Paper-hanger's companion: comprising tools, pastes, preparatory work; selection and hanging of wall-papers; distemper painting and cornice-tinting; stencil work; replacing sash-cord and broken window-panes; and useful wrinkles and receipts.

Mode of access: Internet.

Operator, organizational, direct and general support, depot maintenance manual including repair parts : chassis, trailer, 2 1/2 ton, drop axle, 2 wheel FSN 2330-897-9002 (make and model unspecified) ... FSN 2330-087-2883.

"April 1969."

A laboratory evaluation of trash racks for drop inlets /

Includes bibliographical references.

A critical review of the literature on pressure drop in noncircular ducts and annuli.

Cover title.

Baird Carillon. Hanging the Bourdon bell

Albert Kahn, architect. Built 1936.

Baird Carillon. Hanging the Bourdon bell

Albert Kahn, architect. Built 1936.

Mercury in the California environment, July 1970-July 1971 /

Mode of access: Internet.

Researches into the action of mercury, podophyllin, and taraxacum on the biliary secretion : being the report of the Edinburgh committee of the British Medical Association /

Mode of access: Internet.

Report on Crosby Creek erosion studies by models of drop structures located at junction of Crosby Creek and Canisteo River, Hornell, N. Y. : tests /

Typescript (carbon copy).

Method for generation of homogeneous multicellular tumor spheroids applicable to a wide variety of cell types

Multicellular tumor spheroids (MCTS) are used as organotypic models of normal and solid tumor tissue. Traditional techniques for generating MCTS, such as growth on nonadherent surfaces, in suspension, or on scaffolds, have a number of drawbacks, including the need for manual selection to achieve a homogeneous population and the use of nonphysiological matrix compounds. In this study we describe a mild method for the generation of MCTS, in which individual spheroids form in hanging drops suspended from a microtiter plate. The method has been successfully applied to a broad range of cell lines and shows nearly 100% efficiency (i.e., one spheroid per drop). Using the hepatoma cell line, HepG2, the hanging drop method generated well-rounded MCTS with a narrow size distribution (coefficient of variation [CV] 10% to 15%, compared with 40% to 60% for growth on nonadherent surfaces). Structural analysis of HepG2 and a mammary gland adenocarcinoma cell line, MCF-7, composed spheroids, revealed highly organized, three-dimensional, tissue-like structures with an extensive extracellular matrix. The hanging drop method represents an attractive alternative for MCTS production, because it is mild, can be applied to a wide variety of cell lines, and can produce spheroids of a homogeneous size without the need for sieving or manual selection. The method has applications for basic studies of physiology and metabolism, tumor biology, toxicology, cellular organization, and the development of bioartificial tissue. (C) 2003 Wiley Periodicals, Inc.

Design of artificial myocardial microtissues

Cultivation technologies promoting organization of mammalian cells in three dimensions are essential for gene-function analyses as well as drug testing and represent the first step toward the design of tissue replacements and bioartificial organs. Embedded in a three-dimensional environment, cells are expected to develop tissue-like higher order intercellular structures (cell-cell contacts, extracellular matrix) that orchestrate cellular functions including proliferation, differentiation, apoptosis, and angiogenesis with unmatched quality. We have refined the hanging drop cultivation technology to pioneer beating heart microtissues derived from pure primary rat and mouse cardiomyocyte cultures as well as mixed populations reflecting the cell type composition of rodent hearts. Phenotypic characterization combined with detailed analysis of muscle-specific cell traits, extracellular matrix components, as well as endogenous vascular endothelial growth factor (VEGF) expression profiles of heart microtissues revealed (1) a linear cell number-microtissue size correlation, (2) intermicrotissue superstructures, (3) retention of key cardiomyocyte-specific cell qualities, (4) a sophisticated extracellular matrix, and (5) a high degree of self-organization exemplified by the tendency of muscle structures to assemble at the periphery of these myocardial spheroids. Furthermore (6), myocardial spheroids support endogenous VEGF expression in a size-dependent manner that will likely promote vascularization of heart microtissues produced from defined cell mixtures as well as support connection to the host vascular system after implantation. As cardiomyocytes are known to be refractory to current transfection technologies we have designed lentivirus-based transduction strategies to lead the way for genetic engineering of myocardial microtissues in a clinical setting.