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Prabhakar R. Gudla

Researcher at National Institutes of Health

Publications -  20
Citations -  644

Prabhakar R. Gudla is an academic researcher from National Institutes of Health. The author has contributed to research in topics: Chromosome Territory & X chromosome. The author has an hindex of 9, co-authored 20 publications receiving 477 citations.

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Human T-cell leukemia virus type 1 p8 protein increases cellular conduits and virus transmission

TL;DR: The ability of p8 to simultaneously anergize and cluster T cells, together with its induction of cellular conduits, secures virus propagation while avoiding the host's immune surveillance.
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Allele-specific nuclear positioning of the monoallelically expressed astrocyte marker GFAP

TL;DR: This work directly probed the relationship between nuclear positioning and gene activity by comparing the location of the active and inactive copies of a monoallelically expressed gene in single cell nuclei and shows that the functionally distinct alleles occupy differential radial positions within the cell nucleus and differentially associate with intranuclear compartments.
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Transcriptional Bursting and Co-bursting Regulation by Steroid Hormone Release Pattern and Transcription Factor Mobility

TL;DR: It is demonstrated that transcription factor (TF) nuclear mobility determines burst duration, whereas its bound fraction determines burst frequency, and a striking co-bursting pattern between TSs located at proximal and distal positions in the nucleus is uncovered.
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Dynamic imaging of nascent RNA reveals general principles of transcription dynamics and stochastic splice site selection.

TL;DR: In this paper, a quasi-genome-scale platform for observing synthesis and processing kinetics of single nascent RNA molecules in real time is established, and all observed genes show transcriptional bursting.
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TCR Microclusters Pre-Exist and Contain Molecules Necessary for TCR Signal Transduction

TL;DR: The existence of TCR microclusters prior to ligand binding in a state that is conducive for the initiation of downstream signaling could explain, in part, the rapid kinetics with which TCR signal transduction occurs.