Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 12 of 83 entries
Sorted by: Best Match Show Resources per page
Nomen est Omen: do antidepressants increase p11 or S100A10?.

Journal of biomedical discovery and collaboration

Manev H, Manev R.
PMID: 16722532
J Biomed Discov Collab. 2006 Apr 13;1:5. doi: 10.1186/1747-5333-1-5.

Occasionally, multiple names are given to the same gene/protein. When this happens, different names can be used in subsequent publications, for example in different research areas, sometimes with little or no awareness that the same entity known under a...

Cite
Manev H, Manev R. Nomen est Omen: do antidepressants increase p11 or S100A10?. J Biomed Discov Collab. 2006;1:5doi: 10.1186/1747-5333-1-5.
Manev, H., & Manev, R. (2006). Nomen est Omen: do antidepressants increase p11 or S100A10?. Journal of biomedical discovery and collaboration, 15. https://doi.org/10.1186/1747-5333-1-5
Manev, Hari, and Manev, Radmila. "Nomen est Omen: do antidepressants increase p11 or S100A10?." Journal of biomedical discovery and collaboration vol. 1 (2006): 5. doi: https://doi.org/10.1186/1747-5333-1-5
Manev H, Manev R. Nomen est Omen: do antidepressants increase p11 or S100A10?. J Biomed Discov Collab. 2006 Apr 13;1:5. doi: 10.1186/1747-5333-1-5. PMID: 16722532; PMCID: PMC1481606.
Copy Download .nbib Format: NLM
"Prostate cancer proteomics" database.

Acta naturae

Shishkin SS, Kovalyov LI, Kovalyova MA, Lisitskaya KV, Eremina LS, Ivanov AV, Gerasimov EV, Sadykhov EG, Ulasova NY, Sokolova OS, Toropygin IY, Popov VO.
PMID: 22649669
Acta Naturae. 2010 Oct;2(4):95-104.

A database of Prostate Cancer Proteomics has been created by using the results of a proteomic study of human prostate carcinoma and benign hyperplasia tissues, and of some human-cultured cell lines (PCP, http://ef.inbi.ras.ru). PCP consists of 7 interrelated modules,...

Cite
Shishkin SS, Kovalyov LI, Kovalyova MA, et al. "Prostate cancer proteomics" database. Acta Naturae. 2010;2(4):95-104
Shishkin, S. S., Kovalyov, L. I., Kovalyova, M. A., Lisitskaya, K. V., Eremina, L. S., Ivanov, A. V., Gerasimov, E. V., Sadykhov, E. G., Ulasova, N. Y., Sokolova, O. S., Toropygin, I. Y., & Popov, V. O. (2010). "Prostate cancer proteomics" database. Acta naturae, 2(4), 95-104.
Shishkin, S S, et al. ""Prostate cancer proteomics" database." Acta naturae vol. 2,4 (2010): 95-104.
Shishkin SS, Kovalyov LI, Kovalyova MA, Lisitskaya KV, Eremina LS, Ivanov AV, Gerasimov EV, Sadykhov EG, Ulasova NY, Sokolova OS, Toropygin IY, Popov VO. "Prostate cancer proteomics" database. Acta Naturae. 2010 Oct;2(4):95-104. PMID: 22649669; PMCID: PMC3347584.
Copy Download .nbib Format: NLM
Pediatric Granular Cell Tumor of the Breast: An uncommon neoplasm in an uncommon site and age group.

Autopsy & case reports

Baishya P, Das J, Shangpliang D, Dey B, Marbaniang E, Lynser D, Khonglah Y, Raphael V.
PMID: 31372359
Autops Case Rep. 2019 Jul 12;9(3):e2019099. doi: 10.4322/acr.2019.099. eCollection 2019.

Granular cell tumor (GCT) is a rare soft tissue neoplasm of Schwann cell origin. Most cases occur in adults; however, the precise incidence is unknown in children. GCT is usually a slow-growing, painless tumor involving the skin and soft...

