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Douglas P Mortlock

Showing results (31-40 of 41) with videos related to

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 29, 2017
A Novel Human <i>CAMK2A</i> Mutation Disrupts Dendritic Morphology and Synaptic Transmission, and Causes ASD-Related BehaviorsJason R Stephenson, Xiaohan Wang, Tyler L Perfitt, et al.
The Journal of Cell Biology|June 20, 2007
TGF-beta signaling is essential for joint morphogenesisAnna Spagnoli, Lynda O'Rear, Ronald L Chandler, et al.
Molecular and Cellular Biology|April 12, 2012
UG4 enhancer-driven GATA-2 and bone morphogenetic protein 4 complementation remedies the CAKUT phenotype in Gata2 hypomorphic mutant miceKeiko Ainoya, Takashi Moriguchi, Shin'ya Ohmori, et al.
Stem Cells (Dayton, Ohio)|June 3, 2016
Hypoxia and Reactive Oxygen Species Homeostasis in Mesenchymal Progenitor Cells Define a Molecular Mechanism for Fracture NonunionEmma Muinos-López, Purificación Ripalda-Cemboráin, Tania López-Martínez, et al.
BMC Genomics|August 9, 2007
SNPs in Multi-species Conserved Sequences (MCS) as useful markers in association studies: a practical approachJacob L McCauley, Shannon J Kenealy, Elliott H Margulies, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 6, 2014
Calcific aortic valve disease: a consensus summary from the Alliance of Investigators on Calcific Aortic Valve DiseaseKatherine E Yutzey, Linda L Demer, Simon C Body, et al.
Cell Reports|May 13, 2017
A Chimeric Egfr Protein Reporter Mouse Reveals Egfr Localization and Trafficking In VivoYu-Ping Yang, Haiting Ma, Alina Starchenko, et al.
American Journal of Human Genetics|August 5, 2017
Human Germline Genome EditingKelly E Ormond, Douglas P Mortlock, Derek T Scholes, et al.
Science Signaling|February 21, 2019
Disabling the Gβγ-SNARE interaction disrupts GPCR-mediated presynaptic inhibition, leading to physiological and behavioral phenotypesZack Zurawski, Analisa D Thompson Gray, Lillian J Brady, et al.
Plos Genetics|November 19, 2013
Recurrent tissue-specific mtDNA mutations are common in humansDavid C Samuels, Chun Li, Bingshan Li, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 29, 2017
A Novel Human <i>CAMK2A</i> Mutation Disrupts Dendritic Morphology and Synaptic Transmission, and Causes ASD-Related BehaviorsJason R Stephenson, Xiaohan Wang, Tyler L Perfitt, et al.
The Journal of Cell Biology|June 20, 2007
TGF-beta signaling is essential for joint morphogenesisAnna Spagnoli, Lynda O'Rear, Ronald L Chandler, et al.
Molecular and Cellular Biology|April 12, 2012
UG4 enhancer-driven GATA-2 and bone morphogenetic protein 4 complementation remedies the CAKUT phenotype in Gata2 hypomorphic mutant miceKeiko Ainoya, Takashi Moriguchi, Shin'ya Ohmori, et al.
Stem Cells (Dayton, Ohio)|June 3, 2016
Hypoxia and Reactive Oxygen Species Homeostasis in Mesenchymal Progenitor Cells Define a Molecular Mechanism for Fracture NonunionEmma Muinos-López, Purificación Ripalda-Cemboráin, Tania López-Martínez, et al.
BMC Genomics|August 9, 2007
SNPs in Multi-species Conserved Sequences (MCS) as useful markers in association studies: a practical approachJacob L McCauley, Shannon J Kenealy, Elliott H Margulies, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 6, 2014
Calcific aortic valve disease: a consensus summary from the Alliance of Investigators on Calcific Aortic Valve DiseaseKatherine E Yutzey, Linda L Demer, Simon C Body, et al.
Cell Reports|May 13, 2017
A Chimeric Egfr Protein Reporter Mouse Reveals Egfr Localization and Trafficking In VivoYu-Ping Yang, Haiting Ma, Alina Starchenko, et al.
American Journal of Human Genetics|August 5, 2017
Human Germline Genome EditingKelly E Ormond, Douglas P Mortlock, Derek T Scholes, et al.
Science Signaling|February 21, 2019
Disabling the Gβγ-SNARE interaction disrupts GPCR-mediated presynaptic inhibition, leading to physiological and behavioral phenotypesZack Zurawski, Analisa D Thompson Gray, Lillian J Brady, et al.
Plos Genetics|November 19, 2013
Recurrent tissue-specific mtDNA mutations are common in humansDavid C Samuels, Chun Li, Bingshan Li, et al.
Pageof 5