Showing results (1091-1100 of 1,886) with videos related to

Sort By:
Pageof 189
Proceedings of the National Academy of Sciences of the United States of America|April 8, 2014
Brain galanin system genes interact with life stresses in depression-related phenotypesGabriella Juhasz, Gabor Hullam, Nora Eszlari, et al.
Science (New York, N.Y.)|February 21, 2004
Formation of secondary organic aerosols through photooxidation of isopreneMagda Claeys, Bim Graham, Gyorgy Vas, et al.
Patient Education and Counseling|March 9, 2021
How well do healthcare professionals know of the priorities of their older patients regarding treatment outcomes?Suzanne Festen, Mariken E Stegmann, Annemiek Prins, et al.
Blood Purification|August 19, 2004
Characterization of the DialGuard device for endotoxin removal in hemodialysisSusan Szathmary, Edit Hegyi, Marie-Claude Amoureux, et al.
International Journal of Molecular Sciences|January 23, 2024
Embers of the Past: Early Childhood Traumas Interact with Variation in P2RX7 Gene Implicated in Neuroinflammation on Markers of Current Suicide RiskZsuliet Kristof, Zsofia Gal, Dora Torok, et al.
Current Microbiology|January 7, 2015
Induction of osmoadaptive mechanisms and modulation of cellular physiology help Bacillus licheniformis strain SSA 61 adapt to salt stressSangeeta Paul, Chetana Aggarwal, Jyoti Kumar Thakur, et al.
BMC Pulmonary Medicine|December 17, 2014
Expiratory flow rate, breath hold and anatomic dead space influence electronic nose ability to detect lung cancerAndras Bikov, Marton Hernadi, Beata Zita Korosi, et al.
Cytotherapy|November 26, 2009
Targeted antagonism of CXCR4 mobilizes progenitor cells under investigation for cardiovascular diseaseArnon Blum, Richard W Childs, Aleah Smith, et al.
Chemical Science|June 30, 2017
Probing pattern and dynamics of disulfide bridges using synthesis and NMR of an ion channel blocker peptide toxin with multiple diselenide bondsKrisztina Fehér, István Timári, Kinga Rákosi, et al.
Experimental and Molecular Pathology|May 25, 2020
Maternal mosaicism underlies the inheritance of a rare germline AKT3 variant which is responsible for megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome in two Roma half-siblingsRenata Szalai, Bela I Melegh, Agnes Till, et al.
Pageof 189