Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome
作者： Danny Liaw , Debbie J. Marsh , Jing Li , Patricia L. M. Dahia , Steven I. Wang
DOI: 10.1038/NG0597-64
关键词:
摘要: … nature genetics volume 16 may 1997 … Mulvihill, JJ & McKeen, EA Discussion: genetics of mutiple primary tumors: a clinical etiological approach illustrated by three patients. Cancer 40, …
utsystem.edu
nature.com参考文章(16)
M A Spence, A M Luger, D N Orth, R S Sparkes, S L Davenport, H E Carlson, T W Burns, Cowden disease: gene marker studies and measurements of epidermal growth factor. American Journal of Human Genetics. ,vol. 38, pp. 908- 917 ,(1986)
Nicholas K Tonks, Benjamin G Neel, From form to function: signaling by protein tyrosine phosphatases. Cell. ,vol. 87, pp. 365- 368 ,(1996) , 10.1016/S0092-8674(00)81357-4
John J. Mulvihill, Elisabeth A. McKeen, Discussion: Genetics of multiple primary tumors.A clinical etiologic approach illustrated by three patients Cancer. ,vol. 40, pp. 1867- 1871 ,(1977) , 10.1002/1097-0142(197710)40:4+<1867::AID-CNCR2820400816>3.0.CO;2-P
Eric B. Fauman, Mark A. Saper, Structure and function of the protein tyrosine phosphatases Trends in Biochemical Sciences. ,vol. 21, pp. 413- 417 ,(1996) , 10.1016/S0968-0004(96)10059-1
Th. M. Starink, J. P. W. van der Veen, F. Arwert, L. P. de Waal, G. G.de Lange, J. J. P. Gille, A. W. Eriksson, The Cowden syndrome: a clinical and genetic study in 21 patients Clinical Genetics. ,vol. 29, pp. 222- 233 ,(2008) , 10.1111/J.1399-0004.1986.TB00816.X
KENNETH M. LLOYD, Cowden's Disease Annals of Internal Medicine. ,vol. 58, pp. 136- 142 ,(1963) , 10.7326/0003-4819-58-1-136
Peter A. Steck, Mark A. Pershouse, Samar A. Jasser, W.K. Alfred Yung, Huai Lin, Azra H. Ligon, Lauren A. Langford, Michelle L. Baumgard, Thomas Hattier, Thaylon Davis, Cheryl Frye, Rong Hu, Bradley Swedlund, David H.R. Teng, Sean V. Tavtigian, Identification of a candidate tumour suppressor gene, MMAC1 , at chromosome 10q23.3 that is mutated in multiple advanced cancers Nature Genetics. ,vol. 15, pp. 356- 362 ,(1997) , 10.1038/NG0497-356
Charis Eng, David Clayton, Isabelle Schuffenecker, Gilbert Lenoir, Gilbert Cote, Robert F Gagel, Hans Kristian Ploos Van Amstel, Cornelis JM Lips, Isamu Nishisho, Shin-Ichiro Takai, Debbie J Marsh, Bruce G Robinson, Karin Frank-Raue, Friedhelm Raue, Feiyu Xue, Walter W Noll, Cristina Romei, Furio Pacini, Monika Fink, Bruno Niederle, Jan Zedenius, Magnus Nordenskjöld, Paul Komminoth, Geoffrey N Hendy, Hossein Gharib, Stephen N Thibodeau, André Lacroix, Andrea Frilling, Bruce AJ Ponder, Lois M Mulligan, The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis JAMA: The Journal of the American Medical Association. ,vol. 276, pp. 1575- 1579 ,(1996) , 10.1001/JAMA.276.19.1575
Jan Zedenius, George W. Padberg, Charis Eng, Catharina Larsson, Debbie J. Marsh, Michel Longy, Zimu Zheng, Hannie Kremer, Differential loss of heterozygosity in the region of the Cowden locus within 10q22-23 in follicular thyroid adenomas and carcinomas Cancer Research. ,vol. 57, pp. 500- 503 ,(1997)
MR Nelen, GW Padberg, EAJ Peeters, AY Lin, B van den Helm, RR Frants, V Goulon, AM Goldstein, MMM van Reen, DF Eastern, RA Eeles, S Hodgson, JJ Mulvihill, VA Murday, MA Tucker, ECM Mariman, TM Starink, BAJ Ponder, HH Ropers, H Kremer, M Longy, C Eng, None, Localization of the gene for Cowden disease to chromosome 10q22-23 Nature Genetics. ,vol. 13, pp. 114- 116 ,(1996) , 10.1038/NG0596-114