BBSome function is required for both the morphogenesis and maintenance of the photoreceptor outer segment
Hsu, Ying, Garrison, Janelle E, Kim, Gunhee, Schmitz, Addison R, Searby, Charles C, Zhang, Qihong, Datta, Poppy, Nishimura, Darryl Y, Seo, Seongjin, Sheffield, Val C
Published in PLoS genetics (19.10.2017)
Published in PLoS genetics (19.10.2017)
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Journal Article
Absence of BBSome function leads to astrocyte reactivity in the brain
Singh, Minati, Garrison, Janelle E, Wang, Kai, Sheffield, Val C
Published in Molecular brain (09.05.2019)
Published in Molecular brain (09.05.2019)
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Journal Article
Mutations in C8ORF37 cause Bardet Biedl syndrome (BBS21)
Heon, Elise, Kim, Gunhee, Qin, Sophie, Garrison, Janelle E, Tavares, Erika, Vincent, Ajoy, Nuangchamnong, Nina, Scott, C Anthony, Slusarski, Diane C, Sheffield, Val C
Published in Human molecular genetics (01.06.2016)
Published in Human molecular genetics (01.06.2016)
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Journal Article
The absence of BBSome function decreases synaptogenesis and causes ectopic synapse formation in the retina
Hsu, Ying, Garrison, Janelle E, Seo, Seongjin, Sheffield, Val C
Published in Scientific reports (20.05.2020)
Published in Scientific reports (20.05.2020)
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Journal Article
Keeping an Eye on Bardet-Biedl Syndrome: A Comprehensive Review of the Role of Bardet-Biedl Syndrome Genes in the Eye
Weihbrecht, Katie, Goar, Wesley A, Pak, Thomas, Garrison, Janelle E, DeLuca, Adam P, Stone, Edwin M, Scheetz, Todd E, Sheffield, Val C
Published in Medical research archives (01.09.2017)
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Published in Medical research archives (01.09.2017)
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