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Showing results (31-40 of 51) with videos related to

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Biorxiv : the Preprint Server for Biology|February 12, 2026
Automated Ventricle Assessment via Three-dimensional Anatomical Reconstruction (AVA-TAR): a computational toolkit for autonomous lateral ventricle assessment in preclinical hydrocephalus modelsSundeep Chakladar, Shelei Pan, Owen Limbrick, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 2024
Multiomics profiling of mouse polycystic kidney disease progression at a single-cell resolutionYoshiharu Muto, Yasuhiro Yoshimura, Haojia Wu, et al.
Biorxiv : the Preprint Server for Biology|June 10, 2024
Multi-omics profiling of mouse polycystic kidney disease progression at a single cell resolutionYoshiharu Muto, Yasuhiro Yoshimura, Haojia Wu, et al.
Cytoskeleton (Hoboken, N.J.)|October 31, 2024
The Heterotaxy Gene CCDC11 Is Important for Cytokinesis via RhoA RegulationSaurabh S Kulkarni, Rachel E Stephenson, Sarah Amalraj, et al.
Biorxiv : the Preprint Server for Biology|February 26, 2024
Ultrastructure expansion microscopy (U-ExM) of mouse and human kidneys for analysis of subcellular structuresEwa Langner, Pongpratch Puapatanakul, Rachel Pudlowski, et al.
Cytoskeleton (Hoboken, N.J.)|May 8, 2024
Ultrastructure expansion microscopy (U-ExM) of mouse and human kidneys for analysis of subcellular structuresEwa Langner, Pongpratch Puapatanakul, Rachel Pudlowski, et al.
Kidney International|May 27, 2017
Anticystogenic activity of a small molecule PAK4 inhibitor may be a novel treatment for autosomal dominant polycystic kidney diseaseVicki J Hwang, Xia Zhou, Xiaonan Chen, et al.
American Journal of Physiology. Renal Physiology|October 4, 2018
Arginine reprogramming in ADPKD results in arginine-dependent cystogenesisJosephine F Trott, Vicki J Hwang, Tatsuto Ishimaru, et al.
Pediatric Research|July 4, 2018
Functional characterization of biallelic RTTN variants identified in an infant with microcephaly, simplified gyral pattern, pontocerebellar hypoplasia, and seizuresJennifer A Wambach, Daniel J Wegner, Ping Yang, et al.
Biorxiv : the Preprint Server for Biology|April 2, 2024
Loss of an extensive ciliary connectome induces proteostasis and cell fate switching in a severe motile ciliopathySteven L Brody, Jiehong Pan, Tao Huang, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

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Pageof 6
Biorxiv : the Preprint Server for Biology|February 12, 2026
Automated Ventricle Assessment via Three-dimensional Anatomical Reconstruction (AVA-TAR): a computational toolkit for autonomous lateral ventricle assessment in preclinical hydrocephalus modelsSundeep Chakladar, Shelei Pan, Owen Limbrick, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 15, 2024
Multiomics profiling of mouse polycystic kidney disease progression at a single-cell resolutionYoshiharu Muto, Yasuhiro Yoshimura, Haojia Wu, et al.
Biorxiv : the Preprint Server for Biology|June 10, 2024
Multi-omics profiling of mouse polycystic kidney disease progression at a single cell resolutionYoshiharu Muto, Yasuhiro Yoshimura, Haojia Wu, et al.
Cytoskeleton (Hoboken, N.J.)|October 31, 2024
The Heterotaxy Gene CCDC11 Is Important for Cytokinesis via RhoA RegulationSaurabh S Kulkarni, Rachel E Stephenson, Sarah Amalraj, et al.
Biorxiv : the Preprint Server for Biology|February 26, 2024
Ultrastructure expansion microscopy (U-ExM) of mouse and human kidneys for analysis of subcellular structuresEwa Langner, Pongpratch Puapatanakul, Rachel Pudlowski, et al.
Cytoskeleton (Hoboken, N.J.)|May 8, 2024
Ultrastructure expansion microscopy (U-ExM) of mouse and human kidneys for analysis of subcellular structuresEwa Langner, Pongpratch Puapatanakul, Rachel Pudlowski, et al.
Kidney International|May 27, 2017
Anticystogenic activity of a small molecule PAK4 inhibitor may be a novel treatment for autosomal dominant polycystic kidney diseaseVicki J Hwang, Xia Zhou, Xiaonan Chen, et al.
American Journal of Physiology. Renal Physiology|October 4, 2018
Arginine reprogramming in ADPKD results in arginine-dependent cystogenesisJosephine F Trott, Vicki J Hwang, Tatsuto Ishimaru, et al.
Pediatric Research|July 4, 2018
Functional characterization of biallelic RTTN variants identified in an infant with microcephaly, simplified gyral pattern, pontocerebellar hypoplasia, and seizuresJennifer A Wambach, Daniel J Wegner, Ping Yang, et al.
Biorxiv : the Preprint Server for Biology|April 2, 2024
Loss of an extensive ciliary connectome induces proteostasis and cell fate switching in a severe motile ciliopathySteven L Brody, Jiehong Pan, Tao Huang, et al.
Pageof 6