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Stem Cells Translational Medicine|May 23, 2023
Propensity of Patient-Derived iPSCs for Retinal Differentiation: Implications for Autologous Cell ReplacementJessica A Cooke, Andrew P Voigt, Michael A Collingwood, et al.
The European Respiratory Journal|January 15, 2021
Functional lower airways genomic profiling of the microbiome to capture active microbial metabolismImran Sulaiman, Benjamin G Wu, Yonghua Li, et al.
JACC. Advances|December 5, 2024
Spontaneous Coronary Artery Dissection: Current Knowledge, Research Gaps, and Innovative Research Initiatives: JACC Advances Expert PanelDaniela Crousillat, Amy Sarma, Malissa Wood, et al.
Molecular Endocrinology (Baltimore, Md.)|August 26, 1998
Common mutations in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients of different originsH S Scott, M Heino, P Peterson, et al.
Journal of Medicinal Chemistry|October 7, 2014
Circumventing seizure activity in a series of G protein coupled receptor 119 (GPR119) agonistsJames S Scott, Suzanne S Bowker, Katy J Brocklehurst, et al.
Diabetes Research and Clinical Practice|February 23, 2026
Chronic complication risk and benefits of fenofibrate in type 2 diabetes by a PPARα polymorphism (rs6008845, C/T): a FIELD trial substudyAndrzej S Januszewski, Michael L H Huang, Abubakar Mangani, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 8, 2021
Identification of fluoxetine as a direct NLRP3 inhibitor to treat atrophic macular degenerationMeenakshi Ambati, Ivana Apicella, Shao-Bin Wang, et al.
Psychotherapy Research : Journal of the Society for Psychotherapy Research|November 10, 2023
Therapeutic techniques and session impact: A practice-research network study in private practiceLouis G Castonguay, Soo Jeong Youn, James F Boswell, et al.
Bioorganic & Medicinal Chemistry Letters|December 7, 2007
A new series of neutral 5-substituted 4-anilinoquinazolines as potent, orally active inhibitors of erbB2 receptor tyrosine kinaseBernard Barlaam, Peter Ballard, Robert H Bradbury, et al.
Journal of Molecular Medicine (Berlin, Germany)|March 22, 2002
Mutations in the TMPRSS3 gene are a rare cause of childhood nonsyndromic deafness in Caucasian patientsMarie Wattenhofer, Mario Vincenzo Di Iorio, Raquel Rabionet, et al.
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