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Inflammatory myofibroblastic tumors harbor multiple potentially actionable kinase fusions

Cancer discovery, 2014-08, Vol.4 (8), p.889-895

2014

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Imaging features of alveolar soft-part sarcoma: a report from Children's Oncology Group Study ARST0332

American journal of roentgenology (1976), 2014-12, Vol.203 (6), p.1345-1352

2014

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Alveolar soft part sarcoma and granular cell tumor: an immunohistochemical comparison study

Human pathology, 2014-05, Vol.45 (5), p.1039-1044

2014

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Alveolar rhabdomyosarcomas in conditional Pax3:Fkhr mice: cooperativity of Ink4a/ARF and Trp53 loss of function

Genes & development, 2004-11, Vol.18 (21), p.2614-2626

2004

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Undifferentiated Sarcomas in Children Harbor Clinically Relevant Oncogenic Fusions and Gene Copy-Number Alterations: A Report from the Children's Oncology Group

Clinical cancer research, 2018-08, Vol.24 (16), p.3888-3897

2018

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IgG4 plasma cells in inflammatory myofibroblastic tumor: inflammatory marker or pathogenic link?

Modern pathology, 2011-04, Vol.24 (4), p.606-612

2011

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ALK1 and p80 Expression and Chromosomal Rearrangements Involving 2p23 in Inflammatory Myofibroblastic Tumor

Modern pathology, 2001-06, Vol.14 (6), p.569-576

2001

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Solitary, multifocal and generalized myofibromas: clinicopathological and immunohistochemical features of 114 cases

Histopathology, 2012-05, Vol.60 (6B), p.E1-E11

2012

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Expression of ALK1 and p80 in Inflammatory Myofibroblastic Tumor and Its Mesenchymal Mimics: A Study of 135 Cases

Modern pathology, 2002-09, Vol.15 (9), p.931-938

2002

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Survivin expression and prognostic significance in pediatric malignant peripheral nerve sheath tumors (MPNST)

PloS one, 2013-11, Vol.8 (11), p.e80456-e80456

2013

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Differentiating Ewing's sarcoma from other round blue cell tumors using a RT-PCR translocation panel on formalin-fixed paraffin-embedded tissues

Modern pathology, 2007-03, Vol.20 (3), p.397-404

2007

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Granular cell tumors overexpress TFE3 without corollary gene rearrangement—Reply

Human pathology, 2015-08, Vol.46 (8), p.1243-1243

2015

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Undifferentiated sarcoma: does it exist? A clinicopathologic study of 7 pediatric cases and review of literature

Human pathology, 2009-11, Vol.40 (11), p.1600-1610

2009

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Inflammatory myofibroblastic tumor: comparison of clinicopathologic, histologic, and immunohistochemical features including ALK expression in atypical and aggressive cases

The American journal of surgical pathology, 2007-04, Vol.31 (4), p.509-520

2007

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Lipoblastoma (LPB): a clinicopathologic and immunohistochemical analysis of 59 cases

The American journal of surgical pathology, 2009-11, Vol.33 (11), p.1705-1712

2009

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Signal transduction pathway analysis in desmoid‐type fibromatosis: Transforming growth factor–β, COX2 and sex steroid receptors

Cancer science, 2012-12, Vol.103 (12), p.2173-2180

2012

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Methylthioadenosine phosphorylase and activated insulin-like growth factor-1 receptor/insulin receptor: potential therapeutic targets in chordoma

The Journal of pathology, 2010-04, Vol.220 (5), p.608-617

2010

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Fibroblastic and Myofibroblastic Tumors in Children and Adolescents

Pediatric and developmental pathology, 2012-01, Vol.15 (1_suppl), p.127-180

2012

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Epithelioid inflammatory myofibroblastic sarcoma: An aggressive intra-abdominal variant of inflammatory myofibroblastic tumor with nuclear membrane or perinuclear ALK

The American journal of surgical pathology, 2011-01, Vol.35 (1), p.135-144

2011

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Composite uterine neoplasm with embryonal rhabdomyosarcoma and primitive neuroectodermal tumor components: rhabdomyosarcoma with divergent differentiation, variant of primitive neuroectodermal tumor, or unique entity?

