Pages that link to "Q36838783"
Jump to navigation
Jump to search
The following pages link to Inactivation of a transfected gene in human fibroblasts can occur by deletion, amplification, phenotypic switching, or methylation (Q36838783):
Displaying 18 items.
- De novo methylation of the MyoD1 CpG island during the establishment of immortal cell lines (Q33738027) (← links)
- 5-azacytidine induces transgene silencing by DNA methylation in Chinese hamster cells (Q33957840) (← links)
- Nucleotide-sequence-specific de novo methylation in a somatic murine cell line (Q34302576) (← links)
- Deletion of stably integrated DNA is suppressed by cadmium and zinc (Q34323263) (← links)
- Concepts and strategies for human gene therapy (Q35816188) (← links)
- Acetylation-induced transcription is required for active DNA demethylation in methylation-silenced genes. (Q36315629) (← links)
- Carcinogenic nickel silences gene expression by chromatin condensation and DNA methylation: a new model for epigenetic carcinogens (Q36550875) (← links)
- Ubiquitous and tenacious methylation of the CpG site in codon 248 of the p53 gene may explain its frequent appearance as a mutational hot spot in human cancer (Q36655587) (← links)
- High-frequency changes in transcriptional activity in polyomavirus-transformed cell lines (Q36916073) (← links)
- An evaluation of receptor-mediated gene transfer using synthetic DNA-ligand complexes (Q40655841) (← links)
- DNA methylation, heterochromatin and epigenetic carcinogens (Q40899609) (← links)
- A newly adapted pulsed-field gel electrophoresis technique allows to detect distinct types of DNA damage at low frequencies in human dermal fibroblasts upon exposure to non-toxic H2O2 concentrations (Q40919858) (← links)
- Transgenic Chinese hamster V79 cell lines which exhibit variable levels of gpt mutagenesis (Q41205633) (← links)
- Characterization of a mammalian cell line that exhibits spontaneous and ultraviolet light-induced hypermutability while retaining resistance to cell killing by ultraviolet light. (Q41341028) (← links)
- In vivo system for characterizing clonal variation and tissue-specific gene regulatory factors based on function (Q41395109) (← links)
- Spontaneous CHO APRT heterozygotes reflect high-frequency, allele-specific deletion of the chromosome Z4 APRT gene (Q44468796) (← links)
- 1306 (Q54581459) (← links)
- An Interaction Network of the Human SEPT9 Established by Quantitative Mass Spectrometry. (Q64890703) (← links)