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Results 1 to 25 of 35

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CDC4/FBXW7 and the 'just enough' model of tumourigenesisDAVIS, Hayley; TOMLINSON, Ian.Journal of pathology (Print). 2012, Vol 227, Num 2, pp 131-135, issn 0022-3417, 5 p.Article

Prognostic implications of NOTCH1 and FBXW7 mutations in adult acute T-lymphoblastic leukemiaBAIDUS, Claudia D; THIBAUT, Julia; THIEL, Eckhard et al.Haematologica (Roma). 2009, Vol 94, Num 10, pp 1383-1390, issn 0390-6078, 8 p.Article

FBXW7 and DNA copy number instabilityBYRD, Kristin N; HUEY, Bing; ROYDASGUPTA, Ritu et al.Breast cancer research and treatment. 2008, Vol 109, Num 1, pp 47-54, issn 0167-6806, 8 p.Article

FBXW7/hCDC4 is a general tumor suppressor in human cancerAKHOONDI, Shahab; DAHUI SUN; MUELLER-HOLZNER, Elisabeth et al.Cancer research (Baltimore). 2007, Vol 67, Num 19, pp 9006-9012, issn 0008-5472, 7 p.Article

FBXW7 mutations typically found in human cancers are distinct from null alleles and disrupt lung developmentDAVIS, Hayley; LEWIS, Annabelle; SPENCER-DENE, Bradley et al.Journal of pathology (Print). 2011, Vol 224, Num 2, pp 180-189, issn 0022-3417, 10 p.Article

The favorable effect of activating NOTCH1 receptor mutations on long-term outcome in T-ALL patients treated on the ALL-BFM 2000 protocol can be separated from FBXW7 loss of function : Prognostic effects of NOTCH1 activing mutations in pediatrics T-ALL is treatment dependentKOX, C; ZIMMERMANN, M; MUCKENTHALER, M. U et al.Leukemia. 2010, Vol 24, Num 12, pp 2005-2013, issn 0887-6924, 9 p.Article

NOTCH1 and/or FBXW7 mutations predict for initial good prednisone response but not for improved outcome in pediatric T-cell acute lymphoblastic leukemia patients treated on DCOG or COALL protocols : Prognostic effects of NOTCH1 activing mutations in pediatrics T-ALL is treatment dependentZUURBIER, L; HOMMINGA, I; HORSTMANN, M et al.Leukemia. 2010, Vol 24, Num 12, pp 2014-2022, issn 0887-6924, 9 p.Article

Loss of FBXW7, a cell cycle regulating gene, in colorectal cancer: clinical significanceIWATSUKI, Masaaki; MIMORI, Koshi; MORI, Masaki et al.International journal of cancer (Print). 2010, Vol 126, Num 8, pp 1828-1837, issn 0020-7136, 10 p.Article

Tumor suppressor Fbxw7 regulates TGFβ signaling by targeting TGIF1 for degradationBENGOECHEA-ALONSO, M. T; ERICSSON, J.Oncogene (Basingstoke). 2010, Vol 29, Num 38, pp 5322-5328, issn 0950-9232, 7 p.Article

Copy number loss of FBXW7 is related to gene expression and poor prognosis in esophageal squamous cell carcinomaYOKOBORI, Takehiko; MIMORI, Koshi; ONOYAMA, Ichiro et al.International journal of oncology. 2012, Vol 41, Num 1, pp 253-259, issn 1019-6439, 7 p.Article

NOTCH1 and FBXW7 mutations have a favorable impact on early response to treatment, but not on outcome, in children with T-cell acute lymphoblastic leukemia (T-ALL) treated on EORTC trials 58881 and 58951 : Prognostic effects of NOTCH1 activing mutations in pediatrics T-ALL is treatment dependentCLAPPIER, E; COLLETTE, S; BOUTARD, P et al.Leukemia. 2010, Vol 24, Num 12, pp 2023-2031, issn 0887-6924, 9 p.Article

Overexpression of microRNA-223 regulates the ubiquitin ligase FBXW7 in oesophageal squamous cell carcinomaKURASHIGE, J; WATANABE, M; LWATSUKI, M et al.British journal of cancer. 2012, Vol 106, Num 1, pp 182-188, issn 0007-0920, 7 p.Article