Cite
Baishya P, Das J, Shangpliang D, et al. Pediatric Granular Cell Tumor of the Breast: An uncommon neoplasm in an uncommon site and age group. Autops Case Rep. 2019;9(3):e2019099doi: 10.4322/acr.2019.099.
Baishya, P., Das, J., Shangpliang, D., Dey, B., Marbaniang, E., Lynser, D., Khonglah, Y., & Raphael, V. (2019). Pediatric Granular Cell Tumor of the Breast: An uncommon neoplasm in an uncommon site and age group. Autopsy & case reports, 9(3), e2019099. https://doi.org/10.4322/acr.2019.099
Baishya, Pakesh, et al. "Pediatric Granular Cell Tumor of the Breast: An uncommon neoplasm in an uncommon site and age group." Autopsy & case reports vol. 9,3 (2019): e2019099. doi: https://doi.org/10.4322/acr.2019.099
Baishya P, Das J, Shangpliang D, Dey B, Marbaniang E, Lynser D, Khonglah Y, Raphael V. Pediatric Granular Cell Tumor of the Breast: An uncommon neoplasm in an uncommon site and age group. Autops Case Rep. 2019 Jul 12;9(3):e2019099. doi: 10.4322/acr.2019.099. eCollection 2019. PMID: 31372359; PMCID: PMC6629270.
Copy Download .nbib Format: NLM
S100 Proteins As an Important Regulator of Macrophage Inflammation.

Frontiers in immunology

Xia C, Braunstein Z, Toomey AC, Zhong J, Rao X.
PMID: 29379499
Front Immunol. 2018 Jan 05;8:1908. doi: 10.3389/fimmu.2017.01908. eCollection 2017.

The S100 proteins, a family of calcium-binding cytosolic proteins, have a broad range of intracellular and extracellular functions through regulating calcium balance, cell apoptosis, migration, proliferation, differentiation, energy metabolism, and inflammation. The intracellular functions of S100 proteins involve interaction...

Cite
Xia C, Braunstein Z, Toomey AC, et al. S100 Proteins As an Important Regulator of Macrophage Inflammation. Front Immunol. 2018;8:1908doi: 10.3389/fimmu.2017.01908.
Xia, C., Braunstein, Z., Toomey, A. C., Zhong, J., & Rao, X. (2017). S100 Proteins As an Important Regulator of Macrophage Inflammation. Frontiers in immunology, 81908. https://doi.org/10.3389/fimmu.2017.01908
Xia, Chang, et al. "S100 Proteins As an Important Regulator of Macrophage Inflammation." Frontiers in immunology vol. 8 (2017): 1908. doi: https://doi.org/10.3389/fimmu.2017.01908
Xia C, Braunstein Z, Toomey AC, Zhong J, Rao X. S100 Proteins As an Important Regulator of Macrophage Inflammation. Front Immunol. 2018 Jan 05;8:1908. doi: 10.3389/fimmu.2017.01908. eCollection 2017. PMID: 29379499; PMCID: PMC5770888.
Copy Download .nbib Format: NLM
S100A12 and S100A8/9 proteins are biomarkers of articular disease activity in Blau syndrome.

Rheumatology (Oxford, England)

Wang L, Rosé CD, Foley KP, Anton J, Bader-Meunier B, Brissaud P, Chédeville G, Cimaz R, Fernández-Martín J, Guly C, Hachulla E, Harjacek M, Mackensen F, Merino R, Modesto C, Naranjo Hernández A, Pajot C, Ramanan AV, Thatayatikom A, Thomée C, Vastert S, Votta BJ, Bertin J, Wouters CH.
PMID: 29635517
Rheumatology (Oxford). 2018 Jul 01;57(7):1299-1304. doi: 10.1093/rheumatology/key090.

OBJECTIVE: To identify biomarkers of articular and ocular disease activity in patients with Blau syndrome (BS).METHODS: Multiplex plasma protein arrays were performed in five BS patients and eight normal healthy volunteers (NHVs). Plasma S100A12 and S100A8/9 were subsequently measured...

Cite
Wang L, Rosé CD, Foley KP, et al. S100A12 and S100A8/9 proteins are biomarkers of articular disease activity in Blau syndrome. Rheumatology (Oxford). 2018;57(7):1299-1304doi: 10.1093/rheumatology/key090.
Wang, L., Rosé, C. D., Foley, K. P., Anton, J., Bader-Meunier, B., Brissaud, P., Chédeville, G., Cimaz, R., Fernández-Martín, J., Guly, C., Hachulla, E., Harjacek, M., Mackensen, F., Merino, R., Modesto, C., Naranjo Hernández, A., Pajot, C., Ramanan, A. V., Thatayatikom, A., Thomée, C., Vastert, S., Votta, B. J., Bertin, J., & Wouters, C. H. (2018). S100A12 and S100A8/9 proteins are biomarkers of articular disease activity in Blau syndrome. Rheumatology (Oxford, England), 57(7), 1299-1304. https://doi.org/10.1093/rheumatology/key090
Wang, Lin, et al. "S100A12 and S100A8/9 proteins are biomarkers of articular disease activity in Blau syndrome." Rheumatology (Oxford, England) vol. 57,7 (2018): 1299-1304. doi: https://doi.org/10.1093/rheumatology/key090
Wang L, Rosé CD, Foley KP, Anton J, Bader-Meunier B, Brissaud P, Chédeville G, Cimaz R, Fernández-Martín J, Guly C, Hachulla E, Harjacek M, Mackensen F, Merino R, Modesto C, Naranjo Hernández A, Pajot C, Ramanan AV, Thatayatikom A, Thomée C, Vastert S, Votta BJ, Bertin J, Wouters CH. S100A12 and S100A8/9 proteins are biomarkers of articular disease activity in Blau syndrome. Rheumatology (Oxford). 2018 Jul 01;57(7):1299-1304. doi: 10.1093/rheumatology/key090. PMID: 29635517.
Copy Download .nbib Format: NLM
S100 proteins as therapeutic targets.

