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1. Full Text INI1-deficient tumors: Diagnostic features and molecular genetics
by Hollmann, Travis J and Hornick, Jason L
The American journal of surgical pathology, ISSN 0147-5185, 10/2011, Volume 35, Issue 10, pp. e47 - e63
malignant rhabdoid tumor | SMARCB1 | epithelioid sarcoma | schwannomatosis | SNF5 | soft tissue tumors | renal medullarycarcinoma | INI1 | Pathology | Life Sciences & Biomedicine | Surgery | Science & Technology | Myoepithelioma - metabolism | Kidney Neoplasms - genetics | Soft Tissue Neoplasms - diagnosis | Humans | Transcription Factors - deficiency | Carcinoma, Medullary - diagnosis | Carcinoma, Medullary - metabolism | Kidney Neoplasms - metabolism | DNA-Binding Proteins - deficiency | Kidney Neoplasms - diagnosis | DNA-Binding Proteins - metabolism | SMARCB1 Protein | Biomarkers, Tumor - metabolism | Sarcoma - diagnosis | Cytogenetic Analysis | Rhabdoid Tumor - metabolism | Sarcoma - genetics | Soft Tissue Neoplasms - genetics | Epithelioid Cells - pathology | Myoepithelioma - diagnosis | Chondrosarcoma - diagnosis | Chromosomal Proteins, Non-Histone - metabolism | Carcinoma, Medullary - genetics | Nerve Sheath Neoplasms - diagnosis | Soft Tissue Neoplasms - metabolism | Nerve Sheath Neoplasms - metabolism | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Chromosomal Proteins, Non-Histone - deficiency | Chromosomal Proteins, Non-Histone - genetics | Epithelioid Cells - metabolism | Immunohistochemistry - methods | Sarcoma - metabolism | Transcription Factors - metabolism | Rhabdoid Tumor - genetics | Rhabdoid Tumor - diagnosis | Index Medicus
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2. Full Text SMARCA4 (BRG1) Loss of Expression Is a Useful Marker for the Diagnosis of Ovarian Small Cell Carcinoma of the Hypercalcemic Type (Ovarian Rhabdoid Tumor): A Comprehensive Analysis of 116 Rare Gynecologic Tumors, 9 Soft Tissue Tumors, and 9 Melanomas
by Karanian-Philippe, Marie and Velasco, Valérie and Longy, Michel and Floquet, Anne and Arnould, Laurent and Coindre, Jean-Michel and Le Naoures-Méar, Cécile and Averous, Gerlinde and Guyon, Frédéric and MacGrogan, Gaëtan and Croce, Sabrina
The American journal of surgical pathology, ISSN 0147-5185, 09/2015, Volume 39, Issue 9, pp. 1197 - 1205
Rhabdoid tumor | Ovary | INI1/SMARCB1 | SMARCA4/BRG1 | Small cell carcinoma hypercalcemic type | Pathology | Life Sciences & Biomedicine | Surgery | Science & Technology | Immunohistochemistry | Predictive Value of Tests | Carcinoma, Small Cell - genetics | Nuclear Proteins - analysis | Humans | Middle Aged | Ovarian Neoplasms - pathology | Sarcoma, Ewing - pathology | Granulosa Cell Tumor - pathology | Rhabdoid Tumor - pathology | Bone Neoplasms - pathology | Ovarian Neoplasms - genetics | Young Adult | Carcinoma, Small Cell - chemistry | Sarcoma, Endometrial Stromal - pathology | Soft Tissue Neoplasms - chemistry | Melanoma - genetics | Bone Neoplasms - chemistry | Adult | Female | Bone Neoplasms - genetics | Melanoma - chemistry | Soft Tissue Neoplasms - genetics | Hypercalcemia - genetics | Diagnosis, Differential | Ovarian Neoplasms - chemistry | Sarcoma, Ewing - chemistry | Hypercalcemia - pathology | Endometrial Neoplasms - chemistry | Biomarkers, Tumor - analysis | Rhabdoid Tumor - chemistry | Hypercalcemia - metabolism | Melanoma - pathology | Sarcoma, Endometrial Stromal - chemistry | Rhabdoid Tumor - genetics | Biopsy | Adolescent | Soft Tissue Neoplasms - pathology | DNA Helicases - analysis | Endometrial Neoplasms - pathology | Granulosa Cell Tumor - chemistry | Biomarkers, Tumor - genetics | Transcription Factors - analysis | Carcinoma, Small Cell - pathology | Neoplasm Staging | Sarcoma, Ewing - genetics | Index Medicus
