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A scaffold-level genome assembly of a minute pirate bug, Orius laevigatus (Hemiptera: Anthocoridae), and a comparative analysis of insecticide resistance-related gene families with hemipteran crop pests.

BMC genomics

Bailey E, Field L, Rawlings C, King R, Mohareb F, Pak KH, Hughes D, Williamson M, Ganko E, Buer B, Nauen R.
PMID: 35012450
BMC Genomics. 2022 Jan 11;23(1):45. doi: 10.1186/s12864-021-08249-y.

BACKGROUND: Orius laevigatus, a minute pirate bug, is a highly effective beneficial predator of crop pests including aphids, spider mites and thrips in integrated pest management (IPM) programmes. No genomic information is currently available for O. laevigatus, as is...

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Bailey E, Field L, Rawlings C, et al. A scaffold-level genome assembly of a minute pirate bug, Orius laevigatus (Hemiptera: Anthocoridae), and a comparative analysis of insecticide resistance-related gene families with hemipteran crop pests. BMC Genomics. 2022;23(1):45doi: 10.1186/s12864-021-08249-y.
Bailey, E., Field, L., Rawlings, C., King, R., Mohareb, F., Pak, K. H., Hughes, D., Williamson, M., Ganko, E., Buer, B., & Nauen, R. (2022). A scaffold-level genome assembly of a minute pirate bug, Orius laevigatus (Hemiptera: Anthocoridae), and a comparative analysis of insecticide resistance-related gene families with hemipteran crop pests. BMC genomics, 23(1), 45. https://doi.org/10.1186/s12864-021-08249-y
Bailey, Emma, et al. "A scaffold-level genome assembly of a minute pirate bug, Orius laevigatus (Hemiptera: Anthocoridae), and a comparative analysis of insecticide resistance-related gene families with hemipteran crop pests." BMC genomics vol. 23,1 (2022): 45. doi: https://doi.org/10.1186/s12864-021-08249-y
Bailey E, Field L, Rawlings C, King R, Mohareb F, Pak KH, Hughes D, Williamson M, Ganko E, Buer B, Nauen R. A scaffold-level genome assembly of a minute pirate bug, Orius laevigatus (Hemiptera: Anthocoridae), and a comparative analysis of insecticide resistance-related gene families with hemipteran crop pests. BMC Genomics. 2022 Jan 11;23(1):45. doi: 10.1186/s12864-021-08249-y. PMID: 35012450.
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Fine-Tuning the Biological Profile of Multitarget Mitochondriotropic Antioxidants for Neurodegenerative Diseases.

Antioxidants (Basel, Switzerland)

Chavarria D, Da Silva O, Benfeito S, Barreiro S, Garrido J, Cagide F, Soares P, Remião F, Brazzolotto X, Nachon F, Oliveira PJ, Dias J, Borges F.
PMID: 33672269
Antioxidants (Basel). 2021 Feb 23;10(2). doi: 10.3390/antiox10020329.

Neurotransmitter depletion and mitochondrial dysfunction are among the multiple pathological events that lead to neurodegeneration. Following our previous studies related with the development of multitarget mitochondriotropic antioxidants, this study aims to evaluate whether the π-system extension on the chemical...

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Chavarria D, Da Silva O, Benfeito S, et al. Fine-Tuning the Biological Profile of Multitarget Mitochondriotropic Antioxidants for Neurodegenerative Diseases. Antioxidants (Basel). 2021;10(2)doi: 10.3390/antiox10020329.
Chavarria, D., Da Silva, O., Benfeito, S., Barreiro, S., Garrido, J., Cagide, F., Soares, P., Remião, F., Brazzolotto, X., Nachon, F., Oliveira, P. J., Dias, J., & Borges, F. (2021). Fine-Tuning the Biological Profile of Multitarget Mitochondriotropic Antioxidants for Neurodegenerative Diseases. Antioxidants (Basel, Switzerland), 10(2), . https://doi.org/10.3390/antiox10020329
Chavarria, Daniel, et al. "Fine-Tuning the Biological Profile of Multitarget Mitochondriotropic Antioxidants for Neurodegenerative Diseases." Antioxidants (Basel, Switzerland) vol. 10,2 (2021). doi: https://doi.org/10.3390/antiox10020329
Chavarria D, Da Silva O, Benfeito S, Barreiro S, Garrido J, Cagide F, Soares P, Remião F, Brazzolotto X, Nachon F, Oliveira PJ, Dias J, Borges F. Fine-Tuning the Biological Profile of Multitarget Mitochondriotropic Antioxidants for Neurodegenerative Diseases. Antioxidants (Basel). 2021 Feb 23;10(2). doi: 10.3390/antiox10020329. PMID: 33672269; PMCID: PMC7926627.
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Hybrid Quinoline-Thiosemicarbazone Therapeutics as a New Treatment Opportunity for Alzheimer's Disease‒Synthesis, In Vitro Cholinesterase Inhibitory Potential and Computational Modeling Analysis.

