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Nanostructural adsorption of vanadium oxide on functionalized graphene: a DFT study.

Physical chemistry chemical physics : PCCP

Ayissi S, Palotás K, Qin H, Yang L, Charpentier PA.
PMID: 27731430
Phys Chem Chem Phys. 2016 Oct 26;18(42):29208-29217. doi: 10.1039/c6cp03967g.

Rutile-monoclinic phase transitions of vanadium oxide (VO

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Ayissi S, Palotás K, Qin H, et al. Nanostructural adsorption of vanadium oxide on functionalized graphene: a DFT study. Phys Chem Chem Phys. 2016;18(42):29208-29217doi: 10.1039/c6cp03967g.
Ayissi, S., Palotás, K., Qin, H., Yang, L., & Charpentier, P. A. (2016). Nanostructural adsorption of vanadium oxide on functionalized graphene: a DFT study. Physical chemistry chemical physics : PCCP, 18(42), 29208-29217. https://doi.org/10.1039/c6cp03967g
Ayissi, Serge, et al. "Nanostructural adsorption of vanadium oxide on functionalized graphene: a DFT study." Physical chemistry chemical physics : PCCP vol. 18,42 (2016): 29208-29217. doi: https://doi.org/10.1039/c6cp03967g
Ayissi S, Palotás K, Qin H, Yang L, Charpentier PA. Nanostructural adsorption of vanadium oxide on functionalized graphene: a DFT study. Phys Chem Chem Phys. 2016 Oct 26;18(42):29208-29217. doi: 10.1039/c6cp03967g. PMID: 27731430.
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Sorafenib induces cathepsin B-mediated apoptosis of bladder cancer cells by regulating the Akt/PTEN pathway. The Akt inhibitor, perifosine, enhances the sorafenib-induced cytotoxicity against bladder cancer cells.

Oncoscience

Amantini C, Morelli MB, Santoni M, Soriani A, Cardinali C, Farfariello V, Eleuteri AM, Bonfili L, Mozzicafreddo M, Nabissi M, Cascinu S, Santoni G.
PMID: 26097873
Oncoscience. 2015 Mar 23;2(4):395-409. doi: 10.18632/oncoscience.147. eCollection 2015.

Sorafenib, a tyrosine kinase inhibitor, has been demonstrated to exert anti-tumor effects. However, the molecular mechanisms underlying its effects on bladder cancer remain unknown. Here, we evaluated the mechanisms responsible for the sorafenib-induced anti-tumor effects on 5637 and T24...

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Amantini C, Morelli MB, Santoni M, et al. Sorafenib induces cathepsin B-mediated apoptosis of bladder cancer cells by regulating the Akt/PTEN pathway. The Akt inhibitor, perifosine, enhances the sorafenib-induced cytotoxicity against bladder cancer cells. Oncoscience. 2015;2(4):395-409doi: 10.18632/oncoscience.147.
Amantini, C., Morelli, M. B., Santoni, M., Soriani, A., Cardinali, C., Farfariello, V., Eleuteri, A. M., Bonfili, L., Mozzicafreddo, M., Nabissi, M., Cascinu, S., & Santoni, G. (2015). Sorafenib induces cathepsin B-mediated apoptosis of bladder cancer cells by regulating the Akt/PTEN pathway. The Akt inhibitor, perifosine, enhances the sorafenib-induced cytotoxicity against bladder cancer cells. Oncoscience, 2(4), 395-409. https://doi.org/10.18632/oncoscience.147
Amantini, Consuelo, et al. "Sorafenib induces cathepsin B-mediated apoptosis of bladder cancer cells by regulating the Akt/PTEN pathway. The Akt inhibitor, perifosine, enhances the sorafenib-induced cytotoxicity against bladder cancer cells." Oncoscience vol. 2,4 (2015): 395-409. doi: https://doi.org/10.18632/oncoscience.147
Amantini C, Morelli MB, Santoni M, Soriani A, Cardinali C, Farfariello V, Eleuteri AM, Bonfili L, Mozzicafreddo M, Nabissi M, Cascinu S, Santoni G. Sorafenib induces cathepsin B-mediated apoptosis of bladder cancer cells by regulating the Akt/PTEN pathway. The Akt inhibitor, perifosine, enhances the sorafenib-induced cytotoxicity against bladder cancer cells. Oncoscience. 2015 Mar 23;2(4):395-409. doi: 10.18632/oncoscience.147. eCollection 2015. PMID: 26097873; PMCID: PMC4468325.
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Acetylation of cell wall is required for structural integrity of the leaf surface and exerts a global impact on plant stress responses.

