Chuyan Ying

Severe cardiomyopathy in mice lacking dystrophin and MyoD

Megeney, Lynn A., Kablar, Boris, Perry, Robert L. S., Ying, Chuyan, May, Linda, Rudnicki, Michael A.

The mdx mouse, a mouse model of Duchenne muscular dystrophy, carries a loss-of-function mutation in dystrophin, a component of the membrane-associated dystrophin–glycoprotein complex. Unlike...

Strain-Dependent Myeloid Hyperplasia, Growth Deficiency, and Accelerated Cell Cycle in Mice Lacking the Rb-Related p107 Gene

LeCouter, Jennifer E., Kablar, Boris, Hardy, W. Rodney, Ying, Chuyan, Megeney, Lynn A., May, Linda L., ...

To investigate the function of the Rb-related p107 gene, a null mutation in p107 was introduced into the germ line of mice and bred into a BALB/cJ genetic background. Mice lacking p107 were viable...

Severe cardiomyopathy in mice lacking dystrophin and MyoD

Megeney, Lynn A., Kablar, Boris, Perry, Robert L. S., Ying, Chuyan, May, Linda, Rudnicki, Michael A.

The mdx mouse, a mouse model of Duchenne muscular dystrophy, carries a loss-of-function mutation in dystrophin, a component of the membrane-associated dystrophin–glycoprotein complex. Unlike...

Strain-Dependent Myeloid Hyperplasia, Growth Deficiency, and Accelerated Cell Cycle in Mice Lacking the Rb-Related p107 Gene

LeCouter, Jennifer E., Kablar, Boris, Hardy, W. Rodney, Ying, Chuyan, Megeney, Lynn A., May, Linda L., ...

To investigate the function of the Rb-related p107 gene, a null mutation in p107 was introduced into the germ line of mice and bred into a BALB/cJ genetic background. Mice lacking p107 were viable...