Parallels of Craniofacial Maldevelopment in Down Syndrome and Ts65Dn Mice (2000)
Joan T. Richtsmeier, Laura L. Baxter, Roger H. Reeves
Mouse genetic models can be used to dissect molecular mechanisms that result in human disease. This approach requires detection and demonstration of compelling parallels between phenotypes in mouse...
Mutation of melanosome protein RAB38 in chocolate mice
Loftus, Stacie K., Larson, Denise M., Baxter, Laura L., Antonellis, Anthony, Chen, Yidong, Wu, Xufeng, ...
Mutations of genes needed for melanocyte function can result in oculocutaneous albinism. Examination of similarities in human gene expression patterns by using microarray analysis reveals that RAB38,...
Defective cerebellar response to mitogenic Hedgehog signaling in Down's syndrome mice
Roper, Randall J., Baxter, Laura L., Saran, Nidhi G., Klinedinst, Donna K., Beachy, Philip A., Reeves, Roger H.
Trisomy 21 is the cause of Down's syndrome (DS) which is characterized by a number of phenotypes, including a brain which is small and hypocellular compared to that of euploid individuals. The...
Mutation of melanosome protein RAB38 in chocolate mice
Loftus, Stacie K., Larson, Denise M., Baxter, Laura L., Antonellis, Anthony, Chen, Yidong, Wu, Xufeng, ...
Mutations of genes needed for melanocyte function can result in oculocutaneous albinism. Examination of similarities in human gene expression patterns by using microarray analysis reveals that RAB38,...
Defective cerebellar response to mitogenic Hedgehog signaling in Down's syndrome mice
Roper, Randall J., Baxter, Laura L., Saran, Nidhi G., Klinedinst, Donna K., Beachy, Philip A., Reeves, Roger H.
Trisomy 21 is the cause of Down's syndrome (DS) which is characterized by a number of phenotypes, including a brain which is small and hypocellular compared to that of euploid individuals. The...