Molecules (Basel, Switzerland)

Zaib S, Munir R, Younas MT, Kausar N, Ibrar A, Aqsa S, Shahid N, Asif TT, Alsaab HO, Khan I.
PMID: 34770983
Molecules. 2021 Oct 30;26(21). doi: 10.3390/molecules26216573.

Alzheimer's disease (AD) is a progressive neurodegenerative disorder and the leading cause of dementia worldwide. The limited pharmacological approaches based on cholinesterase inhibitors only provide symptomatic relief to AD patients. Moreover, the adverse side effects such as nausea, vomiting,...

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Zaib S, Munir R, Younas MT, et al. Hybrid Quinoline-Thiosemicarbazone Therapeutics as a New Treatment Opportunity for Alzheimer's Disease‒Synthesis, In Vitro Cholinesterase Inhibitory Potential and Computational Modeling Analysis. Molecules. 2021;26(21)doi: 10.3390/molecules26216573.
Zaib, S., Munir, R., Younas, M. T., Kausar, N., Ibrar, A., Aqsa, S., Shahid, N., Asif, T. T., Alsaab, H. O., & Khan, I. (2021). Hybrid Quinoline-Thiosemicarbazone Therapeutics as a New Treatment Opportunity for Alzheimer's Disease‒Synthesis, In Vitro Cholinesterase Inhibitory Potential and Computational Modeling Analysis. Molecules (Basel, Switzerland), 26(21), . https://doi.org/10.3390/molecules26216573
Zaib, Sumera, et al. "Hybrid Quinoline-Thiosemicarbazone Therapeutics as a New Treatment Opportunity for Alzheimer's Disease‒Synthesis, In Vitro Cholinesterase Inhibitory Potential and Computational Modeling Analysis." Molecules (Basel, Switzerland) vol. 26,21 (2021). doi: https://doi.org/10.3390/molecules26216573
Zaib S, Munir R, Younas MT, Kausar N, Ibrar A, Aqsa S, Shahid N, Asif TT, Alsaab HO, Khan I. Hybrid Quinoline-Thiosemicarbazone Therapeutics as a New Treatment Opportunity for Alzheimer's Disease‒Synthesis, In Vitro Cholinesterase Inhibitory Potential and Computational Modeling Analysis. Molecules. 2021 Oct 30;26(21). doi: 10.3390/molecules26216573. PMID: 34770983; PMCID: PMC8587653.
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Apoptotic Effect of Novel Benzimidazole Derivatives Bearing Pyridyl/Pyrimidinyl Piperazine Moiety.

Anti-cancer agents in medicinal chemistry

Çiftçi G, Temel HE, Yurttaş L.
PMID: 34238172
Anticancer Agents Med Chem. 2021 Jul 07; doi: 10.2174/1871520621666210708095110. Epub 2021 Jul 07.

BACKGROUND: Benzimidazole derivatives bearing pyridyl/pyrimidinyl piperazine moiety has attracted attention in medicinal chemistry and modern drug discovery since it exhibited a variety of biological activities, including anticancer activity.OBJECTIVE: In this study, we have designed and synthesized novel 1-[2-oxo-2-(4-substituted phenyl)ethyl]benzimidazol-2-yl)methyl...

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Çiftçi G, Temel HE, Yurttaş L. Apoptotic Effect of Novel Benzimidazole Derivatives Bearing Pyridyl/Pyrimidinyl Piperazine Moiety. Anticancer Agents Med Chem. 2021;doi: 10.2174/1871520621666210708095110.
Çiftçi, G., Temel, H. E., & Yurttaş, L. (2021). Apoptotic Effect of Novel Benzimidazole Derivatives Bearing Pyridyl/Pyrimidinyl Piperazine Moiety. Anti-cancer agents in medicinal chemistry, . https://doi.org/10.2174/1871520621666210708095110
Çiftçi, Gulsen, et al. "Apoptotic Effect of Novel Benzimidazole Derivatives Bearing Pyridyl/Pyrimidinyl Piperazine Moiety." Anti-cancer agents in medicinal chemistry vol. (2021). doi: https://doi.org/10.2174/1871520621666210708095110
Çiftçi G, Temel HE, Yurttaş L. Apoptotic Effect of Novel Benzimidazole Derivatives Bearing Pyridyl/Pyrimidinyl Piperazine Moiety. Anticancer Agents Med Chem. 2021 Jul 07; doi: 10.2174/1871520621666210708095110. Epub 2021 Jul 07. PMID: 34238172.
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Attenuation of spatial memory in 5xFAD mice by targeting cholinesterases, oxidative stress and inflammatory signaling using 2-(hydroxyl-(2-nitrophenyl)methyl)cyclopentanone.

