Eng C - Search Results

1

Germline PTEN mutations in Cowden syndrome-like families.

Marsh DJ, Dahia PL, Caron S, Kum JB, Frayling IM, Tomlinson IP, Hughes KS, Eeles RA, Hodgson SV, Murday VA, Houlston R, Eng C. Marsh DJ, et al. Among authors: eng c. J Med Genet. 1998 Nov;35(11):881-5. doi: 10.1136/jmg.35.11.881. J Med Genet. 1998. PMID: 9832031 Free PMC article.

2

Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogene.

Mulligan LM, Eng C, Attié T, Lyonnet S, Marsh DJ, Hyland VJ, Robinson BG, Frilling A, Verellen-Dumoulin C, Safar A, et al. Mulligan LM, et al. Among authors: eng c. Hum Mol Genet. 1994 Dec;3(12):2163-7. doi: 10.1093/hmg/3.12.2163. Hum Mol Genet. 1994. PMID: 7881414

3

Familial cancer syndromes.

Eng C, Stratton M, Ponder B, Murday V, Easton D, Sacks N, Watson M, Eeles R. Eng C, et al. Lancet. 1994 Mar 19;343(8899):709-13. doi: 10.1016/s0140-6736(94)91585-7. Lancet. 1994. PMID: 7907684 No abstract available.

4

Cowden syndrome and Lhermitte-Duclos disease in a family: a single genetic syndrome with pleiotropy?

Eng C, Murday V, Seal S, Mohammed S, Hodgson SV, Chaudary MA, Fentiman IS, Ponder BA, Eeles RA. Eng C, et al. J Med Genet. 1994 Jun;31(6):458-61. doi: 10.1136/jmg.31.6.458. J Med Genet. 1994. PMID: 8071972 Free PMC article.

5

Germline and somatic mutations in an oncogene: RET mutations in inherited medullary thyroid carcinoma.

Marsh DJ, Andrew SD, Eng C, Learoyd DL, Capes AG, Pojer R, Richardson AL, Houghton C, Mulligan LM, Ponder BA, Robinson BG. Marsh DJ, et al. Among authors: eng c. Cancer Res. 1996 Mar 15;56(6):1241-3. Cancer Res. 1996. PMID: 8640806

6

Localization of the gene for Cowden disease to chromosome 10q22-23.

Nelen MR, Padberg GW, Peeters EA, Lin AY, van den Helm B, Frants RR, Coulon V, Goldstein AM, van Reen MM, Easton DF, Eeles RA, Hodgsen S, Mulvihill JJ, Murday VA, Tucker MA, Mariman EC, Starink TM, Ponder BA, Ropers HH, Kremer H, Longy M, Eng C. Nelen MR, et al. Among authors: eng c. Nat Genet. 1996 May;13(1):114-6. doi: 10.1038/ng0596-114. Nat Genet. 1996. PMID: 8673088 Free article.

7

Somatic mutations in the RET proto-oncogene in sporadic medullary thyroid carcinoma.

Marsh DJ, Learoyd DL, Andrew SD, Krishnan L, Pojer R, Richardson AL, Delbridge L, Eng C, Robinson BG. Marsh DJ, et al. Among authors: eng c. Clin Endocrinol (Oxf). 1996 Mar;44(3):249-57. doi: 10.1046/j.1365-2265.1996.681503.x. Clin Endocrinol (Oxf). 1996. PMID: 8729519

8

Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas.

Eng C, Crossey PA, Mulligan LM, Healey CS, Houghton C, Prowse A, Chew SL, Dahia PL, O'Riordan JL, Toledo SP, et al. Eng C, et al. J Med Genet. 1995 Dec;32(12):934-7. doi: 10.1136/jmg.32.12.934. J Med Genet. 1995. PMID: 8825918 Free PMC article.

9

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis.

Eng C, Clayton D, Schuffenecker I, Lenoir G, Cote G, Gagel RF, van Amstel HK, Lips CJ, Nishisho I, Takai SI, Marsh DJ, Robinson BG, Frank-Raue K, Raue F, Xue F, Noll WW, Romei C, Pacini F, Fink M, Niederle B, Zedenius J, Nordenskjöld M, Komminoth P, Hendy GN, Mulligan LM, et al. Eng C, et al. JAMA. 1996 Nov 20;276(19):1575-9. JAMA. 1996. PMID: 8918855

10

Mutation analysis of glial cell line-derived neurotrophic factor (GDNF), a ligand for the RET/GDNF receptor alpha complex, in sporadic phaeochromocytomas.

Dahia PL, Toledo SP, Mulligan LM, Maher ER, Grossman AB, Eng C. Dahia PL, et al. Among authors: eng c. Cancer Res. 1997 Jan 15;57(2):310-3. Cancer Res. 1997. PMID: 9000574

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