David Tobin
@tobinlab.bsky.social
2.9K followers 1.2K following 16 posts
Scientist at Duke studying tuberculosis, host susceptibility to infection, and mycobacterial pathogenesis. Views are my own and do not represent those of my employer.
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Reposted by David Tobin
Reposted by David Tobin
uocmicrobiology.bsky.social
UChicago Microbiology is searching for tenured or tenure-track faculty working in host-pathogens interactions, viral and bacterial pathogenesis, and emerging infectious diseases. Come join our vibrant Department! microbiology.uchicago.edu
Apply here apply.interfolio.com/174404
Department of Microbiology | The University of Chicago
microbiology.uchicago.edu
Reposted by David Tobin
science.org
NSF today released instructions for the next round of applicants to its Graduate Research Fellowship Program. A key group—second-year Ph.D. students—is no longer eligible, and students who are still able to apply will face an unusually narrow timeframe. https://scim.ag/3KlQkQk
‘Completely shattered.’ Changes to NSF’s graduate student fellowship spur outcry
The announcement comes months later than usual, leaving many would-be applicants stranded
www.science.org
Reposted by David Tobin
jcellsci.bsky.social
Eric Peterman @errricpeterman.bsky.social, Jeffrey Rasmussen @jraslab.bsky.social @uwbiology.bsky.social & colleagues discover that microtubules regulate tissue-level navigation in skin-resident macrophages.
journals.biologists.com/jcs/article/...
Article: journals.biologists.com/jcs/article/...
Reposted by David Tobin
Reposted by David Tobin
scifri.bsky.social
Today, scientists know that genetics plays a role in many conditions and diseases. But back in the ’90s, geneticist Mary-Claire King was the first to link a gene to an inherited form of a common cancer.
A Trailblazing Geneticist Reflects On Her Life And Work
Dr. Mary-Claire King was the first to link a gene to hereditary cancer risk with the identification of BRCA1. She was just getting started.
buff.ly
Reposted by David Tobin
baym.lol
Immigrants, particularly on H1Bs, are the lifeblood of American innovation. If you wanted to hurt US competitiveness in the next century, I can think of few more effective ways than a move like this

Even when found illegal, the mere intent will have irreparably harmed our future
Reposted by David Tobin
tuuliel.bsky.social
Yup. This was me 10 years ago.
ncweaver.skerry-tech.com
Why is this horrible for Universities?

Just about everyone who isn't a citizen or green card holder already who's hired for a tenure track faculty position is hired through an H1B and then, after 3-5 years, applies for a green card.

This is literally "No more foreign professors can be hired"
gergely.pragmaticengineer.com
Those on an H1B cannot return to the US from tomorrow (Sunday) unless paying $100K. This is an out-of-the blue presidential action. We’ll see software engineers stranded abroad.

One easy to predict outcome: those on US visas will travel less… for work, for conferences etc.
Reposted by David Tobin
reichlinmelnick.bsky.social
Article here. There are still MANY questions about how this new INA 212(f) entry suspension will be implemented, and the government has put out frighteningly little official information. Many people will be watching carefully.

www.nytimes.com/2025/09/19/u...
Trump Says the U.S. Will Institute $100,000 Fee for Skilled Worker Visas
www.nytimes.com
Reposted by David Tobin
donmoyn.bsky.social
"Now an extraordinarily successful scientific research system — one that took decades to build, has saved millions of lives and generated billions of dollars in profits for American companies and investors — is being dismantled before our eyes."
markhisted.org
Shutting down the war on cancer.

“New presidential administrations have usually gone out of their way to make transitions at the NIH as seamless as possible so as not to disrupt ongoing research…”

Right. That’s not what is happening now. Must-read article.

