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Leading the pack: Best practices in comparative canine cancer genomics to inform human oncology.
- Published in:
- Veterinary & Comparative Oncology, 2023, v. 21, n. 4, p. 565, doi. 10.1111/vco.12935
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- Publication type:
- Article
Which is better for cDNA-microarray-based classification: ratios or direct intensities.
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- Bioinformatics, 2004, v. 20, n. 16, p. 2513, doi. 10.1093/bioinformatics/bth272
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- Publication type:
- Article
A Framework for Promoting Diversity, Equity, and Inclusion in Genetics and Genomics Research.
- Published in:
- JAMA Health Forum, 2022, v. 3, n. 1, p. e220603, doi. 10.1001/jamahealthforum.2022.0603
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- Publication type:
- Article
Genome-wide linkage scan for prostate cancer susceptibility genes in men with aggressive disease: significant evidence for linkage at chromosome 15q12.
- Published in:
- Human Genetics, 2006, v. 119, n. 4, p. 400, doi. 10.1007/s00439-006-0149-6
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- Publication type:
- Article
A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region.
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- 2005
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- Correction notice
Interaction effect of PTEN and CDKN1B chromosomal regions on prostate cancer linkage.
- Published in:
- Human Genetics, 2004, v. 115, n. 3, p. 255
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- Publication type:
- Article
Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13.
- Published in:
- Human Genetics, 2003, v. 113, n. 3, p. 293, doi. 10.1007/s00439-003-0967-8
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- Publication type:
- Article
Polymorphic GGC repeats in the androgen receptor gene are associated with hereditary and sporadic prostate cancer risk.
- Published in:
- Human Genetics, 2002, v. 110, n. 2, p. 122, doi. 10.1007/s00439-001-0662-6
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- Publication type:
- Article
Evidence for a prostate cancer linkage to chromosome 20 in 159 hereditary prostate cancer families.
- Published in:
- Human Genetics, 2001, v. 108, n. 5, p. 430, doi. 10.1007/s004390100513
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- Publication type:
- Article
Linkage of prostate cancer susceptibility loci to chromosome 1.
- Published in:
- Human Genetics, 2001, v. 108, n. 4, p. 335, doi. 10.1007/s004390100488
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- Publication type:
- Article
Genome-wide expression changes induced by HTLV-1 Tax: evidence for MLK-3 mixed lineage kinase involvement in Tax-mediated NF-κB activation.
- Published in:
- Oncogene, 2001, v. 20, n. 33, p. 4484, doi. 10.1038/sj.onc.1204513
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- Publication type:
- Article
The p44<sup>S10</sup> locus, encoding a subunit of the proteasome regulatory particle, is amplified during progression of cutaneous malignant melanoma.
- Published in:
- Oncogene, 2000, v. 19, n. 11, p. 1419, doi. 10.1038/sj.onc.1203462
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- Publication type:
- Article
Linkage and association of CYP17 gene in hereditary and sporadic prostate cancer.
- Published in:
- International Journal of Cancer, 2001, v. 95, n. 6, p. 354, doi. 10.1002/1097-0215(20011120)95:6<354::AID-IJC1062>3.0.CO;2-3
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- Publication type:
- Article
Genome-wide association study identifies novel loci associated with serum level of vitamin B12 in Chinese men.
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- Human Molecular Genetics, 2012, v. 21, n. 11, p. 2610, doi. 10.1093/hmg/dds062
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- Publication type:
- Article
DYNAMICAL ANALYSIS OF DRUG EFFICACY AND MECHANISM OF ACTION USING GFP REPORTERS.
- Published in:
- Journal of Biological Systems, 2012, v. 20, n. 4, p. 403, doi. 10.1142/S0218339012400049
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- Publication type:
- Article
Genomic landscapes of canine splenic angiosarcoma (hemangiosarcoma) contain extensive heterogeneity within and between patients.
