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T Strachan

Showing results (131-140 of 138) with videos related to

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Cell|August 9, 2016
GPCR-G Protein-β-Arrestin Super-Complex Mediates Sustained G Protein SignalingAlex R B Thomsen, Bianca Plouffe, Thomas J Cahill, et al.
Nature|July 14, 2016
Allosteric nanobodies reveal the dynamic range and diverse mechanisms of G-protein-coupled receptor activationDean P Staus, Ryan T Strachan, Aashish Manglik, et al.
Nature Genetics|January 1, 1997
Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene familyQ Y Li, R A Newbury-Ecob, J A Terrett, et al.
Human Genetics|May 26, 1998
Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactylyF R Vargas, E Roessler, K Gaudenz, et al.
Nature Chemical Biology|July 12, 2016
Conformationally selective RNA aptamers allosterically modulate the β2-adrenoceptorAlem W Kahsai, James W Wisler, Jungmin Lee, et al.
Cell|January 9, 2018
Structure of the Nanobody-Stabilized Active State of the Kappa Opioid ReceptorTao Che, Susruta Majumdar, Saheem A Zaidi, et al.
American Journal of Human Genetics|April 6, 2000
Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome geneD M Hagan, A J Ross, T Strachan, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 29, 2017
Allosteric "beta-blocker" isolated from a DNA-encoded small molecule librarySeungkirl Ahn, Alem W Kahsai, Biswaranjan Pani, et al.
Pageof 14

Showing results (131-140 of 138) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 138 results.
Cell|August 9, 2016
GPCR-G Protein-β-Arrestin Super-Complex Mediates Sustained G Protein SignalingAlex R B Thomsen, Bianca Plouffe, Thomas J Cahill, et al.
Nature|July 14, 2016
Allosteric nanobodies reveal the dynamic range and diverse mechanisms of G-protein-coupled receptor activationDean P Staus, Ryan T Strachan, Aashish Manglik, et al.
Nature Genetics|January 1, 1997
Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene familyQ Y Li, R A Newbury-Ecob, J A Terrett, et al.
Human Genetics|May 26, 1998
Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactylyF R Vargas, E Roessler, K Gaudenz, et al.
Nature Chemical Biology|July 12, 2016
Conformationally selective RNA aptamers allosterically modulate the β2-adrenoceptorAlem W Kahsai, James W Wisler, Jungmin Lee, et al.
Cell|January 9, 2018
Structure of the Nanobody-Stabilized Active State of the Kappa Opioid ReceptorTao Che, Susruta Majumdar, Saheem A Zaidi, et al.
American Journal of Human Genetics|April 6, 2000
Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome geneD M Hagan, A J Ross, T Strachan, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 29, 2017
Allosteric "beta-blocker" isolated from a DNA-encoded small molecule librarySeungkirl Ahn, Alem W Kahsai, Biswaranjan Pani, et al.
Pageof 14