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ETV transcriptional upregulation is more reliable than RNA sequencing algorithms and FISH in diagnosing round cell sarcomas with CIC gene rearrangements.
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- Genes, Chromosomes & Cancer, 2017, v. 56, n. 6, p. 501, doi. 10.1002/gcc.22454
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- Article
Copy number profiling in von hippel-lindau disease renal cell carcinoma.
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- Genes, Chromosomes & Cancer, 2011, v. 50, n. 7, p. 479, doi. 10.1002/gcc.20865
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- Article
Characterization of a 3;6 translocation associated with renal cell carcinoma.
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- Genes, Chromosomes & Cancer, 2007, v. 46, n. 4, p. 311, doi. 10.1002/gcc.20403
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- Article
Opposite association of two PPARG variants with cancer: overrepresentation of H449H in endometrial carcinoma cases and underrepresentation of P12A in renal cell carcinoma cases.
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- Human Genetics, 2001, v. 109, n. 2, p. 146, doi. 10.1007/s004390100563
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- Article
Frequent RASSF1A tumor suppressor gene promoter methylation in Wilms' tumor and colorectal cancer.
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- Oncogene, 2002, v. 21, n. 47, p. 7277, doi. 10.1038/sj.onc.1205922
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- Article
Tumor specific promoter region methylation of the human homologue of the Drosophila Roundabout gene DUTT1 (ROBO1) in human cancers.
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- Oncogene, 2002, v. 21, n. 19, p. 3020, doi. 10.1038/sj.onc.1205421
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- Article
RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours.
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- Oncogene, 2001, v. 20, n. 51, p. 7573, doi. 10.1038/sj.onc.1204968
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- Article
Methylation associated inactivation of RASSF1A from region 3p21.3 in lung, breast and ovarian tumours.
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- Oncogene, 2001, v. 20, n. 12, p. 1509, doi. 10.1038/sj.onc.1204175
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- Article
Homozygous deletions at 3p12 in breast and lung cancer.
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- Oncogene, 1998, v. 17, n. 13, p. 1723, doi. 10.1038/sj.onc.1202103
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- Article
Cloning of a breast cancer homozygous deletion junction narrows the region of search for a 3p21.3 tumor suppressor gene.
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- Oncogene, 1998, v. 16, n. 24, p. 3151, doi. 10.1038/sj.onc.1201858
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- Article
RASSF Family Proteins.
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- Molecular Biology International, 2012, p. 1, doi. 10.1155/2012/938916
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- Article
Association studies of genetic variation in the WFS1 gene and type 2 diabetes in U.K. populations.
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- 2002
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- Publication type:
- journal article
A cluster of genes located in 1p36 are down-regulated in neuroblastomas with poor prognosis, but not due to CpG island methylation.
- Published in:
- Molecular Cancer, 2005, v. 4, p. 10, doi. 10.1186/1476-4598-4-10
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- Article
Molecular characterization of a large homozygous deletion in the small cell lung cancer cell line U2020: A strategy for cloning the putative tumor suppressor gene.
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- Genes, Chromosomes & Cancer, 1992, v. 5, n. 2, p. 119, doi. 10.1002/gcc.2870050205
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- Article
Germline SDHB Mutations and Familial Renal Cell Carcinoma.
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- JNCI: Journal of the National Cancer Institute, 2008, v. 100, n. 17, p. 1260, doi. 10.1093/jnci/djn254
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- Article
CpG island promoter hypermethylation of a novel Ras-effector gene RASSF2A is an early event in colon carcinogenesis and correlates inversely with K-ras mutations.
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- Oncogene, 2005, v. 24, n. 24, p. 3987, doi. 10.1038/sj.onc.1208566
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- Article
Frequent epigenetic inactivation of RASSF1A and BLU genes located within the critical 3p21.3 region in gliomas.
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- Oncogene, 2004, v. 23, n. 13, p. 2408, doi. 10.1038/sj.onc.1207407
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- Article
Frequent epigenetic inactivation of the RASSF1A tumor suppressor gene in Hodgkin's lymphoma.
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- Oncogene, 2004, v. 23, n. 6, p. 1326, doi. 10.1038/sj.onc.1207313
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- Article
Multigene methylation analysis of Wilms' tumour and adult renal cell carcinoma.
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- Oncogene, 2003, v. 22, n. 43, p. 6794, doi. 10.1038/sj.onc.1206914
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- Article
Frequent epigenetic inactivation of the SLIT2 gene in gliomas.
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- Oncogene, 2003, v. 22, n. 29, p. 4611, doi. 10.1038/sj.onc.1206687
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- Article
Epigenetic inactivation of the candidate 3p21.3 suppressor gene BLU in human cancers.
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- Oncogene, 2003, v. 22, n. 10, p. 1580, doi. 10.1038/sj.onc.1206243
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- Article
NORE1A, a homologue of RASSF1A tumour suppressor gene is inactivated in human cancers.
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- Oncogene, 2003, v. 22, n. 6, p. 947, doi. 10.1038/sj.onc.1206191
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- Article
Frequent epigenetic inactivation of the RASSF1A tumour suppressor gene in testicular tumours and distinct methylation profiles of seminoma and nonseminoma testicular germ cell tumours.
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- Oncogene, 2003, v. 22, n. 3, p. 461, doi. 10.1038/sj.onc.1206119
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- Article
Detection of RASSF1A aberrant promoter hypermethylation in sputum from chronic smokers and ductal carcinoma in situ from breast cancer patients.
