scispace - formally typeset
K

Karen L. Reddy

Researcher at Johns Hopkins University

Publications -  44
Citations -  3555

Karen L. Reddy is an academic researcher from Johns Hopkins University. The author has contributed to research in topics: Nuclear lamina & Chromatin. The author has an hindex of 21, co-authored 41 publications receiving 3173 citations. Previous affiliations of Karen L. Reddy include Howard Hughes Medical Institute & University of Chicago.

Papers
More filters
Journal ArticleDOI

Transcriptional repression mediated by repositioning of genes to the nuclear lamina

TL;DR: Three-dimensional DNA-immunoFISH is devised for inducible tethering of genes to the inner nuclear membrane (INM) and targeted adenine methylation is used to show that, as is the case for the model system, inactive immunoglobulin loci at the nuclear periphery are contacted by INM and lamina proteins.
Journal ArticleDOI

vrille, Pdp1, and dClock form a second feedback loop in the Drosophila circadian clock

TL;DR: It is shown here that VRI and PDP1 proteins feed back and directly regulate dClock expression, comprising a second feedback loop in the Drosophila clock that gives rhythmic expression of dClock, and probably of other genes, to generate accurate circadian rhythms.
Journal ArticleDOI

DNA Sequence-Dependent Compartmentalization and Silencing of Chromatin at the Nuclear Lamina

TL;DR: Genomic repositioning assays show that LADs, spanning the developmentally regulated IgH and Cyp3a loci contain discrete DNA regions that associate chromatin with the nuclear lamina and repress gene activity in fibroblasts, revealing a mechanism that couples nuclear compartmentalization of chromatin domains with the control of gene activity.
Journal ArticleDOI

Directed targeting of chromatin to the nuclear lamina is mediated by chromatin state and A-type lamins

TL;DR: Localization of specific chromatin domains to the nuclear lamina is mediated by YY1 and lamin A/C and is dependent on a specific histone modification profile.
Journal ArticleDOI

Regulation of B cell fate commitment and immunoglobulin heavy-chain gene rearrangements by Ikaros.

TL;DR: It is shown that the transcription factor EBF restored the generation of CD19+ pro–B cells from Ikaros-deficient hematopoietic progenitors, and is an obligate component of a network that regulates B cell fate commitment and immunoglobulin heavy-chain gene recombination.