Qinrong Zhang

This study shows that inhibiting Notch signaling and forcing cell cycle re-entry in Müller glia promotes their reprogramming into neurons in uninjured mouse retina.

NeAT improves in vivo two-photon imaging by correcting optical aberrations and motion without external training data.

The paper introduces FACED 2.0, a high-speed imaging technique that enables simultaneous voltage and calcium activity recording in vivo across large neuronal populations.

This study uses 2-photon fluorescence microscopy to examine lens suture structures in wildtype and KLPH-KO mice, revealing altered suture patterns and pathological features in the knockout model.

This paper shows how cortical pyramidal neurons balance synaptic flexibility and stability by differentially regulating plasticity at oblique and basal dendrites.

This study uses adaptive optical two-photon fluorescence microscopy to investigate retinal microvascular and neuronal pathologies in vivo, revealing microvascular lesions and pharmacological effects.