Characterization of a new BALL cell line with constitutional defect of the Notch signaling pathway
暂无分享,去创建一个
M. Chilosi | M. Krampera | P. T. Kamga | M. Bonifacio | G. Bassi | M. Midolo | Massimo | Delledonne | G. D. Collo | Giulio Bassi
[1] W. Chung,et al. Deep Genetic Connection Between Cancer and Developmental Disorders , 2016, Human mutation.
[2] M. Krampera,et al. Notch signalling drives bone marrow stromal cell-mediated chemoresistance in acute myeloid leukemia , 2016, Oncotarget.
[3] H. Cavé,et al. Acute lymphoblastic leukemia in the context of RASopathies. , 2016, European journal of medical genetics.
[4] Yoichi Matsubara,et al. Recent advances in RASopathies , 2015, Journal of Human Genetics.
[5] Laura M. Heiser,et al. Tumor-Derived Cell Lines as Molecular Models of Cancer Pharmacogenomics , 2015, Molecular Cancer Research.
[6] C. Récher,et al. A robust and rapid xenograft model to assess efficacy of chemotherapeutic agents for human acute myeloid leukemia , 2015, Blood Cancer Journal.
[7] C. Mullighan. The genomic landscape of acute lymphoblastic leukemia in children and young adults. , 2014, Hematology. American Society of Hematology. Education Program.
[8] J. Sage,et al. From fly wings to targeted cancer therapies: a centennial for notch signaling. , 2014, Cancer cell.
[9] T. Golde,et al. γ-Secretase inhibitors and modulators. , 2013, Biochimica et biophysica acta.
[10] R. Gniadecki,et al. Proteasome inhibition as a novel mechanism of the proapoptotic activity of γ‐secretase inhibitor I in cutaneous T‐cell lymphoma , 2013, The British journal of dermatology.
[11] Hideki Uosaki,et al. Non-canonical Notch signaling: emerging role and mechanism. , 2012, Trends in cell biology.
[12] A. Ferrando,et al. Preclinical Analysis of the γ-Secretase Inhibitor PF-03084014 in Combination with Glucocorticoids in T-cell Acute Lymphoblastic Leukemia , 2012, Molecular Cancer Therapeutics.
[13] I. Krantz,et al. NOTCH2 mutations in Alagille syndrome , 2011, Journal of Medical Genetics.
[14] G. Pizzolo,et al. Notch-3 and Notch-4 signaling rescue from apoptosis human B-ALL cells in contact with human bone marrow-derived mesenchymal stromal cells. , 2011, Blood.
[15] T. Mazel,et al. GSI-I (Z-LLNle-CHO) inhibits γ-secretase and the proteosome to trigger cell death in precursor-B acute lymphoblastic leukemia , 2011, Leukemia.
[16] B. Ezquieta,et al. Myeloproliferative Disorder in Noonan Syndrome , 2011, Journal of pediatric hematology/oncology.
[17] D. Haber,et al. Cell line-based platforms to evaluate the therapeutic efficacy of candidate anticancer agents , 2010, Nature Reviews Cancer.
[18] H. Hasle. Malignant Diseases in Noonan Syndrome and Related Disorders , 2009, Hormone Research in Paediatrics.
[19] Jing Chen,et al. ToppGene Suite for gene list enrichment analysis and candidate gene prioritization , 2009, Nucleic Acids Res..
[20] V. Detours,et al. Human cancer cell lines: Experimental models for cancer cells in situ? For cancer stem cells? , 2009, Biochimica et biophysica acta.
[21] J. McCarthy,et al. Presenilin-dependent regulated intramembrane proteolysis and γ-secretase activity , 2009, Cellular and Molecular Life Sciences.
[22] S. Blacklow,et al. The molecular logic of Notch signaling – a structural and biochemical perspective , 2008, Journal of Cell Science.
[23] Bart De Moor,et al. Endeavour update: a web resource for gene prioritization in multiple species , 2008, Nucleic Acids Res..
[24] N. Yoo,et al. Mutational analysis of NOTCH1, 2, 3 and 4 genes in common solid cancers and acute leukemias , 2007, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.
[25] D. Curtis,et al. Presenilin diversifies its portfolio. , 2007, Trends in genetics : TIG.
[26] Martin J Firth,et al. Authenticity and drug resistance in a panel of acute lymphoblastic leukaemia cell lines , 2006, British Journal of Cancer.
[27] I. Krantz,et al. NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder of the notch signaling pathway. , 2006, American journal of human genetics.
[28] L. Gibson,et al. Stromal cells regulate survival of B-lineage leukemic cells during chemotherapy. , 2000, Blood.
[29] Colin C. Collins,et al. Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1 , 1997, Nature Genetics.
[30] T. Hongo,et al. In vitro drug sensitivity testing can predict induction failure and early relapse of childhood acute lymphoblastic leukemia. , 1997, Blood.
[31] C. Guerra,et al. Modeling RASopathies with Genetically Modified Mouse Models. , 2017, Methods in molecular biology.
[32] D. Kovacs,et al. The many substrates of presenilin/γ-secretase. , 2011, Journal of Alzheimer's disease : JAD.
[33] Iannis Aifantis,et al. γ-secretase inhibitors reverse glucocorticoid resistance in T cell acute lymphoblastic leukemia , 2009, Nature Medicine.
[34] Hong Sun,et al. Analysis of transformation and tumorigenicity using mouse embryonic fibroblast cells. , 2007, Methods in molecular biology.
[35] S. Korsmeyer,et al. Human acute leukemia cell line with the t(4;11) chromosomal rearrangement exhibits B lineage and monocytic characteristics. , 1985, Blood.