Germline and somatic SMARCA4 mutations characterize small cell carcinoma of the ovary, hypercalcemic type
暂无分享,去创建一个
R. Siebert | A. Berchuck | H. Mackay | W. Foulkes | B. Clarke | V. Georgoulias | T. Ulbright | N. Hamel | J. Nadaf | J. Majewski | S. Albrecht | Y. Riazalhosseini | K. Pavlakis | M. Hasselblatt | I. Nagel | M. Tischkowitz | J. Arseneau | D. Grynspan | E. Tomiak | E. Saloustros | M. Longy | W. McCluggage | S. Castellino | L. Witkowski | S. Fahiminiya | E. Castellsagué | M. Wu | J. Lamovec | R. Karabakhtsian | F. Ueland | B. Rivera | C. Stewart | M. Arseneault | L. Roth | Avi Saskin | C. Gilpin | Rachel Silva-Smith | Elizabeth Reilly | Jian Carrot-Zhang | François Plourde | Anna Margiolaki | Tracey A Bender | Mona K. Wu | C. Stewart | Jian Carrot-Zhang
[1] W. Hahn,et al. Residual Complexes Containing SMARCA2 (BRM) Underlie the Oncogenic Drive of SMARCA4 (BRG1) Mutation , 2014, Molecular and Cellular Biology.
[2] W. Grajkowska,et al. Ovarian small cell carcinoma of hypercalcemic type - evidence of germline origin and SMARCA4 gene inactivation. a pilot study. , 2013, Polish journal of pathology : official journal of the Polish Society of Pathologists.
[3] W. Foulkes,et al. DICER1 hotspot mutations in non-epithelial gonadal tumours , 2013, British Journal of Cancer.
[4] W. Foulkes,et al. Familial rhabdoid tumour 'avant la lettre'—from pathology review to exome sequencing and back again , 2013, The Journal of pathology.
[5] J. Yokota,et al. A synthetic lethality-based strategy to treat cancers harboring a genetic deficiency in the chromatin remodeling factor BRG1. , 2013, Cancer research.
[6] C. Stiller,et al. Extracranial rhabdoid tumours: what we have learned so far and future directions. , 2013, The Lancet. Oncology.
[7] Y. Fukushima,et al. Clinical correlations of mutations affecting six components of the SWI/SNF complex: Detailed description of 21 patients and a review of the literature , 2013, American journal of medical genetics. Part A.
[8] G. Crabtree,et al. Proteomic and bioinformatic analysis of mammalian SWI/SNF complexes identifies extensive roles in human malignancy , 2013, Nature Genetics.
[9] D. Huntsman,et al. Small cell ovarian carcinoma: genomic stability and responsiveness to therapeutics , 2013, Orphanet Journal of Rare Diseases.
[10] D. Eccles,et al. Loss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomas , 2013, Nature Genetics.
[11] S. Ishikawa,et al. Lung cancer with loss of BRG1/BRM, shows epithelial mesenchymal transition phenotype and distinct histologic and genetic features , 2013, Cancer science.
[12] Jonathan R. Pollack,et al. The Spectrum of SWI/SNF Mutations, Ubiquitous in Human Cancers , 2013, PloS one.
[13] O. Gharbi,et al. Small Cell Carcinoma of the Ovary of Hypercalcemic Type: A Case Report , 2012, Case reports in oncological medicine.
[14] J. Carpten,et al. Deep Clonal Profiling of Formalin Fixed Paraffin Embedded Clinical Samples , 2012, PloS one.
[15] R. Spang,et al. Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing , 2012, Nature Genetics.
[16] Kristian Cibulskis,et al. A remarkably simple genome underlies highly malignant pediatric rhabdoid cancers. , 2012, The Journal of clinical investigation.
[17] Benjamin E. Gross,et al. The cBio cancer genomics portal: an open platform for exploring multidimensional cancer genomics data. , 2012, Cancer discovery.
[18] D. Evans,et al. Frequency of SMARCB1 mutations in familial and sporadic schwannomatosis , 2012, neurogenetics.
[19] David T. W. Jones,et al. Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma , 2012, Nature.
[20] C. Roberts,et al. SWI/SNF nucleosome remodellers and cancer , 2011, Nature Reviews Cancer.
[21] R. Siebert,et al. Nonsense mutation and inactivation of SMARCA4 (BRG1) in an atypical teratoid/rhabdoid tumor showing retained SMARCB1 (INI1) expression. , 2011, The American journal of surgical pathology.
