Gender dimorphism and age of onset in malignant peripheral nerve sheath tumor preclinical models and human patients
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L. Tran | S. Dry | W. Tap | J. Nakashima | Hong Wu | Elizabeth Shurell | Yunfeng Li | F. Eilber | N. Federman | Kathleen B Smith | Brenna M Tam | B. Tam | K. B. Smith
[1] L. Tran,et al. Gender dimorphism and age of onset in malignant peripheral nerve sheath tumor preclinical models and human patients , 2014, BMC Cancer.
[2] Michael D. Brooks,et al. Sexually dimorphic RB inactivation underlies mesenchymal glioblastoma prevalence in males. , 2014, The Journal of clinical investigation.
[3] Jilong Yang,et al. Genomic and molecular aberrations in malignant peripheral nerve sheath tumor and their roles in personalized target therapy. , 2013, Surgical oncology.
[4] K. S. Hall,et al. Survival meta-analyses for >1800 malignant peripheral nerve sheath tumor patients with and without neurofibromatosis type 1 , 2012, Neuro-oncology.
[5] N. Warrington,et al. Why does Jack, and not Jill, break his crown? Sex disparity in brain tumors , 2012, Biology of Sex Differences.
[6] T. de Ravel,et al. Atypical neurofibromas in neurofibromatosis type 1 are premalignant tumors , 2011, Genes, chromosomes & cancer.
[7] G. Scott,et al. Microarray Comparative Genomic Hybridization Detection of Copy Number Changes in Desmoplastic Melanoma and Malignant Peripheral Nerve Sheath Tumor , 2011, The American Journal of dermatopathology.
[8] D. Evans,et al. Malignant peripheral nerve sheath tumours in NF1: improved survival in women and in recent years. , 2011, European journal of cancer.
[9] Wei Zhang,et al. Genomic and Molecular Characterization of Malignant Peripheral Nerve Sheath Tumor Identifies the IGF1R Pathway as a Primary Target for Treatment , 2011, Clinical Cancer Research.
[10] R. Dubrow,et al. Demographic variation in incidence of adult glioma by subtype, United States, 1992-2007 , 2011, BMC Cancer.
[11] C. Fischer,et al. Sex-biased suppression of chemically induced neural carcinogenesis in congenic BDIX.BDIV-Mss4a rats. , 2011, Physiological genomics.
[12] B. Scheithauer,et al. Array-Based Comparative Genomic Hybridization Identifies CDK4 and FOXM1 Alterations as Independent Predictors of Survival in Malignant Peripheral Nerve Sheath Tumor , 2011, Clinical Cancer Research.
[13] M. Wallace,et al. Analysis of steroid hormone effects on xenografted human NF1 tumor schwann cells , 2010, Cancer biology & therapy.
[14] R. Dikshit,et al. Malignant peripheral nerve sheath tumors: clinicopathological profile of 63 cases diagnosed at a tertiary cancer referral center in Mumbai, India. , 2010, Indian journal of pathology & microbiology.
[15] K. S. Hall,et al. Genomic changes in chromosomes 10, 16, and X in malignant peripheral nerve sheath tumors identify a high-risk patient group. , 2010, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[16] S. Gabriel,et al. Integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR, and NF1. , 2010, Cancer cell.
[17] S. Dry,et al. Quantitative F18‐fluorodeoxyglucose positron emission tomography accurately characterizes peripheral nerve sheath tumors as malignant or benign , 2010, Cancer.
[18] Andrew H. Beck,et al. Genome‐wide transcriptome analyses reveal p53 inactivation mediated loss of miR‐34a expression in malignant peripheral nerve sheath tumours , 2010, The Journal of pathology.
[19] S. Dry,et al. PTEN dosage is essential for neurofibroma development and malignant transformation , 2009, Proceedings of the National Academy of Sciences.
[20] C. Fischer,et al. Genetic basis of sex-specific resistance to neuro-oncogenesis in (BDIX × BDIV) F2 rats , 2009, Mammalian Genome.
[21] K. S. Hall,et al. Identification of p53 as a strong predictor of survival for patients with malignant peripheral nerve sheath tumors. , 2009, Neuro-oncology.
