Specific mutations in the beta-catenin gene (CTNNB1) correlate with local recurrence in sporadic desmoid tumors.
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Desmoid tumors: clinical features and treatment options: a case report and a review of literatureChildren's Oncology Group's 2013 blueprint for research: Soft tissue sarcomasNovel uses of immunohistochemistry in the diagnosis and classification of soft tissue tumorsAdvances in sarcoma diagnostics and treatmentThe challenge of developmental therapeutics for adrenocortical carcinomaSoft tissue sarcoma nomograms and their incorporation into practice.Current perspectives on desmoid tumors: the mayo clinic approachExtensive survey of STAT6 expression in a large series of mesenchymal tumors.CTNNB1 S45F mutation predicts poor efficacy of meloxicam treatment for desmoid tumors: a pilot study.β-catenin/Wnt signalling pathway in fibromatosis, metaplastic carcinomas and phyllodes tumours of the breast.Nuclear β-Catenin Expression is Frequent in Sinonasal Hemangiopericytoma and Its Mimics.High frequency of beta-catenin heterozygous mutations in extra-abdominal fibromatosis: a potential molecular tool for disease management.Adult desmoid tumors: biology, management and ongoing trials.A prognostic nomogram for prediction of recurrence in desmoid fibromatosis.Spontaneous regression of primary abdominal wall desmoid tumors: more common than previously thought.Sporadic desmoid-type fibromatosis: a stepwise approach to a non-metastasising neoplasm--a position paper from the Italian and the French Sarcoma Group.Clinical outcomes of systemic therapy for patients with deep fibromatosis (desmoid tumor).Desmoid tumours: our experience of six cases and review of literature.Chemotherapy in patients with desmoid tumors: a study from the French Sarcoma Group (FSG).Desmoid tumors: clinical features and treatment options for advanced diseaseManagement and recurrence patterns of desmoids tumors: a multi-institutional analysis of 211 patients.Isolated limb perfusion using tumour necrosis factor α and melphalan in patients with advanced aggressive fibromatosis.The Wnt/β-catenin pathway in human fibrotic-like diseases and its eligibility as a therapeutic target.Optimal therapy for desmoid tumors: current options and challenges for the future.New, tolerable γ-secretase inhibitor takes desmoid down a notch.Genetic analysis of colon tumors induced by a dietary carcinogen PhIP in CYP1A humanized mice: Identification of mutation of β-catenin/Ctnnb1 as the driver gene for the carcinogenesis.Primary asymptomatic desmoid tumor of the mesentery.Next-generation sequencing is highly sensitive for the detection of beta-catenin mutations in desmoid-type fibromatoses.Long-term outcome of sporadic and FAP-associated desmoid tumors treated with high-dose selective estrogen receptor modulators and sulindac: a single-center long-term observational study in 134 patients.Near universal detection of alterations in CTNNB1 and Wnt pathway regulators in desmoid-type fibromatosis by whole-exome sequencing and genomic analysis.Tailored Beta-catenin mutational approach in extra-abdominal sporadic desmoid tumor patients without therapeutic intervention.Pathology of gastrointestinal stromal tumors.Desmoid fibromatosis in pediatric patients: management based on a retrospective analysis of 59 patients and a review of the literature.Dual targeting of mTOR and aurora-A kinase for the treatment of uterine Leiomyosarcoma.Targeting the Notch pathway: A potential therapeutic approach for desmoid tumorsMeta-analysis of the influence of surgical margin and adjuvant radiotherapy on local recurrence after resection of sporadic desmoid-type fibromatosis.Safety and efficacy of high-dose tamoxifen and sulindac for desmoid tumor in children: results of a Children's Oncology Group (COG) phase II study.A nonrandom association of gastrointestinal stromal tumor (GIST) and desmoid tumor (deep fibromatosis): case series of 28 patients.Role of β-catenin expression in paediatric mesenchymal lesions: a tissue microarray-based immunohistochemical study.Postoperative retroperitoneal desmoid tumor mimics recurrent gastrointestinal stromal tumor: a case report.
P2860
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P2860
Specific mutations in the beta-catenin gene (CTNNB1) correlate with local recurrence in sporadic desmoid tumors.
description
2008 nî lūn-bûn
@nan
2008 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Specific mutations in the beta ...... ce in sporadic desmoid tumors.
@ast
Specific mutations in the beta ...... ce in sporadic desmoid tumors.
@en
Specific mutations in the beta-catenin gene
@nl
type
label
Specific mutations in the beta ...... ce in sporadic desmoid tumors.
@ast
Specific mutations in the beta ...... ce in sporadic desmoid tumors.
@en
Specific mutations in the beta-catenin gene
@nl
prefLabel
Specific mutations in the beta ...... ce in sporadic desmoid tumors.
@ast
Specific mutations in the beta ...... ce in sporadic desmoid tumors.
@en
Specific mutations in the beta-catenin gene
@nl
P2093
P2860
P1476
Specific mutations in the beta ...... nce in sporadic desmoid tumors
@en
P2093
Carla L Warneke
Daniel Tuvin
Dolores Lopez-Terrada
Empar Mayordomo-Aranda
Raphael E Pollock
Shohrae Hajibashi
Sultan Habeeb
Svetlana Bolshakov
P2860
P304
P356
10.2353/AJPATH.2008.080475
P407
P577
2008-10-02T00:00:00Z