Michael Andrews

<i>Bbs2</i> -null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin

Darryl Nishimura, Melissa A. Fath, Robert F. Mullins et al. · Proceedings of the National Academy of Sciences · 2004 · 368 citations

Medicine, Genetics, Molecular Genetics +15

Bardet–Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assembly

Kirk Mykytyn, Robert F. Mullins, Michael Andrews et al. · Proceedings of the National Academy of Sciences · 2004 · 346 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A knockin mouse model of the Bardet–Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesity

Roger E. Davis, Ruth E. Swiderski, Kamal Rahmouni et al. · Proceedings of the National Academy of Sciences · 2007 · 265 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Mkks-null mice have a phenotype resembling Bardet–Biedl syndrome

Melissa A. Fath, Robert F. Mullins, Charles Searby et al. · Human Molecular Genetics · 2005 · 186 citations

Life Sciences, Genetics, Molecular Genetics +17

Developmental time course distinguishes changes in spontaneous and light-evoked retinal ganglion cell activity in <i>rd1</i> and <i>rd10</i> mice

Steven F. Stasheff, Malini Shankar, Michael Andrews · Journal of Neurophysiology · 2011 · 116 citations

Medicine, Neurobiology, Neuroscience +17