Gotowe bibliografie tematyczne / S100A12

Spis treści

  1. Artykuły w czasopismach
  2. Rozprawy doktorskie
  3. Książki
  4. Części książek
  5. Streszczenia konferencji
  6. Raporty organizacyjne

Gotowa bibliografia na temat „S100A12”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 1 lutego 2022

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Artykuły w czasopismach na temat "S100A12"

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Broome, Ann-Marie, David Ryan, and Richard L. Eckert. "S100 Protein Subcellular Localization During Epidermal Differentiation and Psoriasis." Journal of Histochemistry & Cytochemistry 51, no. 5 (May 2003): 675–85. http://dx.doi.org/10.1177/002215540305100513.

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S100 proteins are calcium-activated signaling proteins that interact with target proteins to modulate biological processes. Our present studies compare the level of expression, and cellular localization of S100A7, S100A8, S100A9, S100A10, and S100A11 in normal and psoriatic epidermis. S100A7 and S100A11 are present in the basal and spinous layers in normal epidermis. These proteins appear in the nucleus and cytoplasm in basal cells but are associated with the plasma membrane in spinous cells. S100A10 is present in basal and spinous cells, in the cytoplasm, and is associated with the plasma mem
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McLachlan, Julia L., Alastair J. Sloan, Anthony J. Smith, Gabriel Landini, and Paul R. Cooper. "S100 and Cytokine Expression in Caries." Infection and Immunity 72, no. 7 (July 2004): 4102–8. http://dx.doi.org/10.1128/iai.72.7.4102-4108.2004.

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ABSTRACT The molecular immune response of the pulpal tissue during chronic carious infection is poorly characterized. Our objective was to examine the expression of potential molecular mediators of pulpal inflammation, correlate their levels with disease severity, and determine the cellular localization of key molecules. Results indicated that there was significantly increased transcriptional activity in carious compared to healthy pulp, and the increase correlated positively with disease severity. Semiquantitative reverse transcriptase PCR analysis in 10 carious and 10 healthy pulpal tissue s
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Leach, Steven T., Hazel M. Mitchell, Carolyn L. Geczy, Philip M. Sherman, and Andrew S. Day. "S100 Calgranulin Proteins S100A8, S100A9 and S100A12 are Expressed in the Inflamed Gastric Mucosa ofHelicobacter Pylori-Infected Children." Canadian Journal of Gastroenterology 22, no. 5 (2008): 461–64. http://dx.doi.org/10.1155/2008/308942.

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The expression of the inflammatory S100 calgranulin proteins (S100A8, S100A9 and S100A12) in normal andHelicobacter pylori-infected gastric mucosa of children were examined. S100A8, S100A9 and S100A12, which were virtually absent in normal gastric mucosa, were highly expressed inH pylori-infected mucosa. This expression correlated with the severity of gastritis (r=0.9422, P<0.05). S100 calgranulins may be involved in bacterial-induced gastritis and may limit bacterial growth.
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Tardif, Mélanie R., Julie Andrea Chapeton-Montes, Alma Posvandzic, Nathalie Pagé, Caroline Gilbert, and Philippe A. Tessier. "Secretion of S100A8, S100A9, and S100A12 by Neutrophils Involves Reactive Oxygen Species and Potassium Efflux." Journal of Immunology Research 2015 (2015): 1–16. http://dx.doi.org/10.1155/2015/296149.

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S100A8/A9 (calprotectin) and S100A12 proinflammatory mediators are found at inflammatory sites and in the serum of patients with inflammatory or autoimmune diseases. These cytoplasmic proteins are secreted by neutrophils at sites of inflammation via alternative secretion pathways of which little is known. This study examined the nature of the stimuli leading to S100A8/A9 and S100A12 secretion as well as the mechanism involved in this alternative secretion pathway. Chemotactic agents, cytokines, and particulate molecules were used to stimulate human neutrophils. MSU crystals, PMA, and H2O2induc
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SHISHIBORI, Tsuyoshi, Yuhta OYAMA, Osamu MATSUSHITA, Kayoko YAMASHITA, Hiromi FURUICHI, Akinobu OKABE, Hajime MAETA, Yuiro HATA, and Ryoji KOBAYASHI. "Three distinct anti-allergic drugs, amlexanox, cromolyn and tranilast, bind to S100A12 and S100A13 of the S100 protein family." Biochemical Journal 338, no. 3 (March 8, 1999): 583–89. http://dx.doi.org/10.1042/bj3380583.