Biophysical reviews

Bresnick AR.
PMID: 30382555
Biophys Rev. 2018 Dec;10(6):1617-1629. doi: 10.1007/s12551-018-0471-y. Epub 2018 Oct 31.

The human genome codes for 21 S100 protein family members, which exhibit cell- and tissue-specific expression patterns. Despite sharing a high degree of sequence and structural similarity, the S100 proteins bind a diverse range of protein targets and contribute...

Cite
Bresnick AR. S100 proteins as therapeutic targets. Biophys Rev. 2018;10(6):1617-1629doi: 10.1007/s12551-018-0471-y.
Bresnick, A. R. (2018). S100 proteins as therapeutic targets. Biophysical reviews, 10(6), 1617-1629. https://doi.org/10.1007/s12551-018-0471-y
Bresnick, Anne R. "S100 proteins as therapeutic targets." Biophysical reviews vol. 10,6 (2018): 1617-1629. doi: https://doi.org/10.1007/s12551-018-0471-y
Bresnick AR. S100 proteins as therapeutic targets. Biophys Rev. 2018 Dec;10(6):1617-1629. doi: 10.1007/s12551-018-0471-y. Epub 2018 Oct 31. PMID: 30382555; PMCID: PMC6297089.
Copy Download .nbib Format: NLM
Epigenetic regulation of S100 protein expression.

Clinical epigenetics

Leśniak W.
PMID: 21949546
Clin Epigenetics. 2011 Aug;2(2):77-83. doi: 10.1007/s13148-011-0023-9. Epub 2011 Feb 22.

S100 proteins are small, calcium-binding proteins whose genes are localized in a cluster on human chromosome 1. Through their ability to interact with various protein partners in a calcium-dependent manner, the S100 proteins exert their influence on many vital...

Cite
Leśniak W. Epigenetic regulation of S100 protein expression. Clin Epigenetics. 2011;2(2):77-83doi: 10.1007/s13148-011-0023-9.
Leśniak, W. (2011). Epigenetic regulation of S100 protein expression. Clinical epigenetics, 2(2), 77-83. https://doi.org/10.1007/s13148-011-0023-9
Leśniak, Wiesława. "Epigenetic regulation of S100 protein expression." Clinical epigenetics vol. 2,2 (2011): 77-83. doi: https://doi.org/10.1007/s13148-011-0023-9
Leśniak W. Epigenetic regulation of S100 protein expression. Clin Epigenetics. 2011 Aug;2(2):77-83. doi: 10.1007/s13148-011-0023-9. Epub 2011 Feb 22. PMID: 21949546; PMCID: PMC3156319.
Copy Download .nbib Format: NLM
Toll-Like Receptors, Associated Biochemical Signaling Networks, and S100 Ligands.

Shock (Augusta, Ga.)

Gupta S, Tsoporis JN, Jia SH, Dos Santos CC, Parker TG, Marshall JC.
PMID: 33350801
Shock. 2021 Aug 01;56(2):167-177. doi: 10.1097/SHK.0000000000001704.

ABSTRACT: Host cells recognize molecules that signal danger using pattern recognition receptors (PRRs). Toll-like receptors (TLRs) are the most studied class of PRRs and detect pathogen-associated molecular patterns and danger-associated molecular patterns. Cellular TLR activation and signal transduction can...