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3. Full Text Rhabdoid Tumor of the Kidney in The National Wilms' Tumor Study: Age at Diagnosis As a Prognostic Factor
by Gail E. Tomlinson and Norman E. Breslow and Jeffrey Dome and Katherine Adams Guthrie and Pat Norkool and Sierra Li and Patrick R.M. Thomas and Elizabeth Perlman and J. Bruce Beckwith and Giulio J. D'Angio and Daniel M. Green
Journal of clinical oncology, ISSN 0732-183X, 10/2005, Volume 23, Issue 30, pp. 7641 - 7645
Life Sciences & Biomedicine | Oncology | Science & Technology | Tumors of the urinary system | Nephrology. Urinary tract diseases | Biological and medical sciences | Kidneys | Medical sciences | Tumors | Doxorubicin - therapeutic use | Rhabdoid Tumor - drug therapy | Age Distribution | Prognosis | Humans | Child, Preschool | Rhabdoid Tumor - radiotherapy | Infant | Male | Survival Rate | Treatment Outcome | Combined Modality Therapy | Antibiotics, Antineoplastic - therapeutic use | Female | Rhabdoid Tumor - diagnosis | Neoplasm Staging | Child | Infant, Newborn | Index Medicus
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4. Full Text SMARCB1-deficient Tumors of Childhood: A Practical Guide
by Pawel, Bruce R
1/2018, Volume 21, Issue 1, 23
SMARCB1 | immunohistochemistry | pediatric neoplasms | rhabdoid | oncology | Pathology | Pediatrics | Life Sciences & Biomedicine | Science & Technology | Neoplasms - metabolism | Kidney Neoplasms - genetics | Biomarkers, Tumor - deficiency | Humans | Chordoma - metabolism | Gene Expression Regulation, Neoplastic | SMARCB1 Protein - genetics | Kidney Neoplasms - metabolism | Neoplasms - diagnosis | Neoplasms, Neuroepithelial - pathology | Rhabdoid Tumor - pathology | Chordoma - pathology | Kidney Neoplasms - diagnosis | Neoplasms, Neuroepithelial - diagnosis | Neoplasms - genetics | Neurilemmoma - genetics | Nerve Sheath Neoplasms - pathology | Neoplasms, Neuroepithelial - genetics | Sarcoma - diagnosis | Rhabdoid Tumor - metabolism | SMARCB1 Protein - deficiency | Sarcoma - genetics | Carcinoma - pathology | Child | Chordoma - genetics | Diagnosis, Differential | Nerve Sheath Neoplasms - genetics | Nerve Sheath Neoplasms - diagnosis | Carcinoma - diagnosis | Nerve Sheath Neoplasms - metabolism | Sarcoma - pathology | Neoplasms, Neuroepithelial - metabolism | Neurilemmoma - pathology | Sarcoma - metabolism | Rhabdoid Tumor - genetics | Neurilemmoma - metabolism | Carcinoma - genetics | Kidney Neoplasms - pathology | Biomarkers, Tumor - genetics | Rhabdoid Tumor - diagnosis | Carcinoma - metabolism | Chordoma - diagnosis | Neoplasms - pathology | Neurilemmoma - diagnosis | Index Medicus
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5. Full Text Clinicopathologic prognostic factors in childhood atypical teratoid and rhabdoid tumor of the central nervous system: A multicenter study
by Dufour, Christelle and Beaugrand, Annick and Le Deley, Marie Cécile and Bourdeaut, Franck and André, Nicolas and Leblond, Pierre and Bertozzi, Anne-Isabelle and Frappaz, Didier and Rialland, Xavier and Fouyssac, Fanny and Edan, Christine and Grill, Jacques and Quidot, Marion and Varlet, Pascale
Cancer, ISSN 0008-543X, 08/2012, Volume 118, Issue 15, pp. 3812 - 3821
