标题
Germline mutations and somatic inactivation of TRIM28 in Wilms tumour
作者
关键词
Nephroblastoma, DNA methylation, Frameshift mutation, Gene expression, Histology, Heterozygosity, Kidneys, Somatic mutation
出版物
PLoS Genetics
Volume 14, Issue 6, Pages e1007399
出版商
Public Library of Science (PLoS)
发表日期
2018-06-19
DOI
10.1371/journal.pgen.1007399
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Biallelic TRIP13 mutations predispose to Wilms tumor and chromosome missegregation
- (2017) Shawn Yost et al. NATURE GENETICS
- A Children's Oncology Group and TARGET initiative exploring the genetic landscape of Wilms tumor
- (2017) Samantha Gadd et al. NATURE GENETICS
- Differential regulation of mouse and human nephron progenitors by the Six family of transcriptional regulators
- (2016) Lori L. O'Brien et al. DEVELOPMENT
- Analysis of protein-coding genetic variation in 60,706 humans
- (2016) Monkol Lek et al. NATURE
- DICER1 pleuropulmonary blastoma familial tumour predisposition syndrome: What the paediatric urologist needs to know
- (2016) Alice Faure et al. Journal of Pediatric Urology
- Interactomic analysis of REST/NRSF and implications of its functional links with the transcription suppressor TRIM28 during neuronal differentiation
- (2016) Namgyu Lee et al. Scientific Reports
- Recurrent DGCR8, DROSHA, and SIX Homeodomain Mutations in Favorable Histology Wilms Tumors
- (2015) Amy L. Walz et al. CANCER CELL
- Mutations in the SIX1/2 Pathway and the DROSHA/DGCR8 miRNA Microprocessor Complex Underlie High-Risk Blastemal Type Wilms Tumors
- (2015) Jenny Wegert et al. CANCER CELL
- Improving our resolution of kidney morphogenesis across time and space
- (2015) Melissa H Little CURRENT OPINION IN GENETICS & DEVELOPMENT
- The WTX Tumor Suppressor Interacts with the Transcriptional Corepressor TRIM28
- (2015) Woo Jae Kim et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- A global reference for human genetic variation
- (2015) Richard A. Gibbs et al. NATURE
- Mutations in the transcriptional repressor REST predispose to Wilms tumor
- (2015) Shazia S Mahamdallie et al. NATURE GENETICS
- limma powers differential expression analyses for RNA-sequencing and microarray studies
- (2015) Matthew E. Ritchie et al. NUCLEIC ACIDS RESEARCH
- Proteomic analysis of embryonic kidney development: Heterochromatin proteins as epigenetic regulators of nephrogenesis
- (2015) Gry H. Dihazi et al. Scientific Reports
- TRIM28 Controls Genomic Imprinting through Distinct Mechanisms during and after Early Genome-wide Reprogramming
- (2015) Katherine A. Alexander et al. Cell Reports
- Clinically Relevant Subsets Identified by Gene Expression Patterns Support a Revised Ontogenic Model of Wilms Tumor: A Children's Oncology Group Study
- (2015) Samantha Gadd et al. NEOPLASIA
- Inferring copy number and genotype in tumour exome data
- (2014) Kaushalya C Amarasinghe et al. BMC GENOMICS
- Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumour
- (2014) Sandra Hanks et al. Nature Communications
- Somatic mutations in DROSHA and DICER1 impair microRNA biogenesis through distinct mechanisms in Wilms tumours
- (2014) Dinesh Rakheja et al. Nature Communications
- A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff
- (2012) Pablo Cingolani et al. FLY
- Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility
- (2012) Dewi Astuti et al. NATURE GENETICS
- NCBI GEO: archive for functional genomics data sets—update
- (2012) Tanya Barrett et al. NUCLEIC ACIDS RESEARCH
- Trim28 Is Required for Epigenetic Stability During Mouse Oocyte to Embryo Transition
- (2012) D. M. Messerschmidt et al. SCIENCE
- The GUDMAP database - an online resource for genitourinary research
- (2011) S. D. Harding et al. DEVELOPMENT
- Extending the phenotypes associated withDICER1mutations
- (2011) William D. Foulkes et al. HUMAN MUTATION
- Ensembl variation resources
- (2010) Yuan Chen et al. BMC GENOMICS
- Fast and accurate short read alignment with Burrows-Wheeler transform
- (2009) H. Li et al. BIOINFORMATICS
- Subsets of Very Low Risk Wilms Tumor Show Distinctive Gene Expression, Histologic, and Clinical Features
- (2009) S. T. Sredni et al. CLINICAL CANCER RESEARCH
- WTXinactivation is a frequent, but late event in Wilms tumors without apparent clinical impact
- (2009) Jenny Wegert et al. GENES CHROMOSOMES & CANCER
- Canonical WNT signalling determines lineage specificity in Wilms tumour
- (2009) R Fukuzawa et al. ONCOGENE
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreAdd your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload Now