Frontiers in plant science

Nafisi M, Stranne M, Fimognari L, Atwell S, Martens HJ, Pedas PR, Hansen SF, Nawrath C, Scheller HV, Kliebenstein DJ, Sakuragi Y.
PMID: 26257757
Front Plant Sci. 2015 Jul 22;6:550. doi: 10.3389/fpls.2015.00550. eCollection 2015.

The epidermis on leaves protects plants from pathogen invasion and provides a waterproof barrier. It consists of a layer of cells that is surrounded by thick cell walls, which are partially impregnated by highly hydrophobic cuticular components. We show...

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Nafisi M, Stranne M, Fimognari L, et al. Acetylation of cell wall is required for structural integrity of the leaf surface and exerts a global impact on plant stress responses. Front Plant Sci. 2015;6:550doi: 10.3389/fpls.2015.00550.
Nafisi, M., Stranne, M., Fimognari, L., Atwell, S., Martens, H. J., Pedas, P. R., Hansen, S. F., Nawrath, C., Scheller, H. V., Kliebenstein, D. J., & Sakuragi, Y. (2015). Acetylation of cell wall is required for structural integrity of the leaf surface and exerts a global impact on plant stress responses. Frontiers in plant science, 6550. https://doi.org/10.3389/fpls.2015.00550
Nafisi, Majse, et al. "Acetylation of cell wall is required for structural integrity of the leaf surface and exerts a global impact on plant stress responses." Frontiers in plant science vol. 6 (2015): 550. doi: https://doi.org/10.3389/fpls.2015.00550
Nafisi M, Stranne M, Fimognari L, Atwell S, Martens HJ, Pedas PR, Hansen SF, Nawrath C, Scheller HV, Kliebenstein DJ, Sakuragi Y. Acetylation of cell wall is required for structural integrity of the leaf surface and exerts a global impact on plant stress responses. Front Plant Sci. 2015 Jul 22;6:550. doi: 10.3389/fpls.2015.00550. eCollection 2015. PMID: 26257757; PMCID: PMC4510344.
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Chronic inflammatory demyelinating polyneuropathy associated with diabetes mellitus.

Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences

Fatehi F, Nafissi S, Basiri K, Amiri M, Soltanzadeh A.
PMID: 24174953
J Res Med Sci. 2013 May;18(5):438-41.

Various forms of neuropathy are seen diabetic patients; chronic inflammatory demyelinating polyneuropathy (CIDP) seems not to be infrequent neuropathy in patients suffering from diabetes and it seems to be more common than in the general population; on the contrary,...

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Fatehi F, Nafissi S, Basiri K, et al. Chronic inflammatory demyelinating polyneuropathy associated with diabetes mellitus. J Res Med Sci. 2013;18(5):438-41
Fatehi, F., Nafissi, S., Basiri, K., Amiri, M., & Soltanzadeh, A. (2013). Chronic inflammatory demyelinating polyneuropathy associated with diabetes mellitus. Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences, 18(5), 438-41.
Fatehi, Farzad, et al. "Chronic inflammatory demyelinating polyneuropathy associated with diabetes mellitus." Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences vol. 18,5 (2013): 438-41.
Fatehi F, Nafissi S, Basiri K, Amiri M, Soltanzadeh A. Chronic inflammatory demyelinating polyneuropathy associated with diabetes mellitus. J Res Med Sci. 2013 May;18(5):438-41. PMID: 24174953; PMCID: PMC3810582.
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Electronic switching of single silicon atoms by molecular field effects.