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- Oncogene, 2003, v. 22, n. 1, p. 147, doi. 10.1038/sj.onc.1206057
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- Article
Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibility.
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- Nature Genetics, 2012, v. 44, n. 3, p. 277, doi. 10.1038/ng.1071
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- Article
Global Profiling in Vestibular Schwannomas Shows Critical Deregulation of MicroRNAs and Upregulation in Those Included in Chromosomal Region 14q32.
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- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0065868
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- Article
Genomic and transcriptomic characterisation of undifferentiated pleomorphic sarcoma of bone.
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- Journal of Pathology, 2019, v. 247, n. 2, p. 166, doi. 10.1002/path.5176
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- Article
Genetic analyses of undifferentiated small round cell sarcoma identifies a novel sarcoma subtype with a recurrent CRTC1‐SS18 gene fusion.
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- Journal of Pathology, 2018, v. 245, n. 2, p. 186, doi. 10.1002/path.5071
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- Article
Expression of HIF-1α, HIF-2α (EPAS1), and Their Target Genes in Paraganglioma and Pheochromocytoma with VHL and SDH Mutations.
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- 2006
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- Publication type:
- journal article
Genetic analysis of mitochondrial complex II subunits SDHD, SDHB and SDHC in paraganglioma and phaeochromocytoma susceptibility.
- Published in:
- Clinical Endocrinology, 2003, v. 59, n. 6, p. 728, doi. 10.1046/j.1365-2265.2003.01914.x
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- Article
Profiling of Somatic Mutations in Phaeochromocytoma and Paraganglioma by Targeted Next Generation Sequencing Analysis.
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- International Journal of Endocrinology, 2015, v. 2015, p. 1, doi. 10.1155/2015/138573
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- Article
cDNA Cloning and Expression of the Human Homolog of the Sea Urchin fascin and Drosophila singed Genes Which Encodes an Actin-Bundling Protein.
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- DNA & Cell Biology, 1994, v. 13, n. 8, p. 821, doi. 10.1089/dna.1994.13.821
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- Article
Stability of the CpG island methylator phenotype during glioma progression and identification of methylated loci in secondary glioblastomas.
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- BMC Cancer, 2014, v. 14, p. 1, doi. 10.1186/1471-2407-14-506
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- Article
Stability of the CpG island methylator phenotype during glioma progression and identification of methylated loci in secondary glioblastomas
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- BMC Cancer, 2014, v. 14, n. 1, p. 506, doi. 10.1186/1471-2407-14-506
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- Article
WFS1/wolframin mutations, Wolfram syndrome, and associated diseases.
- Published in:
- Human Mutation, 2001, v. 17, n. 5, p. 357, doi. 10.1002/humu.1110
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- Article
Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: Correlations with phenotype.
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- Human Mutation, 1995, v. 5, n. 1, p. 66, doi. 10.1002/humu.1380050109
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- Publication type:
- Article
Epigenetic inactivation of RASSF1A in lung and breast cancers and malignant phenotype suppression.
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- 2001
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- Publication type:
- journal article
The role of RASSF1A methylation in cancer.
- Published in:
- Disease Markers, 2007, v. 23, n. 1-2, p. 73, doi. 10.1155/2007/291538
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- Publication type:
- Article
Birt Hogg-Dubé syndrome-associated FLCN mutations disrupt protein stability.
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- Human Mutation, 2011, v. 32, n. 8, p. 921, doi. 10.1002/humu.21519
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- Publication type:
- Article
Genome-wide methylation analyses identifies Non-coding RNA genes dysregulated in breast tumours that metastasise to the brain.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-05050-z
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- Publication type:
- Article
OP13 IDENTIFICATION OF GENES EPIGENETICALLY DEREGULATED IN BRAIN METASTASIS FROM PRIMARY BREAST TUMOURS.
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- Neuro-Oncology, 2014, v. 16, n. suppl_6, p. vi18, doi. 10.1093/neuonc/nou251.13
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- Article
Molecular genetic analysis of the 3p — syndrome.
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- Human Molecular Genetics, 1994, v. 3, n. 6, p. 903
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- Article
Detailed mapping of germline deletions of the von Hippel—Lindau disease tumour suppressor gene.
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- Human Molecular Genetics, 1994, v. 3, n. 4, p. 595
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- Publication type:
- Article
Three polymorphic dinucleotide repeats near the von Hippel Lindau (VHL) disease gene on human chromosome 3:D3S587; D3S1317; D3S1435.
- Published in:
- Human Molecular Genetics, 1993, v. 2, n. 8, p. 1326
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- Publication type:
- Article
Identification of 5 novel genes methylated inbreast and other epithelial cancers.
- Published in:
- Molecular Cancer, 2010, v. 9, p. 51, doi. 10.1186/1476-4598-9-51
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- Publication type:
- Article
A Genome-wide screen identifies frequentlymethylated genes in haematological andepithelial cancers.
- Published in:
- Molecular Cancer, 2010, v. 9, p. 44, doi. 10.1186/1476-4598-9-44
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- Publication type:
- Article
CpG methylation profiling in VHL related and VHL unrelated renal cell carcinoma.
- Published in:
- Molecular Cancer, 2009, v. 8, p. 1, doi. 10.1186/1476-4598-8-31
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- Publication type:
- Article