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Gerhard Sengle

Showing results (71-80 of 83) with videos related to

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Nature Communications|November 1, 2017
Odd skipped-related 1 identifies a population of embryonic fibro-adipogenic progenitors regulating myogenesis during limb developmentPedro 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 isoformsInsa 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 syndromePrithviraj 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 necroptosisHarshal 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 CaldesmonGalyna 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 structureRodrigo Barbosa de Souza, Luara Lucena Cassiano, Philipp Barnowski, et al.
Scientific Reports|December 17, 2025
An improved porcine model of infrarenal abdominal aortic aneurysmMarta 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 infiltrationViola 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 fibroblastsKonrad 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 syndromeLore Pottie, Christin S Adamo, Aude Beyens, et al.
Pageof 9

Showing results (71-80 of 83) with videos related to

Sort By:
Pageof 9
Nature Communications|November 1, 2017
Odd skipped-related 1 identifies a population of embryonic fibro-adipogenic progenitors regulating myogenesis during limb developmentPedro 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 isoformsInsa 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 syndromePrithviraj 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 necroptosisHarshal 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 CaldesmonGalyna 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 structureRodrigo Barbosa de Souza, Luara Lucena Cassiano, Philipp Barnowski, et al.
Scientific Reports|December 17, 2025
An improved porcine model of infrarenal abdominal aortic aneurysmMarta 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 infiltrationViola 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 fibroblastsKonrad 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 syndromeLore Pottie, Christin S Adamo, Aude Beyens, et al.
Pageof 9