Detalhe da pesquisa
1.
Novel low-grade renal spindle cell neoplasm with HEY1::NCOA2 fusion that is distinct from mesenchymal chondrosarcoma.
Genes Chromosomes Cancer
; 62(3): 171-175, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36416671
2.
Myoepithelial carcinoma of the parotid gland with a novel CTCF::NCOA2 fusion.
Genes Chromosomes Cancer
; 62(3): 161-166, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36331420
3.
GAB1::ABL1 fusions define a distinctive soft tissue neoplasm, with variable perineurial differentiation, and a predilection for children and young adults.
Genes Chromosomes Cancer
; 62(8): 449-459, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-36744864
4.
CD43-positive, EWSR1::FLI1 -rearranged Soft Tissue Sarcoma in a Pediatric Patient With History of B-Cell Acute Lymphoblastic Leukemia.
J Pediatr Hematol Oncol
; 45(5): e635-e638, 2023 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37027334
5.
Tyrosine kinase-altered spindle cell neoplasms with EGFR internal tandem duplications.
Genes Chromosomes Cancer
; 61(10): 616-621, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35593751
6.
ALK rearrangements in infantile fibrosarcoma-like spindle cell tumours of soft tissue and kidney.
Histopathology
; 80(4): 698-707, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-34843129
7.
Spindle cell neoplasm with EML4-ALK gene fusion presenting as an intraosseous vertebral mass.
Genes Chromosomes Cancer
; 60(4): 282-286, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33170538
8.
Characterization of novel USP6 gene rearrangements in a subset of so-called cellular fibroma of tendon sheath.
Mod Pathol
; 34(1): 13-19, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32661296
9.
Calcified chondroid mesenchymal neoplasms with FN1-receptor tyrosine kinase gene fusions including FGFR2, FGFR1, MERTK, NTRK1, and TEK: a molecular and clinicopathologic analysis.
Mod Pathol
; 34(7): 1373-1383, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33727696
10.
Novel BRAF gene fusions and activating point mutations in spindle cell sarcomas with histologic overlap with infantile fibrosarcoma.
Mod Pathol
; 34(8): 1530-1540, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33850302
11.
EWSR1-PATZ1-rearranged sarcoma: a report of nine cases of spindle and round cell neoplasms with predilection for thoracoabdominal soft tissues and frequent expression of neural and skeletal muscle markers.
Mod Pathol
; 34(4): 770-785, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33012788
12.
A novel MBTD1-PHF1 gene fusion in endometrial stromal sarcoma: A case report and literature review.
Genes Chromosomes Cancer
; 59(7): 428-432, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32237188
13.
Gene fusion analysis in renal cell carcinoma by FusionPlex RNA-sequencing and correlations of molecular findings with clinicopathological features.
Genes Chromosomes Cancer
; 59(1): 40-49, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-31400230
14.
ALK rearranged renal cell carcinoma (ALK-RCC): a multi-institutional study of twelve cases with identification of novel partner genes CLIP1, KIF5B and KIAA1217.
Mod Pathol
; 33(12): 2564-2579, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-32467651
15.
Recurrent RET gene fusions in paediatric spindle mesenchymal neoplasms.
Histopathology
; 76(7): 1032-1041, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-31994201
16.
6q25.1 (TAB2) microdeletion is a risk factor for hypoplastic left heart: a case report that expands the phenotype.
BMC Cardiovasc Disord
; 20(1): 137, 2020 03 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-32183715
17.
Detecting disease-defining gene fusions in unclassified round cell sarcomas using anchored multiplex PCR/targeted RNA next-generation sequencing-Molecular and clinicopathological characterization of 16 cases.
Genes Chromosomes Cancer
; 58(10): 713-722, 2019 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31033080
18.
Amplification of DNA damage-inducible transcript 3 (DDIT3) is associated with myxoid liposarcoma-like morphology and homologous lipoblastic differentiation in dedifferentiated liposarcoma.
Mod Pathol
; 32(4): 585-592, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30420727
19.
Compound heterozygosity for a frameshift mutation and an upstream deletion that reduces expression of SERPINH1 in siblings with a moderate form of osteogenesis imperfecta.
Am J Med Genet A
; 179(8): 1466-1475, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31179625
20.
Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndrome.
Am J Med Genet A
; 179(9): 1783-1790, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31294511