Thesis (M. Phil.)--University of Hong Kong, 2001. / Includes bibliographical references.

Thesis (Ph. D.)--Lehigh University, 2003. / Includes vita. Includes bibliographical references (leaves 162-172).

Thesis (M.S.)--University of Wyoming, 2008. / Title from PDF title page (viewed on Mar. 9, 2010). Includes bibliographical references (p. 173-182).

Thesis (Ph. D.)--University of Texas at Austin, 2003. / Supervisor: Dennis G. Deppe. Vita. Includes bibliographical references. Available also from UMI Company.

Proefachrift--Technische Hogeschool, Delft. / Bibliography: p. 139-142.

Thesis (Ph. D.)--Johns Hopkins University, 1918. / Cover title. Vita. "Author's abstract of this paper issued by the [Wistar institute] Bibliographic service, May 5." "Reprinted from the Journal of experimental zoölogy, vol. 31, no. 1, July, 1920." Bibliography: p. 114-116.

Thesis (Ph. D.)--Chemistry and Biochemistry, Georgia Institute of Technology, 2009. / Committee Chair: Weck, Marcus; Committee Member: Christopher Jones; Committee Member: Jean-Luc Bredas; Committee Member: Joseph Perry; Committee Member: Laren M. Tolbert. Part of the SMARTech Electronic Thesis and Dissertation Collection.

Thesis (M.S. in Meteorology and Physical Oceanography)--Naval Postgraduate School, March 2003. / Thesis advisor(s): Philip A. Durkee. Includes bibliographical references (p. 57-59). Also available online.

Thesis (Ph. D.)--University of Texas at Austin, 2001. / Vita. Includes bibliographical references (leaves 156-171). Available also in a digital version from Dissertation Abstracts.

Little numerical analysis has been done on fluorescence lifetime imaging \emph{in-vivo}. Here, a 3D fluorescence Monte Carlo model is used to evaluate a microvasculature geometry obtained via two-photon microscopy. I found that a bulk-vascularization assumption does not provide an accurate picture of penetration depth of the collected fluorescence signal. Instead the degree of absorption difference between extravascular and intravascular space, as well as the absorption difference between excitation and emission wavelengths must be taken into account to determine the depth distribution. Additionally, I found that using targeted illumination can provide for superior surface vessel sensitivity over wide-field illumination, with small area detection offering an even greater amount of sensitivity to surface vasculature. Depth sensitivity can be enhanced by either increasing the detector area or increasing the illumination area. Finally, it is shown that the excitation wavelength and vessel size can affect intra-vessel sampling distribution, as well as the amount of signal that originates from inside the vessel under targeted illumination conditions. / text