The Childhood Solid Tumor Network: A new resource for the developmental biology and oncology research communities.
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[1] A. Pappo,et al. Pediatric solid tumor genomics and developmental pliancy , 2015, Oncogene.
[2] Li Ding,et al. The Genomic Landscape of Childhood and Adolescent Melanoma , 2014, The Journal of investigative dermatology.
[3] Erin K. Hedlund,et al. Genomic landscape of Ewing sarcoma defines an aggressive subtype with co-association of STAG2 and TP53 mutations. , 2014, Cancer discovery.
[4] Li Ding,et al. Recurrent somatic structural variations contribute to tumorigenesis in pediatric osteosarcoma. , 2014, Cell reports.
[5] F. Berthold,et al. Neuroblastoma in older children, adolescents and young adults: A report from the International Neuroblastoma Risk Group project , 2014, Pediatric blood & cancer.
[6] Heather L. Mulder,et al. Targeting oxidative stress in embryonal rhabdomyosarcoma. , 2013, Cancer cell.
[7] Michael A. Dyer,et al. Neuroblastoma: developmental biology, cancer genomics and immunotherapy , 2013, Nature Reviews Cancer.
[8] D. Finkelstein,et al. Cross-species genomic and epigenomic landscape of retinoblastoma , 2013, Oncotarget.
[9] Jenine K. Harris,et al. Incidence of Childhood and Adolescent Melanoma in the United States: 1973–2009 , 2013, Pediatrics.
[10] F. Speleman,et al. MYCN and ALKF1174L are sufficient to drive neuroblastoma development from neural crest progenitor cells , 2013, Oncogene.
[11] Giovanni Parmigiani,et al. Integrated genomic analyses identify ARID1A and ARID1B alterations in the childhood cancer neuroblastoma , 2012, Nature Genetics.
[12] L. Spector,et al. The epidemiology of hepatoblastoma , 2012, Pediatric blood & cancer.
[13] J. Graff,et al. A mouse model of rhabdomyosarcoma originating from the adipocyte lineage. , 2012, Cancer cell.
[14] R. Stallings,et al. LIN28B induces neuroblastoma and enhances MYCN levels via let-7 suppression , 2012, Nature Genetics.
[15] Li Ding,et al. The Pediatric Cancer Genome Project , 2012, Nature Genetics.
[16] Mauro Delorenzi,et al. PAX3/FOXO1 fusion gene status is the key prognostic molecular marker in rhabdomyosarcoma and significantly improves current risk stratification. , 2012, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[17] D. Neuberg,et al. Activated ALK collaborates with MYCN in neuroblastoma pathogenesis. , 2012, Cancer cell.
[18] Jinghui Zhang,et al. Association of age at diagnosis and genetic mutations in patients with neuroblastoma. , 2012, JAMA.
[19] M. Ladanyi,et al. Molecular pathogenesis of Ewing sarcoma: new therapeutic and transcriptional targets. , 2012, Annual review of pathology.
[20] Matthew W. Wilson,et al. A Novel Retinoblastoma Therapy from Genomic and Epigenetic Analyses , 2011, Nature.
[21] U. Dirksen,et al. Risk of recurrence and survival after relapse in patients with Ewing sarcoma , 2011, Pediatric blood & cancer.
[22] J. Sage,et al. Coexpression of normally incompatible developmental pathways in retinoblastoma genesis. , 2011, Cancer cell.
[23] J. Neuhaus,et al. Clinical features and outcomes in patients with extraskeletal ewing sarcoma , 2011, Cancer.
[24] J. Maris. Recent advances in neuroblastoma. , 2010, The New England journal of medicine.
[25] O. Delattre,et al. Fusion gene-negative alveolar rhabdomyosarcoma is clinically and molecularly indistinguishable from embryonal rhabdomyosarcoma. , 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[26] S. Ognjanovic,et al. Trends in childhood rhabdomyosarcoma incidence and survival in the United States, 1975‐2005 , 2009, Cancer.
[27] P. Gunaratne,et al. Histologic subtypes of hepatoblastoma are characterized by differential canonical Wnt and Notch pathway activation in DLK+ precursors. , 2009, Human pathology.
[28] S. Ogawa,et al. Oncogenic mutations of ALK kinase in neuroblastoma , 2008, Nature.
[29] John M. Maris,et al. Identification of ALK as a major familial neuroblastoma predisposition gene , 2008, Nature.
[30] D. Gary Gilliland,et al. Activating mutations in ALK provide a therapeutic target in neuroblastoma , 2008, Nature.
[31] F. Alt,et al. Conditional mouse osteosarcoma, dependent on p53 loss and potentiated by loss of Rb, mimics the human disease. , 2008, Genes & development.
