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Showing results (751-760 of 866) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|October 7, 2011
Priming of hypoxia-inducible factor by neuronal nitric oxide synthase is essential for adaptive responses to severe anemiaAlbert K Y Tsui, Philip A Marsden, C David Mazer, et al.
Hypertension (Dallas, Tex. : 1979)|January 15, 2019
B-Cell Deficiency Lowers Blood Pressure in MiceLuke S Dingwell, Eric A Shikatani, Rickvinder Besla, et al.
Human Molecular Genetics|January 25, 2015
Non-manifesting AHI1 truncations indicate localized loss-of-function tolerance in a severe Mendelian disease geneSolaf M Elsayed, Jennifer B Phillips, Raoul Heller, et al.
Cell|March 5, 2019
Quiescence Modulates Stem Cell Maintenance and Regenerative Capacity in the Aging BrainGeorgios Kalamakis, Daniel Brüne, Srikanth Ravichandran, et al.
Clinical Genetics|March 19, 2010
A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expressionE Wilch, H Azaiez, R A Fisher, et al.
Human Molecular Genetics|July 10, 2021
KCND2 variants associated with global developmental delay differentially impair Kv4.2 channel gatingYongqiang Zhang, Georgios Tachtsidis, Claudia Schob, et al.
Human Molecular Genetics|February 19, 2013
Mutations in NEK8 link multiple organ dysplasia with altered Hippo signalling and increased c-MYC expressionValeska Frank, Sandra Habbig, Malte P Bartram, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 27, 2019
Biallelic mutation of human <i>SLC6A6</i> encoding the taurine transporter TAUT is linked to early retinal degenerationMarkus N Preising, Boris Görg, Christoph Friedburg, et al.
The Journal of Experimental Medicine|November 14, 2012
A novel role of sphingosine 1-phosphate receptor S1pr1 in mouse thrombopoiesisLin Zhang, Martin Orban, Michael Lorenz, et al.
Elife|September 20, 2015
TALPID3 controls centrosome and cell polarity and the human ortholog KIAA0586 is mutated in Joubert syndrome (JBTS23)Louise A Stephen, Hasan Tawamie, Gemma M Davis, et al.
Pageof 87

Showing results (751-760 of 866) with videos related to

Sort By:
Pageof 87
Proceedings of the National Academy of Sciences of the United States of America|October 7, 2011
Priming of hypoxia-inducible factor by neuronal nitric oxide synthase is essential for adaptive responses to severe anemiaAlbert K Y Tsui, Philip A Marsden, C David Mazer, et al.
Hypertension (Dallas, Tex. : 1979)|January 15, 2019
B-Cell Deficiency Lowers Blood Pressure in MiceLuke S Dingwell, Eric A Shikatani, Rickvinder Besla, et al.
Human Molecular Genetics|January 25, 2015
Non-manifesting AHI1 truncations indicate localized loss-of-function tolerance in a severe Mendelian disease geneSolaf M Elsayed, Jennifer B Phillips, Raoul Heller, et al.
Cell|March 5, 2019
Quiescence Modulates Stem Cell Maintenance and Regenerative Capacity in the Aging BrainGeorgios Kalamakis, Daniel Brüne, Srikanth Ravichandran, et al.
Clinical Genetics|March 19, 2010
A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expressionE Wilch, H Azaiez, R A Fisher, et al.
Human Molecular Genetics|July 10, 2021
KCND2 variants associated with global developmental delay differentially impair Kv4.2 channel gatingYongqiang Zhang, Georgios Tachtsidis, Claudia Schob, et al.
Human Molecular Genetics|February 19, 2013
Mutations in NEK8 link multiple organ dysplasia with altered Hippo signalling and increased c-MYC expressionValeska Frank, Sandra Habbig, Malte P Bartram, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 27, 2019
Biallelic mutation of human <i>SLC6A6</i> encoding the taurine transporter TAUT is linked to early retinal degenerationMarkus N Preising, Boris Görg, Christoph Friedburg, et al.
The Journal of Experimental Medicine|November 14, 2012
A novel role of sphingosine 1-phosphate receptor S1pr1 in mouse thrombopoiesisLin Zhang, Martin Orban, Michael Lorenz, et al.
Elife|September 20, 2015
TALPID3 controls centrosome and cell polarity and the human ortholog KIAA0586 is mutated in Joubert syndrome (JBTS23)Louise A Stephen, Hasan Tawamie, Gemma M Davis, et al.
Pageof 87