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Val C Sheffield

Showing results (31-40 of 193) with videos related to

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Investigative Ophthalmology & Visual Science|April 7, 2017
Restoration of Aqueous Humor Outflow Following Transplantation of iPSC-Derived Trabecular Meshwork Cells in a Transgenic Mouse Model of GlaucomaWei Zhu, Ankur Jain, Oliver W Gramlich, et al.
American Journal of Physiology. Renal Physiology|November 26, 2010
Inactivation of Bardet-Biedl syndrome genes causes kidney defectsDeng-Fu Guo, Andreas M Beyer, Baoli Yang, et al.
Developmental Biology|June 19, 2014
Functional characterization of Prickle2 and BBS7 identify overlapping phenotypes yet distinct mechanismsXue Mei, Trudi A Westfall, Qihong Zhang, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 7, 2002
Novel mutation in the TIMP3 gene causes Sorsby fundus dystrophySamuel G Jacobson, Artur V Cideciyan, Jean Bennett, et al.
Function (Oxford, England)|January 15, 2024
POMC Neuron BBSome Regulation of Body Weight is Independent of its Ciliary FunctionDeng-Fu Guo, Paul A Williams, Connor Laule, et al.
Bone|May 13, 2016
Bardet-Biedl syndrome 3 regulates the development of cranial base midline structuresMakiri Kawasaki, Yayoi Izu, Tadayoshi Hayata, et al.
Plos One|April 4, 2014
Ciliopathy is differentially distributed in the brain of a Bardet-Biedl syndrome mouse modelKhristofor Agassandian, Milan Patel, Marianna Agassandian, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Ocular phenotypes of three genetic variants of Bardet-Biedl syndromeElise Héon, Carol Westall, Rivka Carmi, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 11, 2007
Complement factor H polymorphism p.Tyr402His and cuticular DrusenMichael A Grassi, James C Folk, Todd E Scheetz, et al.
Human Molecular Genetics|January 10, 2006
Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia functionHsan-Jan Yen, Marwan K Tayeh, Robert F Mullins, et al.
Pageof 20

Showing results (31-40 of 193) with videos related to

Sort By:
Pageof 20
Investigative Ophthalmology & Visual Science|April 7, 2017
Restoration of Aqueous Humor Outflow Following Transplantation of iPSC-Derived Trabecular Meshwork Cells in a Transgenic Mouse Model of GlaucomaWei Zhu, Ankur Jain, Oliver W Gramlich, et al.
American Journal of Physiology. Renal Physiology|November 26, 2010
Inactivation of Bardet-Biedl syndrome genes causes kidney defectsDeng-Fu Guo, Andreas M Beyer, Baoli Yang, et al.
Developmental Biology|June 19, 2014
Functional characterization of Prickle2 and BBS7 identify overlapping phenotypes yet distinct mechanismsXue Mei, Trudi A Westfall, Qihong Zhang, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 7, 2002
Novel mutation in the TIMP3 gene causes Sorsby fundus dystrophySamuel G Jacobson, Artur V Cideciyan, Jean Bennett, et al.
Function (Oxford, England)|January 15, 2024
POMC Neuron BBSome Regulation of Body Weight is Independent of its Ciliary FunctionDeng-Fu Guo, Paul A Williams, Connor Laule, et al.
Bone|May 13, 2016
Bardet-Biedl syndrome 3 regulates the development of cranial base midline structuresMakiri Kawasaki, Yayoi Izu, Tadayoshi Hayata, et al.
Plos One|April 4, 2014
Ciliopathy is differentially distributed in the brain of a Bardet-Biedl syndrome mouse modelKhristofor Agassandian, Milan Patel, Marianna Agassandian, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Ocular phenotypes of three genetic variants of Bardet-Biedl syndromeElise Héon, Carol Westall, Rivka Carmi, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 11, 2007
Complement factor H polymorphism p.Tyr402His and cuticular DrusenMichael A Grassi, James C Folk, Todd E Scheetz, et al.
Human Molecular Genetics|January 10, 2006
Bardet-Biedl syndrome genes are important in retrograde intracellular trafficking and Kupffer's vesicle cilia functionHsan-Jan Yen, Marwan K Tayeh, Robert F Mullins, et al.
Pageof 20