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To investigate the roles of calcium-binding proteins in degranulation, we used three anti-allergic drugs, amlexanox, cromolyn and tranilast, which inhibit IgE-mediated degranulation of mast cells, as molecular probes in affinity chromatography. All of these drugs, which have different structures but similar function, scarcely bound to calmodulin in bovine lung extract, but bound to the same kinds of calcium-binding proteins, such as the 10-kDa proteins isolated in this study, calcyphosine and annexins I–V. The 10-kDa proteins obtained on three drug-coupled resins and on phenyl-Sepharose were a
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BASIKA, TATIANA, NATALIA MUÑOZ, CECILIA CASARAVILLA, FLORENCIA IRIGOÍN, CARLOS BATTHYÁNY, MARIANA BONILLA, GUSTAVO SALINAS, et al. "Phagocyte-specific S100 proteins in the local response to theEchinococcus granulosuslarva." Parasitology 139, no. 2 (January 5, 2012): 271–83. http://dx.doi.org/10.1017/s003118201100179x.

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SUMMARYInfection by larvalEchinococcus granulosusis usually characterized by tight inflammatory control. However, various degrees of chronic granulomatous inflammation are also observed, reaching a high point in infection of cattle by the most prevalent parasite strain worldwide, which is not well adapted to this host species. In this context, epithelioid and multinucleated giant macrophages surround the parasite, and the secreted products of these cells often associate with the larval wall. The phagocyte-specific S100 proteins, S100A8, S100A9 and S100A12, are important non-conventionally secr
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Zeng, Meng-Lu, Xian-Jin Zhu, Jin Liu, Peng-Chong Shi, Yan-Li Kang, Zhen Lin, and Ying-Ping Cao. "An Integrated Bioinformatic Analysis of the S100 Gene Family for the Prognosis of Colorectal Cancer." BioMed Research International 2020 (November 26, 2020): 1–15. http://dx.doi.org/10.1155/2020/4746929.

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Background. S100 family genes exclusively encode at least 20 calcium-binding proteins, which possess a wide spectrum of intracellular and extracellular functions in vertebrates. Multiple lines of evidences suggest that dysregulated S100 proteins are associated with human malignancies including colorectal cancer (CRC). However, the diverse expression patterns and prognostic roles of distinct S100 genes in CRC have not been fully elucidated. Methods. In the current study, we analyzed the mRNA expression levels of S100 family genes and proteins and their associations with the survival of CRC pati
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Thames, Brittany E., James W. Barr, Jan S. Suchodolski, Jörg M. Steiner, and Romy M. Heilmann. "Prospective evaluation of S100A12 and S100A8/A9 (calprotectin) in dogs with sepsis or the systemic inflammatory response syndrome." Journal of Veterinary Diagnostic Investigation 31, no. 4 (June 6, 2019): 645–51. http://dx.doi.org/10.1177/1040638719856655.

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Pattern recognition receptors (e.g., S100A12 or S100A8/A9) hold promise as inflammatory biomarkers. We prospectively determined and compared serum S100A12 and S100A8/A9 concentrations in dogs with sepsis ( n = 11) or systemic inflammatory response syndrome (SIRS; n = 8) over a 3-d period with each other, healthy controls ( n = 50), and other clinical and clinicopathologic variables. Serum S100A12 and S100A8/A9 concentrations were significantly higher in dogs with sepsis or SIRS (all p < 0.05) at the time of hospital admission (day 1) compared to healthy controls, with no differences between
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Peterova, Eva, Jan Bures, Paula Moravkova, and Darina Kohoutova. "Tissue mRNA for S100A4, S100A6, S100A8, S100A9, S100A11 and S100P Proteins in Colorectal Neoplasia: A Pilot Study." Molecules 26, no. 2 (January 14, 2021): 402. http://dx.doi.org/10.3390/molecules26020402.

