Mutations in the transcriptional repressor REST predispose to Wilms tumor
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C. Shaw | S. Seal | N. Rahman | N. Sebire | A. Renwick | S. Hanks | S. Mahamdallie | Elise Ruark | T. Westbrook | C. Stiller | J. Birch | T. McLean | E. Sheridan | G. Levitt | J. Hale | Thomas F. Westbrook | Kristen L. Karlin | Shawn E. Yost | M. Capra | J. Gray | J. Kingston | A. Zachariou | Alexander Renwick | Emma Ramsay | Anna Elliott | Elizabeth R Perdeaux
[1] Michael T. Rock. Lessons for the Rest , 2016 .
[2] S. Seal,et al. The ICR1000 UK exome series: a resource of gene variation in an outbred population , 2015, F1000Research.
[3] Kathy Pritchard-Jones,et al. The yin and yang of kidney development and Wilms’ tumors , 2015, Genes & development.
[4] C. Shaw,et al. The oncogenic STP axis promotes triple-negative breast cancer via degradation of the REST tumor suppressor. , 2014, Cell reports.
[5] S. Seal,et al. Germline mutations in the PAF1 complex gene CTR9 predispose to Wilms tumour , 2014, Nature Communications.
[6] G. McVean,et al. Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications , 2014, Nature Genetics.
[7] David A. Bennett,et al. REST and Stress Resistance in Aging and Alzheimer’s Disease , 2014, Nature.
[8] Peter Donnelly,et al. Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer , 2012, Nature.
[9] Martin Goodson,et al. Stampy: a statistical algorithm for sensitive and fast mapping of Illumina sequence reads. , 2011, Genome research.
[10] A. Bithell. REST: transcriptional and epigenetic regulator. , 2011, Epigenomics.
[11] U Schumacher,et al. Regulation of the NRSF/REST gene by methylation and CREB affects the cellular phenotype of small-cell lung cancer , 2010, Oncogene.
[12] Mingming Jia,et al. COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer , 2010, Nucleic Acids Res..
[13] Rory Johnson,et al. The role of REST in transcriptional and epigenetic dysregulation in Huntington's disease , 2010, Neurobiology of Disease.
[14] Xavier Estivill,et al. DYRK1A-dosage imbalance perturbs NRSF/REST levels, deregulating pluripotency and embryonic stem cell fate in Down syndrome. , 2008, American journal of human genetics.
[15] I. Wood,et al. Chromatin crosstalk in development and disease: lessons from REST , 2007, Nature Reviews Genetics.
[16] N. Rahman,et al. Surveillance for Wilms tumour in at-risk children: pragmatic recommendations for best practice , 2006, Archives of Disease in Childhood.
[17] N. Rahman,et al. Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour , 2006, Journal of Medical Genetics.
[18] J. Haefliger,et al. IB1/JIP-1 controls JNK activation and increased during prostatic LNCaP cells neuroendocrine differentiation. , 2005, Cellular signalling.
[19] G. Mandel,et al. REST and Its Corepressors Mediate Plasticity of Neuronal Gene Chromatin throughout Neurogenesis , 2005, Cell.
[20] N. Rahman,et al. Frequency and heritability of WT1 mutations in nonsyndromic Wilms' tumor patients: a UK Children's Cancer Study Group Study. , 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[21] C. Becker,et al. Reduced expression of the neuron restrictive silencer factor permits transcription of glycine receptor α1 subunit in small-cell lung cancer cells , 2003, Oncogene.
[22] N. Rahman,et al. Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2 , 2000, British Journal of Cancer.
[23] L. Strong,et al. Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors. , 1998, Cancer research.
[24] Nazneen Rahman,et al. Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12–q21 , 1996, Nature Genetics.