Coexpression of normally incompatible developmental pathways in retinoblastoma genesis
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Retinoblastoma tumor suppressor functions shared by stem cell and cancer cell strategiesTransgenic Models in Retinoblastoma ResearchPediatric solid tumor genomics and developmental pliancySchedule-Dependent Antiangiogenic and Cytotoxic Effects of Chemotherapy on Vascular Endothelial and Retinoblastoma CellsCRISPR/Cas9 mediated knockout of rb1 and rbl1 leads to rapid and penetrant retinoblastoma development in Xenopus tropicalisMutation spectrum of RB1 mutations in retinoblastoma cases from Singapore with implications for genetic management and counsellingGenetic and Epigenetic Discoveries in Human RetinoblastomaFunctional dissection of the role of UHRF1 in the regulation of retinoblastoma methylome.Analysis of MDM2 and MDM4 single nucleotide polymorphisms, mRNA splicing and protein expression in retinoblastoma.Retinoblastoma. Fifty years of progress. The LXXI Edward Jackson Memorial Lecture.Chromatin remodelers HELLS and UHRF1 mediate the epigenetic deregulation of genes that drive retinoblastoma tumor progression.Targeting the p53 pathway in retinoblastoma with subconjunctival Nutlin-3a.Inhibition of pluripotency networks by the Rb tumor suppressor restricts reprogramming and tumorigenesis.Progress in Small Molecule Therapeutics for the Treatment of Retinoblastoma.Loss of photoreceptorness and gain of genomic alterations in retinoblastoma reveal tumor progression.The retinoblastoma tumor suppressor and stem cell biology.Single-cell profiling of developing and mature retinal neurons.Preclinical Models Provide Scientific Justification and Translational Relevance for Moving Novel Therapeutics into Clinical Trials for Pediatric Cancer.BMP-binding protein twisted gastrulation is required in mammary gland epithelium for normal ductal elongation and myoepithelial compartmentalization.Brg1 coordinates multiple processes during retinogenesis and is a tumor suppressor in retinoblastoma.Epigenetic changes in pediatric solid tumors: promising new targets.Retinoblastoma: concerning its initiation and treatment.Cross-species genomic and epigenomic landscape of retinoblastoma.A drug repositioning approach identifies tricyclic antidepressants as inhibitors of small cell lung cancer and other neuroendocrine tumors.L1 increases adhesion-mediated proliferation and chemoresistance of retinoblastoma.Coordination of proliferation and neuronal differentiation by the retinoblastoma protein family.RB1 gene inactivation by chromothripsis in human retinoblastomaTALENs and CRISPR/Cas9 fuel genetically engineered clinically relevant Xenopus tropicalis tumor models.The Childhood Solid Tumor Network: A new resource for the developmental biology and oncology research communities.We contain multitudes: the protean face of retinoblastoma.Application of an RNA amplification method for reliable single-cell transcriptome analysis.A novel retinoblastoma therapy from genomic and epigenetic analyses.Co-deleting Pten with Rb in retinal progenitor cells in mice results in fully penetrant bilateral retinoblastomas.Retinoblastoma cells activate the AKT pathway and are vulnerable to the PI3K/mTOR inhibitor NVP-BEZ235.Retinoblastoma Progression.Organ size control is dominant over Rb family inactivation to restrict proliferation in vivo.Cancer: The origin of human retinoblastoma.MDM2 but not MDM4 promotes retinoblastoma cell proliferation through p53-independent regulation of MYCN translation.Cooperation between Rb and Arf in suppressing mouse retinoblastoma.Animal models in retinoblastoma research.
P2860
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P2860
Coexpression of normally incompatible developmental pathways in retinoblastoma genesis
description
2011 nî lūn-bûn
@nan
2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Coexpression of normally incompatible developmental pathways in retinoblastoma genesis
@ast
Coexpression of normally incompatible developmental pathways in retinoblastoma genesis
@en
Coexpression of normally incompatible developmental pathways in retinoblastoma genesis
@nl
type
label
Coexpression of normally incompatible developmental pathways in retinoblastoma genesis
@ast
Coexpression of normally incompatible developmental pathways in retinoblastoma genesis
@en
Coexpression of normally incompatible developmental pathways in retinoblastoma genesis
@nl
prefLabel
Coexpression of normally incompatible developmental pathways in retinoblastoma genesis
@ast
Coexpression of normally incompatible developmental pathways in retinoblastoma genesis
@en
Coexpression of normally incompatible developmental pathways in retinoblastoma genesis
@nl
P2093
P2860
P3181
P1433
P1476
Coexpression of normally incompatible developmental pathways in retinoblastoma genesis
@en
P2093
Carlos Rodriguez-Galindo
Cori Bradley
Dianna Johnson
Fred Krafcik
Guillermina Lozano
Jacqueline Flores-Otero
Jeff Trimarchi
Jiakun Zhang
Justina McEvoy
P2860
P304
P3181
P356
10.1016/J.CCR.2011.07.005
P407
P50
P577
2011-08-16T00:00:00Z