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- PLoS ONE, 2022, v. 17, n. 7, p. 1, doi. 10.1371/journal.pone.0264986
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- Publication type:
- Article
GeneLink: a database to facilitate genetic studies of complex traits.
- Published in:
- BMC Genomics, 2004, v. 5, p. 81, doi. 10.1186/1471-2164-5-81
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- Publication type:
- Article
Deletion mapping suggests that the 1p22 melanoma susceptibility gene is a tumor suppressor localized to a 9‐mb interval.
- Published in:
- Genes, Chromosomes & Cancer, 2004, v. 41, n. 1, p. 56, doi. 10.1002/gcc.20056
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- Publication type:
- Article
Chromosome arm-specific multicolor FISH.
- Published in:
- Genes, Chromosomes & Cancer, 2001, v. 30, n. 1, p. 105, doi. 10.1002/1098-2264(2000)9999:9999<::AID-GCC1068>3.0.CO;2-9
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- Publication type:
- Article
Recurrent chromosome alterations in hepatocellular carcinoma detected by comparative genomic hybridization.
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- Genes, Chromosomes & Cancer, 2000, v. 29, n. 2, p. 110, doi. 10.1002/1098-2264(2000)9999:9999<::AID-GCC1022>3.0.CO;2-V
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- Publication type:
- Article
Chromosome abnormalities in ovarian adenocarcinoma: III. Using breakpoint data to infer and test mathematical models for oncogenesis.
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- Genes, Chromosomes & Cancer, 2000, v. 28, n. 1, p. 106, doi. 10.1002/(SICI)1098-2264(200005)28:1<106::AID-GCC13>3.0.CO;2-S
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- Publication type:
- Article
Gain of 9p in the pathogenesis of polycythemia vera.
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- Genes, Chromosomes & Cancer, 1998, v. 22, n. 4, p. 321, doi. 10.1002/(SICI)1098-2264(199808)22:4<321::AID-GCC8>3.0.CO;2-X
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- Publication type:
- Article
Increased chromosome 20 copy number detected by fluorescence in situ hybridization (FISH) in malignant melanoma.
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- Genes, Chromosomes & Cancer, 1997, v. 19, n. 4, p. 278, doi. 10.1002/(SICI)1098-2264(199708)19:4<278::AID-GCC11>3.0.CO;2-C
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- Publication type:
- Article
Simple numeric abnormalities as primary karyotype changes in ovarian carcinoma.
- Published in:
- Genes, Chromosomes & Cancer, 1994, v. 10, n. 4, p. 262, doi. 10.1002/gcc.2870100407
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- Publication type:
- Article
Molecular cytogenetic analysis of i(12p)-negative human male germ cell tumors.
- Published in:
- Genes, Chromosomes & Cancer, 1993, v. 8, n. 4, p. 230, doi. 10.1002/gcc.2870080405
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- Publication type:
- Article
Molecular mapping of the oncogene MYB and rearrangements in malignant melanoma.
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- Genes, Chromosomes & Cancer, 1989, v. 1, n. 1, p. 88, doi. 10.1002/gcc.2870010114
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- Publication type:
- Article
Canine osteosarcoma genome sequencing identifies recurrent mutations in DMD and the histone methyltransferase gene SETD2.
- Published in:
- Communications Biology, 2019, v. 2, n. 1, p. N.PAG, doi. 10.1038/s42003-019-0487-2
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- Publication type:
- Article
The BioIntelligence Framework: a new computational platform for biomedical knowledge computing.
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- Journal of the American Medical Informatics Association, 2013, v. 20, n. 1, p. 128, doi. 10.1136/amiajnl-2011-000646
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- Publication type:
- Article
Re-expression of SMARCA4/BRG1 in small cell carcinoma of ovary, hypercalcemic type (SCCOHT) promotes an epithelial-like gene signature through an AP-1-dependent mechanism.
