Molecular karyotyping of human hepatocellular carcinoma using single-nucleotide polymorphism arrays. - Wikidata - awgldk - TriplyDB

Molecular karyotyping of human hepatocellular carcinoma using single-nucleotide polymorphism arrays.

Molecular karyotyping of human hepatocellular carcinoma using single-nucleotide polymorphism arrays.

http://www.wikidata.org/entity/Q51939495

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Homozygously deleted gene DACH1 regulates tumor-initiating activity of glioma cells The application of single nucleotide polymorphism microarrays in cancer research The significance of PITX2 overexpression in human colorectal cancer Molecular classification and novel targets in hepatocellular carcinoma: recent advancements New genetic biomarkers predicting azathioprine blood concentrations in combination therapy with 5-aminosalicylic acid Quantification of SLIT-ROBO transcripts in hepatocellular carcinoma reveals two groups of genes with coordinate expression Genetic and epigenetic silencing of SCARA5 may contribute to human hepatocellular carcinoma by activating FAK signaling.Clinical omics analysis of colorectal cancer incorporating copy number aberrations and gene expression data.Genetic and epigenetic characteristics of human multiple hepatocellular carcinoma.Collagen triple helix repeat containing 1 is overexpressed in hepatocellular carcinoma and promotes cell proliferation and motility.Identification of drivers from cancer genome diversity in hepatocellular carcinoma.Digital karyotyping reveals probable target genes at 7q21.3 locus in hepatocellular carcinoma.Co-activation of epidermal growth factor receptor and c-MET defines a distinct subset of lung adenocarcinomas.Loss of imprinting and allelic switching at the DLK1-MEG3 locus in human hepatocellular carcinoma.Dynamic changes in the copy number of pluripotency and cell proliferation genes in human ESCs and iPSCs during reprogramming and time in culture.Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays.miR-10b exerts oncogenic activity in human hepatocellular carcinoma cells by targeting expression of CUB and sushi multiple domains 1 (CSMD1)Genome-wide DNA copy number analysis in pancreatic cancer using high-density single nucleotide polymorphism arrays.Microarray-based analysis for hepatocellular carcinoma: from gene expression profiling to new challenges.Focal gains of VEGFA and molecular classification of hepatocellular carcinoma High-dimensional biology to comprehend hepatocellular carcinoma.Human embryonic stem cells and genomic instability.The consequences of uniparental disomy and copy number neutral loss-of-heterozygosity during human development and cancer.Mediators of induced pluripotency and their role in cancer cells - current scientific knowledge and future perspectives.Diagnostic challenges in the myelodysplastic syndromes: the current and future role of genetic and immunophenotypic studies.Use of SNPs in cancer predisposition analysis, diagnosis and prognosis: tools and prospects.Screening of liver-targeted drugs.Exploration of liver cancer genomes.Achilles' heel of pluripotent stem cells: genetic, genomic and epigenetic variations during prolonged culture.Deregulation of RB1 expression by loss of imprinting in human hepatocellular carcinoma.Overexpression of ZAC impairs glucose-stimulated insulin translation and secretion in clonal pancreatic beta-cells.Decreased expression of XPO4 is associated with poor prognosis in hepatocellular carcinoma.Human embryonic stem cells reveal recurrent genomic instability at 20q11.21.Genome-wide detection of recurring sites of uniparental disomy in follicular and transformed follicular lymphoma.NOXIN as a cofactor of DNA polymerase-primase complex could promote hepatocellular carcinoma.Multiple genes identified as targets for 20q13.12-13.33 gain contributing to unfavorable clinical outcomes in patients with hepatocellular carcinoma.Exportin 4 gene expression and DNA promoter methylation status in chronic hepatitis B virus infection.Down-regulation of tyrosine aminotransferase at a frequently deleted region 16q22 contributes to the pathogenesis of hepatocellular carcinoma.Uniparentalism in sporadic colorectal cancer is independent of imprint status, and coordinate for chromosomes 14 and 18.Analysis of genetic damage and gene polymorphism in hepatocellular carcinoma (HCC) patients in a South Indian population.

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P2860

Molecular karyotyping of human hepatocellular carcinoma using single-nucleotide polymorphism arrays.

http://www.wikidata.org/entity/Q51939495

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Molecular karyotyping of human ...... ucleotide polymorphism arrays.

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Molecular karyotyping of human ...... ucleotide polymorphism arrays.

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Aburatani H

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Igarashi H

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Ishikawa S

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Kamimura N

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Midorikawa Y

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P2860

hZAC encodes a zinc finger protein with antiproliferative properties and maps to a chromosomal region frequently lost in cancer

Methylation-specific PCR: a novel PCR assay for methylation status of CpG islands

Genome-wide detection of allelic imbalance using human SNPs and high-density DNA arrays.

Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation

LOT1 (PLAGL1/ZAC1), the candidate tumor suppressor gene at chromosome 6q24-25, is epigenetically regulated in cancer

Altered expression and loss of heterozygosity of the LOT1 gene in ovarian cancer

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome

Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors

Nonrandom chromosomal numerical abnormality predicting prognosis of gastric cancer: a retrospective study of 51 cases using pathology archives.

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