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Nature Communications
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November 1, 2017
Odd skipped-related 1 identifies a population of embryonic fibro-adipogenic progenitors regulating myogenesis during limb development
Pedro Vallecillo-García, Mickael Orgeur, Sophie Vom Hofe-Schneider, et al.
Disease Models & Mechanisms
|
February 26, 2015
Modeling autosomal recessive cutis laxa type 1C in mice reveals distinct functions for Ltbp-4 isoforms
Insa Bultmann-Mellin, Anne Conradi, Alexandra C Maul, et al.
Scientific Reports
|
June 25, 2026
Aortic asprosin overexpression does not ameliorate disease pathophysiology in a murine model of Marfan syndrome
Prithviraj Manohar Vijaya Shetty, Andrea Matzen, Susanne Hille, et al.
Cell Death & Disease
|
February 11, 2026
Loss of MLKL impairs abdominal aortic aneurysm development by attenuating smooth muscle cell necroptosis
Harshal Nemade, Dennis Mehrkens, Hannah Sophia Lottermoser, et al.
Journal of the American Heart Association
|
January 19, 2026
Regulation of Vascular Tone of Preglomerular Renal Vasculature by Caldesmon
Galyna Pryymachuk, Viktor V Velyanov, Nikola R Lazarov, et al.
Scientific Reports
|
July 22, 2025
Exploring thoracic aorta ECM alterations in Marfan syndrome: insights into aorta wall structure
Rodrigo Barbosa de Souza, Luara Lucena Cassiano, Philipp Barnowski, et al.
Scientific Reports
|
December 17, 2025
An improved porcine model of infrarenal abdominal aortic aneurysm
Marta Stei, Per Arkenberg, Theresa Uebing, et al.
Frontiers in Immunology
|
November 24, 2025
Hyaluronan synthase 3 deficiency lowers the incidence of ruptures of abdominal aortic aneurysms by reducing monocyte infiltration
Viola Niemann, Fedor Brack, Luca Rolauer, et al.
The Journal of Clinical Investigation
|
September 17, 2024
ADAMTS12 promotes fibrosis by restructuring extracellular matrix to enable activation of injury-responsive fibroblasts
Konrad Hoeft, Lars Koch, Susanne Ziegler, et al.
American Journal of Human Genetics
|
May 15, 2021
Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome
Lore Pottie, Christin S Adamo, Aude Beyens, et al.
Page
of 9
Search research articles
Search
Showing results (71-80 of 83) with videos related to
Sort By:
Page
of 9
Nature Communications
|
November 1, 2017
Odd skipped-related 1 identifies a population of embryonic fibro-adipogenic progenitors regulating myogenesis during limb development
Pedro Vallecillo-García, Mickael Orgeur, Sophie Vom Hofe-Schneider, et al.
Disease Models & Mechanisms
|
February 26, 2015
Modeling autosomal recessive cutis laxa type 1C in mice reveals distinct functions for Ltbp-4 isoforms
Insa Bultmann-Mellin, Anne Conradi, Alexandra C Maul, et al.
Scientific Reports
|
June 25, 2026
Aortic asprosin overexpression does not ameliorate disease pathophysiology in a murine model of Marfan syndrome
Prithviraj Manohar Vijaya Shetty, Andrea Matzen, Susanne Hille, et al.
Cell Death & Disease
|
February 11, 2026
Loss of MLKL impairs abdominal aortic aneurysm development by attenuating smooth muscle cell necroptosis
Harshal Nemade, Dennis Mehrkens, Hannah Sophia Lottermoser, et al.
Journal of the American Heart Association
|
January 19, 2026
Regulation of Vascular Tone of Preglomerular Renal Vasculature by Caldesmon
Galyna Pryymachuk, Viktor V Velyanov, Nikola R Lazarov, et al.
Scientific Reports
|
July 22, 2025
Exploring thoracic aorta ECM alterations in Marfan syndrome: insights into aorta wall structure
Rodrigo Barbosa de Souza, Luara Lucena Cassiano, Philipp Barnowski, et al.
Scientific Reports
|
December 17, 2025
An improved porcine model of infrarenal abdominal aortic aneurysm
Marta Stei, Per Arkenberg, Theresa Uebing, et al.
Frontiers in Immunology
|
November 24, 2025
Hyaluronan synthase 3 deficiency lowers the incidence of ruptures of abdominal aortic aneurysms by reducing monocyte infiltration
Viola Niemann, Fedor Brack, Luca Rolauer, et al.
The Journal of Clinical Investigation
|
September 17, 2024
ADAMTS12 promotes fibrosis by restructuring extracellular matrix to enable activation of injury-responsive fibroblasts
Konrad Hoeft, Lars Koch, Susanne Ziegler, et al.
American Journal of Human Genetics
|
May 15, 2021
Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome
Lore Pottie, Christin S Adamo, Aude Beyens, et al.
Page
of 9