[32] J. Maris,et al. Prevalence and functional consequence of PHOX2B mutations in neuroblastoma , 2008, Oncogene.
[33] M. Dyer,et al. Retinoblastoma: from the two-hit hypothesis to targeted chemotherapy. , 2007, Cancer research.
[34] M. Washington,et al. Protocol for the examination of specimens from pediatric patients with hepatoblastoma. , 2007, Archives of pathology & laboratory medicine.
[35] M. Dyer,et al. Neuronal differentiation and synaptogenesis in retinoblastoma. , 2007, Cancer research.
[36] M. Hicks,et al. Clinicopathologic features of osteosarcoma in patients with Rothmund-Thomson syndrome. , 2007, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[37] W. Furman,et al. Familial adenomatous polyposis in two brothers with hepatoblastoma: Implications for diagnosis and screening , 2006, Pediatric blood & cancer.
[38] K K Matthay,et al. Evidence for an age cutoff greater than 365 days for neuroblastoma risk group stratification in the Children's Oncology Group. , 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[39] B. Pollock,et al. The spectrum of APC mutations in children with hepatoblastoma from familial adenomatous polyposis kindreds. , 2005, The Journal of pediatrics.
[40] T. Fears,et al. Pediatric melanoma: risk factor and survival analysis of the surveillance, epidemiology and end results database. , 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[41] M. Tucker,et al. Risk of new cancers after radiotherapy in long-term survivors of retinoblastoma: an extended follow-up. , 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[42] A. Munnich,et al. PHOX2B genotype allows for prediction of tumor risk in congenital central hypoventilation syndrome. , 2005, American journal of human genetics.
[43] M. Dyer,et al. The search for the retinoblastoma cell of origin , 2005, Nature Reviews Cancer.
[44] E. Rappaport,et al. Germline PHOX2B mutation in hereditary neuroblastoma. , 2004, American journal of human genetics.
[45] Jonathan Gray,et al. Rb regulates proliferation and rod photoreceptor development in the mouse retina , 2004, Nature Genetics.
[46] A. Pappo. Melanoma in children and adolescents. , 2003, European journal of cancer.
[47] G. Brodeur. Neuroblastoma: biological insights into a clinical enigma , 2003, Nature Reviews Cancer.
[48] Charles J. Sherr,et al. The INK4a/ARF network in tumour suppression , 2001, Nature Reviews Molecular Cell Biology.
[49] James R. Anderson,et al. Rhabdomyosarcoma and Undifferentiated Sarcoma in the First Two Decades of Life: A Selective Review of Intergroup Rhabdomyosarcoma Study Group Experience and Rationale for Intergroup Rhabdomyosarcoma Study V , 2001, Journal of pediatric hematology/oncology.
[50] J. Foley,et al. Beta-catenin mutations and protein accumulation in all hepatoblastomas examined from B6C3F1 mice treated with anthraquinone or oxazepam. , 2000, Cancer research.
[51] F. Barr. Chromosomal translocations involving paired box transcription factors in human cancer. , 1997, The international journal of biochemistry & cell biology.
[52] G. Mohapatra,et al. Targeted expression of MYCN causes neuroblastoma in transgenic mice , 1997, The EMBO journal.
[53] W. McWhirter,et al. Risk factors for childhood melanoma in Queensland, Australia , 1997, International journal of cancer.
[54] C. Cepko,et al. Cell fate determination in the vertebrate retina. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[55] S. Friend,et al. Germline mutations of the p53 tumor suppressor gene in children with osteosarcoma. , 1994, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[56] A. Huvos,et al. Osteogenic sarcoma with clinically detectable metastasis at initial presentation. , 1993, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[57] G. Thomas,et al. Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours , 1992, Nature.
[58] D. Slamon,et al. Frequency and structure of p53 rearrangements in human osteosarcoma. , 1990, Cancer research.
[59] C. Sapienza,et al. A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting , 1989 .
[60] R. Ellsworth,et al. Second tumors in nonirradiated bilateral retinoblastoma. , 1979, American journal of ophthalmology.
[61] D. L. Stewart,et al. Receptive field characteristics of striate cortical neurons in the rabbit. , 1971, Brain research.
[62] Robert W. Williams,et al. Eye, retina, and visual system of the mouse , 2008 .
[63] L. Ries,et al. Cancer incidence and survival among children and adolescents: United States SEER Program 1975-1995. , 1999 .
[64] G. Perilongo,et al. Liver tumours. Commentary , 1999 .
[65] H. Shimada,et al. Histopathology of childhood sarcomas, Intergroup Rhabdomyosarcoma Studies I and II: clinicopathologic correlation. , 1988, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.