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Laboratory Investigation, ISSN 0023-6837, 09/2015, Volume 95, Issue 9, pp. 1071 - 1076
Journal Article
International Journal of Biochemistry and Cell Biology, ISSN 1357-2725, 08/2014, Volume 53, Issue Apr 8, pp. 475 - 481
Benign fibrous histiocytoma (BFH) is a mesenchymal tumor that most often occurs in the skin (so-called dermatofibroma), but may also appear in soft tissues... 
CD63 | LAMTOR1 | Cell membrane | Gene fusion | Endosomes | Podoplanin | DERMATOFIBROMA | APOPTOSIS | ACTIVATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | FAMILY | CELL BIOLOGY | GENE | ROLES | PKC-DELTA | GROWTH | SKIN | Humans | Middle Aged | Protein Kinase C beta - genetics | Male | Oncogene Proteins, Fusion - isolation & purification | Protein Kinase C beta - isolation & purification | Histiocytoma, Benign Fibrous - pathology | Adult | Female | Tetraspanin 30 - genetics | Histiocytoma, Benign Fibrous - genetics | Membrane Proteins - isolation & purification | Chromosome Banding | Membrane Glycoproteins - isolation & purification | Endosomes - genetics | Signal Transduction | Membrane Proteins - genetics | In Situ Hybridization, Fluorescence | Endosomes - pathology | Protein Kinase C-delta - isolation & purification | Membrane Glycoproteins - genetics | Carrier Proteins - genetics | Tetraspanin 30 - isolation & purification | Oncogene Proteins, Fusion - genetics | Carrier Proteins - isolation & purification | Polymorphism, Single Nucleotide | Protein Kinase C-delta - genetics | Proteins | RNA | Stem cells | Medical genetics | Fluorescence | Amino acids | Protein kinases | Genetic polymorphisms | Protein binding | Clinical Medicine | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Orthopedics | Medicinska och farmaceutiska grundvetenskaper | Klinisk medicin | Cancer and Oncology | Ortopedi | Cancer och onkologi
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 2013, Volume 68, Issue 2, pp. 189.e1 - 189.e21
Cutaneous findings are not uncommonly a concomitant finding in patients afflicted with gastrointestinal (GI) diseases. The dermatologic manifestations may... 
Cowden syndrome | hereditary and nonhereditary gastrointestinal malignancies | Muir-Torre syndrome | gastrointestinal disorders | hamartomatous polyposis syndrome | Cronkhite-Canada syndrome | Bannayan-Riley-Ruvalcaba syndrome | cutaneous manifestations | Peutz-Jeghers syndrome | Lynch syndrome | paraneoplastic syndrome | PEUTZ-JEGHERS-SYNDROME | RILEY-RUVALCABA-SYNDROME | HEREDITARY COLORECTAL-CANCER | DERMATOLOGY | PERIANAL PAGETS-DISEASE | LESER-TRELAT SIGN | MUIR-TORRE-SYNDROME | NECROLYTIC MIGRATORY ERYTHEMA | FAMILIAL ADENOMATOUS POLYPOSIS | PARANEOPLASTICA BAZEX-SYNDROME | MALIGNANT ACANTHOSIS NIGRICANS | Paraneoplastic Syndromes - genetics | Dermatomyositis - genetics | Carcinoma, Basal Cell - genetics | Colorectal Neoplasms - genetics | Humans | Hypotrichosis - genetics | Gastrointestinal Neoplasms - complications | Acanthosis Nigricans - genetics | Gastrointestinal Neoplasms - pathology | Skin Diseases, Genetic - etiology | Adenomatous Polyposis Coli - genetics | Histiocytoma, Benign Fibrous - genetics | PTEN Phosphohydrolase - genetics | Hamartoma Syndrome, Multiple - genetics | Necrolytic Migratory Erythema - diagnosis | Necrolytic Migratory Erythema - genetics | Intestinal Polyposis - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Malignant Carcinoid Syndrome - genetics | Gastrointestinal Diseases - complications | Peutz-Jeghers Syndrome - genetics | Gastrointestinal Diseases - genetics | Paraneoplastic Syndromes - complications | Hamartoma Syndrome, Multiple - diagnosis | Skin Neoplasms - genetics | Skin Neoplasms - secondary | Colorectal Neoplasms, Hereditary Nonpolyposis - etiology | Mutation
Journal Article
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 Article
Modern Pathology, ISSN 0893-3952, 03/2003, Volume 16, Issue 3, pp. 256 - 262
Journal Article
The Journal of Pathology, ISSN 0022-3417, 07/2004, Volume 203, Issue 3, pp. 822 - 830
Journal Article
Journal Article