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Journal of Clinical Oncology, ISSN 0732-183X, 05/2010, Volume 28, Issue 13, pp. 2151 - 2158
Journal Article
BMC Cancer, ISSN 1471-2407, 02/2014, Volume 14, Issue 1, pp. 139 - 139
Journal Article
Cancer Cell, ISSN 1535-6108, 12/2013, Volume 24, Issue 6, pp. 710 - 724
Journal Article
Modern Pathology, ISSN 0893-3952, 04/2012, Volume 25, Issue 4, pp. 602 - 614
Embryonal rhabdomyosarcoma of the uterine cervix is an uncommon presentation of the most common soft-tissue sarcoma in the first decades of life. Unlike... 
adenosarcoma | uterine cervix | pleuropulmonary blastoma | DICER1 | Sertoli-Leydig cell tumor | embryonal rhabdomyosarcoma | PLEUROPULMONARY BLASTOMA REGISTRY | FEMALE GENITAL-TRACT | MALIGNANT ECTOMESENCHYMOMA | LEYDIG CELL TUMOR | DICER1 MUTATIONS | PATHOLOGY | SARCOMA BOTRYOIDES | MULLERIAN ADENOSARCOMA | HETEROLOGOUS ELEMENTS | YOUNG-ADULT POPULATION | OF-THE-LITERATURE | Immunohistochemistry | Rhabdomyosarcoma, Embryonal - chemistry | Humans | Child, Preschool | Infant | Uterine Cervical Neoplasms - pathology | Sertoli-Leydig Cell Tumor - pathology | Rhabdomyosarcoma, Embryonal - genetics | Young Adult | Time Factors | Rhabdomyosarcoma, Embryonal - therapy | Adult | Female | Cell Differentiation | Child | Rhabdomyosarcoma, Embryonal - pathology | Uterine Cervical Neoplasms - therapy | Genetic Predisposition to Disease | Ribonuclease III - genetics | Biomarkers, Tumor - analysis | Sertoli-Leydig Cell Tumor - genetics | Neoplasm Recurrence, Local | Pulmonary Blastoma - pathology | Treatment Outcome | Uterine Cervical Neoplasms - genetics | Sertoli-Leydig Cell Tumor - therapy | DEAD-box RNA Helicases - genetics | Disease-Free Survival | Pulmonary Blastoma - therapy | Phenotype | Adolescent | Biomarkers, Tumor - genetics | Uterine Cervical Neoplasms - chemistry | Mutation | Pulmonary Blastoma - genetics | Pulmonary Blastoma - chemistry | Sertoli-Leydig Cell Tumor - chemistry | Sertoli–Leydig cell tumor
Journal Article
Cancer Research, ISSN 0008-5472, 05/2006, Volume 66, Issue 9, pp. 4742 - 4749
Rhabdomyosarcoma (RIMS) is a highly malignant soft-tissue tumor of childhood deriving from skeletal muscle cells. RMS can be classified in two major histologic... 
GROWTH-FACTOR RECEPTOR | MUTANT MICE | ACTIVATION | FUSION | ONCOLOGY | MUSCLE DEVELOPMENT | C-MET | IN-VIVO | PAX3 | SATELLITE CELLS | EXPRESSION | Paired Box Transcription Factors - genetics | NIH 3T3 Cells | RNA, Small Interfering - genetics | Up-Regulation | Humans | Receptors, Growth Factor - antagonists & inhibitors | Apoptosis - genetics | Receptors, Growth Factor - genetics | Rhabdomyosarcoma, Embryonal - genetics | Rhabdomyosarcoma, Alveolar - therapy | RNA Interference | Rhabdomyosarcoma, Alveolar - metabolism | Cell Transformation, Neoplastic - genetics | Rhabdomyosarcoma, Embryonal - therapy | RNA, Small Interfering - biosynthesis | Female | Hepatocyte Growth Factor | Rhabdomyosarcoma, Alveolar - pathology | Cell Growth Processes - genetics | Rhabdomyosarcoma, Embryonal - pathology | Proto-Oncogene Proteins - antagonists & inhibitors | PAX3 Transcription Factor | Transduction, Genetic | Rhabdomyosarcoma, Alveolar - genetics | Neoplasm Invasiveness | Proto-Oncogene Proteins c-met | Gene Silencing | Proto-Oncogene Proteins - genetics | Forkhead Transcription Factors - genetics | Receptors, Growth Factor - physiology | Animals | Rhabdomyosarcoma, Embryonal - metabolism | Mice, Nude | Oncogene Proteins, Fusion - genetics | Proto-Oncogene Proteins - physiology | Forkhead Box Protein O1 | Mice | HeLa Cells | Cell Transformation, Neoplastic - pathology
Journal Article
Pediatric Blood & Cancer, ISSN 1545-5009, 04/2017, Volume 64, Issue 4, p. n/a
Journal Article
Annals of Surgical Oncology, ISSN 1068-9265, 10/2014, Volume 21, Issue 11, pp. 3579 - 3586
Journal Article
Current Oncology Reports, ISSN 1523-3790, 11/2010, Volume 12, Issue 6, pp. 402 - 410
Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma of childhood. The two most common histologic variants are the embryonal and alveolar subtypes.... 
Embryonal | Medicine & Public Health | Alveolar | Sarcoma | Stem cell | Rhabdomyosarcoma | Childhood | Oncology | Rapamycin | Insulin-like growth factor | UNITED-STATES | GROUP-III RHABDOMYOSARCOMA | PROGNOSTIC-FACTORS | INTERGROUP-RHABDOMYOSARCOMA | CHILDRENS ONCOLOGY GROUP | STUDY-IV | ONCOLOGY | EMBRYONAL RHABDOMYOSARCOMA | ALVEOLAR RHABDOMYOSARCOMA | EXPRESSION | SOFT-TISSUE SARCOMA | Antineoplastic Combined Chemotherapy Protocols - administration & dosage | Prognosis | Soft Tissue Neoplasms - diagnosis | Humans | Child, Preschool | Male | Rhabdomyosarcoma, Embryonal - diagnosis | Secondary Prevention | Rhabdomyosarcoma, Embryonal - genetics | TOR Serine-Threonine Kinases - antagonists & inhibitors | Neoplasm Metastasis | Rhabdomyosarcoma, Alveolar - diagnosis | Rhabdomyosarcoma, Alveolar - therapy | Neoplastic Stem Cells - metabolism | Rhabdomyosarcoma, Embryonal - therapy | Neoplastic Stem Cells - pathology | Tomography | Female | Rhabdomyosarcoma, Alveolar - pathology | Child | Rhabdomyosarcoma, Embryonal - pathology | Soft Tissue Neoplasms - genetics | Soft Tissue Neoplasms - therapy | Rhabdomyosarcoma, Alveolar - genetics | Risk Factors | Survival Rate | Clinical Trials as Topic | Combined Modality Therapy | Signal Transduction - genetics | Disease Progression | Protein Kinase Inhibitors - administration & dosage | Sirolimus - administration & dosage | Animals | Signal Transduction - drug effects | Soft Tissue Neoplasms - pathology | Mice | Mesenchymal Stromal Cells - pathology | Neoplasm Staging | Chemotherapy | Stem cells | Cancer
Journal Article
Journal of the College of Physicians and Surgeons Pakistan, ISSN 1022-386X, 2014, Volume 24, pp. S224 - S226
Journal Article