[22] Benjamin J. Raphael,et al. Integrated Genomic Analyses of Ovarian Carcinoma , 2011, Nature.
[23] K. Münstedt,et al. Small cell carcinoma of the ovary of the hypercalcaemic type: an analysis of clinical and prognostic aspects of a rare disease on the basis of cases published in the literature , 2011, Archives of Gynecology and Obstetrics.
[24] Helga Thorvaldsdóttir,et al. Integrative Genomics Viewer , 2011, Nature Biotechnology.
[25] M. DePristo,et al. The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. , 2010, Genome research.
[26] H. Hakonarson,et al. ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data , 2010, Nucleic acids research.
[27] R. Siebert,et al. Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome. , 2010, American journal of human genetics.
[28] J. Petty,et al. Familial small cell carcinoma of the ovary , 2009, Pediatric blood & cancer.
[29] Gonçalo R. Abecasis,et al. The Sequence Alignment/Map format and SAMtools , 2009, Bioinform..
[30] O. Tawfik,et al. Aberrant expression of SWI/SNF catalytic subunits BRG1/BRM is associated with tumor development and increased invasiveness in prostate cancers , 2007, The Prostate.
[31] G. Fleischhack,et al. Ovarian small cell carcinoma of the hypercalcemic type in children and adolescents , 2006, Cancer.
[32] R. Siebert,et al. FISH analysis for the detection of lymphoma-associated chromosomal abnormalities in routine paraffin-embedded tissue. , 2006, The Journal of molecular diagnostics : JMD.
[33] P. Clement,et al. Selected miscellaneous ovarian lesions: small cell carcinomas, mesothelial lesions, mesenchymal and mixed neoplasms, and non-neoplastic lesions , 2005, Modern Pathology.
[34] W. McCluggage,et al. Ovarian Neoplasms Composed of Small Round Cells: A Review , 2004, Advances in anatomic pathology.
[35] McCluggage Wg. Ovarian Neoplasms Composed of Small Round Cells: A Review , 2004 .
[36] E. Oliva,et al. An Immunohistochemical Analysis of Ovarian Small Cell Carcinoma of Hypercalcemic Type , 2004, International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists.
[37] T. Poggio,et al. Prediction of central nervous system embryonal tumour outcome based on gene expression , 2002, Nature.
[38] D. Teng,et al. BRG1, a component of the SWI-SNF complex, is mutated in multiple human tumor cell lines. , 2000, Cancer research.
[39] M. Longy,et al. Familial cluster of ovarian small cell carcinoma: a new mendelian entity? , 1996, Journal of medical genetics.
[40] J. Lamovec,et al. Familial occurrence of small-cell carcinoma of the ovary. , 1995, Archives of pathology & laboratory medicine.
[41] E. Oliva,et al. Small Cell Carcinoma of the Ovary, Hypercalcemic Type: A Clinicopathological Analysis of 150 Cases , 1994, The American journal of surgical pathology.
[42] C. Mangioni,et al. Primary ovarian small cell carcinoma: four more cases. , 1993, Gynecologic oncology.
[43] R. Scully,et al. Primary Ovarian Small Cell Carcinoma of Pulmonary Type: A Clinicopathologic, Immunohistologic, and Flow Cytometric Analysis of 11 Cases , 1992, The American journal of surgical pathology.
[44] R. Scully. Classification of human ovarian tumors. , 1987, Environmental health perspectives.
[45] A. Talerman,et al. Poorly differentiated (small cell) carcinoma of the ovary in young women: evidence supporting a germ cell origin. , 1987, Human pathology.
[46] S. Krane,et al. Differential cyclic AMP responses to calcitonin among human ovarian carcinoma cell lines: A calcitonin‐responsive line derived from a rare tumor type , 1986, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.
[47] T. Kudo,et al. A greatly simplified method of establishing B-lymphoblastoid cell lines. , 1978, Cancer research.
[48] Harlan I. Firminger,et al. Atlas of tumor pathology , 1954 .
[49] Atlas of Tumor Pathology , 1954 .
[50] A. McKenna,et al. The genetic landscape of clinical resistance to RAF inhibition in metastatic melanoma. , 2014, Cancer discovery.
[51] H. Nagatsuka,et al. Genetic and epigenetic alterations of BRG1 promote oral cancer development. , 2005, International journal of oncology.
[52] Claude-Alain H. Roten,et al. Theoretical and practical advances in genome halving , 2004 .
[53] Gilmore Hr,et al. Armed Forces Institute of Pathology. , 1968, Oral surgery, oral medicine, and oral pathology.