Detalhe da pesquisa
1.
Glioneuronal tumor with ATRX alteration, kinase fusion and anaplastic features (GTAKA): a molecularly distinct brain tumor type with recurrent NTRK gene fusions.
Acta Neuropathol
; 145(5): 667-680, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36933012
2.
Targeted next-generation sequencing of EUS-guided through-the-needle-biopsy sampling from pancreatic cystic lesions.
Gastrointest Endosc
; 97(1): 50-58.e4, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35964683
3.
Real-World Data on Combined EGFR-TKI and Crizotinib Treatment for Acquired and De Novo MET Amplification in Patients with Metastatic EGFR-Mutated NSCLC.
Int J Mol Sci
; 24(17)2023 Aug 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-37685884
4.
Constitutional POLE variants causing a phenotype reminiscent of constitutional mismatch repair deficiency.
Hum Mutat
; 43(1): 85-96, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34816535
5.
Correlation of MET-Receptor Overexpression with MET Gene Amplification and Patient Outcome in Malignant Mesothelioma.
Int J Mol Sci
; 22(23)2021 Nov 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-34884673
6.
P53, Somatostatin receptor 2a and Chromogranin A immunostaining as prognostic markers in high grade gastroenteropancreatic neuroendocrine neoplasms.
BMC Cancer
; 20(1): 27, 2020 Jan 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31924180
7.
Changing ALK-TKI-Resistance Mechanisms in Rebiopsies of ALK-Rearranged NSCLC: ALK- and BRAF-Mutations Followed by Epithelial-Mesenchymal Transition.
Int J Mol Sci
; 21(8)2020 Apr 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-32325863
8.
Regional Differences in Neuroinflammation-Associated Gene Expression in the Brain of Sporadic Creutzfeldt-Jakob Disease Patients.
Int J Mol Sci
; 22(1)2020 Dec 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-33375642
9.
KRAS mutations in the parental tumour accelerate in vitro growth of tumoroids established from colorectal adenocarcinoma.
Int J Exp Pathol
; 100(1): 12-18, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30884019
10.
Next-generation sequencing of endoscopic ultrasound guided microbiopsies from pancreatic cystic neoplasms.
Histopathology
; 75(5): 767-771, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31278869
11.
A high-throughput analysis of the IDH1(R132H) protein expression in pituitary adenomas.
Pituitary
; 19(4): 407-14, 2016 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-27097804
12.
Multi-center evaluation of the novel fully-automated PCR-based Idylla™ BRAF Mutation Test on formalin-fixed paraffin-embedded tissue of malignant melanoma.
Exp Mol Pathol
; 99(3): 485-91, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26407762
13.
Validation of the VisionArray® Chip Assay for HPV DNA Testing in Histology Specimens of Oropharyngeal Squamous Cell Carcinoma.
Head Neck Pathol
; 18(1): 27, 2024 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38536624
14.
Multicenter evaluation of an automated, multiplex, RNA-based molecular assay for detection of ALK, ROS1, RET fusions and MET exon 14 skipping in NSCLC.
Virchows Arch
; 484(4): 677-686, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38492039
15.
Sinonasal DLBCL: molecular profiling identifies subtypes with distinctive prognosis and targetable genetic features.
Blood Adv
; 8(8): 1946-1957, 2024 Apr 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-38324724
16.
Microduplication of 15q13.3 and Xq21.31 in a family with Tourette syndrome and comorbidities.
Am J Med Genet B Neuropsychiatr Genet
; 162B(8): 825-31, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23894120
17.
DNA methylation profile of human dura and leptomeninges.
J Neuropathol Exp Neurol
; 82(7): 641-649, 2023 06 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-37203418
18.
Validation of a Novel EUS-FNB-Derived Organoid Co-Culture System for Drug Screening in Patients with Pancreatic Cancer.
Cancers (Basel)
; 15(14)2023 Jul 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-37509338
19.
Gene expression analysis during progression of malignant meningioma compared to benign meningioma.
J Neurosurg
; 138(5): 1302-1312, 2023 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36115056
20.
Deletions and rearrangements of the H19/IGF2 enhancer region in patients with Silver-Russell syndrome and growth retardation.
J Med Genet
; 48(5): 308-11, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21278389