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Mark E Lindsay

Showing results (61-70 of 78) with videos related to

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Elife|October 28, 2015
A deleterious gene-by-environment interaction imposed by calcium channel blockers in Marfan syndromeJefferson J Doyle, Alexander J Doyle, Nicole K Wilson, et al.
Journal of the American College of Cardiology|August 4, 2018
Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and DissectionMarjolijn Renard, Catherine Francis, Rajarshi Ghosh, et al.
Iscience|November 30, 2023
Treatment of calcific arterial disease via enhancement of autophagy using GSK343Christian L Lino Cardenas, Wanlin Jiang, Lova P Kajuluri, et al.
The Journal of Clinical Investigation|December 21, 2013
Angiotensin II-dependent TGF-β signaling contributes to Loeys-Dietz syndrome vascular pathogenesisElena M Gallo, David C Loch, Jennifer P Habashi, et al.
Biorxiv : the Preprint Server for Biology|February 9, 2026
Smooth Muscle Dysfunction Drives Cerebrovascular Reserve Failure and End-Organ Brain InjuryTakahiko Imai, Vijai Krishnan, James H Lai, et al.
American Journal of Medical Quality : the Official Journal of the American College of Medical Quality|January 15, 2013
Improving hypertension control in diabetes: a multisite quality improvement project that applies a 3-step care bundle to a chronic disease care model for diabetes with hypertensionMark E Lindsay, Michael J Hovan, James R Deming, et al.
Nature Genetics|October 2, 2012
Mutations in the TGF-β repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysmAlexander J Doyle, Jefferson J Doyle, Seneca L Bessling, et al.
Nature Genetics|June 13, 2022
Genetic analysis of right heart structure and function in 40,000 peopleJames P Pirruccello, Paolo Di Achille, Victor Nauffal, et al.
European Journal of Human Genetics : EJHG|July 12, 2024
Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlationsEva Vanbelleghem, Tim Van Damme, Aude Beyens, et al.
Nature Genetics|July 10, 2012
Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysmMark E Lindsay, Dorien Schepers, Nikhita Ajit Bolar, et al.
Pageof 8

Showing results (61-70 of 78) with videos related to

Sort By:
Pageof 8
Elife|October 28, 2015
A deleterious gene-by-environment interaction imposed by calcium channel blockers in Marfan syndromeJefferson J Doyle, Alexander J Doyle, Nicole K Wilson, et al.
Journal of the American College of Cardiology|August 4, 2018
Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and DissectionMarjolijn Renard, Catherine Francis, Rajarshi Ghosh, et al.
Iscience|November 30, 2023
Treatment of calcific arterial disease via enhancement of autophagy using GSK343Christian L Lino Cardenas, Wanlin Jiang, Lova P Kajuluri, et al.
The Journal of Clinical Investigation|December 21, 2013
Angiotensin II-dependent TGF-β signaling contributes to Loeys-Dietz syndrome vascular pathogenesisElena M Gallo, David C Loch, Jennifer P Habashi, et al.
Biorxiv : the Preprint Server for Biology|February 9, 2026
Smooth Muscle Dysfunction Drives Cerebrovascular Reserve Failure and End-Organ Brain InjuryTakahiko Imai, Vijai Krishnan, James H Lai, et al.
American Journal of Medical Quality : the Official Journal of the American College of Medical Quality|January 15, 2013
Improving hypertension control in diabetes: a multisite quality improvement project that applies a 3-step care bundle to a chronic disease care model for diabetes with hypertensionMark E Lindsay, Michael J Hovan, James R Deming, et al.
Nature Genetics|October 2, 2012
Mutations in the TGF-β repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysmAlexander J Doyle, Jefferson J Doyle, Seneca L Bessling, et al.
Nature Genetics|June 13, 2022
Genetic analysis of right heart structure and function in 40,000 peopleJames P Pirruccello, Paolo Di Achille, Victor Nauffal, et al.
European Journal of Human Genetics : EJHG|July 12, 2024
Myhre syndrome in adulthood: clinical variability and emerging genotype-phenotype correlationsEva Vanbelleghem, Tim Van Damme, Aude Beyens, et al.
Nature Genetics|July 10, 2012
Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysmMark E Lindsay, Dorien Schepers, Nikhita Ajit Bolar, et al.
Pageof 8