Buys CH - Search Results

1

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

2

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

3

No mutations found by RET mutation scanning in sporadic and hereditary neuroblastoma.

Hofstra RM, Cheng NC, Hansen C, Stulp RP, Stelwagen T, Clausen N, Tommerup N, Caron H, Westerveld A, Versteeg R, Buys CH. Hofstra RM, et al. Among authors: buys ch. Hum Genet. 1996 Mar;97(3):362-4. doi: 10.1007/BF02185773. Hum Genet. 1996. PMID: 8786083

4

Involvement of multiple loci on chromosome 3 in renal cell cancer development.

van den Berg A, Buys CH. van den Berg A, et al. Among authors: buys ch. Genes Chromosomes Cancer. 1997 Jun;19(2):59-76. doi: 10.1002/(sici)1098-2264(199706)19:2<59::aid-gcc1>3.3.co;2-o. Genes Chromosomes Cancer. 1997. PMID: 9171996 Review.

5

Absence of mutations in the RET gene in acute myeloid leukemia.

Visser M, Hofstra RM, Stulp RP, Wu Y, Buys CH, Willemze R, Landegent JE. Visser M, et al. Among authors: buys ch. Ann Hematol. 1997 Sep;75(3):87-90. doi: 10.1007/s002770050319. Ann Hematol. 1997. PMID: 9368476

6

A novel point mutation in the intracellular domain of the ret protooncogene in a family with medullary thyroid carcinoma.

Hofstra RM, Fattoruso O, Quadro L, Wu Y, Libroia A, Verga U, Colantuoni V, Buys CH. Hofstra RM, et al. Among authors: buys ch. J Clin Endocrinol Metab. 1997 Dec;82(12):4176-8. doi: 10.1210/jcem.82.12.4439. J Clin Endocrinol Metab. 1997. PMID: 9398735

7

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

8

Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease.

Angrist M, Bolk S, Thiel B, Puffenberger EG, Hofstra RM, Buys CH, Cass DT, Chakravarti A. Angrist M, et al. Among authors: buys ch. Hum Mol Genet. 1995 May;4(5):821-30. doi: 10.1093/hmg/4.5.821. Hum Mol Genet. 1995. PMID: 7633441

9

A gene in the chromosomal region 3p21 with greatly reduced expression in lung cancer is similar to the gene for ubiquitin-activating enzyme.

Kok K, Hofstra R, Pilz A, van den Berg A, Terpstra P, Buys CH, Carritt B. Kok K, et al. Among authors: buys ch. Proc Natl Acad Sci U S A. 1993 Jul 1;90(13):6071-5. doi: 10.1073/pnas.90.13.6071. Proc Natl Acad Sci U S A. 1993. PMID: 8327486 Free PMC article.

10

A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome).

Hofstra RM, Osinga J, Tan-Sindhunata G, Wu Y, Kamsteeg EJ, Stulp RP, van Ravenswaaij-Arts C, Majoor-Krakauer D, Angrist M, Chakravarti A, Meijers C, Buys CH. Hofstra RM, et al. Among authors: buys ch. Nat Genet. 1996 Apr;12(4):445-7. doi: 10.1038/ng0496-445. Nat Genet. 1996. PMID: 8630503 Free article.

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