Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Demirhan Kobat"'
Autor:
Chris Xu, Catharine G. Clark, Chris B. Schaffer, Ke Wang, Frank W. Wise, Demirhan Kobat, Nicholas G. Horton
Publikováno v:
Nature photonics
Two-photon fluorescence microscopy (2PM)1 enables scientists in various fields including neuroscience2,3, embryology4, and oncology5 to visualize in vivo and ex vivo tissue morphology and physiology at a cellular level deep within scattering tissue.
Publikováno v:
Nature Photonics. 7:33-37
A parallel implementation of multifocal multiphoton modulation microscopy allows simultaneous phosphorescent lifetime and intensity imaging in vivo at speeds 100 times faster than conventional configurations. Three-dimensional imaging of a phosphores
Autor:
David R. Rivera, Christopher M. Brown, Ina Pavlova, Watt W. Webb, Chris Xu, Demirhan Kobat, Dimitre G. Ouzounov
Publikováno v:
Proceedings of the National Academy of Sciences. 108:17598-17603
We present a compact and flexible endoscope (3-mm outer diameter, 4-cm rigid length) that utilizes a miniaturized resonant/nonresonant fiber raster scanner and a multielement gradient-index lens assembly for two-photon excited intrinsic fluorescence
Publikováno v:
Nature photonics
Multiphoton microscopy (MPM) is widely used for optical sectioning deep in scattering tissue, in vivo [1–2]. Phosphorescence lifetime imaging microscopy (PLIM) [3] is a powerful technique for obtaining biologically relevant chemical information thr
Autor:
Scott S. Howard, Chris Xu, Eric R. DeLeon, Demirhan Kobat, Nicholas G. Horton, Kenneth R. Olsen, Adam Straub, Aamir A. Khan
Publikováno v:
Optics in the Life Sciences.
Multiphoton Microscopy and Phosphorescence Lifetime Microscopy are combined to produce full-frame lifetime resolved 3D images in vivo. Parallel excitation and acquisition of two-photon emission is achieved via a frequency multiplexed multi-foci excit
Publikováno v:
Optics in the Life Sciences.
In vivo images of the mouse brain were recorded through an unthinned, intact skull using three-photon fluorescence microscopy at 1700 nm. Images of brain vasculature 900 μm below the surface of the skull were obtained.
Publikováno v:
Scopus-Elsevier
We demonstrate deep tissue three-photon microscopy at the new spectral window of 1700 nm. We imaged vasculature and RFP-tagged neurons up to 1 mm below the cortical surface, and RFP-tagged neurons below an unthinned skull.
Publikováno v:
Scopus-Elsevier
We demonstrate non-invasive, high-resolution, in vivo imaging of subcortical structures (the external capsule (EC) and hippocampus) within an intact mouse brain using three-photon fluorescence microscopy at the new spectral window of 1700 nm.
Publikováno v:
Journal of biomedical optics. 16(10)
Deep tissue in vivo two-photon fluorescence imaging of cortical vasculature in a mouse brain using 1280-nm excitation is presented. A record imaging depth of 1.6 mm in mouse cortex is achieved in vivo, approximately reaching the fundamental depth lim
Publikováno v:
SPIE Proceedings.
A miniaturized scanning mechanism is a crucial component in the creation of endoscopes for microscopic imaging. Several groups have developed resonant sca nners (e.g., spiral or Lissajous scan pa ttern), but these suffer from limitations in non-unifo