Peacocke M - Search Results

1

The role of MMAC1 mutations in early-onset breast cancer: causative in association with Cowden syndrome and excluded in BRCA1-negative cases.

Tsou HC, Teng DH, Ping XL, Brancolini V, Davis T, Hu R, Xie XX, Gruener AC, Schrager CA, Christiano AM, Eng C, Steck P, Ott J, Tavtigian SV, Peacocke M. Tsou HC, et al. Among authors: peacocke m. Am J Hum Genet. 1997 Nov;61(5):1036-43. doi: 10.1086/301607. Am J Hum Genet. 1997. PMID: 9345101 Free PMC article.

2

Molecular basis of variegate porphyria: a de novo insertion mutation in the protoporphyrinogen oxidase gene.

Lam H, Dragan L, Tsou HC, Merk H, Peacocke M, Goerz G, Sassa S, Poh-Fitzpatrick M, Bickers DR, Christiano AM. Lam H, et al. Among authors: peacocke m. Hum Genet. 1997 Jan;99(1):126-9. doi: 10.1007/s004390050325. Hum Genet. 1997. PMID: 9003509

3

Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome.

Liaw D, Marsh DJ, Li J, Dahia PL, Wang SI, Zheng Z, Bose S, Call KM, Tsou HC, Peacocke M, Eng C, Parsons R. Liaw D, et al. Among authors: peacocke m. Nat Genet. 1997 May;16(1):64-7. doi: 10.1038/ng0597-64. Nat Genet. 1997. PMID: 9140396

4

Clinical and pathological features of breast disease in Cowden's syndrome: an underrecognized syndrome with an increased risk of breast cancer.

Schrager CA, Schneider D, Gruener AC, Tsou HC, Peacocke M. Schrager CA, et al. Among authors: peacocke m. Hum Pathol. 1998 Jan;29(1):47-53. doi: 10.1016/s0046-8177(98)90389-6. Hum Pathol. 1998. PMID: 9445133 Free article.

5

The genetic basis of Cowden's syndrome: three novel mutations in PTEN/MMAC1/TEP1.

Tsou HC, Ping XL, Xie XX, Gruener AC, Zhang H, Nini R, Swisshelm K, Sybert V, Diamond TM, Sutphen R, Peacocke M. Tsou HC, et al. Among authors: peacocke m. Hum Genet. 1998 Apr;102(4):467-73. doi: 10.1007/s004390050723. Hum Genet. 1998. PMID: 9600246

6

Identification of PTEN mutations in five families with Bannayan-Zonana syndrome.

Tok Celebi J, Chen FF, Zhang H, Ping XL, Tsou HC, Peacocke M. Tok Celebi J, et al. Among authors: peacocke m. Exp Dermatol. 1999 Apr;8(2):134-9. doi: 10.1111/j.1600-0625.1999.tb00361.x. Exp Dermatol. 1999. PMID: 10232405

7

PTEN/MMAC1 mutations in hepatocellular carcinomas.

Yao YJ, Ping XL, Zhang H, Chen FF, Lee PK, Ahsan H, Chen CJ, Lee PH, Peacocke M, Santella RM, Tsou HC. Yao YJ, et al. Among authors: peacocke m. Oncogene. 1999 May 20;18(20):3181-5. doi: 10.1038/sj.onc.1202659. Oncogene. 1999. PMID: 10340391

8

Phenotypic findings of Cowden syndrome and Bannayan-Zonana syndrome in a family associated with a single germline mutation in PTEN.

Celebi JT, Tsou HC, Chen FF, Zhang H, Ping XL, Lebwohl MG, Kezis J, Peacocke M. Celebi JT, et al. Among authors: peacocke m. J Med Genet. 1999 May;36(5):360-4. J Med Genet. 1999. PMID: 10353779 Free PMC article.

9

Germline PTEN mutations in three families with Cowden syndrome.

Celebi JT, Ping XL, Zhang H, Remington T, Sulica VI, Tsou HC, Peacocke M. Celebi JT, et al. Among authors: peacocke m. Exp Dermatol. 2000 Apr;9(2):152-6. doi: 10.1034/j.1600-0625.2000.009002152.x. Exp Dermatol. 2000. PMID: 10772390

10

Association of splicing defects in PTEN leading to exon skipping or partial intron retention in Cowden syndrome.

Celebi JT, Wanner M, Ping XL, Zhang H, Peacocke M. Celebi JT, et al. Among authors: peacocke m. Hum Genet. 2000 Sep;107(3):234-8. doi: 10.1007/s004390000362. Hum Genet. 2000. PMID: 11071384

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