CA-70519/CA/NCI NIH HHS/United States[Grant Number] - Search Results

Year	Number of Results
1997	1
1998	3
1999	3
2000	2
2001	1
2022	0

1

Identification of PTEN mutations in metastatic melanoma specimens.

Celebi JT, Shendrik I, Silvers DN, Peacocke M. Celebi JT, et al. J Med Genet. 2000 Sep;37(9):653-7. doi: 10.1136/jmg.37.9.653. J Med Genet. 2000. PMID: 10978354 Free PMC article.

2

Similarities of cutaneous and breast pathology in Cowden's Syndrome.

Schrager CA, Schneider D, Gruener AC, Tsou HC, Peacocke M. Schrager CA, et al. Exp Dermatol. 1998 Dec;7(6):380-90. doi: 10.1111/j.1600-0625.1998.tb00338.x. Exp Dermatol. 1998. PMID: 9858141

3

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. Exp Dermatol. 1999 Apr;8(2):134-9. doi: 10.1111/j.1600-0625.1999.tb00361.x. Exp Dermatol. 1999. PMID: 10232405

4

Mutation report: identification of a germline mutation in keratin 17 in a family with pachyonychia congenita type 2.

Celebi JT, Tanzi EL, Yao YJ, Michael EJ, Peacocke M. Celebi JT, et al. J Invest Dermatol. 1999 Nov;113(5):848-50. doi: 10.1046/j.1523-1747.1999.00762.x. J Invest Dermatol. 1999. PMID: 10571744 Free article.

5

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. J Med Genet. 1999 May;36(5):360-4. J Med Genet. 1999. PMID: 10353779 Free PMC article.

6

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. Hum Pathol. 1998 Jan;29(1):47-53. doi: 10.1016/s0046-8177(98)90389-6. Hum Pathol. 1998. PMID: 9445133 Free article.

7

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. Hum Genet. 1998 Apr;102(4):467-73. doi: 10.1007/s004390050723. Hum Genet. 1998. PMID: 9600246

8

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. Am J Hum Genet. 1997 Nov;61(5):1036-43. doi: 10.1086/301607. Am J Hum Genet. 1997. PMID: 9345101 Free PMC article.

9

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. Hum Genet. 2000 Sep;107(3):234-8. doi: 10.1007/s004390000362. Hum Genet. 2000. PMID: 11071384

10

Identification of a PTEN mutation in a family with Cowden syndrome and Bannayan-Zonana syndrome.

Wanner M, Celebi JT, Peacocke M. Wanner M, et al. J Am Acad Dermatol. 2001 Feb;44(2):183-7. doi: 10.1067/mjd.2001.110390. J Am Acad Dermatol. 2001. PMID: 11174374

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