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Stephanie M Ware

Showing results (51-60 of 146) with videos related to

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Developmental Biology|January 31, 2012
An essential and highly conserved role for Zic3 in left-right patterning, gastrulation and convergent extension morphogenesisAshley E Cast, Chunlei Gao, Jeffrey D Amack, et al.
Journal of Genetic Counseling|August 24, 2016
Bicuspid Aortic Valve: a Review with Recommendations for Genetic CounselingSamantha L Freeze, Benjamin J Landis, Stephanie M Ware, et al.
Genome Biology|September 23, 2011
SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencingMuhammad Tariq, John W Belmont, Seema Lalani, et al.
Progress in Pediatric Cardiology|February 16, 2018
Noncompaction cardiomyopathy and heterotaxy syndromeHugo R Martinez, Stephanie M Ware, Marcus S Schamberger, et al.
Developmental Biology|June 9, 2020
SHROOM3 is downstream of the planar cell polarity pathway and loss-of-function results in congenital heart defectsMatthew D Durbin, James O'Kane, Samuel Lorentz, et al.
Human Molecular Genetics|January 11, 2013
Zic3 is required in the migrating primitive streak for node morphogenesis and left-right patterningMardi J Sutherland, Shuyun Wang, Malgorzata E Quinn, et al.
American Journal of Medical Genetics. Part A|April 27, 2016
Analysis of TGFBR1*6A variant in individuals evaluated for Marfan syndromeAllyson E Somers, Robert B Hinton, Valentina Pilipenko, et al.
Pediatrics|September 17, 2014
Twins with progressive thoracic aortic aneurysm, recurrent dissection and ACTA2 mutationStephanie M Ware, Amy Shikany, Benjamin J Landis, et al.
Human Mutation|September 28, 2018
Novel pathogenic variants in filamin C identified in pediatric restrictive cardiomyopathyJeffrey Schubert, Muhammad Tariq, Gabrielle Geddes, et al.
American Journal of Medical Genetics. Part A|February 9, 2016
Clinically relevant variants identified in thoracic aortic aneurysm patients by research exome sequencingJeffrey A Schubert, Benjamin J Landis, Amy R Shikany, et al.
Pageof 15

Showing results (51-60 of 146) with videos related to

Sort By:
Pageof 15
Developmental Biology|January 31, 2012
An essential and highly conserved role for Zic3 in left-right patterning, gastrulation and convergent extension morphogenesisAshley E Cast, Chunlei Gao, Jeffrey D Amack, et al.
Journal of Genetic Counseling|August 24, 2016
Bicuspid Aortic Valve: a Review with Recommendations for Genetic CounselingSamantha L Freeze, Benjamin J Landis, Stephanie M Ware, et al.
Genome Biology|September 23, 2011
SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencingMuhammad Tariq, John W Belmont, Seema Lalani, et al.
Progress in Pediatric Cardiology|February 16, 2018
Noncompaction cardiomyopathy and heterotaxy syndromeHugo R Martinez, Stephanie M Ware, Marcus S Schamberger, et al.
Developmental Biology|June 9, 2020
SHROOM3 is downstream of the planar cell polarity pathway and loss-of-function results in congenital heart defectsMatthew D Durbin, James O'Kane, Samuel Lorentz, et al.
Human Molecular Genetics|January 11, 2013
Zic3 is required in the migrating primitive streak for node morphogenesis and left-right patterningMardi J Sutherland, Shuyun Wang, Malgorzata E Quinn, et al.
American Journal of Medical Genetics. Part A|April 27, 2016
Analysis of TGFBR1*6A variant in individuals evaluated for Marfan syndromeAllyson E Somers, Robert B Hinton, Valentina Pilipenko, et al.
Pediatrics|September 17, 2014
Twins with progressive thoracic aortic aneurysm, recurrent dissection and ACTA2 mutationStephanie M Ware, Amy Shikany, Benjamin J Landis, et al.
Human Mutation|September 28, 2018
Novel pathogenic variants in filamin C identified in pediatric restrictive cardiomyopathyJeffrey Schubert, Muhammad Tariq, Gabrielle Geddes, et al.
American Journal of Medical Genetics. Part A|February 9, 2016
Clinically relevant variants identified in thoracic aortic aneurysm patients by research exome sequencingJeffrey A Schubert, Benjamin J Landis, Amy R Shikany, et al.
Pageof 15