Somatic Mutations of the CDC4 (FBXW7) Gene in Hereditary Colorectal TumorsMIYAKI, Michiko; YAMAGUCHI, Tatsuro; LIJIMA, Takeru et al.Oncology. 2009, Vol 76, Num 6, pp 430-434, issn 0030-2414, 5 p.Article

Role of Fbxw7 in the maintenance of normal stem cells and cancer-initiating cellsTAKEISHI, S; NAKAYAMA, K. I.British journal of cancer. 2014, Vol 111, Num 6, pp 1054-1059, issn 0007-0920, 6 p.Article

MicroRNA-223 functions as an oncogene in human gastric cancer by targeting FBXW7/hCdc4JINHAI LI; YUANYUAN GUO; XIAODI LIANG et al.Journal of cancer research and clinical oncology. 2012, Vol 138, Num 5, pp 763-774, issn 0171-5216, 12 p.Article

Prognostic Implications of NOTCH1 and FBXW7 Mutations in Adults With T-Cell Acute Lymphoblastic Leukemia Treated on the MRC UKALLXII/ECOG E2993 ProtocolMANSOUR, Marc R; SULIS, Maria L; PAIETTA, Elisabeth et al.Journal of clinical oncology. 2009, Vol 27, Num 26, pp 4352-4356, issn 0732-183X, 5 p.Article

Fbxw7 contributes to tumor suppression by targeting multiple proteins for ubiquitin-dependent degradationFUJII, Yo; YADA, Masayoshi; NISHIYAMA, Masaaki et al.Cancer science. 2006, Vol 97, Num 8, pp 729-736, issn 1347-9032, 8 p.Article

p53-Altered FBXW7 Expression Determines Poor Prognosis in Gastric Cancer CasesYOKOBORI, Takehiko; MIMORI, Koshi; IWATSUKI, Masaaki et al.Cancer research (Chicago, Ill.). 2009, Vol 69, Num 9, pp 3788-3794, issn 0008-5472, 7 p.Article

Fbxw7/Cdc4 is a p53-dependent, haploinsufficient tumour suppressor geneMAO, Jian-Hua; PEREZ-IOSADA, Jesus; WU, Di et al.Nature (London). 2004, Vol 432, Num 7018, pp 775-779, issn 0028-0836, 5 p.Article

FBXW7 Mutations in Melanoma and a New Therapeutic ParadigmAYDIN, Iraz T; MELAMED, Rachel D; CELEBI, Julide Tok et al.Journal of the National Cancer Institute. 2014, Vol 106, Num 6, issn 0027-8874, dju107.1-dju107.8Article

Clinical Impact of NOTCH1 and/or FBXW7 Mutations, FLASH Deletion, and TCR Status in Pediatric T-Cell Lymphoblastic LymphomaCALLENS, Celine; BALEYDIER, Frederic; BARUCHEL, André et al.Journal of clinical oncology. 2012, Vol 30, Num 16, pp 1966-1973, issn 0732-183X, 8 p.Article

The tumor suppressor gene hCDC4 is frequently mutated in human T-cell acute lymphoblastic leukemia with functional consequences for notch signalingMALYUKOVA, Alena; DOHDA, Takeaki; VON DER LEHR, Natalie et al.Cancer research (Baltimore). 2007, Vol 67, Num 12, pp 5611-5616, issn 0008-5472, 6 p.Article

Sequential mutations in Notch1, Fbxw7, and Tp53 in radiation-induced mouse thymic lymphomasJEN, Kuang-Yu; IHN YOUNG SONG; KARL LUKE BANTA et al.Blood. 2012, Vol 119, Num 3, pp 805-809, issn 0006-4971, 5 p.Article

Pediatric-inspired intensified therapy of adult T-ALL reveals the favorable outcome of NOTCH1/FBXW7 mutations, but not of low ERG/BAALC expression: a GRAALL studyABDELALI, Raouf Ben; ASNAFI, Vahid; ESCOFFRE-BARBE, Martine et al.Blood. 2011, Vol 118, Num 19, pp 5099-5107, issn 0006-4971, 9 p.Article

Subtype-Specific FBXW7 Mutation and MYCN Copy Number Gain in Wilms' TumorWILLIAMS, Richard D; AL-SAADI, Reem; HUBANK, Mike et al.Clinical cancer research (Print). 2010, Vol 16, Num 7, pp 2036-2045, issn 1078-0432, 10 p.Article

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