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Insights from the sequence similarity of Zika virus proteins with the Human nerve proteins.

Bioinformation

Marsakatla P, Suneetha S, Lee J, Swaminathan PD, Vasudevan L, Supriya R, Suneetha LM.
PMID: 30108415
Bioinformation. 2018 May 31;14(5):194-200. doi: 10.6026/97320630014194. eCollection 2018.

Massive peptide sharing between the Zika virus polyprotein and host tissue proteins could elicit significant host-pathogen interactions and cross-reactions leading to autoimmune diseases. This study found similarities in the Zika V proteins and human nerve tissue proteins. 63 human...

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Marsakatla P, Suneetha S, Lee J, et al. Insights from the sequence similarity of Zika virus proteins with the Human nerve proteins. Bioinformation. 2018;14(5):194-200doi: 10.6026/97320630014194.
Marsakatla, P., Suneetha, S., Lee, J., Swaminathan, P. D., Vasudevan, L., Supriya, R., & Suneetha, L. M. (2018). Insights from the sequence similarity of Zika virus proteins with the Human nerve proteins. Bioinformation, 14(5), 194-200. https://doi.org/10.6026/97320630014194
Marsakatla, Prasanna, et al. "Insights from the sequence similarity of Zika virus proteins with the Human nerve proteins." Bioinformation vol. 14,5 (2018): 194-200. doi: https://doi.org/10.6026/97320630014194
Marsakatla P, Suneetha S, Lee J, Swaminathan PD, Vasudevan L, Supriya R, Suneetha LM. Insights from the sequence similarity of Zika virus proteins with the Human nerve proteins. Bioinformation. 2018 May 31;14(5):194-200. doi: 10.6026/97320630014194. eCollection 2018. PMID: 30108415; PMCID: PMC6077820.
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How scientists use Slack.

Nature

Perkel JM.
PMID: 28054618
Nature. 2016 Dec 29;541(7635):123-124. doi: 10.1038/541123a.

No abstract available.

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Perkel JM. How scientists use Slack. Nature. 2016;541(7635):123-124doi: 10.1038/541123a.
Perkel, J. M. (2016). How scientists use Slack. Nature, 541(7635), 123-124. https://doi.org/10.1038/541123a
Perkel, Jeffrey M. "How scientists use Slack." Nature vol. 541,7635 (2016): 123-124. doi: https://doi.org/10.1038/541123a
Perkel JM. How scientists use Slack. Nature. 2016 Dec 29;541(7635):123-124. doi: 10.1038/541123a. PMID: 28054618.
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Developing stem cell-based therapies for neural repair.

Frontiers in cellular neuroscience

Parish CL, Thompson LH.
PMID: 24204332
Front Cell Neurosci. 2013 Nov 05;7:198. doi: 10.3389/fncel.2013.00198. eCollection 2013.

No abstract available.

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Parish CL, Thompson LH. Developing stem cell-based therapies for neural repair. Front Cell Neurosci. 2013;7:198doi: 10.3389/fncel.2013.00198.
Parish, C. L., & Thompson, L. H. (2013). Developing stem cell-based therapies for neural repair. Frontiers in cellular neuroscience, 7198. https://doi.org/10.3389/fncel.2013.00198
Parish, Clare L, and Thompson, Lachlan H. "Developing stem cell-based therapies for neural repair." Frontiers in cellular neuroscience vol. 7 (2013): 198. doi: https://doi.org/10.3389/fncel.2013.00198
Parish CL, Thompson LH. Developing stem cell-based therapies for neural repair. Front Cell Neurosci. 2013 Nov 05;7:198. doi: 10.3389/fncel.2013.00198. eCollection 2013. PMID: 24204332; PMCID: PMC3817926.
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Nesfatin-1 and its effects on different systems.

Hippokratia

Ayada C, Toru Ü, Korkut Y.
PMID: 26435639
Hippokratia. 2015 Jan-Mar;19(1):4-10.

Nesfatin-1 is a peptide secreted by peripheral tissues, central and peripheral nervous system. It is involved in the regulation of energy homeostasis related with food regulation and water intake. Nesfatin-1 can pass through the blood-brain barrier in both directions....

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Ayada C, Toru Ü, Korkut Y. Nesfatin-1 and its effects on different systems. Hippokratia. 2015;19(1):4-10
Ayada, C., Toru, �. �., & Korkut, Y. (2015). Nesfatin-1 and its effects on different systems. Hippokratia, 19(1), 4-10.
Ayada, C, et al. "Nesfatin-1 and its effects on different systems." Hippokratia vol. 19,1 (2015): 4-10.
Ayada C, Toru Ü, Korkut Y. Nesfatin-1 and its effects on different systems. Hippokratia. 2015 Jan-Mar;19(1):4-10. PMID: 26435639; PMCID: PMC4574585.
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Altered neuronal markers following treatment with mood stabilizer and antipsychotic drugs indicate an increased likelihood of neurotransmitter release.

Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology

Scarr E, Dean B.
PMID: 23429852
Clin Psychopharmacol Neurosci. 2012 Apr;10(1):25-33. doi: 10.9758/cpn.2012.10.1.25. Epub 2012 Apr 30.

OBJECTIVE: Given the ability of mood stabilizers and antipsychotics to promote cell proliferation, we wanted to determine the effects of these drugs on neuronal markers previously reported to be altered in subjects with psychiatric disorders.METHODS: Male Sprauge-Dawley rats were...

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Scarr E, Dean B. Altered neuronal markers following treatment with mood stabilizer and antipsychotic drugs indicate an increased likelihood of neurotransmitter release. Clin Psychopharmacol Neurosci. 2012;10(1):25-33doi: 10.9758/cpn.2012.10.1.25.
Scarr, E., & Dean, B. (2012). Altered neuronal markers following treatment with mood stabilizer and antipsychotic drugs indicate an increased likelihood of neurotransmitter release. Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology, 10(1), 25-33. https://doi.org/10.9758/cpn.2012.10.1.25
Scarr, Elizabeth, and Dean, Brian. "Altered neuronal markers following treatment with mood stabilizer and antipsychotic drugs indicate an increased likelihood of neurotransmitter release." Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology vol. 10,1 (2012): 25-33. doi: https://doi.org/10.9758/cpn.2012.10.1.25
Scarr E, Dean B. Altered neuronal markers following treatment with mood stabilizer and antipsychotic drugs indicate an increased likelihood of neurotransmitter release. Clin Psychopharmacol Neurosci. 2012 Apr;10(1):25-33. doi: 10.9758/cpn.2012.10.1.25. Epub 2012 Apr 30. PMID: 23429852; PMCID: PMC3569157.
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Showing 1 to 5 of 5 entries