Systematic study of nonmagnetic resistance changes due to electrical pulsing in single metal layers and metal/antiferromagnet bilayers

Autor: Jacot, B. J., Krishnaswamy, G., Sala, G., Avci, C. O., Vélez, S., Gambardella, P., Lambert, C. -H.

Publikováno v: Journal of Applied Physics 128, 173902 (2020)

Intense current pulses are often required to operate microelectronic and spintronic devices. Notably, strong current pulses have been shown to induce magnetoresistance changes attributed to domain reorientation in antiferromagnet/heavy metal bilayers

Externí odkaz: http://arxiv.org/abs/2011.13413

Structural and spectroscopic characterization, reactivity study and charge transfer analysis of the newly synthetized 2-(6-hydroxy-1-benzofuran-3-yl) acetic acid

Autor: Murthy, P. Krishna, Krishnaswamy, G., Armaković, Stevan, Armaković, Sanja J., Suchetan, P.A., Desai, Nivedita R., Suneetha, V., SreenivasaRao, R., Bhargavi, G., Aruna Kumar, D.B.

Publikováno v: In Journal of Molecular Structure 15 June 2018 1162:81-95

Healthcare utilization and clinical characteristics of genetic epilepsy in electronic health records.

Autor: Boßelmann CM; Genomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA.; Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, OH 44195, USA., Ivaniuk A; Genomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA.; Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, OH 44195, USA., St John M; Genomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA.; Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, OH 44195, USA., Taylor SC; Neurological Institute, Cleveland Clinic, Cleveland, OH 44195, USA., Krishnaswamy G; Neurological Institute, Cleveland Clinic, Cleveland, OH 44195, USA., Milinovich A; Department of Quantitative Health Sciences, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA., Leu C; Genomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA.; Department of Clinical and Experimental Epilepsy, Institute of Neurology, University College London, London, WC1N 3BG, UK.; Department of Neurology, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.; Center for Neurogenetics, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA., Gupta A; Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, OH 44195, USA., Pestana-Knight EM; Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, OH 44195, USA., Najm I; Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, OH 44195, USA., Lal D; Genomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195, USA.; Epilepsy Center, Neurological Institute, Cleveland Clinic, Cleveland, OH 44195, USA.; Department of Neurology, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.; Center for Neurogenetics, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.; Stanley Center for Psychiatric Research, Broad Institute of Harvard and M.I.T., Cambridge, MA 02142, USA.; Cologne Center for Genomics (CCG), University of Cologne, 50931 Cologne, Germany.

Publikováno v: Brain communications [Brain Commun] 2024 Mar 14; Vol. 6 (2), pp. fcae090. Date of Electronic Publication: 2024 Mar 14 (Print Publication: 2024).

Highly Facile, Regio‐ and Stereoselective Synthesis of Spiropyrrolidine‐5‐aza‐2‐oxindole Derivatives through Multicomponent 1,3‐Dipolar Cycloaddition Reaction and Their In‐Vitro and In‐Silico Biological Studies

Autor: Shinoj Kumar, P. P.¹ (AUTHOR), Krishnaswamy, G.² (AUTHOR), Desai, Nivedita R.¹ (AUTHOR), Sreenivasa, S.³ (AUTHOR), Aruna Kumar, D. B.^1,2 (AUTHOR) nirmaldb@gamil.com

Publikováno v: ChemistrySelect. 9/21/2021, Vol. 6 Issue 35, p9407-9414. 8p.

MOLECULAR IODINE CATALYZED SOLVENT FREE ONE POT SYNTHESIS, CHARACTERIZATION, INSILICO ADME, hERG ANALYSIS, MOLECULAR DOCKING STUDIES AND DFT ANALYSIS OF 2- SUBSTITUTED 4,5-DIPHENYL-1H-IMIDAZOLE DERIVATIVES

Autor: Sreenivasa S., Sridhar M. A., Fathima Zohra, Shivaraja G., Krishnaswamy G., Venugopal K. B., Vanajakshi H. V., Usha G. H., Yeshwanth M., Lohith T. N., Pruthviraj K.

Publikováno v: Journal of Advanced Scientific Research. 12:211-229

In the present investigation, a series of 2-substituted 4,5-Diphenyl-1H-imidazoles (3a-f) were prepared via one pot Debus-Radziszwski multicomponent condensation reaction using molecular iodine as a catalyst. Synthesis involves one pot reaction of be

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0b01a8fbcc8e3007a15e325a6d7f8555
https://doi.org/10.55218/jasr.202112428