-42. doi: 10.1016/0888-7543(91)90060-r. Genomics. 1991. PMID: 1685475

10

An evolutionary rearrangement of the Xp11.3-11.23 region in 3p21.3, a region frequently deleted in a variety of cancers.

Timmer T, Terpstra P, van den Berg A, Veldhuis PM, Ter Elst A, van der Veen AY, Kok K, Naylor SL, Buys CH. Timmer T, et al. Among authors: buys ch. Genomics. 1999 Sep 1;60(2):238-40. doi: 10.1006/geno.1999.5878. Genomics. 1999. PMID: 10486216

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