Detalhe da pesquisa
1.
Comprehensive clinicopathological, molecular, and methylation analysis of mesenchymal tumors with NTRK and other kinase gene aberrations.
J Pathol
; 263(1): 61-73, 2024 05.
Artigo
Inglês
| MEDLINE | ID: mdl-38332737
2.
TFG::MET-rearranged soft tissue tumor: A rare infantile neoplasm with a distinct low-grade triphasic morphology.
Genes Chromosomes Cancer
; 62(5): 290-296, 2023 05.
Artigo
Inglês
| MEDLINE | ID: mdl-36464850
3.
Eosinophilic vacuolated tumor (EVT) of kidney demonstrates sporadic TSC/MTOR mutations: next-generation sequencing multi-institutional study of 19 cases.
Mod Pathol
; 35(3): 344-351, 2022 03.
Artigo
Inglês
| MEDLINE | ID: mdl-34521993
4.
Identification of tumors with NRG1 rearrangement, including a novel putative pathogenic UNC5D-NRG1 gene fusion in prostate cancer by data-drilling a de-identified tumor database.
Genes Chromosomes Cancer
; 60(7): 474-481, 2021 07.
Artigo
Inglês
| MEDLINE | ID: mdl-33583086
5.
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
Inglês
| MEDLINE | ID: mdl-33012788
6.
Targeted next generation sequencing of MLH1-deficient, MLH1 promoter hypermethylated, and BRAF/RAS-wild-type colorectal adenocarcinomas is effective in detecting tumors with actionable oncogenic gene fusions.
Genes Chromosomes Cancer
; 59(10): 562-568, 2020 10.
Artigo
Inglês
| MEDLINE | ID: mdl-32427409
7.
Papillary thyroid carcinoma with prominent myofibroblastic stromal component: clinicopathologic, immunohistochemical and next-generation sequencing study of seven cases.
Mod Pathol
; 33(9): 1702-1711, 2020 09.
Artigo
Inglês
| MEDLINE | ID: mdl-32291398
8.
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
Inglês
| MEDLINE | ID: mdl-32467651
9.
Polypoid Atypical Spitz Tumor With a Fibrosclerotic Stroma, CLIP2-BRAF Fusion, and Homozygous Loss of 9p21.
Am J Dermatopathol
; 42(3): 204-207, 2020 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-31449064
10.
Novel EIF5A-USP6 Gene Fusion in Nodular Fasciitis Associated With Unusual Pathologic Features: A Report of a Case and Review of the Literature.
Am J Dermatopathol
; 42(7): 539-543, 2020 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-31880592
11.
Kaposi Sarcoma in Association With an Extracavitary Primary Effusion Lymphoma Showing Unusual Intravascular Involvement: Report of a Case Harboring a FAM175A Germline Mutation.
Am J Dermatopathol
; 42(1): 55-60, 2020 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-31361614
12.
A Clinicopathological Study of 29 Spitzoid Melanocytic Lesions With ALK Fusions, Including Novel Fusion Variants, Accompanied by Fluorescence In Situ Hybridization Analysis for Chromosomal Copy Number Changes, and Both TERT Promoter and Next-Generation Sequencing Mutation Analysis.
Am J Dermatopathol
; 42(8): 578-592, 2020 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-32701692
13.
S100 and CD34 positive spindle cell tumor with prominent perivascular hyalinization and a novel NCOA4-RET fusion.
Genes Chromosomes Cancer
; 58(9): 680-685, 2019 09.
Artigo
Inglês
| MEDLINE | ID: mdl-30938880
14.
Inflammatory myofibroblastic tumor of the uterus - case report.
Cesk Patol
; 55(4): 239-243, 2019.
Artigo
Inglês
| MEDLINE | ID: mdl-31842556
15.
Correction to: Eosinophilic vacuolated tumor (EVT) of kidney demonstrates sporadic TSC/MTOR mutations: next-generation sequencing multi-institutional study of 19 cases.
Mod Pathol
; 35(2): 289, 2022 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-34728788
16.
Correction to: 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(11): 2092, 2021 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-34112958
17.
Correction to: Eosinophilic vacuolated tumor (EVT) of kidney demonstrates sporadic TSC/MTOR mutations: next-generation sequencing multi-institutional study of 19 cases.
Mod Pathol
; 34(12): 2243, 2021 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-34611304
18.
Complex morphological and molecular genetic examination of amelogenesis imperfecta: a case presentation of two Czech siblings with a non-syndrome form of the disease.
Neuro Endocrinol Lett
; 35(5): 347-51, 2014.
Artigo
Inglês
| MEDLINE | ID: mdl-25275257
19.
High-grade non-intestinal type sinonasal adenocarcinoma with ETV6::NTRK3 fusion, distinct from secretory carcinoma by immunoprofile and morphology.
Virchows Arch
; 483(2): 187-195, 2023 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-37415052
20.
Poorly differentiated extra-axial extraskeletal chordoma diagnosed by methylation profiling: case report and analysis of brachyury expression in SWI/SNF-deficient tumors.
Virchows Arch
; 2023 Aug 18.
Artigo
Inglês
| MEDLINE | ID: mdl-37594643