- Published in:
- eLife, 2021, p. 1, doi. 10.7554/eLife.59073
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- Publication type:
- Article
Stress-specific signatures: expression profiling of p53 wild-type and -null human cells.
- Published in:
- Oncogene, 2005, v. 24, n. 28, p. 4572, doi. 10.1038/sj.onc.1208653
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- Publication type:
- Article
Generation and analysis of melanoma SAGE libraries: SAGE advice on the melanoma transcriptome.
- Published in:
- Oncogene, 2004, v. 23, n. 12, p. 2264, doi. 10.1038/sj.onc.1207337
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- Publication type:
- Article
Gene-expression profiling in human cutaneous melanoma.
- Published in:
- Oncogene, 2003, v. 22, n. 20, p. 3076, doi. 10.1038/sj.onc.1206448
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- Publication type:
- Article
Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma families.
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- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1135, doi. 10.1038/ejhg.2008.72
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- Publication type:
- Article
Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma families.
- Published in:
- 2008
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- Publication type:
- Correction notice
A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 10, p. 1097, doi. 10.1038/sj.ejhg.5201670
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- Publication type:
- Article
A unique malignant T-cell lymphoproliferative disorder with neutropenia simulating hairy cell leukemia.
- Published in:
- 1985
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- Publication type:
- journal article
Characterization of X Chromosome Inactivation Using Integrated Analysis of Whole-Exome and mRNA Sequencing.
- Published in:
- PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0113036
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- Publication type:
- Article
Assessment of <i>PALB2</i> as a Candidate Melanoma Susceptibility Gene.
- Published in:
- PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0100683
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- Publication type:
- Article
A <i>BAP1</i> Mutation in a Danish Family Predisposes to Uveal Melanoma and Other Cancers.
- Published in:
- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0072144
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- Publication type:
- Article
The histone methyltransferase EZH2 is a therapeutic target in small cell carcinoma of the ovary, hypercalcaemic type.
- Published in:
- Journal of Pathology, 2017, v. 242, n. 3, p. 371, doi. 10.1002/path.4912
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- Publication type:
- Article
Dual loss of the SWI/ SNF complex ATPases SMARCA4/ BRG1 and SMARCA2/ BRM is highly sensitive and specific for small cell carcinoma of the ovary, hypercalcaemic type.
- Published in:
- Journal of Pathology, 2016, v. 238, n. 3, p. 389, doi. 10.1002/path.4633
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- Publication type:
- Article
High frequency of BRAF mutations in nevi.
- Published in:
- Nature Genetics, 2003, v. 33, n. 1, p. 19, doi. 10.1038/ng1054
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- Publication type:
- Article
Chipping away at genomic medicine.
- Published in:
- Nature Genetics, 2002, v. 32, p. 462, doi. 10.1038/ng1025
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- Publication type:
- Article
RNASEL Arg462Gln variant is implicated in up to 13% of prostate cancer cases.
- Published in:
- Nature Genetics, 2002, v. 32, n. 4, p. 581, doi. 10.1038/ng1021
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- Publication type:
- Article
Experimentally-derived haplotypes substantially increase the efficiency of linkage disequilibrium studies.
- Published in:
- Nature Genetics, 2001, v. 28, n. 4, p. 361, doi. 10.1038/ng582
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- Publication type:
- Article
Mining melanoma with microarrays.
- Published in:
- 1999
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- Publication type:
- Abstract
Analysis of the mechanisms of drug resistance in cancer by cDNA microarray.
- Published in:
- 1999
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- Publication type:
- Abstract
Nonlinear stochastic determination for gene expressions via cDNA microarrays.
- Published in:
- 1999
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- Publication type:
- Abstract
Determining the quantitative accuracy of cDNA microarrays.
- Published in:
- 1999
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- Publication type:
- Abstract
cDNA microarrays detect activation of a myogenic transcription program by the PAX3-FKHR fusion oncogene.
- Published in:
- 1999
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- Publication type:
- Abstract