atypical teratoid/rhabdoid tumors | prognostic factors | clinical and pathologic features | pediatric oncology | claudin-6 | Biological and medical sciences | Medical sciences | Tumors | Prognosis | Humans | Brain Neoplasms - pathology | Rhabdoid Tumor - mortality | Child, Preschool | Teratoma - diagnosis | Infant | Male | Rhabdoid Tumor - pathology | Female | Teratoma - therapy | Brain Neoplasms - mortality | Child | Infant, Newborn | Brain Neoplasms - diagnosis | Risk Factors | Central Nervous System Neoplasms - therapy | Teratoma - mortality | Rhabdoid Tumor - therapy | Central Nervous System Neoplasms - pathology | Teratoma - pathology | Brain Neoplasms - therapy | Rhabdoid Tumor - diagnosis | Central Nervous System Neoplasms - diagnosis | Central Nervous System Neoplasms - mortality | Care and treatment | Diagnosis | Children | Health aspects | Brain tumors | Central nervous system | Index Medicus | Abridged Index Medicus
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6. Full Text Cancer surveillance in Gorlin syndrome and rhabdoid tumor predisposition syndrome
by Foulkes, William D and Kamihara, Junne and Evans, D. Gareth R and Brugières, Laurence and Bourdeaut, Franck and Molenaar, Jan J and Walsh, Michael F and Brodeur, Garrett M and Diller, Lisa
Clinical cancer research, ISSN 1078-0432, 06/2017, Volume 23, Issue 12, pp. e62 - e67
Life Sciences & Biomedicine | Oncology | Science & Technology | Kidney Neoplasms - genetics | Basal Cell Nevus Syndrome - diagnosis | Brain Neoplasms - diagnosis | Humans | Brain Neoplasms - pathology | Brain Neoplasms - genetics | Child, Preschool | Repressor Proteins - genetics | SMARCB1 Protein - genetics | Chromatin Assembly and Disassembly - genetics | Infant | Rhabdoid Tumor - pathology | Transcription Factors - genetics | Patched-1 Receptor - genetics | Kidney Neoplasms - diagnosis | Basal Cell Nevus Syndrome - pathology | Rhabdoid Tumor - genetics | Germ-Line Mutation | Kidney Neoplasms - pathology | Rhabdoid Tumor - diagnosis | Basal Cell Nevus Syndrome - genetics | Nuclear Proteins - genetics | DNA Helicases - genetics | Brain | Carcinoma | Kidneys | Brain tumors | Abnormalities | Risk | Chromatin remodeling | Hypercalcemia | Cranium | Magnetic resonance imaging | Surveillance | Gorlin syndrome | Hedgehog protein | Medulloblastoma | Carrier lifetime | Mutation | Children | Age | Cancer | Tumors | Index Medicus
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7. Full Text Diffuse and strong cyclin D1 immunoreactivity in clear cell sarcoma of the kidney
by Mirkovic, Jelena and Calicchio, Monica and Fletcher, Christopher D and Perez‐Atayde, Antonio R
Histopathology, ISSN 0309-0167, 09/2015, Volume 67, Issue 3, pp. 306 - 312
Wilms tumour | mesoblastic nephroma | Ewing sarcoma | children | cyclin D1 | rhabdoid tumour | renal clear cell sarcoma | Rhabdoid tumour | Mesoblastic nephroma | Children | Cyclin D1 | Renal clear cell sarcoma | Pathology | Life Sciences & Biomedicine | Science & Technology | Cell Biology | Immunohistochemistry | Cyclin D1 - metabolism | Sarcoma, Clear Cell - diagnosis | Diagnosis, Differential | Nephroma, Mesoblastic - diagnosis | Sarcoma, Ewing - metabolism | Nephroma, Mesoblastic - metabolism | Humans | Child, Preschool | Male | Sarcoma, Ewing - diagnosis | Kidney Neoplasms - metabolism | Neuroblastoma - diagnosis | Kidney Neoplasms - diagnosis | Sarcoma, Clear Cell - pathology | Biomarkers, Tumor - metabolism | Female | Kidney Neoplasms - pathology | Neuroblastoma - metabolism | Rhabdoid Tumor - diagnosis | Sarcoma, Clear Cell - metabolism | Rhabdoid Tumor - metabolism | Wilms Tumor - metabolism | Wilms Tumor - diagnosis | Sarcoma | Endometrial cancer | Tumors | Index Medicus
