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Scientific and Technical Aerospace Reports Volume 39 April 6, 2001

Scientific and Technical Aerospace Reports Volume 39 April 6, 2001

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212<br />

51<br />

LIFE SCIENCES (GENERAL)<br />

Includes general research topics related to plant <strong>and</strong> animal biology (non-human); ecology; microbiology; <strong>and</strong> also the origin, development, structure,<br />

<strong>and</strong> maintenance, of animals <strong>and</strong> plants in space <strong>and</strong> related environmental conditions. For specific topics in life sciences see categories 52<br />

through 55.<br />

<strong>2001</strong>00218<strong>39</strong> Henry Ford Health Systems, Detroit, MI USA<br />

High Fidelity Electronic Display of Digital Mammographs Final Report, 3 Sep. 1996 - 2 Sep. 1998<br />

Flynn, Michael J.; Oct. 1998; 362p; In English<br />

Contract(s)/Grant(s): DAMD17-96-1-6283<br />

Report No.(s): AD-A385649; No Copyright; Avail: CASI; A03, Microfiche; A16, Hardcopy<br />

We have investigated photoemissive structures which can achieve the required display performance of digital mammography.<br />

A design utilizing a thin glass faceplate supported by a glass microcapillary array was evaluated. The original objectives of this<br />

project was to model the performance of emissive structures <strong>and</strong> evaluate designs with high performance. With respect to performance<br />

modeling we have; (1) developed software to describe the electric field <strong>and</strong> the trajectories of electrons <strong>and</strong> used it to study<br />

the effect of the focusing plate electrode, (2) used electron/photon transport computations to characterize the electron backscattering<br />

from phosphor layers, <strong>and</strong> (3) developed a simulation code to study the luminance spread function of emissive structures <strong>and</strong><br />

reported results for conventional CRT structures <strong>and</strong> for thin structures. With respect to the evaluation of potential designs we<br />

have; (1) constructed a vacuum subsystem <strong>and</strong> experimental chamber into which a cathode <strong>and</strong> emissive structure can be mounted,<br />

(2) designed, built <strong>and</strong> tested a unique cone shaped luminance probe that will measure spread function tails on actual emissive<br />

structures. (3) Identified electron charge deposition processes that limit the utility of the originally proposed method using microcapillary<br />

designs.<br />

DTIC<br />

Electric Fields; Display Devices; Photoelectric Emission; Mammary Gl<strong>and</strong>s<br />

<strong>2001</strong>0021843 Georgetown Univ., Medical Center, Washington, DC USA<br />

Cell Cycle Regulation of Estrogen <strong>and</strong> Androgen Receptor Annual Report, 1 Jul. 1999 - 30 Jun. 2000<br />

Martinez, Elisabeth D.; Jul. 2000; 16p; In English<br />

Contract(s)/Grant(s): DAMD17-99-1-9199<br />

Report No.(s): AD-A385514; No Copyright; Avail: CASI; A01, Microfiche; A03, Hardcopy<br />

We seek to identify the phases in the cell cycle during which steroid-activated estrogen <strong>and</strong> <strong>and</strong>rogen receptors are normally<br />

transcriptionally active <strong>and</strong> to determine whether this cell cycle regulation of receptor activity is maintained when cancer-inducing<br />

non- steroidal agents activate the receptors. Our hypothesis is that the activities of steroid-induced ER <strong>and</strong> AR are controlled by<br />

cell cycle regulators <strong>and</strong> that cancer-inducing, non-steroidal activators bypass or alter this regulation of receptor activity giving<br />

rise to aberrant ER <strong>and</strong> AR function. Through these studies we are gaining underst<strong>and</strong>ing of how estrogen <strong>and</strong> <strong>and</strong>rogen receptors<br />

may contribute to the onset of tumors <strong>and</strong> to the development of hormone independent growth. We have found that the activity<br />

of the <strong>and</strong>rogen <strong>and</strong> estrogen receptors is indeed regulated throughout the cell cycle with no activity of the <strong>and</strong>rogen receptor in<br />

the G2/Phase phase <strong>and</strong> low activity of the estrogen receptor in cells which are mainly in S phase. Furthermore, our data indicate<br />

that non-steroidal activators of the receptors may act in a cell type <strong>and</strong> promoter dependent manner as we do not detect receptor<br />

activation by growth factors in our system.<br />

DTIC<br />

Steroids; Estrogens; Sense Organs; Growth; Cancer<br />

<strong>2001</strong>0021844 University of South Florida, Tampa, FL USA<br />

Weight Gain in Breast Cancer Patients on Chemotheraphy: Exploring Hormonal Body Composition <strong>and</strong> Behavioral<br />

Mechanisms Annual Report, 1 Sep. 1998-31 Aug. 1999<br />

Kumar, Nagi B.; Sep. 1999; 10p; In English<br />

Contract(s)/Grant(s): DAMD17-98-1-8240<br />

Report No.(s): AD-A385507; No Copyright; Avail: CASI; A02, Hardcopy; A01, Microfiche<br />

The purpose of this study is to prospectively <strong>and</strong> systematically observe the relative contribution of each viable mechanism<br />

such as nutritional intake, activity levels, body composition, hormonal function, thyroid function, coping mechanisms <strong>and</strong> fatigue<br />

scores during chemotherapy on weight gain in breast cancer patients. If changes in the above factors contribute to weight gain<br />

<strong>and</strong> thus alter prognosis, manipulation of these variables by timely intervention may improve prognosis <strong>and</strong> facilitate recovery<br />

from breast cancer. Progress: As planned <strong>and</strong> described in the Statement of Work, Task 1 of recruitment <strong>and</strong> data collection <strong>and</strong>

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