Skip To Main Content
Barbara L Kee on Muck Rack

Barbara L Kee

As seen in: Color Research & Application, Nature, Cell Press, The Journal of Immunology
Is this you? As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work. Claim your profile

Get in touch with Barbara L

Contact Barbara L, search articles and posts on X, monitor coverage, and track replies from one place.

Learn more about Muck Rack

Actions

Share this page

Is this you?

As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work.
Claim your profile

Articles

Genomic and Transcriptional Mechanisms Governing Innate-like T Lymphocyte Development

|
By Barbara L Kee, Roxroy C. Morgan
| The Journal of Immunology Verified
Thank you for your interest in spreading the word about The Journal of Immunology. NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address. Your Email * Your Name * Send To * Enter multiple addresses on separate lines or separate them with commas.
Open in Who Shared View Duplicates (233) Issue with article?

It’s a Phase That EBF1 Is Going Through

|
By Barbara L Kee
| Cell Press Verified
Lineage-specific programming of chromatin requires transcription factors to bind inaccessible chromatin. Wang et al. find that “pioneering” by the transcription factor EBF1 involves a prion-like domain that enables recruitment of chromatin remodelers and formation of phase-separated condensates. Partitioning of EBF1-bound sites into condensates may coordinate expression of B lineage genes.
Open in Who Shared Issue with article?

The transcription factor BCL-6 controls early development of innate-like T cells

|
By Barbara L Kee, Mihalis Verykokakis, Marianthi Gioulbasani, Alexandros Galaras
| Nature Verified
Abstract Innate T cells, including invariant natural killer T (iNKT) and mucosal-associated innate T (MAIT) cells, are a heterogeneous T lymphocyte population with effector properties preprogrammed during their thymic differentiation. How this program is initiated is currently unclear. Here, we show that the transcription factor BCL-6 was transiently expressed in iNKT cells upon exit from positive selection and was required for their proper development beyond stage 0.
Open in Who Shared Issue with article?
See all 10 articles