Found: 18
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Dedifferentiation in SDH-Deficient Gastrointestinal Stromal Tumor: A Report With Histologic, Immunophenotypic, and Molecular Characterization.
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- Pediatric & Developmental Pathology, 2019, v. 22, n. 5, p. 492, doi. 10.1177/1093526619846222
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- Article
Novel NONO::TFE3 fusion and ALK co-expression identified in a subset of cutaneous microcystic/reticular schwannoma.
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- Virchows Archiv: European Journal of Pathology, 2023, v. 483, n. 2, p. 237, doi. 10.1007/s00428-023-03605-7
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- Article
Keratin‐positive giant cell‐rich tumors of soft tissue with HMGA2::NCOR2 fusions.
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- Journal of Cutaneous Pathology, 2023, v. 50, n. 11, p. 977, doi. 10.1111/cup.14497
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- Article
Combined utility of p16 and BRAF V600E in the evaluation of spitzoid tumors: Superiority to PRAME and correlation with FISH.
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- Journal of Cutaneous Pathology, 2023, v. 50, n. 2, p. 155, doi. 10.1111/cup.14342
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- Article
EWSR1‐SMAD3 rearranged fibroblastic tumor: Case series and review.
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- Journal of Cutaneous Pathology, 2021, v. 48, n. 2, p. 255, doi. 10.1111/cup.13870
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- Article
Targeted next generation sequencing (NGS) to classify melanocytic neoplasms.
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- Journal of Cutaneous Pathology, 2020, v. 47, n. 8, p. 691, doi. 10.1111/cup.13695
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Superficial sarcomas with CIC rearrangement are aggressive neoplasms: A series of eight cases.
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- Journal of Cutaneous Pathology, 2020, v. 47, n. 6, p. 509, doi. 10.1111/cup.13656
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- Article
MET Mutations in Non-small Cell Lung Cancer: Four Case Reports of Mutations at or Near the Splice Junction for Exon 14.
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- Journal of OncoPathology, 2014, v. 2, n. 2, p. 65, doi. 10.13032/tjop.2052-5931.100089
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- Article
Gene Fusion Identification Using Anchor-Based Multiplex PCR and Next-Generation Sequencing.
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- Journal of Applied Laboratory Medicine, 2021, v. 6, n. 4, p. 917, doi. 10.1093/jalm/jfaa230
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- Article
PRRX1–NCOA1‐rearranged fibroblastic tumour: a clinicopathological, immunohistochemical and molecular genetic study of six cases of a potentially under‐recognised, distinctive mesenchymal tumour.
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- Histopathology, 2021, v. 79, n. 6, p. 997, doi. 10.1111/his.14454
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- Article
YAP1–TFE3 gene fusion variant in clear cell stromal tumour of lung: report of two cases in support of a distinct entity.
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- Histopathology, 2021, v. 79, n. 6, p. 940, doi. 10.1111/his.14437
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- Article
Common germline variation in mismatch repair genes and survival after a diagnosis of colorectal cancer.
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- International Journal of Cancer, 2009, v. 124, n. 8, p. 1887, doi. 10.1002/ijc.24120
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- Article
γδ T-Cell Acute Lymphoblastic Leukemia/Lymphoma: Discussion of Two Pediatric Cases and Its Distinction from Other Mature γδ T-Cell Malignancies.
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- Case Reports in Hematology, 2017, p. 1, doi. 10.1155/2017/5873015
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- Article
Common germline polymorphisms in COMT, CYP19A1, ESR1, PGR, SULT1E1 and STS and survival after a diagnosis of breast cancer.
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- International Journal of Cancer, 2009, v. 125, n. 11, p. 2687, doi. 10.1002/ijc.24678
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- Article
Solitary Fibrous Tumor of Breast and Axilla: Clinicopathological Profile of Five Tumors With Comparison of Risk Stratification Models.
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- International Journal of Surgical Pathology, 2024, v. 32, n. 5, p. 895, doi. 10.1177/10668969231204957
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- Article
Genome-Wide Meta-Analysis Identifies Regions on 7p21 (AHR ) and 15q24 (CYP1A2 ) As Determinants of Habitual Caffeine Consumption.
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- PLoS Genetics, 2011, v. 7, n. 4, p. 1, doi. 10.1371/journal.pgen.1002033
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- Article
Diagnostic Utility of a Custom 34-Gene Anchored Multiplex PCR-Based Next-Generation Sequencing Fusion Panel for the Diagnosis of Bone and Soft Tissue Neoplasms With Identification of Novel USP6 Fusion Partners in Aneurysmal Bone Cysts.
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- Archives of Pathology & Laboratory Medicine, 2021, v. 145, n. 7, p. 851, doi. 10.5858/arpa.2020-0336-OA
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- Article
Association Between a Germline OCA2 Polymorphism at Chromosome 15q13.1 and Estrogen Receptor–Negative Breast Cancer Survival.
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- JNCI: Journal of the National Cancer Institute, 2010, v. 102, n. 9, p. 650, doi. 10.1093/jnci/djq057
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- Article