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S100 proteins are involved in the pathogenesis of sporadic colorectal carcinoma through different mechanisms. The aim of our study was to assess tissue mRNA encoding S100 proteins in patients with non-advanced and advanced colorectal adenoma. Mucosal biopsies were taken from the caecum, transverse colon and rectum during diagnostic and/or therapeutic colonoscopy. Another biopsy was obtained from adenomatous tissue in the advanced adenoma group. The tissue mRNA for each S100 protein (S100A4, S100A6, S100A8, S100A9, S100A11 and S100P) was investigated. Eighteen biopsies were obtained from the he
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Åberg, Anna-Maja, Sofia Halin Bergström, Elin Thysell, Lee-Ann Tjon-Kon-Fat, Jonas A. Nilsson, Anders Widmark, Camilla Thellenberg-Karlsson, Anders Bergh, Pernilla Wikström, and Marie Lundholm. "High Monocyte Count and Expression of S100A9 and S100A12 in Peripheral Blood Mononuclear Cells Are Associated with Poor Outcome in Patients with Metastatic Prostate Cancer." Cancers 13, no. 10 (May 17, 2021): 2424. http://dx.doi.org/10.3390/cancers13102424.

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Increasing evidence indicates calcium-binding S100 protein involvement in inflammation and tumor progression. In this prospective study, we evaluated the mRNA levels of two members of this family, S100A9 and S100A12, in peripheral blood mononuclear cells (PBMCs) in a cohort of 121 prostate cancer patients using RT-PCR. Furthermore, monocyte count was determined by flow cytometry. By stratifying patients into different risk groups, according to TNM stage, Gleason score and PSA concentration at diagnosis, expression of S100A9 and S100A12 was found to be significantly higher in patients with meta
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Rozprawy doktorskie na temat "S100A12"

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Goyette, Jesse Davis Medical Sciences Faculty of Medicine UNSW. "The extracellular functions of S100A12." Publisher:University of New South Wales. Medical Sciences, 2008. http://handle.unsw.edu.au/1959.4/41302.

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The S100s comprise a group of Ca2+-binding proteins of the EF-hand superfamily with varied functions. Within this family, three inflammatory-related proteins - S100A8, S100A9 and S100A12 - form a subcluster known as the 'calgranulins'. S100A12 levels are elevated in sera from patients with inflammatory diseases, such as rheumatoid arthritis and inflammatory bowel disease. S100A12 is constitutively expressed in neutrophils and induced in monocytes by LPS and TNFα, and in macrophages by IL-6. S100A12 is a potent monocyte and mast cell chemoattractant and its potentiation of mast cell activation
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Moroz, Olga. "Structural studies on human S100A12." Thesis, University of York, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.403963.

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Chapeton, Montes Julie Andrea. "Caractérisation des voies alternatives de sécrétion des protéines S100A8/A9 et S100A12 par les neutrophiles humains." Master's thesis, Université Laval, 2015. http://hdl.handle.net/20.500.11794/26156.

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Bien que les protéines S100A8/A9 et S100A12 exprimées par les neutrophiles ne possèdent pas de peptide signal, elles sont retrouvées dans le sérum de patients souffrant de diverses maladies inflammatoires. Les mécanismes de sécrétion de ces protéines demeurent peu connus ainsi que les agonistes qui favorisent leur sécrétion. Nous avons donc émis l´hypothèse que plusieurs voies de sécrétion alternative ainsi que plusieurs agonistes des neutrophiles pourraient participer à la libération de ces protéines. Dans un premier temps, nous avons étudié les stimuli capables de provoquer la sécrétion de l
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Mossel, Dieuwertje Marije [Verfasser], and Julia [Akademischer Betreuer] Kzhyshkowska. "Epigenetic regulation of S100A9 and S100A12 expression in monocytes-macrophage system in hyperglycemic conditions / Dieuwertje Marije Mossel ; Betreuer: Julia Kzhyshkowska." Heidelberg : Universitätsbibliothek Heidelberg, 2020. http://d-nb.info/1219303100/34.

