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JCI Insight|January 6, 2026
Structural and functional gastrointestinal abnormalities in ACTA2 R179H mice modeling multisystemic smooth muscle dysfunction syndromeAhmed A Rahman, Rhian Stavely, Leah C Ott, et al.
International Journal of Molecular Sciences|November 13, 2021
Structural and Functional Analysis of Female Sex Hormones against SARS-CoV-2 Cell EntryJorge Alberto Aguilar-Pineda, Mazen Albaghdadi, Wanlin Jiang, et al.
Jvs-Vascular Science|February 7, 2022
Vascular smooth muscle cell phenotype switching in carotid atherosclerosisElizabeth L Chou, Christian L Lino Cardenas, Mark Chaffin, et al.
Journal of the American College of Cardiology|July 28, 2022
Spatially Distinct Genetic Determinants of Aortic Dimensions Influence Risks of Aneurysm and StenosisMahan Nekoui, James P Pirruccello, Paolo Di Achille, et al.
Journal of the National Comprehensive Cancer Network : JNCCN|September 15, 2025
"A Double-Edged Sword": Influence of the 21st Century Cures Act on the Childhood, Adolescent, and Young Adult Cancer Care ExperienceMeghan E Lindsay, Mona Clappier, Sophia de Oliveira, et al.
Radiation Research|February 19, 2020
A Mail Audit Independent Peer Review System for Dosimetry Verification of a Small Animal IrradiatorMary P Gronberg, Ramesh C Tailor, Susan A Smith, et al.
JAMA Cardiology|March 2, 2022
Fibrillar Collagen Variants in Spontaneous Coronary Artery DissectionSeyedeh Maryam Zekavat, Elizabeth L Chou, Melica Zekavat, et al.
Medrxiv : the Preprint Server for Health Sciences|May 19, 2023
Assessment of valvular function in over 47,000 people using deep learning-based flow measurementsShinwan Kany, Joel T Rämö, Cody Hou, et al.
The Journal of Allergy and Clinical Immunology|March 1, 1977
Cromolyn sodium nasal solution in the prophylactic treatment of pollen-induced seasonal allergic rhinitisN I Handelman, G A Friday, H J Schwartz, et al.
American Journal of Medical Genetics. Part A|January 13, 2022
Expanded cardiovascular phenotype of Myhre syndrome includes tetralogy of Fallot suggesting a role for SMAD4 in human neural crest defectsGerarda Cappuccio, Nicola Brunetti-Pierri, Paul Clift, et al.
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