Cite
Gupta S, Tsoporis JN, Jia SH, et al. Toll-Like Receptors, Associated Biochemical Signaling Networks, and S100 Ligands. Shock. 2021;56(2):167-177doi: 10.1097/SHK.0000000000001704.
Gupta, S., Tsoporis, J. N., Jia, S. H., Dos Santos, C. C., Parker, T. G., & Marshall, J. C. (2021). Toll-Like Receptors, Associated Biochemical Signaling Networks, and S100 Ligands. Shock (Augusta, Ga.), 56(2), 167-177. https://doi.org/10.1097/SHK.0000000000001704
Gupta, Sahil, et al. "Toll-Like Receptors, Associated Biochemical Signaling Networks, and S100 Ligands." Shock (Augusta, Ga.) vol. 56,2 (2021): 167-177. doi: https://doi.org/10.1097/SHK.0000000000001704
Gupta S, Tsoporis JN, Jia SH, Dos Santos CC, Parker TG, Marshall JC. Toll-Like Receptors, Associated Biochemical Signaling Networks, and S100 Ligands. Shock. 2021 Aug 01;56(2):167-177. doi: 10.1097/SHK.0000000000001704. PMID: 33350801.
Copy Download .nbib Format: NLM
Trichohyalin-like 1 protein plays a crucial role in proliferation and anti-apoptosis of normal human keratinocytes and squamous cell carcinoma cells.

Cell death discovery

Makino T, Mizawa M, Yoshihisa Y, Yamamoto S, Tabuchi Y, Miyai M, Hibino T, Sasahara M, Shimizu T.
PMID: 33133644
Cell Death Discov. 2020 Oct 27;6:109. doi: 10.1038/s41420-020-00344-5. eCollection 2020.

Epidermal differentiation is a complex process that requires the regulated and sequential expression of various genes. Most fused-type S100 proteins are expressed in the granular layer and it is hypothesized that these proteins may be associated with cornification and...

Cite
Makino T, Mizawa M, Yoshihisa Y, et al. Trichohyalin-like 1 protein plays a crucial role in proliferation and anti-apoptosis of normal human keratinocytes and squamous cell carcinoma cells. Cell Death Discov. 2020;6:109doi: 10.1038/s41420-020-00344-5.
Makino, T., Mizawa, M., Yoshihisa, Y., Yamamoto, S., Tabuchi, Y., Miyai, M., Hibino, T., Sasahara, M., & Shimizu, T. (2020). Trichohyalin-like 1 protein plays a crucial role in proliferation and anti-apoptosis of normal human keratinocytes and squamous cell carcinoma cells. Cell death discovery, 6109. https://doi.org/10.1038/s41420-020-00344-5
Makino, Teruhiko, et al. "Trichohyalin-like 1 protein plays a crucial role in proliferation and anti-apoptosis of normal human keratinocytes and squamous cell carcinoma cells." Cell death discovery vol. 6 (2020): 109. doi: https://doi.org/10.1038/s41420-020-00344-5
Makino T, Mizawa M, Yoshihisa Y, Yamamoto S, Tabuchi Y, Miyai M, Hibino T, Sasahara M, Shimizu T. Trichohyalin-like 1 protein plays a crucial role in proliferation and anti-apoptosis of normal human keratinocytes and squamous cell carcinoma cells. Cell Death Discov. 2020 Oct 27;6:109. doi: 10.1038/s41420-020-00344-5. eCollection 2020. PMID: 33133644; PMCID: PMC7591909.
Copy Download .nbib Format: NLM
Specific cytokines of interleukin-6 family interact with S100 proteins.

Cell calcium

Kazakov AS, Sokolov AS, Permyakova ME, Litus EA, Uversky VN, Permyakov EA, Permyakov SE.
PMID: 34933172
Cell Calcium. 2021 Dec 14;101:102520. doi: 10.1016/j.ceca.2021.102520. Epub 2021 Dec 14.

Cytokines of interleukin-6 (IL-6) family are important signaling proteins involved in various physiological and pathological processes. Earlier, we described interactions between IL-11 and S100P/B proteins from the family of S100 proteins engaged in the pathogenesis of numerous diseases. We...

Cite
Kazakov AS, Sokolov AS, Permyakova ME, et al. Specific cytokines of interleukin-6 family interact with S100 proteins. Cell Calcium. 2021;101:102520doi: 10.1016/j.ceca.2021.102520.
Kazakov, A. S., Sokolov, A. S., Permyakova, M. E., Litus, E. A., Uversky, V. N., Permyakov, E. A., & Permyakov, S. E. (2021). Specific cytokines of interleukin-6 family interact with S100 proteins. Cell calcium, 101102520. https://doi.org/10.1016/j.ceca.2021.102520
Kazakov, Alexey S, et al. "Specific cytokines of interleukin-6 family interact with S100 proteins." Cell calcium vol. 101 (2021): 102520. doi: https://doi.org/10.1016/j.ceca.2021.102520
Kazakov AS, Sokolov AS, Permyakova ME, Litus EA, Uversky VN, Permyakov EA, Permyakov SE. Specific cytokines of interleukin-6 family interact with S100 proteins. Cell Calcium. 2021 Dec 14;101:102520. doi: 10.1016/j.ceca.2021.102520. Epub 2021 Dec 14. PMID: 34933172.
Copy Download .nbib Format: NLM
Early transcriptional changes after UVB treatment in atopic dermatitis include inverse regulation of IL-36γ and IL-37.

