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Lori Carpenter

Showing results (11-20 of 16) with videos related to

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Implementation Science Communications|August 26, 2025
Normalizing daily awakening and breathing coordination at 15 heterogenous ICUs: a multicenter post-implementation surveyAndrew J Knighton, Jacob Kean, Ithan D Peltan, et al.
JAMIA Open|July 11, 2022
An alert tool to promote lung protective ventilation for possible acute respiratory distress syndromeAndrew J Knighton, Kathryn G Kuttler, Pallavi Ranade-Kharkar, et al.
American Journal of Human Genetics|October 23, 2018
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal FeaturesPeter D Turnpenny, Michael J Wright, Melissa Sloman, et al.
American Journal of Human Genetics|December 12, 2018
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal FeaturesPeter D Turnpenny, Michael J Wright, Melissa Sloman, et al.
Research Square|October 16, 2023
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex compositionDavid Picketts, Ghayda Mirzaa, Keqin Yan, et al.
Nature Communications|November 10, 2025
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex compositionGhayda M Mirzaa, Keqin Yan, Raissa Relator, et al.
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Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Implementation Science Communications|August 26, 2025
Normalizing daily awakening and breathing coordination at 15 heterogenous ICUs: a multicenter post-implementation surveyAndrew J Knighton, Jacob Kean, Ithan D Peltan, et al.
JAMIA Open|July 11, 2022
An alert tool to promote lung protective ventilation for possible acute respiratory distress syndromeAndrew J Knighton, Kathryn G Kuttler, Pallavi Ranade-Kharkar, et al.
American Journal of Human Genetics|October 23, 2018
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal FeaturesPeter D Turnpenny, Michael J Wright, Melissa Sloman, et al.
American Journal of Human Genetics|December 12, 2018
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal FeaturesPeter D Turnpenny, Michael J Wright, Melissa Sloman, et al.
Research Square|October 16, 2023
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex compositionDavid Picketts, Ghayda Mirzaa, Keqin Yan, et al.
Nature Communications|November 10, 2025
Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex compositionGhayda M Mirzaa, Keqin Yan, Raissa Relator, et al.
Pageof 2