✦ LIBER ✦

Absence of PPP2R1A mutations in Wilms tumor

✍ Scribed by Ruteshouser, E Cristy; Ashworth, Linda K; Huff, Vicki

Book ID: 110064591
Publisher: Nature Publishing Group
Year: 2001
Tongue: English
Weight: 119 KB
Volume: 20
Category: Article
ISSN: 0950-9232
DOI: 10.1038/sj.onc.1204301

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Correlation of chromosome abnormalities

Correlation of chromosome abnormalities with presence or absence of WT1 deletions/mutations in Wilms tumor

✍ Hisaya Nakadate; Takashi Tsuchiya; Nobuo Maseki; Yoshiro Hatae; Yukiko Tsunemats 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 218 KB 👁 2 views

Of 40 Wilms tumors with chromosome abnormalities, 6 were hypodiploid, 10 were pseudodiploid, 7 were hyperdiploid with 47 to 49 chromosomes, and 17 were hyperdiploid with 50 or more chromosomes, mostly including ϩ12. WT1 deletions/ mutations were found in one hypodiploid, eight pseudodiploid, and one

Mutation analysis of the tumor suppresso

Mutation analysis of the tumor suppressor gene PPP2R1B in human cervical cancer

✍ L.-S. YEH; Y.-Y. HSIEH; J.-G. CHANG; W.W.-C. CHANG; C.-C. CHANG; F.-J. TSAI 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 71 KB

Radiation hybrid mapping of the porcine

Radiation hybrid mapping of the porcine PPP2CA, PPP2CB, PPP2R1A and PPP2R1B genes

✍ X. W. Xu; B. Liu; B. Fan; H. F. Qiu; M. Yerle 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 65 KB

Absence of PPP2R1B gene alterations in p

Absence of PPP2R1B gene alterations in primary ovarian cancers

✍ Campbell, I G; Manolitsas, T 📂 Article 📅 1999 🏛 Nature Publishing Group 🌐 English ⚖ 123 KB

GermlineWT1 mutations in Wilms' tumor pa

GermlineWT1 mutations in Wilms' tumor patients: Preliminary results

✍ Li, Frederick P.; Breslow, Norman E.; Morgan, Jennifer M.; Ghahremani, Majid; Mi 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 450 KB 👁 2 views

We conducted a comparative study of the prevalence of gerrnline WTI mutations in patients with Wilms' tumor. Patients in Group l have familial Wilms' tumor, bilateral disease, associated urogenital anomalies, and/or second cancers. Those in Group 2 are unilateral, sporadic Wilrns' patients without o

Expression and mutation analysis of the

Expression and mutation analysis of the Wilms' tumor 1 gene in human neural tumors

✍ Sally L. Dennis; Shehnaaz S.M. Manji; Darryl P. Carrington; Deborah L. Scarcella 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 French ⚖ 214 KB

## Abstract The Wilms' tumor 1 gene, __WT1__, encodes a zinc‐finger protein that is implicated in the development of Wilms' tumor. Mutant or aberrantly expressed WT1 isoforms have also been described in desmoplastic small round cell tumor, acute leukemias, mesothelioma, breast tumors and melanoma.