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Kehr

Showing results (731-740 of 752) with videos related to

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Nature Communications|May 12, 2021
Probing subwavelength in-plane anisotropy with antenna-assisted infrared nano-spectroscopyZiheng Yao, Xinzhong Chen, Lukas Wehmeier, et al.
Nature Materials|September 15, 2025
Ultraconfined terahertz phonon polaritons in hafnium dichalcogenidesRyan A Kowalski, Niclas S Mueller, Gonzalo Álvarez-Pérez, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2019
Antidepressant-relevant concentrations of the ketamine metabolite (2<i>R</i>,6<i>R</i>)-hydroxynorketamine do not block NMDA receptor functionEric W Lumsden, Timothy A Troppoli, Scott J Myers, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 4, 2021
Dopaminergic neuromodulation of prefrontal cortex activity requires the NMDA receptor coagonist d-serineGlenn Dallérac, Xia Li, Pierre Lecouflet, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2023
Cholinergic regulation of vascular endothelial function by human ChAT<sup>+</sup> T cellsLaura Tarnawski, Vladimir S Shavva, Eric J Kort, et al.
Blood|October 1, 2025
Mucosal calprotectin is associated with severity of aGI-GVHD and poor outcomes after allogeneic stem cell transplantationEkin Ece Gurer Kluge, Elisabeth Meedt, Julia Feicht, et al.
Nature Genetics|November 7, 2018
Multiple transmissions of de novo mutations in familiesHákon Jónsson, Patrick Sulem, Gudny A Arnadottir, et al.
Nature Communications|May 4, 2017
Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2Sigurdis Haraldsdottir, Thorunn Rafnar, Wendy L Frankel, et al.
Human Molecular Genetics|April 12, 2017
A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery diseaseEythor Bjornsson, Hannes Helgason, Gisli Halldorsson, et al.
Nature|September 30, 2017
Parental influence on human germline de novo mutations in 1,548 trios from IcelandHákon Jónsson, Patrick Sulem, Birte Kehr, et al.
Pageof 76

Showing results (731-740 of 752) with videos related to

Sort By:
Pageof 76
Nature Communications|May 12, 2021
Probing subwavelength in-plane anisotropy with antenna-assisted infrared nano-spectroscopyZiheng Yao, Xinzhong Chen, Lukas Wehmeier, et al.
Nature Materials|September 15, 2025
Ultraconfined terahertz phonon polaritons in hafnium dichalcogenidesRyan A Kowalski, Niclas S Mueller, Gonzalo Álvarez-Pérez, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 24, 2019
Antidepressant-relevant concentrations of the ketamine metabolite (2<i>R</i>,6<i>R</i>)-hydroxynorketamine do not block NMDA receptor functionEric W Lumsden, Timothy A Troppoli, Scott J Myers, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 4, 2021
Dopaminergic neuromodulation of prefrontal cortex activity requires the NMDA receptor coagonist d-serineGlenn Dallérac, Xia Li, Pierre Lecouflet, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2023
Cholinergic regulation of vascular endothelial function by human ChAT<sup>+</sup> T cellsLaura Tarnawski, Vladimir S Shavva, Eric J Kort, et al.
Blood|October 1, 2025
Mucosal calprotectin is associated with severity of aGI-GVHD and poor outcomes after allogeneic stem cell transplantationEkin Ece Gurer Kluge, Elisabeth Meedt, Julia Feicht, et al.
Nature Genetics|November 7, 2018
Multiple transmissions of de novo mutations in familiesHákon Jónsson, Patrick Sulem, Gudny A Arnadottir, et al.
Nature Communications|May 4, 2017
Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2Sigurdis Haraldsdottir, Thorunn Rafnar, Wendy L Frankel, et al.
Human Molecular Genetics|April 12, 2017
A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery diseaseEythor Bjornsson, Hannes Helgason, Gisli Halldorsson, et al.
Nature|September 30, 2017
Parental influence on human germline de novo mutations in 1,548 trios from IcelandHákon Jónsson, Patrick Sulem, Birte Kehr, et al.
Pageof 76