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David R Beier

Showing results (61-70 of 88) with videos related to

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G3 (Bethesda, Md.)|June 23, 2022
The arginine methyltransferase Carm1 is necessary for heart developmentSophie Jamet, Seungshin Ha, Tzu-Hua Ho, et al.
Nature Methods|June 16, 2009
Agouti C57BL/6N embryonic stem cells for mouse genetic resourcesStephen J Pettitt, Qi Liang, Xin Y Rairdan, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 13, 2010
The zebrafish foxj1a transcription factor regulates cilia function in response to injury and epithelial stretchNathan E Hellman, Yan Liu, Erin Merkel, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 20, 2012
ENU mutagenesis in mice identifies candidate genes for hypogonadismJeffrey Weiss, Lisa A Hurley, Rebecca M Harris, et al.
Journal of the American Society of Nephrology : JASN|January 1, 2013
Loss of the ciliary kinase Nek8 causes left-right asymmetry defectsDanielle K Manning, Mikhail Sergeev, Roy G van Heesbeen, et al.
Journal of the American Society of Nephrology : JASN|April 5, 2014
Downregulating hedgehog signaling reduces renal cystogenic potential of mouse modelsPamela V Tran, George C Talbott, Annick Turbe-Doan, et al.
Physiological Genomics|January 20, 2005
Interacting genetic loci cause airway hyperresponsivenessKate G Ackerman, Hailu Huang, Hartmut Grasemann, et al.
American Journal of Physiology. Renal Physiology|January 7, 2026
The response to kidney injury is epigenetically regulated through the activation of bivalent genesBenjamin I Tickman, Jacquelyn R McDonald, Ryan McCarthy, et al.
Neural Development|January 11, 2011
A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotypeNoelle D Dwyer, Danielle K Manning, Jennifer L Moran, et al.
Nature Genetics|November 28, 2018
Reply to 'Selective effects of heterozygous protein-truncating variants'Christopher A Cassa, Donate Weghorn, Daniel J Balick, et al.
Pageof 9

Showing results (61-70 of 88) with videos related to

Sort By:
Pageof 9
G3 (Bethesda, Md.)|June 23, 2022
The arginine methyltransferase Carm1 is necessary for heart developmentSophie Jamet, Seungshin Ha, Tzu-Hua Ho, et al.
Nature Methods|June 16, 2009
Agouti C57BL/6N embryonic stem cells for mouse genetic resourcesStephen J Pettitt, Qi Liang, Xin Y Rairdan, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 13, 2010
The zebrafish foxj1a transcription factor regulates cilia function in response to injury and epithelial stretchNathan E Hellman, Yan Liu, Erin Merkel, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 20, 2012
ENU mutagenesis in mice identifies candidate genes for hypogonadismJeffrey Weiss, Lisa A Hurley, Rebecca M Harris, et al.
Journal of the American Society of Nephrology : JASN|January 1, 2013
Loss of the ciliary kinase Nek8 causes left-right asymmetry defectsDanielle K Manning, Mikhail Sergeev, Roy G van Heesbeen, et al.
Journal of the American Society of Nephrology : JASN|April 5, 2014
Downregulating hedgehog signaling reduces renal cystogenic potential of mouse modelsPamela V Tran, George C Talbott, Annick Turbe-Doan, et al.
Physiological Genomics|January 20, 2005
Interacting genetic loci cause airway hyperresponsivenessKate G Ackerman, Hailu Huang, Hartmut Grasemann, et al.
American Journal of Physiology. Renal Physiology|January 7, 2026
The response to kidney injury is epigenetically regulated through the activation of bivalent genesBenjamin I Tickman, Jacquelyn R McDonald, Ryan McCarthy, et al.
Neural Development|January 11, 2011
A forward genetic screen with a thalamocortical axon reporter mouse yields novel neurodevelopment mutants and a distinct emx2 mutant phenotypeNoelle D Dwyer, Danielle K Manning, Jennifer L Moran, et al.
Nature Genetics|November 28, 2018
Reply to 'Selective effects of heterozygous protein-truncating variants'Christopher A Cassa, Donate Weghorn, Daniel J Balick, et al.
Pageof 9