Eng C - Search Results

1

PTEN hamartoma tumour syndrome: variability of an entity.

Merks JH, de Vries LS, Zhou XP, Nikkels P, Barth PG, Eng C, Hennekam RC. Merks JH, et al. Among authors: eng c. J Med Genet. 2003 Oct;40(10):e111. doi: 10.1136/jmg.40.10.e111. J Med Genet. 2003. PMID: 14569134 Free PMC article. No abstract available.

2

PTEN and inherited hamartoma-cancer syndromes.

Eng C, Peacocke M. Eng C, et al. Nat Genet. 1998 Jul;19(3):223. doi: 10.1038/897. Nat Genet. 1998. PMID: 9662392 No abstract available.

3

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.

4

Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotype.

Longy M, Coulon V, Duboué B, David A, Larrègue M, Eng C, Amati P, Kraimps JL, Bottani A, Lacombe D, Bonneau D. Longy M, et al. Among authors: eng c. J Med Genet. 1998 Nov;35(11):886-9. doi: 10.1136/jmg.35.11.886. J Med Genet. 1998. PMID: 9832032 Free PMC article.

5

Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis.

Zhou XP, Marsh DJ, Hampel H, Mulliken JB, Gimm O, Eng C. Zhou XP, et al. Among authors: eng c. Hum Mol Genet. 2000 Mar 22;9(5):765-8. doi: 10.1093/hmg/9.5.765. Hum Mol Genet. 2000. PMID: 10749983

6

Over-representation of PPARgamma sequence variants in sporadic cases of glioblastoma multiforme: preliminary evidence for common low penetrance modifiers for brain tumour risk in the general population.

Zhou XP, Smith WM, Gimm O, Mueller E, Gao X, Sarraf P, Prior TW, Plass C, von Deimling A, Black PM, Yates AJ, Eng C. Zhou XP, et al. Among authors: eng c. J Med Genet. 2000 Jun;37(6):410-4. doi: 10.1136/jmg.37.6.410. J Med Genet. 2000. PMID: 10851250 Free PMC article.

7

Biallelic inactivating mutations and an occult germline mutation of PTEN in primary cervical carcinomas.

Kurose K, Zhou XP, Araki T, Eng C. Kurose K, et al. Among authors: eng c. Genes Chromosomes Cancer. 2000 Oct;29(2):166-72. Genes Chromosomes Cancer. 2000. PMID: 10959096

8

Epigenetic PTEN silencing in malignant melanomas without PTEN mutation.

Zhou XP, Gimm O, Hampel H, Niemann T, Walker MJ, Eng C. Zhou XP, et al. Among authors: eng c. Am J Pathol. 2000 Oct;157(4):1123-8. doi: 10.1016/S0002-9440(10)64627-5. Am J Pathol. 2000. PMID: 11021816 Free PMC article.

9

Transient ectopic expression of PTEN in thyroid cancer cell lines induces cell cycle arrest and cell type-dependent cell death.

Weng LP, Gimm O, Kum JB, Smith WM, Zhou XP, Wynford-Thomas D, Leone G, Eng C. Weng LP, et al. Among authors: eng c. Hum Mol Genet. 2001 Feb 1;10(3):251-8. doi: 10.1093/hmg/10.3.251. Hum Mol Genet. 2001. PMID: 11159944

10

Absence of germline mutations in MINPP1, a phosphatase encoding gene centromeric of PTEN, in patients with Cowden and Bannayan-Riley-Ruvalcaba syndrome without germline PTEN mutations.

Dahia PM, Gimm O, Chi H, Marsh DJ, Reynolds PR, Eng C. Dahia PM, et al. Among authors: eng c. J Med Genet. 2000 Sep;37(9):715-7. doi: 10.1136/jmg.37.9.715. J Med Genet. 2000. PMID: 11182934 Free PMC article. No abstract available.

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