Human pathology, 2013-04, Vol.44 (4), p.656-663

2013

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c-Myc Enhances Sonic Hedgehog-Induced Medulloblastoma Formation from Nestin-Expressing Neural Progenitors in Mice

Neoplasia (New York, N.Y.), 2003-05, Vol.5 (3), p.198-204

2003

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Fibrous hamartoma of infancy: a clinicopathologic analysis of 60 cases

The American journal of surgical pathology, 2014-03, Vol.38 (3), p.394-401

2014

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A Conditional Mouse Model of Synovial Sarcoma: Insights into a Myogenic Origin

Cancer cell, 2007-04, Vol.11 (4), p.375-388

2007

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The rationale for nonsteroidal anti-inflammatory drug therapy for inflammatory myofibroblastic tumors: a Children's Oncology Group study

Journal of pediatric surgery, 2005-06, Vol.40 (6), p.999-1003

2005

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Morphologic and immunophenotypic analysis of desmoid-type fibromatosis after radiation therapy

Human pathology, 2012-09, Vol.43 (9), p.1418-1424

2012

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Inflammatory myofibroblastic tumors harbor multiple potentially actionable kinase fusions

Imaging features of alveolar soft-part sarcoma: a report from Children's Oncology Group Study ARST0332

Alveolar soft part sarcoma and granular cell tumor: an immunohistochemical comparison study

Alveolar rhabdomyosarcomas in conditional Pax3:Fkhr mice: cooperativity of Ink4a/ARF and Trp53 loss of function

Undifferentiated Sarcomas in Children Harbor Clinically Relevant Oncogenic Fusions and Gene Copy-Number Alterations: A Report from the Children's Oncology Group

IgG4 plasma cells in inflammatory myofibroblastic tumor: inflammatory marker or pathogenic link?

ALK1 and p80 Expression and Chromosomal Rearrangements Involving 2p23 in Inflammatory Myofibroblastic Tumor

Solitary, multifocal and generalized myofibromas: clinicopathological and immunohistochemical features of 114 cases

Expression of ALK1 and p80 in Inflammatory Myofibroblastic Tumor and Its Mesenchymal Mimics: A Study of 135 Cases

Survivin expression and prognostic significance in pediatric malignant peripheral nerve sheath tumors (MPNST)

Differentiating Ewing's sarcoma from other round blue cell tumors using a RT-PCR translocation panel on formalin-fixed paraffin-embedded tissues

Granular cell tumors overexpress TFE3 without corollary gene rearrangement—Reply

Undifferentiated sarcoma: does it exist? A clinicopathologic study of 7 pediatric cases and review of literature

Inflammatory myofibroblastic tumor: comparison of clinicopathologic, histologic, and immunohistochemical features including ALK expression in atypical and aggressive cases

Lipoblastoma (LPB): a clinicopathologic and immunohistochemical analysis of 59 cases

Signal transduction pathway analysis in desmoid‐type fibromatosis: Transforming growth factor–β, COX2 and sex steroid receptors

Methylthioadenosine phosphorylase and activated insulin-like growth factor-1 receptor/insulin receptor: potential therapeutic targets in chordoma

Fibroblastic and Myofibroblastic Tumors in Children and Adolescents

Epithelioid inflammatory myofibroblastic sarcoma: An aggressive intra-abdominal variant of inflammatory myofibroblastic tumor with nuclear membrane or perinuclear ALK

Composite uterine neoplasm with embryonal rhabdomyosarcoma and primitive neuroectodermal tumor components: rhabdomyosarcoma with divergent differentiation, variant of primitive neuroectodermal tumor, or unique entity?

c-Myc Enhances Sonic Hedgehog-Induced Medulloblastoma Formation from Nestin-Expressing Neural Progenitors in Mice

Fibrous hamartoma of infancy: a clinicopathologic analysis of 60 cases

A Conditional Mouse Model of Synovial Sarcoma: Insights into a Myogenic Origin

The rationale for nonsteroidal anti-inflammatory drug therapy for inflammatory myofibroblastic tumors: a Children's Oncology Group study

Morphologic and immunophenotypic analysis of desmoid-type fibromatosis after radiation therapy

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