Fletcher, Christopher D.M.
Christopher D. M. Fletcher
Fletcher, Christopher D. M., 19..-....
VIAF ID: 182572 (Personal)
Permalink: http://viaf.org/viaf/182572
Preferred Forms
- 100 0 _ ‡a Christopher D. M. Fletcher
- 200 _ | ‡a Fletcher ‡b Christopher D. M.
- 100 1 _ ‡a Fletcher, Christopher D. M
-
-
- 100 1 _ ‡a Fletcher, Christopher D. M.
- 100 1 _ ‡a Fletcher, Christopher D. M.
-
- 100 1 _ ‡a Fletcher, Christopher D. M.
-
- 100 1 _ ‡a Fletcher, Christopher D. M., ‡d 19..-....
-
-
-
4xx's: Alternate Name Forms (9)
Works
Title | Sources |
---|---|
5-Hydroxymethylcytosine is a nuclear biomarker to assess biological potential in histologically ambiguous heavily pigmented melanocytic neoplasms | |
Adequacy of pathology resident training for employment: a survey report from the Future of Pathology Task Group | |
An atlas of gross pathology | |
Biochemical correlates of thiazolidinedione-induced adipocyte differentiation by high-resolution magic angle spinning NMR spectroscopy | |
Central nervous system involvement in diffuse large B-cell lymphoma: an analysis of risks and prevention strategies in the post-rituximab era. | |
Clinically Relevant Molecular Subtypes in Leiomyosarcoma | |
Coactivated platelet-derived growth factor receptor {alpha} and epidermal growth factor receptor are potential therapeutic targets in intimal sarcoma | |
Consistent SMARCB1 homozygous deletions in epithelioid sarcoma and in a subset of myoepithelial carcinomas can be reliably detected by FISH in archival material | |
Diagnostic histopathology of tumors | |
Diffuse and strong cyclin D1 immunoreactivity in clear cell sarcoma of the kidney. | |
Distinct transcriptional signature and immunoprofile of CIC-DUX4 fusion-positive round cell tumors compared to EWSR1-rearranged Ewing sarcomas: further evidence toward distinct pathologic entities | |
DNA copy number changes in tumors within the spectrum of cellular, atypical, and metastasizing fibrous histiocytoma | |
Efficacy and safety of sunitinib in patients with advanced gastrointestinal stromal tumour after failure of imatinib: a randomised controlled trial | |
Establishment and characterization of MRT cell lines from genetically engineered mouse models and the influence of genetic background on their development. | |
EWSR1-CREB1 is the predominant gene fusion in angiomatoid fibrous histiocytoma | |
Expression of enhancer of zeste homolog 2 (EZH2) protein in histiocytic and dendritic cell neoplasms with evidence for p-ERK1/2-related, but not MYC- or p-STAT3-related cell signaling. | |
Expression of subtype-specific group 1 leiomyosarcoma markers in a wide variety of sarcomas by gene expression analysis and immunohistochemistry | |
GRIA2 is a novel diagnostic marker for solitary fibrous tumour identified through gene expression profiling | |
Hairy Cell Leukemia, Version 2.2018, NCCN Clinical Practice Guidelines in Oncology. | |
High Frequency of Ovarian Cyst Development in Vhl2B/+;Snf5+/- Mice. | |
The histologic spectrum of soft tissue spindle cell tumors with NTRK3 gene rearrangements | |
IgG4 plasma cells in inflammatory myofibroblastic tumor: inflammatory marker or pathogenic link? | |
Indistinguishable genomic profiles and shared prognostic markers in undifferentiated pleomorphic sarcoma and leiomyosarcoma: different sides of a single coin? | |
Investigative pathology: leading the post-genomic revolution | |
Makuro byōri karā atorasu | |
Malignant giant solitary fibrous tumor of the mediastinum. | |
Management of malignant gastrointestinal stromal tumours | |
Mutations in Hedgehog pathway genes in fetal rhabdomyomas | |
n88146204 | |
NCCN Guidelines Insights: Myeloproliferative Neoplasms, Version 2.2018. | |
Neonatal rhabdomyosarcoma misdiagnosed as a congenital hemangioma | |
Novel ZC3H7B-BCOR, MEAF6-PHF1, and EPC1-PHF1 fusions in ossifying fibromyxoid tumors--molecular characterization shows genetic overlap with endometrial stromal sarcoma. | |
Pathobiology of soft tissue tumours | |
Pazopanib for metastatic soft-tissue sarcoma (PALETTE): a randomised, double-blind, placebo-controlled phase 3 trial | |
Phase II study of imatinib in patients with small cell lung cancer. | |
PPARgamma ligands inhibit primary tumor growth and metastasis by inhibiting angiogenesis | |
Primary and secondary kinase genotypes correlate with the biological and clinical activity of sunitinib in imatinib-resistant gastrointestinal stromal tumor | |
Primary gastrointestinal liposarcoma-a clinicopathological study of 8 cases of a rare entity | |
A prognostic model for soft tissue sarcoma of the extremities and trunk wall based on size, vascular invasion, necrosis, and growth pattern. | |
The PTEN and INK4A/ARF tumor suppressors maintain myelolymphoid homeostasis and cooperate to constrain histiocytic sarcoma development in humans | |
Pure epithelioid PEComas (so-called epithelioid angiomyolipoma) of the kidney: A clinicopathologic study of 41 cases: detailed assessment of morphology and risk stratification. | |
A reappraisal of hemangiopericytoma of bone; analysis of cases reclassified as synovial sarcoma and solitary fibrous tumor of bone | |
Recurrent SRF-RELA Fusions Define a Novel Subset of Cellular Myofibroma/Myopericytoma: A Potential Diagnostic Pitfall With Sarcomas With Myogenic Differentiation. | |
Role of BRAFV600E in the first preclinical model of multifocal infiltrating myopericytoma development and microenvironment | |
Sarcomas With CIC-rearrangements Are a Distinct Pathologic Entity With Aggressive Outcome: A Clinicopathologic and Molecular Study of 115 Cases. | |
A Subset of Malignant Mesotheliomas in Young Adults Are Associated With Recurrent EWSR1/FUS-ATF1 Fusions. | |
A system for sharing routine surgical pathology specimens across institutions: the Shared Pathology Informatics Network | |
TERT promoter mutations and prognosis in solitary fibrous tumor. | |
Tumor-specific cooperation of retinoblastoma protein family and Snf5 inactivation | |
Unclassified low grade spindle cell sarcoma with storiform pattern characterized by recurrent novel EWSR1/FUS-NACC1 fusions | |
WHO classification tumors of soft tissue and bone | |
ZFP36-FOSB fusion defines a subset of epithelioid hemangioma with atypical features | |
マクロ病理カラーアトラス |