International immunopharmacology

Ullah R, Ali G, Subhan F, Khan A, Ahsan Halim S, Naveed M, Kalsoom S, Al-Harrasi A.
PMID: 34478946
Int Immunopharmacol. 2021 Nov;100:108083. doi: 10.1016/j.intimp.2021.108083. Epub 2021 Aug 31.

Alzheimer's disease (AD) is classified pathologically as a progressive neurological disorder associated with memory decline. The study was designed to assess the underlying molecular signaling involved in the neuroprotective effect of the 2-(hydroxyl-(2-nitrophenyl)methyl)cyclopentanone (2NCP) as a novel therapeutic agent...

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Ullah R, Ali G, Subhan F, et al. Attenuation of spatial memory in 5xFAD mice by targeting cholinesterases, oxidative stress and inflammatory signaling using 2-(hydroxyl-(2-nitrophenyl)methyl)cyclopentanone. Int Immunopharmacol. 2021;100:108083doi: 10.1016/j.intimp.2021.108083.
Ullah, R., Ali, G., Subhan, F., Khan, A., Ahsan Halim, S., Naveed, M., Kalsoom, S., & Al-Harrasi, A. (2021). Attenuation of spatial memory in 5xFAD mice by targeting cholinesterases, oxidative stress and inflammatory signaling using 2-(hydroxyl-(2-nitrophenyl)methyl)cyclopentanone. International immunopharmacology, 100108083. https://doi.org/10.1016/j.intimp.2021.108083
Ullah, Rahim, et al. "Attenuation of spatial memory in 5xFAD mice by targeting cholinesterases, oxidative stress and inflammatory signaling using 2-(hydroxyl-(2-nitrophenyl)methyl)cyclopentanone." International immunopharmacology vol. 100 (2021): 108083. doi: https://doi.org/10.1016/j.intimp.2021.108083
Ullah R, Ali G, Subhan F, Khan A, Ahsan Halim S, Naveed M, Kalsoom S, Al-Harrasi A. Attenuation of spatial memory in 5xFAD mice by targeting cholinesterases, oxidative stress and inflammatory signaling using 2-(hydroxyl-(2-nitrophenyl)methyl)cyclopentanone. Int Immunopharmacol. 2021 Nov;100:108083. doi: 10.1016/j.intimp.2021.108083. Epub 2021 Aug 31. PMID: 34478946.
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Cholinesterases in Tripartite Neuromuscular Synapse.

Frontiers in molecular neuroscience

Petrov KA, Proskurina SE, Krejci E.
PMID: 35002624
Front Mol Neurosci. 2021 Dec 23;14:811220. doi: 10.3389/fnmol.2021.811220. eCollection 2021.

The neuromuscular junction (NMJ) is a tripartite synapse in which not only presynaptic and post-synaptic cells participate in synaptic transmission, but also terminal Schwann cells (TSC). Acetylcholine (ACh) is the neurotransmitter that mediates the signal between the motor neuron...

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Petrov KA, Proskurina SE, Krejci E. Cholinesterases in Tripartite Neuromuscular Synapse. Front Mol Neurosci. 2021;14:811220doi: 10.3389/fnmol.2021.811220.
Petrov, K. A., Proskurina, S. E., & Krejci, E. (2021). Cholinesterases in Tripartite Neuromuscular Synapse. Frontiers in molecular neuroscience, 14811220. https://doi.org/10.3389/fnmol.2021.811220
Petrov, Konstantin A, et al. "Cholinesterases in Tripartite Neuromuscular Synapse." Frontiers in molecular neuroscience vol. 14 (2021): 811220. doi: https://doi.org/10.3389/fnmol.2021.811220
Petrov KA, Proskurina SE, Krejci E. Cholinesterases in Tripartite Neuromuscular Synapse. Front Mol Neurosci. 2021 Dec 23;14:811220. doi: 10.3389/fnmol.2021.811220. eCollection 2021. PMID: 35002624; PMCID: PMC8733319.
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Showing 157 to 162 of 162 entries