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Ryan P Liegel

Showing results (1-10 of 6) with videos related to

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Molecular Genetics and Metabolism Reports|September 9, 2014
Alkylglycerone phosphate synthase (AGPS) deficient mice: models for rhizomelic chondrodysplasia punctate type 3 (RCDP3) malformation syndromeRyan P Liegel, Adam Ronchetti, D J Sidjanin
BMC Genetics|December 6, 2014
Targeted disruption of Tbc1d20 with zinc-finger nucleases causes cataracts and testicular abnormalities in miceAnna Kyunglim Park, Ryan P Liegel, Adam Ronchetti, et al.
Plos Genetics|August 7, 2019
Differential requirements of tubulin genes in mammalian forebrain developmentElizabeth Bittermann, Zakia Abdelhamed, Ryan P Liegel, et al.
Genesis (New York, N.Y. : 2000)|October 31, 2018
Using human sequencing to guide craniofacial researchRyan P Liegel, Erin Finnerty, Lauren Blizzard, et al.
Development (Cambridge, England)|February 15, 2023
Successful therapeutic intervention in new mouse models of frizzled 2-associated congenital malformationsRyan P Liegel, Megan N Michalski, Sanika Vaidya, et al.
American Journal of Human Genetics|November 19, 2013
Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humansRyan P Liegel, Mark T Handley, Adam Ronchetti, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Molecular Genetics and Metabolism Reports|September 9, 2014
Alkylglycerone phosphate synthase (AGPS) deficient mice: models for rhizomelic chondrodysplasia punctate type 3 (RCDP3) malformation syndromeRyan P Liegel, Adam Ronchetti, D J Sidjanin
BMC Genetics|December 6, 2014
Targeted disruption of Tbc1d20 with zinc-finger nucleases causes cataracts and testicular abnormalities in miceAnna Kyunglim Park, Ryan P Liegel, Adam Ronchetti, et al.
Plos Genetics|August 7, 2019
Differential requirements of tubulin genes in mammalian forebrain developmentElizabeth Bittermann, Zakia Abdelhamed, Ryan P Liegel, et al.
Genesis (New York, N.Y. : 2000)|October 31, 2018
Using human sequencing to guide craniofacial researchRyan P Liegel, Erin Finnerty, Lauren Blizzard, et al.
Development (Cambridge, England)|February 15, 2023
Successful therapeutic intervention in new mouse models of frizzled 2-associated congenital malformationsRyan P Liegel, Megan N Michalski, Sanika Vaidya, et al.
American Journal of Human Genetics|November 19, 2013
Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humansRyan P Liegel, Mark T Handley, Adam Ronchetti, et al.
Pageof 1