Pages that link to "Q40879187"
Jump to navigation
Jump to search
The following pages link to Genome screening by comparative genomic hybridization (Q40879187):
Displaying 50 items.
- Duplication of ATR inhibits MyoD, induces aneuploidy and eliminates radiation-induced G1 arrest (Q24317123) (← links)
- Expression and copy number analysis of TRPS1, EIF3S3 and MYC genes in breast and prostate cancer (Q24645931) (← links)
- Co-amplified genes at 8p12 and 11q13 in breast tumors cooperate with two major pathways in oncogenesis (Q24655172) (← links)
- Accurate quantitation of protein expression and site-specific phosphorylation (Q24671013) (← links)
- Methods for high throughput validation of amplified fragment pools of BAC DNA for constructing high resolution CGH arrays (Q24791257) (← links)
- Applications of microarray technology in breast cancer research (Q24801392) (← links)
- Human molecular cytogenetics: From cells to nucleotides (Q27024633) (← links)
- Application of DNA array technology for diagnostic microbiology (Q27481954) (← links)
- Genome-wide detection of allelic imbalance using human SNPs and high-density DNA arrays (Q28144479) (← links)
- A novel gene family NBPF: intricate structure generated by gene duplications during primate evolution (Q28265563) (← links)
- 18-Fluorodeoxyglucose positron emission tomography (FDG-PET) and the staging of early lung cancer (Q28346531) (← links)
- DNA arrays for analysis of gene expression (Q29617395) (← links)
- An oncogenic role for the phosphorylated h-subunit of human translation initiation factor eIF3 (Q30438861) (← links)
- Identification of recurrent regions of chromosome loss and gain in vestibular schwannomas using comparative genomic hybridisation (Q30495325) (← links)
- Integration of cytogenetic data with genome maps and available probes: present status and future promise (Q30619624) (← links)
- Universal linkage system: an improved method for labeling archival DNA for comparative genomic hybridization (Q30723603) (← links)
- ExpressYourself: A modular platform for processing and visualizing microarray data (Q30806406) (← links)
- Arcyptera fusca and Arcyptera tornosi repetitive DNA families: whole-comparative genomic hybridization (W-CGH) as a novel approach to the study of satellite DNA libraries (Q30837044) (← links)
- Comparative genomic hybridisation (Q30854548) (← links)
- Application of inter-simple sequence repeat PCR to mouse models: assessment of genetic alterations in carcinogenesis (Q30863057) (← links)
- Risk of false positive results in comparative genomic hybridization (Q30881764) (← links)
- Whole genome amplification of DNA from laser capture-microdissected tissue for high-throughput single nucleotide polymorphism and short tandem repeat genotyping (Q31034423) (← links)
- The novel human MOST-1 (C8orf17) gene exhibits tissue specific expression, maps to chromosome 8q24.2, and is overexpressed/amplified in high grade cancers of the breast and prostate (Q33186570) (← links)
- Amplification methods to increase the sensitivity of in situ hybridization: play card(s). (Q33534710) (← links)
- The impact of the new fish technologies on the cytogenetics of haematological malignancies (Q33587586) (← links)
- Genetic alterations in intrahepatic cholangiocarcinoma as revealed by degenerate oligonucleotide primed PCR-comparative genomic hybridization (Q33629688) (← links)
- Comparative genomic hybridization and chromosomal instability in solid tumours (Q33653215) (← links)
- Genomic changes defining the genesis, progression, and malignancy potential in solid human tumors: a phenotype/genotype correlation (Q33668711) (← links)
- Detection of copy number variation from array intensity and sequencing read depth using a stepwise Bayesian model (Q33733665) (← links)
- Assessment of a six gene panel for the molecular detection of circulating tumor cells in the blood of female cancer patients. (Q33762644) (← links)
- Mechanisms and consequences of aneuploidy and chromosome instability in the aging brain (Q33850635) (← links)
- Centrosome amplification and instability occurs exclusively in aneuploid, but not in diploid colorectal cancer cell lines, and correlates with numerical chromosomal aberrations (Q33884941) (← links)
- Methods of molecular analysis: assessing losses and gains in tumours (Q33918898) (← links)
- Selective inactivation of p53 facilitates mouse epithelial tumor progression without chromosomal instability (Q33969381) (← links)
- Chromosome imbalances in familial gliomas detected by comparative genomic hybridization (Q34077480) (← links)
- Comparative genomic hybridization: uses and limitations (Q34079193) (← links)
- Molecular cytogenetics of prostate cancer (Q34080737) (← links)
- Consulting the source code: prospects for gene-based medical diagnostics (Q34086825) (← links)
- Operomics: molecular analysis of tissues from DNA to RNA to protein (Q34093051) (← links)
- Amplification and overexpression of Elongin C gene discovered in prostate cancer by cDNA microarrays. (Q34127887) (← links)
- Aneuploidy and malignancy: an unsolved equation (Q34371170) (← links)
- Role of molecular biology in the follow-up of patients who have Barrett's esophagus (Q34569515) (← links)
- Combined classical and molecular cytogenetic analysis of cancer. (Q34762177) (← links)
- Application of comparative genomic hybridization, spectral karyotyping, and microarray analysis in the identification of subtype-specific patterns of genomic changes in rhabdomyosarcoma (Q34786049) (← links)
- Applications of comparative genomic hybridisation in constitutional chromosome studies (Q35433098) (← links)
- Constitutive heterochromatin polymorphisms in human chromosomes identified by whole comparative genomic hybridization (Q35466906) (← links)
- Quantitative analysis of differences in copy numbers using read depth obtained from PCR-enriched samples and controls (Q35550039) (← links)
- Specific chromosomal aberrations and amplification of the AIB1 nuclear receptor coactivator gene in pancreatic carcinomas (Q35745306) (← links)
- High-throughput copy number analysis of 17q23 in 3520 tissue specimens by fluorescence in situ hybridization to tissue microarrays (Q35747499) (← links)
- Recurrent chromosomal imbalances detected in biopsy material from oral premalignant and malignant lesions by combined tissue microdissection, universal DNA amplification, and comparative genomic hybridization (Q35753191) (← links)