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Cells|June 24, 2022
New Phenylglycinamide Derivatives with Hybrid Structure as Candidates for New Broad-Spectrum AnticonvulsantsMarcin Jakubiec, Michał Abram, Mirosław Zagaja, et al.
BMC Cardiovascular Disorders|February 17, 2022
Preoperative evaluation of pulmonary hypertension in lung transplant candidates: echocardiography versus right heart catheterizationTal Abu, Amos Levi, David Hasdai, et al.
Human Molecular Genetics|February 3, 2009
Depression Case Control (DeCC) Study fails to support involvement of the muscarinic acetylcholine receptor M2 (CHRM2) gene in recurrent major depressive disorderSarah Cohen-Woods, Daria Gaysina, Nick Craddock, et al.
Plos Pathogens|January 26, 2019
LANA oligomeric architecture is essential for KSHV nuclear body formation and viral genome maintenance during latencyAlessandra De Leo, Zhong Deng, Olga Vladimirova, et al.
Vascular Medicine (London, England)|October 26, 2017
Burden of hospitalization in clinically diagnosed peripheral artery disease: A community-based studyAdelaide M Arruda-Olson, Homam Moussa Pacha, Naveed Afzal, et al.
Journal of Acquired Immune Deficiency Syndromes (1999)|July 17, 2015
Brief Report: Cobicistat Compared With Ritonavir as a Pharmacoenhancer for Atazanavir in Combination With Emtricitabine/Tenofovir Disoproxil Fumarate: Week 144 ResultsJoel E Gallant, Ellen Koenig, Jaime F Andrade-Villanueva, et al.
Zoonoses and Public Health|December 30, 2022
Coxiella burnetii (Q-fever) outbreak associated with non-occupational exposure in a semi-urban area of western Croatia in 2022Morana Tomljenovic, Danijela Lakošeljac, Lucija Knežević, et al.
American Journal of Hypertension|April 8, 2011
Hypertension in response to AT1-AA: role of reactive oxygen species in pregnancy-induced hypertensionMarc R Parrish, Kedra Wallace, Kiran B Tam Tam, et al.
Biomedicines|September 23, 2022
A Protein Microarray-Based Respiratory Viral Antigen Testing Platform for COVID-19 SurveillanceSungjun Beck, Rie Nakajima, Algis Jasinskas, et al.
Archives of Otolaryngology--Head & Neck Surgery|December 21, 2005
Deletion of and novel missense mutation in POU3F4 in 2 families segregating X-linked nonsyndromic deafnessAbram P Vore, Eugene H Chang, Jane E Hoppe, et al.
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