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Cancer Cell, ISSN 1535-6108, 02/2013, Volume 23, Issue 2, pp. 249 - 262
Journal Article
American Journal of Surgical Pathology, ISSN 0147-5185, 12/2006, Volume 30, Issue 12, pp. 1502 - 1512
Inflammatory myofibroblastic tumor (IMT) of the urinary tract, also termed postoperative spindle cell nodule, inflammatory pseudotumor, and pseudosarcomatous... 
ALK | Sarcoma | Pseudosarcoma | Bladder | FISH | Urinary tract | Inflammatory myofibroblastic tumor | SURGERY | PSEUDOSARCOMATOUS FIBROMYXOID TUMOR | DIFFERENTIAL-DIAGNOSIS | sarcoma | PLASMA-CELL GRANULOMA | FUSION | ALK EXPRESSION | inflammatory myofibroblastic tumor | urinary tract | PSEUDOTUMOR | PATHOLOGY | LESIONS | ANAPLASTIC LYMPHOMA KINASE | pseudosarcoma | bladder | OF-THE-LITERATURE | Inflammation - pathology | Urologic Diseases - enzymology | Urologic Diseases - genetics | Protein-Tyrosine Kinases - metabolism | Carcinoma, Transitional Cell - enzymology | Humans | Middle Aged | Ureter - enzymology | Child, Preschool | Male | Urinary Bladder - pathology | Urothelium - pathology | Prostate - pathology | Protein-Tyrosine Kinases - genetics | Fibrosarcoma - pathology | Urothelium - enzymology | Aged, 80 and over | Biomarkers, Tumor - metabolism | Adult | Female | Urinary Bladder - enzymology | Child | Carcinoma, Transitional Cell - genetics | Granuloma, Plasma Cell - enzymology | Granuloma, Plasma Cell - genetics | In Situ Hybridization, Fluorescence | Receptor Protein-Tyrosine Kinases | Granuloma, Plasma Cell - pathology | Fibrosarcoma - genetics | Carcinoma, Transitional Cell - pathology | Urologic Diseases - pathology | Adolescent | Aged | Prostate - enzymology | Fibrosarcoma - enzymology | Ureter - pathology
Journal Article
Modern Pathology, ISSN 0893-3952, 09/2002, Volume 15, Issue 9, pp. 931 - 938
Abnormalities of chromosome 2p23 with expression of ALK1 and p80 occur in both inflammatory myofibroblastic tumor (IMT) and anaplastic large cell lymphoma.... 
ALK gene rearrangements | Anaplastic large cell lymphoma | ALK immunohistochemistry | Inflammatory myofibroblastic tumor | DIAGNOSIS | P80(NPM/ALK) | inflammatory myofibroblastic tumor | INVOLVEMENT | 2P23 | PSEUDOTUMOR | LARGE-CELL LYMPHOMA | TPM3-ALK | PATHOLOGY | GENE | SARCOMAS | anaplastic large cell lymphoma | Immunohistochemistry | Humans | Rhabdomyosarcoma - metabolism | Leiomyosarcoma - metabolism | Rhabdomyosarcoma - pathology | Fibrosarcoma - metabolism | Activin Receptors, Type I - biosynthesis | Chromosomes, Human, Pair 2 - genetics | Protein-Tyrosine Kinases - genetics | Fibrosarcoma - pathology | Neoplasms, Muscle Tissue - metabolism | Nerve Sheath Neoplasms - pathology | Histiocytoma, Benign Fibrous - pathology | Leiomyosarcoma - genetics | Child | Soft Tissue Neoplasms - genetics | Neoplasms, Muscle Tissue - pathology | Histiocytoma, Benign Fibrous - genetics | Diagnosis, Differential | Nerve Sheath Neoplasms - genetics | Leiomyosarcoma - pathology | Histiocytoma, Benign Fibrous - metabolism | Carrier Proteins - biosynthesis | Soft Tissue Neoplasms - metabolism | In Situ Hybridization, Fluorescence | Myofibromatosis - metabolism | Nerve Sheath Neoplasms - metabolism | Fibroma - genetics | Myofibromatosis - genetics | Receptor Protein-Tyrosine Kinases | Fibroma - pathology | Bacterial Proteins | Neoplasms, Muscle Tissue - genetics | Fibrosarcoma - genetics | Membrane Proteins - biosynthesis | Activin Receptors, Type II | Fibroma - metabolism | Chromosome Aberrations | Soft Tissue Neoplasms - pathology | Mesoderm - metabolism | Rhabdomyosarcoma - genetics | Mesoderm - pathology | Myofibromatosis - pathology
Journal Article
Journal of Surgical Oncology, ISSN 0022-4790, 04/2015, Volume 111, Issue 5, pp. 513 - 519
Journal Article
Journal Article
Medicine (United States), ISSN 0025-7974, 01/2015, Volume 94, Issue 3, p. e369
Journal Article
Neurosurgery Clinics of North America, ISSN 1042-3680, 01/2013, Volume 24, Issue 1, pp. 67 - 78
Journal Article
Veterinary Pathology, ISSN 0300-9858, 7/2016, Volume 53, Issue 4, pp. 781 - 787
Osteosarcoma (OSA) is a malignant heterogeneous primary bone tumor responsible for up to 90% of all primary bone tumors in dogs. In this study, osteocalcin... 
