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Kaveeta Kaw

Showing results (1-10 of 9) with videos related to

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Arteriosclerosis, Thrombosis, and Vascular Biology|October 8, 2020
Cholesterol-Induced Phenotypic Modulation of Smooth Muscle Cells to Macrophage/Fibroblast-like Cells Is Driven by an Unfolded Protein ResponseAbhijnan Chattopadhyay, Callie S Kwartler, Kaveeta Kaw, et al.
European Heart Journal|June 28, 2023
Smooth muscle α-actin missense variant promotes atherosclerosis through modulation of intracellular cholesterol in smooth muscle cellsKaveeta Kaw, Abhijnan Chattopadhyay, Pujun Guan, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 16, 2022
Preventing Cholesterol-Induced Perk (Protein Kinase RNA-Like Endoplasmic Reticulum Kinase) Signaling in Smooth Muscle Cells Blocks Atherosclerotic Plaque FormationAbhijnan Chattopadhyay, Pujun Guan, Suravi Majumder, et al.
STAR Protocols|April 9, 2025
Protocol for 3D bioprinting of a 3D in vitro model of neuroblastomaMehdi Salar Amoli, Sarah Rezapourdamanab, Linqi Jin, et al.
The Journal of Biological Chemistry|October 3, 2021
Resistance of Acta2<sup>R149C/+</sup> mice to aortic disease is associated with defective release of mutant smooth muscle α-actin from the chaperonin-containing TCP1 folding complexJiyuan Chen, Kaveeta Kaw, Hailong Lu, et al.
American Journal of Medical Genetics. Part A|May 14, 2022
Expanding ACTA2 genotypes with corresponding phenotypes overlapping with smooth muscle dysfunction syndromeAnita Kaw, Kaveeta Kaw, Ellen M Hostetler, et al.
Research Square|October 27, 2023
Augmenting Mitochondrial Respiration in Immature Smooth Muscle Cells with an <i>ACTA2</i> Pathogenic Variant Mitigates Moyamoya-like Cerebrovascular DiseaseAnita Kaw, Ting Wu, Zbigniew Starosolski, et al.
Nature Communications|July 2, 2025
Immature Acta2<sup>R179C/+</sup> smooth muscle cells cause moyamoya-like cerebrovascular lesions in mice prevented by boosting OXPHOSAnita Kaw, Suravi Majumder, Jose E Esparza Pinelo, et al.
JAMA Neurology|November 24, 2015
Whole-Exome Sequencing in Familial Parkinson DiseaseJanice L Farlow, Laurie A Robak, Kurt Hetrick, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Arteriosclerosis, Thrombosis, and Vascular Biology|October 8, 2020
Cholesterol-Induced Phenotypic Modulation of Smooth Muscle Cells to Macrophage/Fibroblast-like Cells Is Driven by an Unfolded Protein ResponseAbhijnan Chattopadhyay, Callie S Kwartler, Kaveeta Kaw, et al.
European Heart Journal|June 28, 2023
Smooth muscle α-actin missense variant promotes atherosclerosis through modulation of intracellular cholesterol in smooth muscle cellsKaveeta Kaw, Abhijnan Chattopadhyay, Pujun Guan, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 16, 2022
Preventing Cholesterol-Induced Perk (Protein Kinase RNA-Like Endoplasmic Reticulum Kinase) Signaling in Smooth Muscle Cells Blocks Atherosclerotic Plaque FormationAbhijnan Chattopadhyay, Pujun Guan, Suravi Majumder, et al.
STAR Protocols|April 9, 2025
Protocol for 3D bioprinting of a 3D in vitro model of neuroblastomaMehdi Salar Amoli, Sarah Rezapourdamanab, Linqi Jin, et al.
The Journal of Biological Chemistry|October 3, 2021
Resistance of Acta2<sup>R149C/+</sup> mice to aortic disease is associated with defective release of mutant smooth muscle α-actin from the chaperonin-containing TCP1 folding complexJiyuan Chen, Kaveeta Kaw, Hailong Lu, et al.
American Journal of Medical Genetics. Part A|May 14, 2022
Expanding ACTA2 genotypes with corresponding phenotypes overlapping with smooth muscle dysfunction syndromeAnita Kaw, Kaveeta Kaw, Ellen M Hostetler, et al.
Research Square|October 27, 2023
Augmenting Mitochondrial Respiration in Immature Smooth Muscle Cells with an <i>ACTA2</i> Pathogenic Variant Mitigates Moyamoya-like Cerebrovascular DiseaseAnita Kaw, Ting Wu, Zbigniew Starosolski, et al.
Nature Communications|July 2, 2025
Immature Acta2<sup>R179C/+</sup> smooth muscle cells cause moyamoya-like cerebrovascular lesions in mice prevented by boosting OXPHOSAnita Kaw, Suravi Majumder, Jose E Esparza Pinelo, et al.
JAMA Neurology|November 24, 2015
Whole-Exome Sequencing in Familial Parkinson DiseaseJanice L Farlow, Laurie A Robak, Kurt Hetrick, et al.
Pageof 1