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Helen May-Simera

Showing results (21-30 of 26) with videos related to

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Nature Communications|June 21, 2014
Ciliopathy-associated gene Cc2d2a promotes assembly of subdistal appendages on the mother centriole during cilia biogenesisShobi Veleri, Souparnika H Manjunath, Robert N Fariss, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 30, 2008
Inhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet-Biedl syndromeJonathan L Tobin, Matt Di Franco, Erica Eichers, et al.
Nature Genetics|August 18, 2004
Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndromeYanli Fan, Muneer A Esmail, Stephen J Ansley, et al.
Cell|May 13, 2004
Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease geneJin Billy Li, Jantje M Gerdes, Courtney J Haycraft, et al.
Nature Genetics|September 20, 2005
Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebratesAlison J Ross, Helen May-Simera, Erica R Eichers, et al.
EMBO Molecular Medicine|March 7, 2022
Early disruption of photoreceptor cell architecture and loss of vision in a humanized pig model of usher syndromesSophia Grotz, Jessica Schäfer, Kirsten A Wunderlich, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Nature Communications|June 21, 2014
Ciliopathy-associated gene Cc2d2a promotes assembly of subdistal appendages on the mother centriole during cilia biogenesisShobi Veleri, Souparnika H Manjunath, Robert N Fariss, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 30, 2008
Inhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet-Biedl syndromeJonathan L Tobin, Matt Di Franco, Erica Eichers, et al.
Nature Genetics|August 18, 2004
Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndromeYanli Fan, Muneer A Esmail, Stephen J Ansley, et al.
Cell|May 13, 2004
Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease geneJin Billy Li, Jantje M Gerdes, Courtney J Haycraft, et al.
Nature Genetics|September 20, 2005
Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebratesAlison J Ross, Helen May-Simera, Erica R Eichers, et al.
EMBO Molecular Medicine|March 7, 2022
Early disruption of photoreceptor cell architecture and loss of vision in a humanized pig model of usher syndromesSophia Grotz, Jessica Schäfer, Kirsten A Wunderlich, et al.
Pageof 3