Journal of the American Chemical Society

Harikumar KR, Polanyi JC, Sloan PA, Ayissi S, Hofer WA.
PMID: 17177429
J Am Chem Soc. 2006 Dec 27;128(51):16791-7. doi: 10.1021/ja062874c.

We have observed on-off switching of scanning tunneling microscope current flow to silicon adatoms of the Si(111)-(7 x 7) surface that are enclosed within a bistable dimeric corral of self-assembled chlorododecane molecules. These thermally activated oscillations amounted to an...

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Harikumar KR, Polanyi JC, Sloan PA, et al. Electronic switching of single silicon atoms by molecular field effects. J Am Chem Soc. 2006;128(51):16791-7doi: 10.1021/ja062874c.
Harikumar, K. R., Polanyi, J. C., Sloan, P. A., Ayissi, S., & Hofer, W. A. (2006). Electronic switching of single silicon atoms by molecular field effects. Journal of the American Chemical Society, 128(51), 16791-7. https://doi.org/10.1021/ja062874c
Harikumar, Krishnan R, et al. "Electronic switching of single silicon atoms by molecular field effects." Journal of the American Chemical Society vol. 128,51 (2006): 16791-7. doi: https://doi.org/10.1021/ja062874c
Harikumar KR, Polanyi JC, Sloan PA, Ayissi S, Hofer WA. Electronic switching of single silicon atoms by molecular field effects. J Am Chem Soc. 2006 Dec 27;128(51):16791-7. doi: 10.1021/ja062874c. PMID: 17177429.
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Granzyme h serum levels variations with both reproductive hormone receptors, and related hormone receptors in breast cancer patients.

Iranian journal of cancer prevention

Tahbaz-Lahafi B, Akbari ME, Amir-Rassouli H, Rahimipour A, Azargashb E, Nafissi N, Jahani F.
PMID: 25250148
Iran J Cancer Prev. 2014;7(1):48-52.

BACKGROUND: Breast Cancer (BC) is the most common cancer in Iranian women, meanwhile the Iranian patients are relatively young. Granzyme H (GZMH) is a functional cytotoxic serine protease of NK cell granules, which expands the cell death-inducing repertoire of...

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Tahbaz-Lahafi B, Akbari ME, Amir-Rassouli H, et al. Granzyme h serum levels variations with both reproductive hormone receptors, and related hormone receptors in breast cancer patients. Iran J Cancer Prev. 2014;7(1):48-52
Tahbaz-Lahafi, B., Akbari, M. E., Amir-Rassouli, H., Rahimipour, A., Azargashb, E., Nafissi, N., & Jahani, F. (2014). Granzyme h serum levels variations with both reproductive hormone receptors, and related hormone receptors in breast cancer patients. Iranian journal of cancer prevention, 7(1), 48-52.
Tahbaz-Lahafi, Behnoosh, et al. "Granzyme h serum levels variations with both reproductive hormone receptors, and related hormone receptors in breast cancer patients." Iranian journal of cancer prevention vol. 7,1 (2014): 48-52.
Tahbaz-Lahafi B, Akbari ME, Amir-Rassouli H, Rahimipour A, Azargashb E, Nafissi N, Jahani F. Granzyme h serum levels variations with both reproductive hormone receptors, and related hormone receptors in breast cancer patients. Iran J Cancer Prev. 2014;7(1):48-52. PMID: 25250148; PMCID: PMC4142953.
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The TRPV1 ion channel regulates thymocyte differentiation by modulating autophagy and proteasome activity.

Oncotarget

Amantini C, Farfariello V, Cardinali C, Morelli MB, Marinelli O, Nabissi M, Santoni M, Bonfili L, Cecarini V, Eleuteri AM, Santoni G.
PMID: 29207602
Oncotarget. 2017 Oct 11;8(53):90766-90780. doi: 10.18632/oncotarget.21798. eCollection 2017 Oct 31.

