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Science Signaling
|
March 3, 2021
SOX9 is required for kidney fibrosis and activates NAV3 to drive renal myofibroblast function
Sayyid Raza, Elliot Jokl, James Pritchett, et al.
HGG Advances
|
October 18, 2025
Two commonly reported incidental variants in OTC are associated with late-onset disease
Steven H Lang, Russell S Lo, Gareth A Cromie, et al.
Cell Reports
|
November 15, 2023
PAK1-dependent mechanotransduction enables myofibroblast nuclear adaptation and chromatin organization during fibrosis
Elliot Jokl, Aoibheann F Mullan, Kara Simpson, et al.
JACC. Cardiovascular Imaging
|
April 20, 2020
Substrate for the Myocardial Inflammation-Heart Failure Hypothesis Identified Using Novel USPIO Methodology
Jakub Lagan, Josephine H Naish, Kara Simpson, et al.
EMBO Molecular Medicine
|
April 25, 2025
Spatial gene regulatory networks driving cell state transitions during human liver disease
Nigel L Hammond, Syed Murtuza Baker, Sokratia Georgaka, et al.
Genome Medicine
|
April 20, 2021
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders
Madelyn A Gillentine, Tianyun Wang, Kendra Hoekzema, et al.
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Search research articles
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Showing results (11-20 of 16) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 16 results.
Science Signaling
|
March 3, 2021
SOX9 is required for kidney fibrosis and activates NAV3 to drive renal myofibroblast function
Sayyid Raza, Elliot Jokl, James Pritchett, et al.
HGG Advances
|
October 18, 2025
Two commonly reported incidental variants in OTC are associated with late-onset disease
Steven H Lang, Russell S Lo, Gareth A Cromie, et al.
Cell Reports
|
November 15, 2023
PAK1-dependent mechanotransduction enables myofibroblast nuclear adaptation and chromatin organization during fibrosis
Elliot Jokl, Aoibheann F Mullan, Kara Simpson, et al.
JACC. Cardiovascular Imaging
|
April 20, 2020
Substrate for the Myocardial Inflammation-Heart Failure Hypothesis Identified Using Novel USPIO Methodology
Jakub Lagan, Josephine H Naish, Kara Simpson, et al.
EMBO Molecular Medicine
|
April 25, 2025
Spatial gene regulatory networks driving cell state transitions during human liver disease
Nigel L Hammond, Syed Murtuza Baker, Sokratia Georgaka, et al.
Genome Medicine
|
April 20, 2021
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders
Madelyn A Gillentine, Tianyun Wang, Kendra Hoekzema, et al.
Page
of 2