Regulation of Osteoclast Differentiation at Multiple Stages by Protein Kinase D Family Kinases
Amanda C. Leightner(University of Minnesota), Eric D. Jensen(University of Minnesota)
Cited by 10
Related Papers
Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3
|Human Molecular Genetics|2009|125
The Meckel syndrome protein meckelin (TMEM67) is a key regulator of cilia function but is not required for tissue planar polarity
|Human Molecular Genetics|2013|63