Results 271 to 280 of about 731,751 (310)

Decellularized Extracellular Matrix Scaffolds to Engineer the Dormant Landscape of Microscopic Colorectal Cancer Liver Metastasis

Advanced Healthcare Materials, EarlyView.
Decellularized liver extracellular matrix scaffolds provide a platform to study dormant liver‐metastatic colorectal cancer. They induce reversible dormancy, in combination with nutrient depletion and low dose chemotherapy, through cell cycle arrest and chemotherapy resistance.
Sabrina N. VandenHeuvel, Lucia L. Nash, Abigail J. Clevenger, Claudia A. Collier, Oscar R. Benavides, Sanjana Roy, Brinlee Goggans, Aelita Salikhova, Anvitha Tharakesh, Svasti Haricharan, Amber N. Stratman, Scott Kopetz, Alex J. Walsh, Shreya A. Raghavan   +13 more
wiley   +1 more source

Pharmacovigilance study of famciclovir in the Food and Drug administration adverse event reporting system database. [PDF]

Sci Rep
Fang R, Zhou Y, Han L, Chen W, Guan N, Li J.   +5 more
europepmc   +1 more source

ROS‐Scavenging Multifunctional Microneedle Patch Facilitating Wound Healing

Advanced Healthcare Materials, EarlyView.
A reactive oxygen species (ROS) scavenging and immunomodulatory microneedle patch based on hyaluronic acid methacrylate (HaMA) and Flightless I (Flii)‐siRNA‐laden arginine functionalized poly (β‐amino ester)/alginate particles is developed for chronic wound healing applications.
Mahshid Kharaziha, Sahar Salehi, Mahshid Shokri, Seyed Mohsen Ahmadi Tafti, Thomas Scheibel   +4 more
wiley   +1 more source

Analysis of Adverse Events Associated With Dental Local Anaesthetics Using Food and Drug Administration Adverse Event Reporting System Data. [PDF]

Int Dent J
Bayram F, Akici A, Apari AM, Aydin V.
europepmc   +1 more source

Comparing drug combinations for graft-versus-host disease prophylaxis using the U.S. Food and Drug Administration Adverse Event Reporting System. [PDF]

Clin Transplant Res
Ogura T, Shiraishi C, Urawa A.
europepmc   +1 more source

Safety assessment of ripretinib: a real-world adverse event analysis from the food and drug administration adverse event reporting system. [PDF]

Front Oncol
Wang S, Chen H, Zhou Y, Chen J, Cao J.
europepmc   +1 more source

Jurisdiction of the Food and Drug Administration to Regulate Tobacco Products Under the Food, Drug, and Cosmetic Act: Food and Drug Administration v. Brown & Williamson Tobacco Corporation et al.

, 2000
Alison J. Lezak
openalex   +1 more source

Fluoroquinolones and risk of nightmares: A literature review and disproportionality analysis using individual case safety reports from Food and Drug Administration Adverse Event Reporting System database. [PDF]

J Psychopharmacol
Omrani MA, Tsobo CT, Chalabianloo N, Ahmadi F, Abdullah SS, Muanda FT.   +5 more
europepmc   +1 more source

Assessing drug lag in new drug approvals by the Iran Food and Drug Administration compared to the U.S. FDA, EMA, and PMDA: A 20-year analysis (2001–2021)

Sama Alipour, Sadra Nadimi Parashkouhi, Mohammadmahdi Mojahedian, Hadi Abbasian   +3 more
openalex   +1 more source