Pages that link to "Q40402337"
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The following pages link to Homozygous deletions and chromosome amplifications in human lung carcinomas revealed by single nucleotide polymorphism array analysis (Q40402337):
Displaying 50 items.
- The diploid genome sequence of an individual human (Q21090194) (← links)
- Chromosomal changes in high- and low-invasive mouse lung adenocarcinoma cell strains derived from early passage mouse lung adenocarcinoma cell strains (Q23916995) (← links)
- Activation of ERBB2 signaling causes resistance to the EGFR-directed therapeutic antibody cetuximab (Q24600031) (← links)
- CaSNP: a database for interrogating copy number alterations of cancer genome from SNP array data (Q24607064) (← links)
- Molecular biology of lung cancer: clinical implications (Q24610335) (← links)
- MET amplification occurs with or without T790M mutations in EGFR mutant lung tumors with acquired resistance to gefitinib or erlotinib (Q24646295) (← links)
- Somatic mutations affect key pathways in lung adenocarcinoma (Q24648102) (← links)
- Integrated analysis of homozygous deletions, focal amplifications, and sequence alterations in breast and colorectal cancers (Q24649562) (← links)
- Characterizing the cancer genome in lung adenocarcinoma (Q24649926) (← links)
- The application of single nucleotide polymorphism microarrays in cancer research (Q24653582) (← links)
- CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosa (Q24655494) (← links)
- Allelic imbalances and microdeletions affecting the PTPRD gene in cutaneous squamous cell carcinomas detected using single nucleotide polymorphism microarray analysis (Q24657188) (← links)
- Fibroblast growth factor (FGF) and FGF receptor-mediated autocrine signaling in non-small-cell lung cancer cells (Q24658237) (← links)
- Oncogenic cooperation and coamplification of developmental transcription factor genes in lung cancer (Q24678477) (← links)
- Allele-specific amplification in cancer revealed by SNP array analysis (Q24811573) (← links)
- CARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays (Q25257143) (← links)
- BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH) (Q25257750) (← links)
- Human genetics of diabetic vascular complications (Q27000709) (← links)
- Allelic dilution obscures detection of a biologically significant resistance mutation in EGFR-amplified lung cancer (Q27851396) (← links)
- Frequent and focal FGFR1 amplification associates with therapeutically tractable FGFR1 dependency in squamous cell lung cancer. (Q27851615) (← links)
- Inhibitor-sensitive FGFR1 amplification in human non-small cell lung cancer (Q27851654) (← links)
- Reactivation of ERK signaling causes resistance to EGFR kinase inhibitors. (Q27851896) (← links)
- Loss-of-Function PTPRD Mutations Lead to Increased STAT3 Activation and Sensitivity to STAT3 Inhibition in Head and Neck Cancer (Q27853197) (← links)
- Insights for hepatitis C virus related hepatocellular carcinoma genetic biomarkers: Early diagnosis and therapeutic intervention (Q28080281) (← links)
- The tyrosine phosphatase PTPRD is a tumor suppressor that is frequently inactivated and mutated in glioblastoma and other human cancers (Q28115840) (← links)
- Lineage dependency and lineage-survival oncogenes in human cancer (Q28253671) (← links)
- Copy-number variation and association studies of human disease (Q28307763) (← links)
- Genomic aberrations in lung adenocarcinoma in never smokers (Q28385032) (← links)
- Genome wide SNP comparative analysis between EGFR and KRAS mutated NSCLC and characterization of two models of oncogenic cooperation in non-small cell lung carcinoma (Q28385454) (← links)
- DNA copy number gains in malignant pleural mesothelioma (Q28395184) (← links)
- Integrative and comparative genomics analysis of early hepatocellular carcinoma differentiated from liver regeneration in young and old (Q28396741) (← links)
- Role of protein tyrosine phosphatases in cancer (Q28741003) (← links)
- Psychomotor retardation with a 1q42.11–q42.12 deletion (Q29048634) (← links)
- Assessing the significance of chromosomal aberrations in cancer: methodology and application to glioma (Q30014823) (← links)
- Advances in understanding cancer genomes through second-generation sequencing (Q30014827) (← links)
- Concurrent loss of heterozygosity and copy number analysis in adenoid cystic carcinoma by SNP genotyping arrays (Q30443218) (← links)
- A survey of copy-number variation detection tools based on high-throughput sequencing data. (Q30573762) (← links)
- Mapping tumor-suppressor genes with multipoint statistics from copy-number-variation data (Q31044207) (← links)
- QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data (Q31104515) (← links)
- Interrogation of genomes by molecular copy-number counting (MCC). (Q33244431) (← links)
- SIGMA: a system for integrative genomic microarray analysis of cancer genomes (Q33267748) (← links)
- Resolving the resolution of array CGH. (Q33271882) (← links)
- Direct inference of SNP heterozygosity rates and resolution of LOH detection (Q33308258) (← links)
- SNPExpress: integrated visualization of genome-wide genotypes, copy numbers and gene expression levels (Q33316565) (← links)
- Major copy proportion analysis of tumor samples using SNP arrays (Q33329722) (← links)
- A flexible rank-based framework for detecting copy number aberrations from array data (Q33403709) (← links)
- Recurrent genomic gains in preinvasive lesions as a biomarker of risk for lung cancer (Q33472669) (← links)
- MiR-107 and MiR-185 can induce cell cycle arrest in human non small cell lung cancer cell lines. (Q33494538) (← links)
- An optimization framework for unsupervised identification of rare copy number variation from SNP array data (Q33511862) (← links)
- A statistical change point model approach for the detection of DNA copy number variations in array CGH data (Q33513807) (← links)