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A Forte

Showing results (181-190 of 187) with videos related to

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Circulation Research|January 28, 2006
Upregulated TRPC1 channel in vascular injury in vivo and its role in human neointimal hyperplasiaB Kumar, K Dreja, S S Shah, et al.
Human Mutation|April 18, 2013
Synonymous mutations in RNASEH2A create cryptic splice sites impairing RNase H2 enzyme function in Aicardi-Goutières syndromeGillian I Rice, Martin A M Reijns, Stephanie R Coffin, et al.
Physical Review Letters|May 27, 2022
Effect of Strongly Magnetized Electrons and Ions on Heat Flow and Symmetry of Inertial Fusion ImplosionsA Bose, J Peebles, C A Walsh, et al.
Nature Genetics|September 25, 2012
Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signatureGillian I Rice, Paul R Kasher, Gabriella M A Forte, et al.
The Lancet. Neurology|November 5, 2013
Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control studyGillian I Rice, Gabriella M A Forte, Marcin Szynkiewicz, et al.
American Journal of Medical Genetics. Part A|January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, et al.
The Review of Scientific Instruments|October 7, 2011
A state observer for the Virgo inverted pendulumT Accadia, F Acernese, P Astone, et al.
Pageof 19

Showing results (181-190 of 187) with videos related to

Sort By:
Pageof 19
You have reached the last page of results.This site can display upto 187 results.
Circulation Research|January 28, 2006
Upregulated TRPC1 channel in vascular injury in vivo and its role in human neointimal hyperplasiaB Kumar, K Dreja, S S Shah, et al.
Human Mutation|April 18, 2013
Synonymous mutations in RNASEH2A create cryptic splice sites impairing RNase H2 enzyme function in Aicardi-Goutières syndromeGillian I Rice, Martin A M Reijns, Stephanie R Coffin, et al.
Physical Review Letters|May 27, 2022
Effect of Strongly Magnetized Electrons and Ions on Heat Flow and Symmetry of Inertial Fusion ImplosionsA Bose, J Peebles, C A Walsh, et al.
Nature Genetics|September 25, 2012
Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signatureGillian I Rice, Paul R Kasher, Gabriella M A Forte, et al.
The Lancet. Neurology|November 5, 2013
Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control studyGillian I Rice, Gabriella M A Forte, Marcin Szynkiewicz, et al.
American Journal of Medical Genetics. Part A|January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, et al.
The Review of Scientific Instruments|October 7, 2011
A state observer for the Virgo inverted pendulumT Accadia, F Acernese, P Astone, et al.
Pageof 19