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Val C Sheffield

Showing results (21-30 of 193) with videos related to

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Survey of Ophthalmology|December 31, 2002
Myocilin glaucomaJohn H Fingert, Edwin M Stone, Val C Sheffield, et al.
The European Journal of Neuroscience|April 17, 2008
Classical and melanopsin photoreception in irradiance detection: negative masking of locomotor activity by lightStewart Thompson, Russell G Foster, Edwin M Stone, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|February 6, 2009
Cartilage abnormalities associated with defects of chondrocytic primary cilia in Bardet-Biedl syndrome mutant miceAnjan P Kaushik, James A Martin, Qihong Zhang, et al.
Human Molecular Genetics|February 2, 2011
Functional analysis of BBS3 A89V that results in non-syndromic retinal degenerationPamela R Pretorius, Mohammed A Aldahmesh, Fowzan S Alkuraya, et al.
Psychiatric Genetics|December 14, 2011
Germline mosaic transmission of a novel duplication of PXDN and MYT1L to two male half-siblings with autismKacie J Meyer, Michael S Axelsen, Val C Sheffield, et al.
Human Molecular Genetics|January 20, 2009
Requirement of Bardet-Biedl syndrome proteins for leptin receptor signalingSeongjin Seo, Deng-Fu Guo, Kevin Bugge, et al.
Plos Genetics|February 20, 2014
The centriolar satellite protein AZI1 interacts with BBS4 and regulates ciliary trafficking of the BBSomeXitiz Chamling, Seongjin Seo, Charles C Searby, et al.
The Journal of Biological Chemistry|May 11, 2018
Transforming growth factor β2 (TGFβ2) signaling plays a key role in glucocorticoid-induced ocular hypertensionRamesh B Kasetti, Prabhavathi Maddineni, Pinkal D Patel, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 10, 2019
Disruption of RPGR protein interaction network is the common feature of RPGR missense variations that cause XLRPQihong Zhang, Joseph C Giacalone, Charles Searby, et al.
American Journal of Human Genetics|April 19, 2011
Primary ciliary dyskinesia caused by homozygous mutation in DNAL1, encoding dynein light chain 1Masha Mazor, Soliman Alkrinawi, Vered Chalifa-Caspi, et al.
Pageof 20

Showing results (21-30 of 193) with videos related to

Sort By:
Pageof 20
Survey of Ophthalmology|December 31, 2002
Myocilin glaucomaJohn H Fingert, Edwin M Stone, Val C Sheffield, et al.
The European Journal of Neuroscience|April 17, 2008
Classical and melanopsin photoreception in irradiance detection: negative masking of locomotor activity by lightStewart Thompson, Russell G Foster, Edwin M Stone, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|February 6, 2009
Cartilage abnormalities associated with defects of chondrocytic primary cilia in Bardet-Biedl syndrome mutant miceAnjan P Kaushik, James A Martin, Qihong Zhang, et al.
Human Molecular Genetics|February 2, 2011
Functional analysis of BBS3 A89V that results in non-syndromic retinal degenerationPamela R Pretorius, Mohammed A Aldahmesh, Fowzan S Alkuraya, et al.
Psychiatric Genetics|December 14, 2011
Germline mosaic transmission of a novel duplication of PXDN and MYT1L to two male half-siblings with autismKacie J Meyer, Michael S Axelsen, Val C Sheffield, et al.
Human Molecular Genetics|January 20, 2009
Requirement of Bardet-Biedl syndrome proteins for leptin receptor signalingSeongjin Seo, Deng-Fu Guo, Kevin Bugge, et al.
Plos Genetics|February 20, 2014
The centriolar satellite protein AZI1 interacts with BBS4 and regulates ciliary trafficking of the BBSomeXitiz Chamling, Seongjin Seo, Charles C Searby, et al.
The Journal of Biological Chemistry|May 11, 2018
Transforming growth factor β2 (TGFβ2) signaling plays a key role in glucocorticoid-induced ocular hypertensionRamesh B Kasetti, Prabhavathi Maddineni, Pinkal D Patel, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 10, 2019
Disruption of RPGR protein interaction network is the common feature of RPGR missense variations that cause XLRPQihong Zhang, Joseph C Giacalone, Charles Searby, et al.
American Journal of Human Genetics|April 19, 2011
Primary ciliary dyskinesia caused by homozygous mutation in DNAL1, encoding dynein light chain 1Masha Mazor, Soliman Alkrinawi, Vered Chalifa-Caspi, et al.
Pageof 20