Abstract: Methods for generating high-yield, high-purity cardiomyocyte progenitors or cardiomyocytes from pluripotent cells are described. Wnt/?-catenin signaling is first activated in pluripotent cells, e.g., by inhibition of Gsk-3 to obtain a first population of cells. Wnt/?-catenin signaling is then inhibited in the first cell population to induce cardiogenesis under fully defined, growth factor free culture conditions.

Abstract: Methods for generating high-yield, high-purity cardiomyocyte progenitors or cardiomyocytes from pluripotent cells are described. Wnt/?-catenin signaling is first activated in pluripotent cells, e.g., by inhibition of Gsk-3 to obtain a first population of cells. Wnt/?-catenin signaling is then inhibited in the first cell population to induce cardiogenesis under fully defined, growth factor free culture conditions.

Abstract: Methods for generating high-yield, high-purity cardiomyocyte progenitors or cardiomyocytes from pluripotent cells are described. Wnt/?-catenin signaling is first activated in pluripotent cells, e.g., by inhibition of Gsk-3 to obtain a first population of cells. Wnt/?-catenin signaling is then inhibited in the first cell population to induce cardiogenesis under fully defined, growth factor free culture conditions.

Abstract: Methods for generating high-yield, high-purity cardiomyocyte progenitors or cardiomyocytes from pluripotent cells are described. Wnt/?-catenin signaling is first activated in pluripotent cells, e.g., by inhibition of Gsk-3 to obtain a first population of cells. Wnt/?-catenin signaling is then inhibited in the first cell population to induce cardiogenesis under fully defined, growth factor free culture conditions.

Abstract: Methods for generating high-yield, high-purity cardiomyocyte progenitors or cardiomyocytes from pluripotent cells are described. Wnt/?-catenin signaling is first activated in pluripotent cells, e.g., by inhibition of Gsk-3 to obtain a first population of cells. Wnt/?-catenin signaling is then inhibited in the first cell population to induce cardiogenesis under fully defined, growth factor free culture conditions.

Abstract: A dynamoelectric machine, such as a totally enclosed fan cooled (TEFC) induction motor has a double-wall bearing housing heat shield that envelops and thermally isolates the bearing housing from the rest of the motor housing interior. The shield defines an air channel between the shield outer and inner walls. Optionally the air channel may be constructed to enable circulating air flow through a shield intake in communication with an air flow source, such as air ducted from the TEFC motor axial cooling fan. The air channel also defines an exhaust. Air flow within the air channel transfers heat out of the motor housing, lowering bearing housing operating temperature. Air flow rate may be varied in response to motor operational parameters.

Abstract: Methods for generating high-yield, high-purity cardiomyocyte progenitors or cardiomyocytes from pluripotent cells are described. Wnt/?-catenin signaling is first activated in pluripotent cells, e.g., by inhibition of Gsk-3 to obtain a first population of cells. Wnt/?-catenin signaling is then inhibited in the first cell population to induce cardiogenesis under fully defined, growth factor free culture conditions.

Abstract: A dynamoelectric machine, such as a totally enclosed fan cooled (TEFC) induction motor has a double-wall bearing housing heat shield that envelops and thermally isolates the bearing housing from the rest of the motor housing interior. The shield defines an air channel between the shield outer and inner walls. Optionally the air channel may be constructed to enable circulating air flow through a shield intake in communication with an air flow source, such as air ducted from the TEFC motor axial cooling fan. The air channel also defines an exhaust. Air flow within the air channel transfers heat out of the motor housing, lowering bearing housing operating temperature. Air flow rate may be varied in response to motor operational parameters.