[22] O. Myhre-Jensen,et al. A consecutive series of 30 malignant schwannomas. Survival in relation to clinico-pathological parameters and treatment. , 2009, Acta pathologica, microbiologica, et immunologica Scandinavica. Section A, Pathology.
[23] Karlyne M. Reilly,et al. Chr 19A/J modifies tumor resistance in a sex- and parent-of-origin-specific manner , 2009, Mammalian Genome.
[24] N. Freedman,et al. Sex Disparities in Cancer Incidence by Period and Age , 2009, Cancer Epidemiology Biomarkers & Prevention.
[25] P. Terrier,et al. Frequent EGFR Positivity and Overexpression in High-Grade Areas of Human MPNSTs , 2008, Sarcoma.
[26] E. Petty,et al. The role of steroid hormones in the NF1 phenotype: Focus on pregnancy , 2008, American journal of medical genetics. Part A.
[27] N. Thomas,et al. Germline and somatic NF1 gene mutation spectrum in NF1‐associated malignant peripheral nerve sheath tumors (MPNSTs) , 2008, Human mutation.
[28] C. Hartmann,et al. MMP-13, p53 in the Progression of Malignant Peripheral Nerve Sheath Tumors , 2007 .
[29] M. Wallace,et al. In vitro studies of steroid hormones in neurofibromatosis 1 tumors and schwann cells , 2007, Molecular carcinogenesis.
[30] R. Benigni. Social sexual inequality and sex difference in cancer incidence. , 2007, Environmental research.
[31] U. Bockmühl,et al. Malignant peripheral nerve sheath tumors of the head and neck: Management of 10 cases and literature review , 2007, Head & neck.
[32] S. Huson,et al. The heterogeneous nature of germline mutations in NF1 patients with malignant peripheral serve sheath tumours (MPNSTs) , 2006, Human mutation.
[33] R. Buchert,et al. Prognostic relevance of FDG PET in patients with neurofibromatosis type-1 and malignant peripheral nerve sheath tumours , 2006, European Journal of Nuclear Medicine and Molecular Imaging.
[34] J. Zeller,et al. Association between benign and malignant peripheral nerve sheath tumors in NF1 , 2005, Neurology.
[35] M. Watson,et al. Gene Expression Profiling Reveals Unique Molecular Subtypes of Neurofibromatosis Type I‐associated and Sporadic Malignant Peripheral Nerve Sheath Tumors , 2004, Brain pathology.
[36] S. Tripp,et al. Malignant Peripheral Nerve Sheath Tumor: A Comparison of Grade, Immunophenotype, and Cell Cycle/Growth Activation Marker Expression in Sporadic and Neurofibromatosis 1-Related Lesions , 2003, The American journal of surgical pathology.
[37] D. Evans,et al. Malignant peripheral nerve sheath tumours in neurofibromatosis 1 , 2002, Journal of medical genetics.
[38] Theresa M. Wizemann,et al. Exploring the biological contributions to human health: does sex matter? , 2001, Journal of women's health & gender-based medicine.
[39] K. Leroy,et al. Malignant peripheral nerve sheath tumors associated with neurofibromatosis type 1: a clinicopathologic and molecular study of 17 patients. , 2001, Archives of dermatology.
[40] J. McCann. Gender differences in cancer that don't make sense--or do they? , 2000, Journal of the National Cancer Institute.
[41] H. Taubert,et al. Gains in chromosomes 7, 8q, 15q and 17q are characteristic changes in malignant but not in benign peripheral nerve sheath tumors from patients with Recklinghausen's disease. , 2000, Cancer letters.
[42] R. Hughes,et al. Evaluation of 18fluorodeoxyglucose positron emission tomography (18FDG PET) in the detection of malignant peripheral nerve sheath tumours arising from within plexiform neurofibromas in neurofibromatosis 1 , 2000, Journal of neurology, neurosurgery, and psychiatry.
[43] A. Ferrari,et al. Malignant peripheral nerve sheath tumors in children: a single-institution twenty-year experience. , 1999, Journal of pediatric hematology/oncology.
[44] F. Haseltine. Does Sex Matter? , 1999, Science.
[45] H. Taubert,et al. Genomic imbalances of 7p and 17q in malignant peripheral nerve sheath tumors are clinically relevant , 1999, Genes, chromosomes & cancer.