bone tumors | osteonectin | osteoid | chondrosarcoma | osteocalcin | canine | immunohistochemistry | osteosarcoma | DIAGNOSIS | PROGNOSTIC-FACTORS | IMMUNOREACTIVITY | IRREGULAR BONES | ANTIGENS | PATHOLOGY | TUMORS | BIOLOGY | DOGS | DECALCIFICATION | VETERINARY SCIENCES | Bone and Bones - pathology | Hemangiosarcoma - metabolism | Hemangiosarcoma - veterinary | Dog Diseases - metabolism | Histiocytic Sarcoma - diagnosis | Antibodies | Extracellular Matrix - metabolism | Fibrosarcoma - metabolism | Osteosarcoma - diagnosis | Bone Neoplasms - pathology | Dog Diseases - pathology | Osteosarcoma - veterinary | Bone Neoplasms - metabolism | Hemangiosarcoma - diagnosis | Sarcoma - veterinary | Fibrosarcoma - pathology | Histiocytic Sarcoma - metabolism | Bone and Bones - metabolism | Sensitivity and Specificity | Biomarkers, Tumor - metabolism | Chondrosarcoma - pathology | Sarcoma - diagnosis | Histiocytic Sarcoma - pathology | Immunohistochemistry - veterinary | Dog Diseases - diagnosis | Bone Neoplasms - veterinary | Osteosarcoma - metabolism | Hemangiosarcoma - pathology | Chondrosarcoma - diagnosis | Diagnosis, Differential | Fibrosarcoma - diagnosis | Bone Neoplasms - diagnosis | Osteocalcin - metabolism | Osteonectin - metabolism | Sarcoma - pathology | Sarcoma - metabolism | Animals | Chondrosarcoma - metabolism | Chondrosarcoma - veterinary | Histiocytic Sarcoma - veterinary | Dogs | Fibrosarcoma - veterinary | Osteosarcoma - pathology
Journal Article
Journal Article
Applied Immunohistochemistry and Molecular Morphology, ISSN 1541-2016, 05/2015, Volume 23, Issue 5, pp. 313 - 326
Pediatric tumors are heterogenous and can be quite varied in appearance. However, those in the infamous "small round blue-cell tumor" group, with their... 
tumors | immunohistochemistry | pediatric | ROUND-CELL TUMORS | SYNOVIAL SARCOMA | ANATOMY & MORPHOLOGY | PATHOLOGY | SARCOMA/PRIMITIVE NEUROECTODERMAL TUMOR | NEUROBLASTOMA PATHOLOGY CLASSIFICATION | WILMS-TUMOR | MALIGNANT RHABDOID TUMORS | SOFT-TISSUE TUMORS | EWINGS-SARCOMA CELLS | MEDICAL LABORATORY TECHNOLOGY | CONGENITAL-INFANTILE FIBROSARCOMA | NERVE SHEATH TUMORS | Immunohistochemistry | Hepatoblastoma - genetics | Wilms Tumor - genetics | Humans | Sarcoma, Ewing - pathology | Rhabdomyosarcoma - pathology | Hepatoblastoma - diagnosis | Sarcoma, Alveolar Soft Part - pathology | Sarcoma, Alveolar Soft Part - genetics | Fibrosarcoma - pathology | Desmoplastic Small Round Cell Tumor - pathology | Child | Wilms Tumor - diagnosis | Neuroblastoma - pathology | Pulmonary Blastoma - diagnosis | Hepatoblastoma - pathology | Fibrosarcoma - diagnosis | Rhabdomyosarcoma - diagnosis | Desmoplastic Small Round Cell Tumor - genetics | Neuroblastoma - genetics | Pulmonary Blastoma - pathology | Immunophenotyping | In Situ Hybridization, Fluorescence | Sarcoma, Ewing - diagnosis | Sarcoma, Synovial - diagnosis | Desmoplastic Small Round Cell Tumor - diagnosis | Neuroblastoma - diagnosis | Wilms Tumor - pathology | Fibrosarcoma - genetics | Phenotype | Sarcoma, Synovial - genetics | Biomarkers, Tumor - genetics | Rhabdomyosarcoma - genetics | Pulmonary Blastoma - genetics | Sarcoma, Ewing - genetics | Sarcoma, Synovial - pathology | Sarcoma, Alveolar Soft Part - diagnosis
Journal Article