Mutation and deletion analysis of the Cowden disease gene, PTEN, in sporadic nonmedullary thyroid tumors.

被引：0
|
作者：
Dahla, PLM
Marsh, DJ
Zheng, Z
Zedenius, J
Komminoth, P
Parsons, R
Longy, M
Larsson, C
Eng, C
机构：
[1] Dana Farber Canc Inst, Boston, MA 02115 USA
[2] Karolinska Hosp, Dept Mol Med, S-10401 Stockholm, Sweden
[3] Karolinska Hosp, Dept Surg, S-10401 Stockholm, Sweden
[4] Univ Zurich, Dept Pathol, CH-8006 Zurich, Switzerland
[5] Columbia Univ, Ctr Canc, Dept Pathol, New York, NY 10027 USA
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 1997年 / 61卷 / 04期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
338
引用
收藏
页码：A63 / A63
页数：1
相关论文
共 50 条
  • [41] Mutation of the MENIN gene in sporadic pancreatic endocrine tumors
    Wang, EH
    Ebrahimi, SA
    Wu, AY
    Kashefi, C
    Passaro, E
    Sawicki, MP
    CANCER RESEARCH, 1998, 58 (19) : 4417 - 4420
  • [42] A deletion mutation of the VHL gene associated with a patient with sporadic von Hippel-Lindau disease
    Jia, Dandan
    Tang, Beisha
    Shi, Yuting
    Wang, Junling
    Sun, Zhanfang
    Chen, Zhao
    Zhang, Li
    Xia, Kun
    Jiang, Hong
    JOURNAL OF CLINICAL NEUROSCIENCE, 2013, 20 (06) : 842 - 847
  • [43] Deletion of PTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden disease
    Arch, EM
    Goodman, BK
    VanWesep, RA
    Liaw, D
    Clarke, K
    Parsons, R
    McKusick, VA
    Geraghty, MT
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1997, 71 (04): : 489 - 493
  • [44] Germline mutations in the PTEN/MMAC1 gene in patients with Cowden disease
    Nelen, MR
    vanStaveren, WCG
    Peeters, EAJ
    BenHassel, M
    Gorlin, RJ
    Hamm, H
    Lindboe, CF
    Fryns, JP
    Sijmons, RH
    Woods, DG
    Mariman, ECM
    Padberg, GW
    Kremer, H
    HUMAN MOLECULAR GENETICS, 1997, 6 (08) : 1383 - 1387
  • [45] Pten loss in the mouse thyroid causes goiter and follicular adenomas:: Insights into thyroid function and Cowden disease pathogenesis
    Yeager, Nicole
    Klein-Szanto, Andres
    Kimura, Shioko
    Di Cristofano, Antonio
    CANCER RESEARCH, 2007, 67 (03) : 959 - 966
  • [46] An atypical patient with Cowden syndrome and PTEN gene mutation presenting with cortical malformation and focal epilepsy
    Elia, Maurizio
    Amato, Carmelo
    Bottitta, Maria
    Grillo, Lucia
    Calabrese, Giuseppe
    Esposito, Maria
    Carotenuto, Marco
    BRAIN & DEVELOPMENT, 2012, 34 (10): : 873 - 876
  • [47] FREQUENCY OF THYROID TUMORS IN PATIENTS WITH PTEN MUTATION AND ASSOCIATED VASCULAR MALFORMATIONS
    Hammill, Adrienne
    Mundt, Erin
    Elluru, Ravi
    Gupta, Anita
    Merrow, Arnold
    Patel, Manish
    Adams, Denise M.
    PEDIATRIC BLOOD & CANCER, 2013, 60 : S35 - S35
  • [48] Mutation analysis of the putative tumor suppression gene PTEN/MMAC1 in sporadic breast cancer
    Chen, ST
    Yu, SY
    Tsai, M
    Yeh, KT
    Wang, JC
    Kao, MC
    Shih, MC
    Chang, JG
    BREAST CANCER RESEARCH AND TREATMENT, 1999, 55 (01) : 85 - 89
  • [49] Enhanced lymphocyte interferon (IFN)-γ responses in a PTEN mutation-negative Cowden disease kindred
    Stevenson, R.
    Fatehullah, A.
    Jagan, I.
    Deevi, R. K.
    Bingham, V.
    Irvine, A. E.
    Armstrong, M.
    Morrison, P. J.
    Dimmick, I.
    Stewart, R.
    Campbell, F. C.
    CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2011, 164 (02): : 202 - 210
  • [50] Cowden's disease:: clinical and molecular genetic findings in a patient with a novel PTEN germline mutation
    Reifenberger, J
    Rauch, L
    Beckmann, MW
    Megahed, M
    Ruzicka, T
    Reifenberger, G
    BRITISH JOURNAL OF DERMATOLOGY, 2003, 148 (05) : 1040 - 1046
12345