[46] L. Dehner,et al. p53 and Ki-67 Proliferating Cell Nuclear Antigen in Benign and Malignant Peripheral Nerve Sheath Tumors in Children , 1999, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.
[47] M Super,et al. A clinical study of type 1 neurofibromatosis in north west England , 1999, Journal of medical genetics.
[48] A. Davis,et al. Neurogenic sarcomas: experience at the University of Toronto. , 1998, Neurosurgery.
[49] M. Bilsky,et al. Subdiaphragmatic and intrathoracic paraspinal malignant peripheral nerve sheath tumors , 1998, Cancer.
[50] H. Inoue,et al. A clinical analysis of malignant schwannoma. , 1997, Acta medica Okayama.
[51] A. Pappo,et al. Malignant peripheral nerve sheath tumors: The St. Jude Children's Research Hospital experience , 1995, Annals of Surgical Oncology.
[52] J. Vauthey,et al. Extremity malignant peripheral nerve sheath tumors (neurogenic sarcomas): A 10-year experience , 1995, Annals of Surgical Oncology.
[53] E. Abemayor,et al. Malignant nerve sheath tumors of the head and neck: A combined experience from two university hospitals , 1991, The Laryngoscope.
[54] R. Hruban,et al. Malignant peripheral nerve sheath tumors of the buttock and lower extremity. A study of 43 cases , 1990, Cancer.
[55] B. Scheithauer,et al. Malignant peripheral nerve sheath tumors. A clinicopathologic study of 120 cases , 1986, Cancer.
[56] M. Enjoji,et al. Malignant peripheral nerve‐sheath tumors (malignant schwannomas): An immunohistochemical study of 29 cases , 1985, The American journal of surgical pathology.
[57] B. Scheithauer,et al. Malignant peripheral nerve sheath tumors with divergent differentiation , 1984, Cancer.
[58] Takashi Nakajima,et al. Malignant Peripheral Nerve Tumors: A Clinicopathological and Flectron Microscopic Study , 1984 .
[59] J. Trojanowski,et al. Malignant tumors of nerve sheath origin , 1980, Cancer.
[60] F. Enzinger,et al. Malignant schwannoma associated with von Recklinghausen's neurofibromatosis , 1979, Virchows Archiv A.
[61] J. Beare. A STUDY OF 43 CASES , 1976 .
[62] G. Swapp,et al. Neurofibromatosis in pregnancy , 1973, The British journal of dermatology.
[63] A. Huvos,et al. Malignant schwannoma. A Clinicopathologic Study , 1973, Cancer.
[64] H. White. Survival in malignant schwannoma. An 18‐year study , 1971, Cancer.
[65] E. Soule,et al. Sarcomas of the peripheral nerves and somatic soft tissues associated with multiple neurofibromatosis (von Recklinghausen's disease) , 1963, Cancer.
[66] E. Soule,et al. Primary malignant neoplasms of nerves (Malignant neurilemomas) in patients without manifestations of multiple neurofibromatosis (von Recklinghausen's disease) , 1963, Cancer.
[67] R. H. Young,et al. RECKLINGHAUSEN'S NEUROFIBROMATOSIS: CLINICAL MANIFESTATIONS IN THIRTY-ONE CASES , 1937 .
[68] A. von Deimling,et al. MMP-13 and p53 in the progression of malignant peripheral nerve sheath tumors. , 2007, Neoplasia.
[69] C. Fischer,et al. Gender‐specific polygenic control of ethylnitrosourea‐induced oncogenesis in the rat peripheral nervous system , 2006, International journal of cancer.
[70] J. Day. Malignant schwannoma. , 2002, Journal of neurosurgery.
[71] V. Muller. Exploring the biological contributions to human health: does sex matter? , 2001, Journal of women's health & gender-based medicine.
[72] Leila Mohammadi,et al. BMC Cancer , 2001 .
[73] F. Mitelman,et al. Cytogenetic characterization of peripheral nerve sheath tumours: a report of the CHAMP study group. , 2000, The Journal of pathology.
[74] T. Nakajima,et al. Malignant peripheral nerve tumors: a clinicopathological and electron microscopic study. , 1984, Japanese journal of clinical oncology.