Harry C. Dietz
Affiliations: | Johns Hopkins University, Baltimore, MD |
Area:
Molecular Biology, Genetics, Cell BiologyGoogle:
"Harry Dietz"Children
Sign in to add traineePamela A. Frischmeyer | grad student | 2001 | Johns Hopkins |
Dan E. Arking | grad student | 2002 | Johns Hopkins |
Neda A. Sharifi | grad student | 2007 | Johns Hopkins |
Mark M. Awad | grad student | 2008 | Johns Hopkins |
Tammy M. Holm | grad student | 2009 | Johns Hopkins |
Kathleen C. Kent | grad student | 2012 | Johns Hopkins |
Stefani C. Fontana | grad student | 2013 | Johns Hopkins |
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Publications
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Velchev JD, Van Laer L, Luyckx I, et al. (2021) Loeys-Dietz Syndrome. Advances in Experimental Medicine and Biology. 1348: 251-264 |
Grattan M, Prince A, Ruman R, et al. (2020) Predictors of Bicuspid Aortic Valve-Associated Aortopathy in Childhood: A Report From the MIBAVA Consortium. Circulation. Cardiovascular Imaging. 13: e009717 |
Li J, Ritelli M, Ma CS, et al. (2019) Chronic mucocutaneous candidiasis and connective tissue disorder in humans with impaired JNK1-dependent responses to IL-17A/F and TGF-β. Science Immunology. 4 |
Bowen CJ, Calderón Giadrosic JF, Burger Z, et al. (2019) Targetable cellular signaling events mediate vascular pathology in vascular Ehlers-Danlos syndrome. The Journal of Clinical Investigation |
Schoenhoff FS, Alejo DE, Black JH, et al. (2019) Management of the aortic arch in patients with Loeys-Dietz syndrome. The Journal of Thoracic and Cardiovascular Surgery |
Kim DH, Beckett JD, Nagpal V, et al. (2019) Calpain 9 as a therapeutic target in TGFβ-induced mesenchymal transition and fibrosis. Science Translational Medicine. 11 |
Shin JY, Beckett JD, Bagirzadeh R, et al. (2019) Epigenetic activation and memory at a enhancer in systemic sclerosis. Science Translational Medicine. 11 |
Habashi JP, MacFarlane EG, Bagirzadeh R, et al. (2019) Oxytocin antagonism prevents pregnancy-associated aortic dissection in a mouse model of Marfan syndrome. Science Translational Medicine. 11 |
Fraser CD, Liu RH, Zhou X, et al. (2019) Valve-sparing aortic root replacement in children: Outcomes from 100 consecutive cases. The Journal of Thoracic and Cardiovascular Surgery. 157: 1100-1109 |
Luyckx I, MacCarrick G, Kempers M, et al. (2019) Confirmation of the role of pathogenic SMAD6 variants in bicuspid aortic valve-related aortopathy. European Journal of Human Genetics : Ejhg. 27: 1044-1053 |