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NFI transcription factors provide chromatin access to maintain stem cell identity while preventing unintended lineage fate choices.
Transcriptional reprogramming by oxidative stress occurs within a predefined chromatin accessibility landscape.
A chromatin-mediated mechanism for specification of conditional transcription factor targets.
The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus.
Chromatin looping defines expression of TAL1, its flanking genes, and regulation in T-ALL.
Molecular mechanisms of motor neuron terminal identity
Progress and challenges in profiling the dynamics of chromatin and transcription factor binding with DNA microarrays.
Pluripotency reprogramming by competent and incompetent POU factors uncovers temporal dependency for Oct4 and Sox2.
Accurate inference of transcription factor binding from DNA sequence and chromatin accessibility data.
Heritable individual-specific and allele-specific chromatin signatures in humans.
DNA sequence-dependent compartmentalization and silencing of chromatin at the nuclear lamina.
SWI/SNF deficiency results in aberrant chromatin organization, mitotic failure, and diminished proliferative capacity.
Zelda is differentially required for chromatin accessibility, transcription factor binding, and gene expression in the early Drosophila embryo.
A common set of DNA regulatory elements shapes Drosophila appendages.
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