Autophagy and the ubiquitin-proteasome system (UPS) control thymus cell homeostasis under resting and endoplasmic reticulum (ER) stress conditions. Several evidence support a cross-talk between UPS and autophagy; abrogation of UPS responses stimulates autophagy, and vice versa the inhibition of...

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Amantini C, Farfariello V, Cardinali C, et al. The TRPV1 ion channel regulates thymocyte differentiation by modulating autophagy and proteasome activity. Oncotarget. 2017;8(53):90766-90780doi: 10.18632/oncotarget.21798.
Amantini, C., Farfariello, V., Cardinali, C., Morelli, M. B., Marinelli, O., Nabissi, M., Santoni, M., Bonfili, L., Cecarini, V., Eleuteri, A. M., & Santoni, G. (2017). The TRPV1 ion channel regulates thymocyte differentiation by modulating autophagy and proteasome activity. Oncotarget, 8(53), 90766-90780. https://doi.org/10.18632/oncotarget.21798
Amantini, Consuelo, et al. "The TRPV1 ion channel regulates thymocyte differentiation by modulating autophagy and proteasome activity." Oncotarget vol. 8,53 (2017): 90766-90780. doi: https://doi.org/10.18632/oncotarget.21798
Amantini C, Farfariello V, Cardinali C, Morelli MB, Marinelli O, Nabissi M, Santoni M, Bonfili L, Cecarini V, Eleuteri AM, Santoni G. The TRPV1 ion channel regulates thymocyte differentiation by modulating autophagy and proteasome activity. Oncotarget. 2017 Oct 11;8(53):90766-90780. doi: 10.18632/oncotarget.21798. eCollection 2017 Oct 31. PMID: 29207602; PMCID: PMC5710883.
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Expression Profiling of Circulating Tumor Cells in Pancreatic Ductal Adenocarcinoma Patients: Biomarkers Predicting Overall Survival.

Frontiers in oncology

Amantini C, Morelli MB, Nabissi M, Piva F, Marinelli O, Maggi F, Bianchi F, Bittoni A, Berardi R, Giampieri R, Santoni G.
PMID: 31552188
Front Oncol. 2019 Sep 10;9:874. doi: 10.3389/fonc.2019.00874. eCollection 2019.

The interest in liquid biopsy is growing because it could represent a non-invasive prognostic or predictive tool for clinical outcome in patients with pancreatic ductal adenocarcinoma (PDAC), an aggressive and lethal disease. In this pilot study, circulating tumor cells...

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Amantini C, Morelli MB, Nabissi M, et al. Expression Profiling of Circulating Tumor Cells in Pancreatic Ductal Adenocarcinoma Patients: Biomarkers Predicting Overall Survival. Front Oncol. 2019;9:874doi: 10.3389/fonc.2019.00874.
Amantini, C., Morelli, M. B., Nabissi, M., Piva, F., Marinelli, O., Maggi, F., Bianchi, F., Bittoni, A., Berardi, R., Giampieri, R., & Santoni, G. (2019). Expression Profiling of Circulating Tumor Cells in Pancreatic Ductal Adenocarcinoma Patients: Biomarkers Predicting Overall Survival. Frontiers in oncology, 9874. https://doi.org/10.3389/fonc.2019.00874
Amantini, Consuelo, et al. "Expression Profiling of Circulating Tumor Cells in Pancreatic Ductal Adenocarcinoma Patients: Biomarkers Predicting Overall Survival." Frontiers in oncology vol. 9 (2019): 874. doi: https://doi.org/10.3389/fonc.2019.00874
Amantini C, Morelli MB, Nabissi M, Piva F, Marinelli O, Maggi F, Bianchi F, Bittoni A, Berardi R, Giampieri R, Santoni G. Expression Profiling of Circulating Tumor Cells in Pancreatic Ductal Adenocarcinoma Patients: Biomarkers Predicting Overall Survival. Front Oncol. 2019 Sep 10;9:874. doi: 10.3389/fonc.2019.00874. eCollection 2019. PMID: 31552188; PMCID: PMC6746928.
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RNA Loading on Nano-Structured Hyperbranched β-Cyclodextrin.

