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High level MYCN amplification and distinct methylation signature define an aggressive subtype of spinal cord ependymoma.
- Published in:
- Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. 1, doi. 10.1186/s40478-020-00973-y
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- Publication type:
- Article
CD30<sup>+</sup> large B cell lymphoma with anaplastic features and complete loss of B cell marker expression arising from follicular lymphoma.
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- Histopathology, 2019, v. 75, n. 4, p. 602, doi. 10.1111/his.13919
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- Publication type:
- Article
Two Cases of Spinal, Extraosseous, Intradural Ewing's Sarcoma/Peripheral Neuroectodermal Tumor: Radiologic, Pathologic, and Molecular Analysis.
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- Journal of Clinical Imaging Science, 2014, v. 4, n. 1, p. 1, doi. 10.4103/2156-7514.126050
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- Publication type:
- Article
Somatic mutations in VHL germline deletion kindred correlate with mild phenotype (This article is a US Government work and, as such, is in the public domain in the United States of America.).
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- Annals of Neurology, 2004, v. 55, n. 2, p. 236
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- Publication type:
- Article
Malignant round cell tumor of bone with EWSR1-NFATC2 gene fusion.
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- Virchows Archiv: European Journal of Pathology, 2014, v. 465, n. 2, p. 233, doi. 10.1007/s00428-014-1613-7
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- Publication type:
- Article
Tumor derived vasculogenesis in von Hippel-Lindau disease-associated tumors.
- Published in:
- Scientific Reports, 2014, p. 1, doi. 10.1038/srep04102
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- Publication type:
- Article
Localization of deletion to a 300 Kb interval of chromosome 11q13 in cervical cancer.
- Published in:
- Oncogene, 2002, v. 21, n. 36, p. 5631, doi. 10.1038/sj.onc.1205698
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- Publication type:
- Article
VASCULOGENESIS IN VON HIPPEL-LINDAU DISEASE ASSOCIATED TUMORS.
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- Neuro-Oncology, 2014, v. 16, n. suppl_3, p. iii9, doi. 10.1093/neuonc/nou206.32
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- Publication type:
- Article
The Human Vitamin D Receptor Gene ( VDR) Is Localized to Region 12cen-q12 by Fluorescent In Situ Hybridization and Radiation Hybrid Mapping: Genetic and Physical VDR Map.
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- Journal of Bone & Mineral Research, 1999, v. 14, n. 7, p. 1163, doi. 10.1359/jbmr.1999.14.7.1163
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- Article
Identification of skin‐infiltrating donor lymphocytes in a case of pre‐engraftment syndrome.
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- Journal of Dermatology, 2023, v. 50, n. 9, p. e282, doi. 10.1111/1346-8138.16785
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- Publication type:
- Article
Von hippel-lindau disease associated pulmonary carcinoid with cranial metastasis.
- Published in:
- 2014
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- Publication type:
- journal article
Amplification and Overexpression of Mutant RET in Multiple Endocrine Neoplasia Type 2-Associated Medullary Thyroid Carcinoma.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 1, p. 459, doi. 10.1210/jc.2002-021254
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- Publication type:
- Article
Pituitary Macroadenoma in a 5-Year-Old: An Early Expression of Multiple Endocrine Neoplasia Type 1*.
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- Journal of Clinical Endocrinology & Metabolism, 2001, v. 86, n. 12, p. 4776
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- Publication type:
- Article
Ovarian Lesions in Carney Complex: Clinical Genetics and Possible Predisposition to Malignancy.
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- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 11, p. 4359, doi. 10.1210/jcem.85.11.6921
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- Publication type:
- Article
Genetic and Histologic Studies of Somatomammotropic Pituitary Tumors in Patients with the “Complex of Spotty Skin Pigmentation, Myxomas, Endocrine Overactivity and Schwannomas” (Carney Complex).
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- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 10, p. 3860, doi. 10.1210/jcem.85.10.6875
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- Publication type:
- Article
Human CYP11B2 (aldosterone synthase) maps to chromosome 8q24.3.
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- Journal of Clinical Endocrinology & Metabolism, 1998, v. 83, n. 3, p. 1033, doi. 10.1210/jcem.83.3.4801
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- Publication type:
- Article
Impact of the methylation classifier and ancillary methods on CNS tumor diagnostics.
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- Neuro-Oncology, 2022, v. 24, n. 4, p. 571, doi. 10.1093/neuonc/noab227
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- Publication type:
- Article
Primary Subcutaneous Spindle Cell Ewing Sarcoma w ith Strong S100 Expression and EWSR1-FLI1 Fusion: A Case Report.
- Published in:
- 2014
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- Publication type:
- Case Study
The Structural Complexity of the Human BORIS Gene in Gametogenesis and Cancer.
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- PLoS ONE, 2010, v. 5, n. 11, p. 1, doi. 10.1371/journal.pone.0013872
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- Publication type:
- Article
Peripheral T‐cell lymphomas expressing CD30 and CD15 expand the spectrum of anaplastic large cell lymphoma, ALK‐negative.
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- British Journal of Haematology, 2024, v. 204, n. 5, p. 1862, doi. 10.1111/bjh.19442
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- Publication type:
- Article
Mutations of the gene encoding the protein kinase A type I-α regulatory subunit in patients with the Carney complex.
