Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome
Liaw, Danny, Marsh, Debbie J, Li, Jing, Dahia, Patricia L. M, Wang, Steven I, Zheng, Zimu, Bose, Shikha, Call, Katherine M, Tsou, Hui C, Peacoke, Monica, Eng, Charis, Parsons, Ramon
Published in Nature genetics (01.05.1997)
Published in Nature genetics (01.05.1997)
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Clinical and pathological features of breast disease in Cowden's syndrome: An underrecognized syndrome with an increased risk of breast cancer
Schrager, Carolina A, Schneider, Douglas, Gruener, Alexandra C, Tsou, Hui C, Peacocke, Monica
Published in Human pathology (1998)
Published in Human pathology (1998)
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Identification of PTEN mutations in metastatic melanoma specimens
Çelebi, Julide Tok, Shendrik, Igor, Silvers, David N, Peacocke, Monica
Published in Journal of medical genetics (01.09.2000)
Published in Journal of medical genetics (01.09.2000)
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Phenotypic findings of Cowden syndrome and Bannayan-Zonana syndrome in a family associated with a single germline mutation in PTEN
Çelebi, Julide Tok, Tsou, Hui C, Chen, Fei Fei, Zhang, Hong, Ping, Xiao Li, Lebwohl, Mark G, Kezis, Jeffrey, Peacocke, Monica
Published in Journal of medical genetics (01.05.1999)
Published in Journal of medical genetics (01.05.1999)
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Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locus
Kolluri, R, Shehabeldin, A, Peacocke, M, Lamhonwah, A M, Teichert-Kuliszewska, K, Weissman, S M, Siminovitch, K A
Published in Human molecular genetics (01.07.1995)
Published in Human molecular genetics (01.07.1995)
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Association of splicing defects in PTEN leading to exon skipping or partial intron retention in Cowden syndrome
CELEBI, Julide Tok, WANNER, Molly, XIAO LI PING, HONG ZHANG, PEACOCKE, Monica
Published in Human genetics (01.09.2000)
Published in Human genetics (01.09.2000)
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The genetic basis of Cowden's syndrome : three novel mutations in PTEN/MMAC1/TEP1
TSOU, H. C, XIAO LI PING, PEACOCKE, M, XIAO XUN XIE, GRUENER, A. C, HONG ZHANG, NINI, R, SWISSHELM, K, SYBERT, V, DIAMOND, T. M, SUTPHEN, R
Published in Human genetics (01.04.1998)
Published in Human genetics (01.04.1998)
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Identification of PTEN mutations in five families with Bannayan-Zonana syndrome
Çelebi, J. Tok, Chen, F. F., Zhang, H., Ping, X. L., Tsou, H. C., Peacocke, M.
Published in Experimental dermatology (01.04.1999)
Published in Experimental dermatology (01.04.1999)
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Germline PTEN mutations in three families with Cowden syndrome
Çelebi, J. T., Ping, X. L., Zhang, H., Remington, T., Sulica, V. I., Tsou, H. C., Peacocke, M.
Published in Experimental dermatology (01.04.2000)
Published in Experimental dermatology (01.04.2000)
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A Biomarker that Identifies Senescent Human Cells in Culture and in Aging Skin in vivo
Dimri, Goberdhan P., Lee, Xinhua, Basile, George, Acosta, Meileen, Scott, Glynis, Roskelley, Calvin, Medrano, Estela E., Linskens, Maarten, Rubelj, Ivica, Pereira-Smith, Olivia, Peacocke, Monica, Campisi, Judith
Published in Proceedings of the National Academy of Sciences - PNAS (26.09.1995)
Published in Proceedings of the National Academy of Sciences - PNAS (26.09.1995)
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A diagnostic assay for the Wiskott-Aldrich syndrome and its variant forms
Siminovitch, K A, Greer, W L, Novogrodsky, A, Axelsson, B, Somani, A K, Peacocke, M
Published in Journal of investigative medicine (01.04.1995)
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Published in Journal of investigative medicine (01.04.1995)
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