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Comprehensive molecular and clinicopathological analysis of vascular malformations: A study of 319 cases.
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- Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 541, doi. 10.1002/gcc.22739
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- Article
Mutational analysis using Sanger and next generation sequencing in sporadic spindle cell hemangiomas: A study of 19 cases.
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- Genes, Chromosomes & Cancer, 2017, v. 56, n. 12, p. 855, doi. 10.1002/gcc.22501
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- Article
Systematic discovery of gene fusions in pediatric cancer by integrating RNA-seq and WGS.
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- BMC Cancer, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12885-023-11054-3
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- Article
Processing of primary microRNAs by the Microprocessor complex.
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- Nature, 2004, v. 432, n. 7014, p. 231, doi. 10.1038/nature03049
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- Article
Correction to: Amplification of the PLAG-family genes—PLAGL1 and PLAGL2—is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification.
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- Acta Neuropathologica, 2023, v. 145, n. 4, p. 511, doi. 10.1007/s00401-023-02538-4
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- Article
Amplification of the PLAG-family genes—PLAGL1 and PLAGL2—is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification.
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- Acta Neuropathologica, 2023, v. 145, n. 1, p. 49, doi. 10.1007/s00401-022-02516-2
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- Publication type:
- Article
GOPC:ROS1 and other ROS1 fusions represent a rare but recurrent drug target in a variety of glioma types.
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- Acta Neuropathologica, 2021, v. 142, n. 6, p. 1065, doi. 10.1007/s00401-021-02369-1
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- Publication type:
- Article
RT-PCR assay to detect FGFR3::TACC3 fusions in formalin-fixed, paraffin-embedded glioblastoma samples.
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- Neuro-Oncology Practice, 2024, v. 11, n. 2, p. 142, doi. 10.1093/nop/npad081
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- Publication type:
- Article
A germline homozygous mutation in the base-excision repair gene NTHL1 causes adenomatous polyposis and colorectal cancer.
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- Nature Genetics, 2015, v. 47, n. 6, p. 668, doi. 10.1038/ng.3287
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- Article
Recommendations for the clinical interpretation and reporting of copy number gains using gene panel NGS analysis in routine diagnostics.
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- 2019
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- Publication type:
- journal article
HER2, chromosome 17 polysomy and DNA ploidy status in breast cancer; a translational study.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-48212-2
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- Publication type:
- Article
EWSR1 —The Most Common Rearranged Gene in Soft Tissue Lesions, Which Also Occurs in Different Bone Lesions: An Updated Review.
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- Diagnostics (2075-4418), 2021, v. 11, n. 6, p. 1093, doi. 10.3390/diagnostics11061093
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- Publication type:
- Article
Evaluating Experimental Bias and Completeness in Comparative Phosphoproteomics Analysis.
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- PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0023276
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- Publication type:
- Article
Molecular profiles of benign and (pre)malignant endometrial lesions.
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- Carcinogenesis, 2017, v. 38, n. 3, p. 329, doi. 10.1093/carcin/bgx008
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- Publication type:
- Article
RDE-2 interacts with MUT-7 to mediate RNA interference in Caenorhabditis elegans.
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- Nucleic Acids Research, 2005, v. 33, n. 1, p. 347, doi. 10.1093/nar/gki183
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- Publication type:
- Article
Molecular Characterization Reveals Subclasses of 1q Gain in Intermediate Risk Wilms Tumors.
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- Cancers, 2022, v. 14, n. 19, p. 4872, doi. 10.3390/cancers14194872
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- Publication type:
- Article
Development of a semi-conductor sequencing-based panel for genotyping of colon and lung cancer by the Onconetwork consortium.
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- BMC Cancer, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12885-015-1015-5
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- Publication type:
- Article
Development of a semi-conductor sequencing-based panel for genotyping of colon and lung cancer by the Onconetwork consortium.
- Published in:
- BMC Cancer, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12885-015-1015-5
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- Publication type:
- Article
Comprehensive routine diagnostic screening to identify predictive mutations, gene amplifications, and microsatellite instability in FFPE tumor material.
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- 2020
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- Publication type:
- journal article
Recurrent mutations in genes involved in nuclear factor-κB signalling in nodal marginal zone lymphoma-diagnostic and therapeutic implications.
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- Histopathology, 2017, v. 70, n. 2, p. 174, doi. 10.1111/his.13015
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- Publication type:
- Article
Immunoglobulin rearrangement analysis from multiple lesions in the same patient using next-generation sequencing.
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- Histopathology, 2015, v. 67, n. 6, p. 843, doi. 10.1111/his.12714
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- Publication type:
- Article
Desmoid-type fibromatosis of the head and neck region in the paediatric population: a clinicopathological and genetic study of seven cases.
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- Histopathology, 2014, v. 64, n. 6, p. 769, doi. 10.1111/his.12323
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- Publication type:
- Article
Presence of C11orf95-MKL2 fusion is a consistent finding in chondroid lipomas: a study of eight cases.
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- Histopathology, 2013, v. 62, n. 6, p. 925, doi. 10.1111/his.12100
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- Publication type:
- Article
Molecular diagnostic tools for the World Health Organization (WHO) 2021 classification of gliomas, glioneuronal and neuronal tumors; an EANO guideline.
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- Neuro-Oncology, 2023, v. 25, n. 10, p. 1731, doi. 10.1093/neuonc/noad100
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- Article