- Published in:
- Nature Genetics, 2000, v. 26, n. 1, p. 89, doi. 10.1038/79238
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- Publication type:
- Article
Trisomy 7-harbouring non-random duplication of the mutant MET allele in hereditary papillary renal carcinomas.
- Published in:
- Nature Genetics, 1998, v. 20, n. 1, p. 66, doi. 10.1038/1727
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- Publication type:
- Article
Common genetic changes in hereditary and sporadic pituitary adenomas detected by comparative genomic hybridization.
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- Genes, Chromosomes & Cancer, 2005, v. 43, n. 1, p. 72, doi. 10.1002/gcc.20162
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- Publication type:
- Article
Cytogenetic, spectral karyotyping, fluorescence in situ hybridization, and comparative genomic hybridization characterization of two new secondary leukemia cell lines with 5q deletions, and MYC and MLL amplification.
- Published in:
- Genes, Chromosomes & Cancer, 2003, v. 37, n. 3, p. 270, doi. 10.1002/gcc.10200
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- Publication type:
- Article
Amplification of 4q21-q22 and the MXR gene in independently derived mitoxantrone-resistant cell lines.
- Published in:
- Genes, Chromosomes & Cancer, 2000, v. 27, n. 1, p. 110, doi. 10.1002/(SICI)1098-2264(200001)27:1<110::AID-GCC14>3.0.CO;2-4
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- Publication type:
- Article
Molecular cytogenetic fingerprinting of esophageal squamous cell carcinoma by comparative genomic hybridization reveals a consistent pattern of chromosomal alterations.
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- Genes, Chromosomes & Cancer, 1999, v. 25, n. 2, p. 160, doi. 10.1002/(SICI)1098-2264(199906)25:2<160::AID-GCC12>3.0.CO;2-U
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- Publication type:
- Article
A Revision of the Lissencephaly and Miller-Dieker Syndrome Critical Regions in Chromosome 17p13.3.
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- Human Molecular Genetics, 1997, v. 6, n. 2, p. 147, doi. 10.1093/hmg/6.2.147
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- Publication type:
- Article
In vivo modeling of metastatic human high-grade serous ovarian cancer in mice.
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- PLoS Genetics, 2020, v. 16, n. 6, p. 1, doi. 10.1371/journal.pgen.1008808
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- Publication type:
- Article
Spinal cord glioneuronal tumor with neuropil-like islands with 1p/19q deletion in an adult with low-grade cerebral oligodendroglioma.
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- 2012
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- Publication type:
- Report
Germline SUCLG2 Variants in Patients With Pheochromocytoma and Paraganglioma.
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- 2022
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- Publication type:
- journal article
Phase I Clinical Trial of an Autologous Dendritic Cell Vaccine Against HER2 Shows Safety and Preliminary Clinical Efficacy.
- Published in:
- Frontiers in Oncology, 2021, v. 11, p. 1, doi. 10.3389/fonc.2021.789078
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- Publication type:
- Article
Somatic point mutation of the wild-type allele detected in tumors of patients with VHL germline deletion.
- Published in:
- Oncogene, 2002, v. 21, n. 8, p. 1167, doi. 10.1038/sj.onc.1205121
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- Publication type:
- Article
Melanoma in patients with GATA2 deficiency.
- Published in:
- Pigment Cell & Melanoma Research, 2018, v. 31, n. 2, p. 337, doi. 10.1111/pcmr.12671
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- Publication type:
- Article
Missense Mutation of the MET Gene Detected in Human Glioma.
- Published in:
- Modern Pathology, 2000, v. 13, n. 9, p. 973, doi. 10.1038/modpathol.3880177
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- Publication type:
- Article
Individual NMDA receptor GluN2 subunit signaling domains differentially regulate the postnatal maturation of hippocampal excitatory synaptic transmission and plasticity but not dendritic morphology.
- Published in:
- Synapse, 2024, v. 78, n. 4, p. 1, doi. 10.1002/syn.22292
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- Publication type:
- Article
Somatic Mutations of the MEN1 Tumor Suppressor Gene Detected in Sporadic Angiofibromas.
- Published in:
- Journal of Investigative Dermatology, 1998, v. 111, n. 3, p. 539, doi. 10.1046/j.1523-1747.1998.00317.x
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- Publication type:
- Article
Cutaneous Tumors in Patients with Multiple Endocrine Neoplasia Type 1 Show Allelic Deletion of...
- Published in:
- Journal of Investigative Dermatology, 1998, v. 110, n. 4, p. 438, doi. 10.1046/j.1523-1747.1998.00140.x
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- Publication type:
- Article
Multilineage involvement of the fusion gene in patients with FIP1L1/PDGFRA-positive hypereosinophilic syndrome.
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- British Journal of Haematology, 2006, v. 132, n. 3, p. 286, doi. 10.1111/j.1365-2141.2005.05863.x
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- Publication type:
- Article
A novel splicing site IRP1 somatic mutation in a patient with pheochromocytoma and JAK2<sup>V617F</sup> positive polycythemia vera: a case report.
- Published in:
- 2018
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- Publication type:
- journal article