Experimental dermatology

Lossius AH, Berents TL, Saetre F, Nilsen HR, Bradley M, Asad S, Haraldsen G, Sundnes O, Holm JØ.
PMID: 33067891
Exp Dermatol. 2021 Feb;30(2):249-261. doi: 10.1111/exd.14217. Epub 2020 Nov 02.

Phototherapy with narrow-band Ultraviolet B (nb-UVB) is a major therapeutic option in atopic dermatitis (AD), yet knowledge of the early molecular responses to this treatment is lacking. The objective of this study was to map the early transcriptional changes...

Cite
Lossius AH, Berents TL, Saetre F, et al. Early transcriptional changes after UVB treatment in atopic dermatitis include inverse regulation of IL-36γ and IL-37. Exp Dermatol. 2020;30(2):249-261doi: 10.1111/exd.14217.
Lossius, A. H., Berents, T. L., Saetre, F., Nilsen, H. R., Bradley, M., Asad, S., Haraldsen, G., Sundnes, O., & Holm, J. �. �. (2021). Early transcriptional changes after UVB treatment in atopic dermatitis include inverse regulation of IL-36γ and IL-37. Experimental dermatology, 30(2), 249-261. https://doi.org/10.1111/exd.14217
Lossius, Astrid H, et al. "Early transcriptional changes after UVB treatment in atopic dermatitis include inverse regulation of IL-36γ and IL-37." Experimental dermatology vol. 30,2 (2021): 249-261. doi: https://doi.org/10.1111/exd.14217
Lossius AH, Berents TL, Saetre F, Nilsen HR, Bradley M, Asad S, Haraldsen G, Sundnes O, Holm JØ. Early transcriptional changes after UVB treatment in atopic dermatitis include inverse regulation of IL-36γ and IL-37. Exp Dermatol. 2021 Feb;30(2):249-261. doi: 10.1111/exd.14217. Epub 2020 Nov 02. PMID: 33067891.
Copy Download .nbib Format: NLM
The contribution of postnatal steroid administration to early brain damage in preterm babies with bronchopulmonary dysplasia.

Turkish journal of medical sciences

Ertuğrul S, Darakci SM, Kaplan İ, Yolbaş İ, Deger İ, Tanrıverdi Yilmaz S, Aktaş Ş.
PMID: 33819976
Turk J Med Sci. 2021 Aug 30;51(4):1917-1923. doi: 10.3906/sag-2101-295.

BACKGROUND/AIM: Postnatal corticosteroids are commonly used to treat bronchopulmonary dysplasia (BPD). We aimed to show whether S100 calcium-binding B (S100B), neuron-specific enolase (NSE), Tau protein or microtubule-associated protein tau (MAPT), and glial fibrillary acid protein (GFAP) levels would provide...

Cite
Ertuğrul S, Darakci SM, Kaplan İ, et al. The contribution of postnatal steroid administration to early brain damage in preterm babies with bronchopulmonary dysplasia. Turk J Med Sci. 2021;51(4):1917-1923doi: 10.3906/sag-2101-295.
Ertuğrul, S., Darakci, S. M., Kaplan, �. �., Yolbaş, �. �., Deger, �. �., Tanrıverdi Yilmaz, S., & Aktaş, �. �. (2021). The contribution of postnatal steroid administration to early brain damage in preterm babies with bronchopulmonary dysplasia. Turkish journal of medical sciences, 51(4), 1917-1923. https://doi.org/10.3906/sag-2101-295
Ertuğrul, Sabahattin, et al. "The contribution of postnatal steroid administration to early brain damage in preterm babies with bronchopulmonary dysplasia." Turkish journal of medical sciences vol. 51,4 (2021): 1917-1923. doi: https://doi.org/10.3906/sag-2101-295
Ertuğrul S, Darakci SM, Kaplan İ, Yolbaş İ, Deger İ, Tanrıverdi Yilmaz S, Aktaş Ş. The contribution of postnatal steroid administration to early brain damage in preterm babies with bronchopulmonary dysplasia. Turk J Med Sci. 2021 Aug 30;51(4):1917-1923. doi: 10.3906/sag-2101-295. PMID: 33819976; PMCID: PMC8569755.
Copy Download .nbib Format: NLM
Showing 1 to 12 of 83 entries