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Page 1
Shape-Memory Effect Enabled by Ligand Substitution and CO2 Affinity in a Flexible SIFSIX Coordination Network.
Song BQ, Shivanna M, Gao MY, Wang SQ, Deng CH, Yang QY, Nikkhah SJ, Vandichel M, Kitagawa S, Zaworotko MJ. Song BQ, et al. Angew Chem Int Ed Engl. 2023 Nov 20;62(47):e202309985. doi: 10.1002/anie.202309985. Epub 2023 Oct 17. Angew Chem Int Ed Engl. 2023. PMID: 37770385
As-synthesized SIFSIX-23-Cu(N) , alpha, transformed to less open, gamma, and closed, beta, phases during activation. beta did not adsorb N(2) (77 K), rather it reverted to alpha induced by CO(2) at 195, 273 and 298 K. CO(2) desorption resulted in alpha', a shape-mem …
As-synthesized SIFSIX-23-Cu(N) , alpha, transformed to less open, gamma, and closed, beta, phases during activation. beta did not adsorb N(2 …
DNA binding properties and cytotoxic effects of two double rollover cycloplatinated (II) complexes on cancer cell lines.
Shabaninejad Z, Nikkhah M, Nabavizadeh SM. Shabaninejad Z, et al. J Inorg Biochem. 2023 Jun;243:112194. doi: 10.1016/j.jinorgbio.2023.112194. Epub 2023 Mar 16. J Inorg Biochem. 2023. PMID: 36966676
By using UV-Visible spectroscopy the intrinsic binding constant (K(b)) of C1 and C2 to DNA were determined as 2.9 10(5) M(-1), and 5.4 10(5) M(-1), respectively. Both the compounds were able to quench the fluorescence of ethidium bromide as a well known DNA intercalator. T …
By using UV-Visible spectroscopy the intrinsic binding constant (K(b)) of C1 and C2 to DNA were determined as 2.9 10(5) M(-1), and 5. …
Delayed functional maturation of human neuronal progenitor cells in vitro.
Lepski G, Maciaczyk J, Jannes CE, Maciaczyk D, Bischofberger J, Nikkhah G. Lepski G, et al. Mol Cell Neurosci. 2011 May;47(1):36-44. doi: 10.1016/j.mcn.2011.02.011. Epub 2011 Feb 26. Mol Cell Neurosci. 2011. PMID: 21362477
Functional maturation was observed only by the fifth/sixth week, preceded by a marked increase in Na+ and K+ currents. In contrast, electrophysiological maturation of rodent precursor cells was observed at the end of the first week in vitro. ...
Functional maturation was observed only by the fifth/sixth week, preceded by a marked increase in Na+ and K+ currents. In contrast, e …
One Atom Can Make All the Difference: Gas-Induced Phase Transformations in Bisimidazole-Linked Diamondoid Coordination Networks.
Koupepidou K, Nikolayenko VI, Sensharma D, Bezrukov AA, Vandichel M, Nikkhah SJ, Castell DC, Oyekan KA, Kumar N, Subanbekova A, Vandenberghe WG, Tan K, Barbour LJ, Zaworotko MJ. Koupepidou K, et al. J Am Chem Soc. 2023 May 10;145(18):10197-10207. doi: 10.1021/jacs.3c01113. Epub 2023 Apr 26. J Am Chem Soc. 2023. PMID: 37099724 Free PMC article.
Specifically, X-dia-4-Co exhibited a gradual phase transformation with a steady increase in the uptake when exposed to CO(2), whereas X-dia-5-Co exhibited a sharp step (type F-IV isotherm) at P/P(0) 0.008 or P 3 bar (195 or 298 K, respectively). Single-crystal X-ray diffra …
Specifically, X-dia-4-Co exhibited a gradual phase transformation with a steady increase in the uptake when exposed to CO(2), whereas X-dia- …
Amyotrophic lateral sclerosis progression: Iran-ALS clinical registry, a multicentre study.
Shamshiri H, Fatehi F, Davoudi F, Mir E, Pourmirza B, Abolfazli R, Etemadifar M, Harirchian MH, Gharagozli K, Ayromlou H, Basiri K, Zamani B, Rohani M, Sedighi B, Roudbari A, Delavar Kasmaei H, Nikkhah K, Ranjbar Naeini A, Nafissi S. Shamshiri H, et al. Amyotroph Lateral Scler Frontotemporal Degener. 2015;16(7-8):506-11. doi: 10.3109/21678421.2015.1074698. Epub 2015 Oct 5. Amyotroph Lateral Scler Frontotemporal Degener. 2015. PMID: 26437387
Pyknodysostosis: A case report of an 8-year-old male with a rare genetic disorder.
Faraji N, Nikkhah F, Goli R, Hassanpour A, Imanzadeh F, Yavari S. Faraji N, et al. Int J Surg Case Rep. 2023 Sep;110:108793. doi: 10.1016/j.ijscr.2023.108793. Epub 2023 Sep 7. Int J Surg Case Rep. 2023. PMID: 37689021 Free PMC article.
It is an autosomal recessive disorder caused by mutations in the gene encoding cathepsin K. Pyknodysostosis is associated with short stature, brittle bones, and distinctive facial features. ...
It is an autosomal recessive disorder caused by mutations in the gene encoding cathepsin K. Pyknodysostosis is associated with short …
16 results