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Our paper "Intravital Two-Photon Microscopy of the Native Thymus" demonstrating in vivo imaging of the native thymus for the first time is finally out. @JoelSpencerLab You can read it here: journals.plos.org/plosone/ar…
Christian Burns retweeted
1/3 We built COMET (Cortex-wide Observational Miniature Epifluorescence Technique), a 3.75-g head-mounted mesoscope for cortex-wide, cellular-resolution calcium imaging in freely moving mice.
φ10-mm FOV, single-cell resolution.
biorxiv.org/content/10.64898…
#neuroscience #miniscope
Christian Burns retweeted
Very excited about this preprint! We use a K-mirror and a tunable lens to flexibly align the two-photon imaging plane with curved biological structures. Great work of PhD student @ShinjinNeuro101, with Fritjof Helmchen, @LucaGodenzini, and many others! biorxiv.org/content/10.64898…
Christian Burns retweeted
Scientists have developed an open-source microlens-array miniature microscope that can image the brains of freely moving mice with both a large field of view and cellular-level resolution. @NBIC_PKU @Orangeroad2017 scim.ag/4hAWwAI
Christian Burns retweeted
Intravital 3-photon microscopy of leukocyte dynamics in the splenic white pulp @CellRepMethods @SMuellerLab @TheDohertyInst
cell.com/cell-reports-method… 🇦🇺
Christian Burns retweeted
スマホで一分子計測する
€350程度で組み立て可能な光学系内蔵の専用の土台にスマホを設置するだけ
研究用の顕微鏡より精度は劣るものの、約250nmの距離であれば見分けることが可能で、微小管の超解像度観察や、RNA結合の検出などにも利用できた #BNTNJC
nature.com/articles/s41467-0…
Christian Burns retweeted
This 'important' Tools and Resources paper establishes a robust live-imaging toolkit to characterize excitatory and inhibitory synaptic dynamics during neuronal development. The methodology and quantitative data are 'convincing' and well validated.
elifesciences.org/articles/1…
Christian Burns retweeted
By utilizing acoustic virtual walls rather than solid boundaries, a new microfluidic platform design minimizes shear stress while guiding particles on a precise trajectory, enabling programmable, high throughput, clog-free particle manipulation. scim.ag/4i013i2
Christian Burns retweeted
We developed a maintainable, large-scale cranial window for NHPs that restores optical access in about an hour without repeat surgery—laying the groundwork for stable, long-term brain & BCI research. We hope this technology will serve as a useful resource
biorxiv.org/content/10.64898…
Christian Burns retweeted
Protocol for In Vivo Two-Photon FCS to Measure Nanocarrier Number and Flow Velocity in Mouse Cerebral Microvasculature:bio-protocol.org/en/bpdetail…
Christian Burns retweeted
They squeezed so much out of a neuron:
Ca²⁺ imaging → organic-solvent clearing → 100-hour whole-brain 2P scan → tracing → rehydration → sectioning → expansion/FISH → multi-round RNA imaging → registration.
doi.org/10.1016/j.cell.2026.…
Christian Burns retweeted
Hybrid solid−liquid optics enable scalable, high-resolution light-sheet microscopy across diverse immersion media go.nature.com/4xdDkQR
MouseMapper
An imaging-omics workflow of whole-mouse analysis
Reaching single-cell resolution!👹
vDISCO WildDISCO whole-mouse optical clearing
+#SpatialProteomics Trigeminal ganglia
Deep learning & VR annotation▶️automated segmentation & quantitative analysis of major organs, peripheral nerves & individual macrophages
@Dorie00 @erturklab @Nature 2026
nature.com/articles/s41586-0…
Christian Burns retweeted
Hello world, meet 1,000× Expansion Microscopy.
1,000,000,000× expansion by volume! A gel that starts at a few centimeters will then expand to the volume of an Olympic swimming pool. biorxiv.org/content/10.64898…
In our new bioRxiv preprint, work carried out between MIT and UMG, led by Helena Hu in collaboration with scientists from the labs of @eboyden3 Ed Boyden, Silvio Rizzoli, and myself, we present Thousandfold Expansion Microscopy.
By enlarging biological specimens across multiple rounds of expansion, molecular-scale features, as small as the distances between adjacent amino acids, can be visualized with conventional optical microscopes.
Democratizing super-resolution microscopy.
Christian Burns retweeted
MOSAIC: a versatile multimodal microscopy that seamlessly transitions between light-sheet, 2-photon, label-free and super-resolution modalities. @Eric_Betzig @ABCUCBerkeley @legant_lab
nature.com/articles/s41592-0…
Quantitative analysis of the full-thickness 3D human cortical microvasculature
h-iDISCO+
Light-sheet fluorescence microscopy
Podocalyxin->Endothelium
αSMA->Smooth muscle cell
Antibodies penetrating ~2 mm covering near full-thickness cortex
tUbeNet deep-learning segmentation
#SciArt
Vanja Curcic lab bioRxiv 2026
biorxiv.org/content/10.64898…
Christian Burns retweeted
Let's get the week started with some knowledge: capillaries act as the ultimate interface between arteries and veins, delivering vital oxygen and nutrients directly to tissues while removing metabolic waste products.
bit.ly/4dMfXWz
Credit: Dr. Gaylene Russell McEvoy
Christian Burns retweeted
Spatial genomics has existed for many years, but it has often been limited by complex imaging systems, specialized equipment, and $$$.
With IRISeq, we wanted to simplify this to a simple PCR rxn. nature.com/articles/s41593-0…
Christian Burns retweeted
#MayThe4th be with you! Meet FORCE1s, a new positive‑going, ultrasensitive voltage indicator. Optimized for 2P imaging at slower acquisition speeds, FORCE1s is easy to use on almost any microscope. Bonus: it even powers 2P miniscope experiments!📄Preprint: biorxiv.org/content/10.64898…
Christian Burns retweeted
New online! TimeVault: a synthetic time capsule for transcriptome storage dlvr.it/TS9Ywy
Christian Burns retweeted
High-fidelity intravital imaging of biological dynamics with latent-space-enhanced digital adaptive optics go.nature.com/41M0qiW





























