Reference health
Two-photon excitation improves multifocal structured illumination microscopy in thick scattering tissue
28/28 checkable references clean · checked 2026-07-23
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
2 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.
The 28 checked references that resolve
resolves10.1038/nmeth929
Sub-diffraction-limit imaging by stochastic optical reconstruction microscopy (STORM)
resolves10.1364/OL.19.000780
Breaking the diffraction resolution limit by stimulated emission: stimulated-emission-depletion fluorescence microscopy
resolves10.1038/nmeth.2025
Resolution doubling in live, multicellular organisms via multifocal structured illumination microscopy
resolves10.1364/AO.38.003562
Effect of a finite-size pinhole on noise performance in single-, two-, and three-photon confocal fluorescence microscopy
resolves10.1364/AO.34.003576
Quantitative comparison of background rejection, signal-to-noise ratio, and resolution in confocal and full-field laser scanning microscopes
resolves10.1002/(SICI)1097-0029(19991101)47:3<210::AID-JEMT7>3.0.CO;2-H
Effect of a confocal pinhole in two-photon microscopy
resolves10.1016/j.cell.2012.10.008
Noninvasive Imaging beyond the Diffraction Limit of 3D Dynamics in Thickly Fluorescent Specimens
resolves10.1046/j.1365-2818.2001.00852.x
High efficiency beam splitter for multifocal multiphoton microscopy
resolves10.1529/biophysj.106.102459
The Power of Single and Multibeam Two-Photon Microscopy for High-Resolution and High-Speed Deep Tissue and Intravital Imaging
resolves10.1364/OL.25.001213
Time-decorrelated multifocal array for multiphoton microscopy and micromachining
resolves10.1046/j.1365-2818.1999.00493.x
Real‐time imaging of two‐photon‐induced fluorescence with a microlens‐array scanner and a regenerative amplifier
resolves10.1364/JOSAA.17.001192
Time multiplexing and parallelization in multifocal multiphoton microscopy
resolves10.1364/OL.30.003353
Optically sectioned fluorescence lifetime imaging using a Nipkow disk microscope and a tunable ultrafast continuum excitation source
resolves10.1073/pnas.1216696110
Improving spinning disk confocal microscopy by preventing pinhole cross-talk for intravital imaging
resolves10.1046/j.1365-2818.1998.00431.x
Real time two‐photon absorption microscopy using multi point excitation
resolves10.1073/pnas.052545099
Fast 100-nm resolution three-dimensional microscope reveals structural plasticity of mitochondria in live yeast
The 2 references without a DOI — listed, not checked
no DOI — not checkedCJR Sheppard, Super-resolution in confocal imaging. Optik (Stuttg) 80, 5354 (1988).
no DOI — not checkedCJR Sheppard, M Gu, Image formation in two-photon fluorescence microscopy. Optik (Stuttg) 86, 104–106 (1990).
What this badge says. CiteStamped means the CHECKABLE references of this
work were clean at the dated check: each resolved to a known work in a public registry, and none
carried a retraction notice at that time. It says nothing about the quality, findings,
or importance of the work itself, and nothing about references deposited without a DOI.
checked 2026-07-23 — re-checked daily as this page is visited; titles and statuses come from Crossref and DataCite and are not part of the signed record
Embed this badge
Both snippets point at the live badge image and link back to this page. The badge re-renders from the daily check, so an embed never goes stale by more than a day of visits.
<a href="https://citestamp.com/citestamped/10.1073/pnas.1314447111"><img src="https://citestamp.com/citestamped/10.1073/pnas.1314447111/badge.svg" alt="CiteStamped reference-health badge" width="460" height="64"></a>
[](https://citestamp.com/citestamped/10.1073/pnas.1314447111)