Avicenna journal of medical biotechnology

Hirbod S, Nafisi S, Maibach HI.
PMID: 29296262
Avicenna J Med Biotechnol. 2018 Jan-Mar;10(1):15-21.

BACKGROUND: β-Cyclodextrin functionalized hyper-branched polyglycerol (HBCD: β-CD-g-PG), a biocompatible polymer, has recently been proposed for delivery of poorly water soluble compounds.METHODS: The present study examines the interaction of HBCD with RNA, utilizing a constant concentration of RNA and different...

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Hirbod S, Nafisi S, Maibach HI. RNA Loading on Nano-Structured Hyperbranched β-Cyclodextrin. Avicenna J Med Biotechnol. 2018;10(1):15-21
Hirbod, S., Nafisi, S., & Maibach, H. I. (2018). RNA Loading on Nano-Structured Hyperbranched β-Cyclodextrin. Avicenna journal of medical biotechnology, 10(1), 15-21.
Hirbod, Sorina, et al. "RNA Loading on Nano-Structured Hyperbranched β-Cyclodextrin." Avicenna journal of medical biotechnology vol. 10,1 (2018): 15-21.
Hirbod S, Nafisi S, Maibach HI. RNA Loading on Nano-Structured Hyperbranched β-Cyclodextrin. Avicenna J Med Biotechnol. 2018 Jan-Mar;10(1):15-21. PMID: 29296262; PMCID: PMC5742648.
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The effect of spinal cord stimulation on pain medication reduction in intractable spine and limb pain: a systematic review of randomized controlled trials and meta-analysis.

Journal of pain research

Pollard EM, Lamer TJ, Moeschler SM, Gazelka HM, Hooten WM, Bendel MA, Warner NS, Murad MH.
PMID: 31118751
J Pain Res. 2019 Apr 30;12:1311-1324. doi: 10.2147/JPR.S186662. eCollection 2019.

No abstract available.

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Pollard EM, Lamer TJ, Moeschler SM, et al. The effect of spinal cord stimulation on pain medication reduction in intractable spine and limb pain: a systematic review of randomized controlled trials and meta-analysis. J Pain Res. 2019;12:1311-1324doi: 10.2147/JPR.S186662.
Pollard, E. M., Lamer, T. J., Moeschler, S. M., Gazelka, H. M., Hooten, W. M., Bendel, M. A., Warner, N. S., & Murad, M. H. (2019). The effect of spinal cord stimulation on pain medication reduction in intractable spine and limb pain: a systematic review of randomized controlled trials and meta-analysis. Journal of pain research, 121311-1324. https://doi.org/10.2147/JPR.S186662
Pollard, E Morgan, et al. "The effect of spinal cord stimulation on pain medication reduction in intractable spine and limb pain: a systematic review of randomized controlled trials and meta-analysis." Journal of pain research vol. 12 (2019): 1311-1324. doi: https://doi.org/10.2147/JPR.S186662
Pollard EM, Lamer TJ, Moeschler SM, Gazelka HM, Hooten WM, Bendel MA, Warner NS, Murad MH. The effect of spinal cord stimulation on pain medication reduction in intractable spine and limb pain: a systematic review of randomized controlled trials and meta-analysis. J Pain Res. 2019 Apr 30;12:1311-1324. doi: 10.2147/JPR.S186662. eCollection 2019. PMID: 31118751; PMCID: PMC6502439.
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Magnetic Resonance Imaging-based biomechanical simulation of cartilage: A systematic review.

Journal of the mechanical behavior of biomedical materials

Seyedpour SM, Nafisi S, Nabati M, Pierce DM, Reichenbach JR, Ricken T.
PMID: 34894500
J Mech Behav Biomed Mater. 2021 Nov 26;126:104963. doi: 10.1016/j.jmbbm.2021.104963. Epub 2021 Nov 26.

