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Val C Sheffield

Showing results (11-20 of 193) with videos related to

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Journal of Pediatric Orthopedics|April 2, 2010
Evaluation of embryonic and perinatal myosin gene mutations and the etiology of congenital idiopathic clubfootWilliam Shyy, Kai Wang, Val C Sheffield, et al.
Scientific Reports|May 21, 2020
The absence of BBSome function decreases synaptogenesis and causes ectopic synapse formation in the retinaYing Hsu, Janelle E Garrison, Seongjin Seo, et al.
Molecular Brain|May 11, 2019
Absence of BBSome function leads to astrocyte reactivity in the brainMinati Singh, Janelle E Garrison, Kai Wang, et al.
American Journal of Physiology. Heart and Circulatory Physiology|September 21, 2010
Contrasting vascular effects caused by loss of Bardet-Biedl syndrome genesAndreas M Beyer, Deng-Fu Guo, Val C Sheffield, et al.
The Journal of Biological Chemistry|April 14, 2012
Intrinsic protein-protein interaction-mediated and chaperonin-assisted sequential assembly of stable bardet-biedl syndrome protein complex, the BBSomeQihong Zhang, Dahai Yu, Seongjin Seo, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 9, 2002
The phenotype in Norwegian patients with Bardet-Biedl syndrome with mutations in the BBS4 geneRuth Riise, Kristina Tornqvist, Alan F Wright, et al.
Human Molecular Genetics|January 10, 2012
BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypesQihong Zhang, Seongjin Seo, Kevin Bugge, et al.
Progress in Retinal and Eye Research|December 20, 2021
Retinal ciliopathies through the lens of Bardet-Biedl Syndrome: Past, present and futureBharatendu Chandra, Moon Ley Tung, Ying Hsu, et al.
Plos One|February 15, 2018
Genotypic and phenotypic characterization of the Sdccag8Tn(sb-Tyr)2161B.CA1C2Ove mouse modelKatie Weihbrecht, Wesley A Goar, Calvin S Carter, et al.
Clinical Orthopaedics and Related Research|January 23, 2009
Evaluation of CAND2 and WNT7a as candidate genes for congenital idiopathic clubfootWilliam Shyy, Frederick Dietz, Matthew B Dobbs, et al.
Pageof 20

Showing results (11-20 of 193) with videos related to

Sort By:
Pageof 20
Journal of Pediatric Orthopedics|April 2, 2010
Evaluation of embryonic and perinatal myosin gene mutations and the etiology of congenital idiopathic clubfootWilliam Shyy, Kai Wang, Val C Sheffield, et al.
Scientific Reports|May 21, 2020
The absence of BBSome function decreases synaptogenesis and causes ectopic synapse formation in the retinaYing Hsu, Janelle E Garrison, Seongjin Seo, et al.
Molecular Brain|May 11, 2019
Absence of BBSome function leads to astrocyte reactivity in the brainMinati Singh, Janelle E Garrison, Kai Wang, et al.
American Journal of Physiology. Heart and Circulatory Physiology|September 21, 2010
Contrasting vascular effects caused by loss of Bardet-Biedl syndrome genesAndreas M Beyer, Deng-Fu Guo, Val C Sheffield, et al.
The Journal of Biological Chemistry|April 14, 2012
Intrinsic protein-protein interaction-mediated and chaperonin-assisted sequential assembly of stable bardet-biedl syndrome protein complex, the BBSomeQihong Zhang, Dahai Yu, Seongjin Seo, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 9, 2002
The phenotype in Norwegian patients with Bardet-Biedl syndrome with mutations in the BBS4 geneRuth Riise, Kristina Tornqvist, Alan F Wright, et al.
Human Molecular Genetics|January 10, 2012
BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypesQihong Zhang, Seongjin Seo, Kevin Bugge, et al.
Progress in Retinal and Eye Research|December 20, 2021
Retinal ciliopathies through the lens of Bardet-Biedl Syndrome: Past, present and futureBharatendu Chandra, Moon Ley Tung, Ying Hsu, et al.
Plos One|February 15, 2018
Genotypic and phenotypic characterization of the Sdccag8Tn(sb-Tyr)2161B.CA1C2Ove mouse modelKatie Weihbrecht, Wesley A Goar, Calvin S Carter, et al.
Clinical Orthopaedics and Related Research|January 23, 2009
Evaluation of CAND2 and WNT7a as candidate genes for congenital idiopathic clubfootWilliam Shyy, Frederick Dietz, Matthew B Dobbs, et al.
Pageof 20