Pathophysiologic and clinical implications of molecular profiles resultant from deletion 5q
暂无分享,去创建一个
L. Arenillas | F. Solé | T. Haferlach | J. Barnard | J. Maciejewski | W. Kern | C. Haferlach | J. Boultwood | A. Pellagatti | V. Visconte | V. Adema | T. Radivoyevitch | M. Meggendorfer | W. Walter | Laura Palomo | M. Mallo | B. Xicoy | S. Hutter | Thomas La Framboise | M. Sekeres | L. Palomo
[1] B. Ebert,et al. Rps14, Csnk1a1 and miRNA145/miRNA146a deficiency cooperate in the clinical phenotype and activation of the innate immune system in the 5q- syndrome , 2019, Leukemia.
[2] You-yang Zhao,et al. β-Catenin Is a Candidate Therapeutic Target for Myeloid Neoplasms with del(5q). , 2017, Cancer research.
[3] Anna L. Brown,et al. DDX41-related myeloid neoplasia. , 2017, Seminars in hematology.
[4] S. Miyano,et al. Dynamics of clonal evolution in myelodysplastic syndromes , 2016, Nature Genetics.
[5] A. Trumpp,et al. Mutational hierarchies in myelodysplastic syndromes dynamically adapt and evolve upon therapy response and failure. , 2016, Blood.
[6] Mario Cazzola,et al. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. , 2016, Blood.
[7] Michelle C. Chen,et al. Rps14 haploinsufficiency causes a block in erythroid differentiation mediated by S100A8 and S100A9 , 2016, Nature Medicine.
[8] C. Hernández-Munain,et al. Functional Consequences for Apoptosis by Transcription Elongation Regulator 1 (TCERG1)-Mediated Bcl-x and Fas/CD95 Alternative Splicing , 2015, PloS one.
[9] S. Miyano,et al. Inherited and Somatic Defects in DDX41 in Myeloid Neoplasms. , 2015, Cancer cell.
[10] G. Mufti,et al. CSNK1A1 mutations and isolated del(5q) abnormality in myelodysplastic syndrome: a retrospective mutational analysis. , 2015, The Lancet. Haematology.
[11] K. Döhner,et al. Frequency and prognostic impact of casein kinase 1A1 mutations in MDS patients with deletion of chromosome 5q , 2015, Leukemia.
[12] Matthew E. Ritchie,et al. limma powers differential expression analyses for RNA-sequencing and microarray studies , 2015, Nucleic acids research.
[13] B. Ebert,et al. Role of casein kinase 1A1 in the biology and targeted therapy of del(5q) MDS. , 2014, Cancer cell.
[14] Weixin Yao,et al. Fully Bayesian logistic regression with hyper-LASSO priors for high-dimensional feature selection , 2014, Journal of Statistical Computation and Simulation.
[15] M. L. Le Beau,et al. Haploinsufficiency of del(5q) genes, Egr1 and Apc, cooperate with Tp53 loss to induce acute myeloid leukemia in mice. , 2014, Blood.
[16] A. Jankowska,et al. Topography, clinical, and genomic correlates of 5q myeloid malignancies revisited. , 2012, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[17] J. Boultwood. The role of haploinsufficiency of RPS14 and p53 activation in the molecular pathogenesis of the 5q- syndrome , 2011, Pediatric reports.
[18] M. DePristo,et al. The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. , 2010, Genome research.
[19] D. Levens,et al. Isolation and Characterization of a Novel H1.2 Complex That Acts as a Repressor of p53-mediated Transcription* , 2008, Journal of Biological Chemistry.
[20] T. Mustelin,et al. A network of p73, p53 and Egr1 is required for efficient apoptosis in tumor cells , 2007, Cell Death and Differentiation.
[21] D. Lane,et al. Regulation of p53 by the Ubiquitin-conjugating Enzymes UbcH5B/C in Vivo* , 2004, Journal of Biological Chemistry.
[22] V. Najfeld,et al. Deletions of PURA, at 5q31, and PURB, at 7p13, in myelodysplastic syndrome and progression to acute myelogenous leukemia , 2001, Leukemia.
[23] G. Mufti,et al. The role of apoptosis, proliferation, and the Bcl-2-related proteins in the myelodysplastic syndromes and acute myeloid leukemia secondary to MDS. , 2000, Blood.
[24] A. Monaco,et al. Novel genes mapping to the critical region of the 5q- syndrome. , 1997, Genomics.
[25] R. Espinosa,et al. Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[26] J. Fryns,et al. Distinct haematological disorder with deletion of long arm of No. 5 chromosome , 1974, Nature.
[27] J. Reinstein,et al. Bap (Sil1) regulates the molecular chaperone BiP by coupling release of nucleotide and substrate , 2017, Nature Structural & Molecular Biology.
[28] Michael F Clarke,et al. Chromosome 5q deletion and epigenetic suppression of the gene encoding α-catenin (CTNNA1) in myeloid cell transformation , 2007, Nature Medicine.
[29] C. Schoch,et al. Clinical, morphological, cytogenetic, and prognostic features of patients with myelodysplastic syndromes and del(5q) including band q31 , 2004, Leukemia.