MRI-based mathematical and computational modeling studies can contribute to a better understanding of the mechanisms governing cartilage's mechanical performance and cartilage disease. In addition, distinct modeling of cartilage is needed to optimize artificial cartilage production. These studies have opened...

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Seyedpour SM, Nafisi S, Nabati M, et al. Magnetic Resonance Imaging-based biomechanical simulation of cartilage: A systematic review. J Mech Behav Biomed Mater. 2021;126:104963doi: 10.1016/j.jmbbm.2021.104963.
Seyedpour, S. M., Nafisi, S., Nabati, M., Pierce, D. M., Reichenbach, J. R., & Ricken, T. (2021). Magnetic Resonance Imaging-based biomechanical simulation of cartilage: A systematic review. Journal of the mechanical behavior of biomedical materials, 126104963. https://doi.org/10.1016/j.jmbbm.2021.104963
Seyedpour, S M, et al. "Magnetic Resonance Imaging-based biomechanical simulation of cartilage: A systematic review." Journal of the mechanical behavior of biomedical materials vol. 126 (2021): 104963. doi: https://doi.org/10.1016/j.jmbbm.2021.104963
Seyedpour SM, Nafisi S, Nabati M, Pierce DM, Reichenbach JR, Ricken T. Magnetic Resonance Imaging-based biomechanical simulation of cartilage: A systematic review. J Mech Behav Biomed Mater. 2021 Nov 26;126:104963. doi: 10.1016/j.jmbbm.2021.104963. Epub 2021 Nov 26. PMID: 34894500.
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Perioperative Opioid Consumption and Clinical Outcomes in Surgical Patients With a Pre-existing Opioid-Based Intrathecal Drug Delivery System.

Anesthesia and analgesia

D'Souza RS, Warner MA, Olatoye OO, Langford BJ, Bruns DL, Schroeder DR, Mauck WD, Schaefer KK, Warner NS.
PMID: 34260427
Anesth Analg. 2022 Jan 01;134(1):35-43. doi: 10.1213/ANE.0000000000005662.

BACKGROUND: Intrathecal drug delivery systems (IDDS) have been utilized for over 3 decades for management of chronic pain and spasticity. Patients with IDDS may present for surgical procedures unrelated to the IDDS device, although data are limited regarding perioperative...

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D'Souza RS, Warner MA, Olatoye OO, et al. Perioperative Opioid Consumption and Clinical Outcomes in Surgical Patients With a Pre-existing Opioid-Based Intrathecal Drug Delivery System. Anesth Analg. 2022;134(1):35-43doi: 10.1213/ANE.0000000000005662.
D'Souza, R. S., Warner, M. A., Olatoye, O. O., Langford, B. J., Bruns, D. L., Schroeder, D. R., Mauck, W. D., Schaefer, K. K., & Warner, N. S. (2022). Perioperative Opioid Consumption and Clinical Outcomes in Surgical Patients With a Pre-existing Opioid-Based Intrathecal Drug Delivery System. Anesthesia and analgesia, 134(1), 35-43. https://doi.org/10.1213/ANE.0000000000005662
D'Souza, Ryan S, et al. "Perioperative Opioid Consumption and Clinical Outcomes in Surgical Patients With a Pre-existing Opioid-Based Intrathecal Drug Delivery System." Anesthesia and analgesia vol. 134,1 (2022): 35-43. doi: https://doi.org/10.1213/ANE.0000000000005662
D'Souza RS, Warner MA, Olatoye OO, Langford BJ, Bruns DL, Schroeder DR, Mauck WD, Schaefer KK, Warner NS. Perioperative Opioid Consumption and Clinical Outcomes in Surgical Patients With a Pre-existing Opioid-Based Intrathecal Drug Delivery System. Anesth Analg. 2022 Jan 01;134(1):35-43. doi: 10.1213/ANE.0000000000005662. PMID: 34260427; PMCID: PMC8678135.
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Showing 1 to 12 of 183 entries