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Mossel, Dieuwertje M. [Verfasser], and Julia [Akademischer Betreuer] Kzhyshkowska. "Epigenetic regulation of S100A9 and S100A12 expression in monocytes-macrophage system in hyperglycemic conditions / Dieuwertje Marije Mossel ; Betreuer: Julia Kzhyshkowska." Heidelberg : Universitätsbibliothek Heidelberg, 2020. http://d-nb.info/1219303100/34.

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Dubois, Christelle. "Confirmation de biomarqueurs pour le pronostic du sepsis et développement de tests rapides High plasma level of S100A8/S100A9 and S100A12 at admission indicates a higher risk of death in septic shock patients Top-down and bottom-up proteomics of circulating S100A8/S100A9 complexes in plasma of septic shock patients." Thesis, Université Paris-Saclay (ComUE), 2019. http://www.theses.fr/2019SACLS521.

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Le sepsis est la 3eme cause de mortalité dans les pays occidentaux, avec un taux de mortalité entre 20 et 50% selon la sévérité. La « prédiction » du devenir clinique du patient est essentielle pour établir le traitement le plus adéquat. Quelques protéines marqueurs de l'inflammation ou d'une infection (CRP, procalcitonine) sont citées pour le suivi des patients en clinique mais manquent de spécificité pour le sepsis. D'autre part, les études « omiques » ont permis de générer des listes de biomarqueurs potentiels du pronostic vital du sepsis. En revanche, aucun n'a encore été validé et/ou conf
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Citadini, Ana Paula da Silva. "Estudos da dinâmica estrutural da proteína ligante de cálcio S100A12 humana e da lisozima T4." Universidade de São Paulo, 2011. http://www.teses.usp.br/teses/disponiveis/76/76132/tde-05072011-134514/.

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O trabalho ora apresentado foi concebido como tendo dois objetivos. O primeiro, mais geral, foi implementar uma nova metodologia para o estudo de mudanças conformacionais em proteínas, ou seja, de sua dinâmica estrutural. A técnica de marcação de spin sítio dirigida aliada à ressonância paramagnética eletrônica (SDSL-RPE) são os pilares desse novo método que faz, agora, parte do conjunto de técnicas disponíveis no Grupo de Biofísica Molecular Sérgio Mascarenhas do Instituto de Física de São Carlos (USP). O segundo objetivo, mais específico, representou o caminho efetivamente tomado para que se
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Reis, Renata Almeida Garcia. "Estudo dinâmico conformacional da proteína calgranulina C (S100A12) mediante interação com íons e receptor RAGE." Universidade de São Paulo, 2012. http://www.teses.usp.br/teses/disponiveis/60/60136/tde-03072012-163222/.

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Calgranulina C (S100A12) é membro da família das proteínas S100 \"EF-hands\" que complexam cálcio. A S100A12 humana é expressa predominantemente por granulócitos e é superexpressa em compartimentos inflamatórios. Níveis séricos elevados de S100A12 são encontrados em pacientes acometidos por distúrbios inflamatórios, neurodegenerativos, metabólicos e neoplasias. A S100A12 intracelular existe como um homodímero anti-paralelo. Cada monômero é composto por um \"EF-hand\" clássico, C-terminal (HI - LI - HII), e um \"EF-hand\" N-terminal, o pseudo \"EF-hand\" (HIII - LIII - HIV). Os \"motifs\" são c
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Augner, Kerstin Verfasser], and Monika [Akademischer Betreuer] [Pischetsrieder. "Auswirkung nicht-enzymatischer posttranslationaler Modifikationen auf Konstitution, Oligomerisierung und Biofunktionalität von S100A12 / Kerstin Augner. Gutachter: Monika Pischetsrieder." Erlangen : Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 2013. http://d-nb.info/1054164886/34.

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Garcia, Assuero Faria. "Estudo da estabilidade estrutural de uma proteína recombinante ligante de zinco e cálcio - Calgranulina C (S100A12) porcina." Universidade de São Paulo, 2007. http://www.teses.usp.br/teses/disponiveis/76/76132/tde-30042007-141038/.

