Feasibility of Repairing Glomerular Basement Membrane Defects in Alport Syndrome

Por Lin, Xiaobo, Suh, Jung Hee, Go, Gloriosa, Miner, Jeffrey H.
Publicado em 2014

Transgenic isolation of skeletal muscle and kidney defects in laminin beta2 mutant mice: Implications for Pierson syndrome

Por Miner, Jeffrey H., Go, Gloriosa, Cunningham, Jeanette, Patton, Bruce L., Jarad, George
Publicado em 2006

Laminin β2 Gene Missense Mutation Produces Endoplasmic Reticulum Stress in Podocytes

Por Chen, Ying Maggie, Zhou, Yuefang, Go, Gloriosa, Marmerstein, Joseph T., Kikkawa, Yamato, Miner, Jeffrey H.
Publicado em 2013

Homozygous and compound heterozygous mutations in ZMPSTE24 cause the laminopathy restrictive dermopathy

Por Moulson, Casey L., Go, Gloriosa, van der Wal, Allard C., Smitt, J. Henk Sillevis, van Hagen, Johanna M., Miner, Jeffrey H.
Publicado em 2005

Discs-large homolog 1 regulates smooth muscle orientation in the mouse ureter

Por Mahoney, Zhen X., Sammut, Bénédicte, Xavier, Ramnik J., Cunningham, Jeanette, Go, Gloriosa, Brim, Karry L., Stappenbeck, Thaddeus S., Miner, Jeffrey H., Swat, Wojciech
Publicado em 2006