🧪
Trump Is Shutting Down the War On Cancer
www.nytimes.com
Reposted by David Tobin
saradakethar.bsky.social
Hey zebrafish folks! Super excited to kick off a speaker spotlight series for the ZDM Conference happening this October in Boston! Watch this space and be sure to retweet!
#zdmsECI #ZDM18
tobinlab.bsky.social
Really interesting work from our neighbor Clare Smith @dukemedschool.bsky.social starting from CC mice and linking Ctsz to TB infection outcome as well as functional variation in human populations (UW, Case Western, Uganda) and expression in human granulomas (@charliejpyle.bsky.social)
plosbiology.org
#Tuberculosis severity varies widely between people; why is this? This study uses the #CollaborativeCross mouse panel to identify the protease #cathepsin Z (CTSZ) as a conserved regulator of #TB outcomes via its influence on CXCL1 in mice & in humans @plosbiology.org 🧪 plos.io/4phwRA8
Human CTSZ variants are associated with TB severity, and CTSZ is present at the host-pathogen interface within human pulmonary Mtb granulomas. Top left: A manually annotated UMAP generated by unsupervised clustering of data from single-cell mRNA-Seq of human biopsy tissue, containing Mtb granulomas from three patients with TB. Top right: Analysis of normalized expression values reveals that CTSZ is specifically induced in granuloma macrophages, particularly in lipid-associated macrophages. Bottom: Brightfield (BF) images and immunofluorescent staining of CTSZ and CD68 within a granuloma biopsy from an individual with pulmonary TB. Goat (Gt) and mouse (Ms) IgG isotype control staining is depicted in the top row. DAPI staining indicates cell nuclei. Scale bar is 60 µM in length.
Reposted by David Tobin
charliejpyle.bsky.social
You can now explore the mRNA expression of your favorite TB gene of interest in our recently published human pulmonary M.tb granuloma single-cell dataset at the Broad Single Cell PORTAL!

@broadinstitute.org
@wallacewly.bsky.social

singlecell.broadinstitute.org/single_cell/...
Paired single-cell and spatial transcriptional profiling reveals a central osteopontin macrophage response mediating tuberculous granuloma formation - Single Cell Portal
Granulomas are classic manifestations of tuberculosis pathogenesis. They result from an ensemble of immune responses to Mycobacterium tuberculosis infection, but the identities, arrangement, cellular interactions, and regulation of the cells that comprise them have thus far been incompletely understood. To better understand the composition of granulomas, we conducted spatial and single-cell RNA sequencing of granulomas in biopsy specimens from patients with tuberculosis. We found that granulomas consist of concentric transcriptional laminae surrounding areas of central necrosis. We identified distinct populations of granuloma-associated stromal cells, fibroblasts, lymphocytes, mast cells, dendritic cells, neutrophils, and macrophages. Furthermore, gene expression among these cell populations differed by location within granulomas. We used inferential analysis to predict dominant granuloma cell-cell interactions, the activity of major signaling pathways, and transcription factor activities. Using spatial deconvolution, we mapped a conserved pattern of cellular organization dominated by macrophages rich in SPP1/osteopontin expression. Trajectory analysis of macrophage subtypes mapped their differentiation and supported the importance of SPP1 to granuloma macrophage polarization. Using the Mycobacterium marinum-zebrafish model, we found that mycobacterial infection induces spp1 expression in macrophages and that spp1 ablation results in granuloma formation defects and reduced survival in adult animals. Cumulatively, we have identified a dominant macrophage granuloma population as well as its central regulatory gene in human samples and confirmed the importance of spp1 to granuloma biology in vivo.
singlecell.broadinstitute.org
Reposted by David Tobin
crampell.bsky.social
The new proposed rule would also effectively end automatic OPT - the program that allows students to work for a short period of time after they graduate (which means e.g. they can accept a position at a US tech company while waiting to enter lottery for a longer-term skilled-worker visa)
Reposted by David Tobin
Reposted by David Tobin
burgesslab.bsky.social
#zebrafish genome update, our T2T assembly of the inbred strain of AB (M-AB) generated by my buddy Nori Sakai has now been released at NCBI and will be a second reference genome for zebrafish (GRCz12ab):
JBQAYU000000000.1 Danio rerio :: NCBI
www.ncbi.nlm.nih.gov
Reposted by David Tobin
debbysilver.bsky.social
Sharing our newest study led by the incredibly talented @federicamosti.bsky.social investigating new molecular mechanisms of human brain development. We discover a human-specific enhancer HAR1984 that influences chromatin looping to promote cortical size and folding! www.biorxiv.org/cgi/content/...
Reposted by David Tobin
alwardlab-ucla.bsky.social
*Please read and share!* My NIH funds at UCLA were suspended last week.
It's hard to find the words to describe the impact of these grant suspensions. I have felt speechless and heartbroken that people in my lab, my friends, colleagues, researchers, trainees, and undergrads 1/9
Reposted by David Tobin
drglam.bsky.social
I just got the notice that all the FlyBase people at Harvard, including me, will be laid off on October 12. I'm devastated.