Timothy W Vogel

Bardet-Biedl syndrome 3 (Bbs3) knockout mouse model reveals common BBS-associated phenotypes and Bbs3 unique phenotypes

V. Sheffield, E. Stone, D. Morgan, 2011, Proceedings of the National Academy of Sciences.

Abnormal development of NG2+PDGFRα+ neural progenitor cells leads to neonatal hydrocephalus in a ciliopathy mouse model

V. Sheffield, P. Nopoulos, D. Thedens, 2012, Nature Medicine.

The role of primary cilia in the pathophysiology of neural tube defects.

C. Carter, S. Robinson, Qihong Zhang, 2012, Neurosurgical focus.

A mouse model of Bardet-Biedl Syndrome has impaired fear memory, which is rescued by lithium treatment

V. Sheffield, J. Wemmie, C. Carter, 2020, bioRxiv.

BBS7 is required for BBSome formation and its absence in mice results in Bardet-Biedl syndrome phenotypes and selective abnormalities in membrane protein trafficking

Val C. Sheffield, Edwin M. Stone, Darryl Nishimura, 2013, Journal of Cell Science.

Light aversion in mice depends on nonimage-forming irradiance detection.

V. Sheffield, E. Stone, A. Russo, 2010, Behavioral neuroscience.

The role of primary cilia in the pathophysiology of neural tube defects.

C. Carter, S. Robinson, Qihong Zhang, 2012, Neurosurgical focus.