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8. Full Text Selective killing of SMARCA2- and SMARCA4-deficient small cell carcinoma of the ovary, hypercalcemic type cells by inhibition of EZH2: In vitro and in vivo preclinical models
by Chan-Penebre, Elayne and Armstrong, Kelli and Drew, Allison and Grassian, Alexandra R and Feldman, Igor and Knutson, Sarah K and Kuplast-Barr, Kristy and Roche, Maria and Campbell, John and Ho, Peter and Copeland, Robert A and Chesworth, Richard and Smith, Jesse J and Keilhack, Heike and Ribich, Scott A
Molecular cancer therapeutics, ISSN 1535-7163, 05/2017, Volume 16, Issue 5, pp. 850 - 860
Life Sciences & Biomedicine | Oncology | Science & Technology | Enhancer of Zeste Homolog 2 Protein - antagonists & inhibitors | Carcinoma, Small Cell - genetics | Humans | Ovarian Neoplasms - pathology | Rhabdoid Tumor - pathology | Ovarian Neoplasms - genetics | Female | Hypercalcemia - drug therapy | Gene Expression Regulation, Neoplastic - drug effects | Nuclear Proteins - genetics | DNA Helicases - genetics | Ovarian Neoplasms - drug therapy | Hypercalcemia - genetics | Rhabdoid Tumor - drug therapy | Diagnosis, Differential | Enhancer of Zeste Homolog 2 Protein - genetics | Histone-Lysine N-Methyltransferase - genetics | Hypercalcemia - pathology | Ovarian Neoplasms - diagnosis | Carcinoma, Small Cell - drug therapy | Transcription Factors - genetics | Carcinoma, Small Cell - diagnosis | Chromosomal Proteins, Non-Histone - genetics | Xenograft Model Antitumor Assays | Animals | Rhabdoid Tumor - genetics | Hypercalcemia - diagnosis | Cell Line, Tumor | Mice | Rhabdoid Tumor - diagnosis | Mutation | Carcinoma, Small Cell - pathology | Medical research | Biotechnology | Ovarian carcinoma | Clinical trials | Tumor cell lines | Gene expression | Anticancer properties | Hypercalcemia | SWI/SNF complex | Xenografts | Histone methyltransferase | Antitumor activity | Inhibition | Cancer | Tumors | Index Medicus
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9. Full Text Familial rhabdoid tumour 'avant la lettre'—from pathology review to exome sequencing and back again
by Witkowski, Leora and Lalonde, Emilie and Zhang, Jian and Albrecht, Steffen and Hamel, Nancy and Cavallone, Luca and May, Sandra Thompson and Nicholson, James C and Coleman, Nicholas and Murray, Matthew J and Tauber, Peter F and Huntsman, David G and Schönberger, Stefan and Yandell, David and Hasselblatt, Martin and Tischkowitz, Marc D and Majewski, Jacek and Foulkes, William D
The Journal of pathology, ISSN 0022-3417, 09/2013, Volume 231, Issue 1, pp. 35 - 43
exome sequencing | ovarian | chromatin remodelling | cancer | rhabdoid tumour | germ cell tumour | SMARCA4 | Chromatin remodelling | Exome sequencing | Rhabdoid tumour | Germ cell tumour | Ovarian | Cancer | Humans | Teratoma - diagnosis | Male | Ovarian Neoplasms - genetics | DNA Mutational Analysis | Diagnostic Errors | Biomarkers, Tumor - metabolism | Female | Ovarian Neoplasms - metabolism | Rhabdoid Tumor - metabolism | Tumor Cells, Cultured | Nuclear Proteins - genetics | DNA Helicases - genetics | Genetic Predisposition to Disease | Ovarian Neoplasms - diagnosis | Nuclear Proteins - metabolism | Transcription Factors - genetics | Transcription Factors - metabolism | DNA Helicases - metabolism | Exome - genetics | Rhabdoid Tumor - genetics | Pedigree | Chromosome Aberrations | Biomarkers, Tumor - genetics | Rhabdoid Tumor - diagnosis | DNA, Neoplasm - genetics | Mutation | Genes, Dominant - genetics | Sequence Analysis, DNA - methods | Genetic aspects | Tumors | Index Medicus
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