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S100A12 porcina é um membro da família das proteínas S100, um grupo de pequenas proteínas ligantes de cálcio caracterizado pela presença de dois motivos “EF-hand”. Estas proteínas estão envolvidas em diversos eventos celulares, como a regulação da fosforilação protéica, atividade enzimática, tamponamento de Ca+2, processos inflamatórios e a polimerização de filamentos intermediários. Adicionalmente, algumas dessas proteínas podem ligar Zn+2, o qual pode afetar a ligação do íon Ca+2, particularmente para as proteínas S100. Neste trabalho, a seqüência gênica que codifica a proteína S100A12 porci
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Książki na temat "S100A12"

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Tirkos, Sam. Investigation of S100A8 and S100A9 as potential genetic modifiers of the pulmonary phenotype in cystic fibrosis mice. Ottawa: National Library of Canada, 2003.

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Merklinger, Sandra Lea. Progression and regression of pulmonary vascular disease related to smooth muscle cell apoptosis, S100A4/Mts1 and fibulin-5. 2005.

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Części książek na temat "S100A12"

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Gressner, A. M., and O. A. Gressner. "S100A12-Protein." In Springer Reference Medizin, 2097. Berlin, Heidelberg: Springer Berlin Heidelberg, 2019. http://dx.doi.org/10.1007/978-3-662-48986-4_2726.

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Gressner, A. M., and O. A. Gressner. "S100A12-Protein." In Lexikon der Medizinischen Laboratoriumsdiagnostik, 1. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49054-9_2726-1.

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Leach, Steven T., and Andrew S. Day. "Enzyme-Linked Immunosorbent Assay to Measure S100A12 in Fecal Samples of Children and Adults." In Methods in Molecular Biology, 755–61. New York, NY: Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9030-6_47.

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Prudovsky, Igor, Thallapuranam Krishnaswamy Suresh Kumar, and Rosario Donato. "S100a13." In Encyclopedia of Signaling Molecules, 4801–4. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-67199-4_101530.

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Prudovsky, Igor, Thallapuranam Krishnaswamy Suresh Kumar, and Rosario Donato. "S100a13." In Encyclopedia of Signaling Molecules, 1–4. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4614-6438-9_101530-1.

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Donato, Rosario, Guglielmo Sorci, and Ileana Giambanco. "S100A6." In Encyclopedia of Signaling Molecules, 4805–13. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-67199-4_101531.

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Donato, Rosario, Guglielmo Sorci, and Ileana Giambanco. "S100A6." In Encyclopedia of Signaling Molecules, 1–10. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4614-6438-9_101531-1.

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Foertsch, Franziska, and Christian Melle. "Analysis of S100A11 in DNA Damage Repair." In Methods in Molecular Biology, 447–60. New York, NY: Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9030-6_28.

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Most, Patrick, Philip Raake, Christophe Weber, Hugo A. Katus, and Sven T. Pleger. "S100A1 Gene Therapy in Small and Large Animals." In Methods in Molecular Biology, 407–20. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-62703-230-8_25.

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Sreejit, Gopalkrishna, Sunil Kiran Nooti, Baskaran Athmanathan, and Prabhakara Reddy Nagareddy. "S100A8/A9 in Myocardial Infarction." In Methods in Molecular Biology, 739–54. New York, NY: Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9030-6_46.

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Streszczenia konferencji na temat "S100A12"

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Kim, Hye Jeong, Karam Kim, Jin Hyun Kang, and Il Yup Chung. "Role of NLRP3 inflammasome and ATP in S100A12-induced MUC5AC production in airway epithelial cells." In ERS International Congress 2018 abstracts. European Respiratory Society, 2018. http://dx.doi.org/10.1183/13993003.congress-2018.pa2185.

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Orczyk, K., and E. Smolewska. "THU0585 Personalised treatment in juvenile idiopathic arthritis – future or fiction? preliminary results of using s100a8a9, s100a12 and vascular endothelial cadherin as diagnostic and prognostic biomarkers." In Annual European Congress of Rheumatology, EULAR 2018, Amsterdam, 13–16 June 2018. BMJ Publishing Group Ltd and European League Against Rheumatism, 2018. http://dx.doi.org/10.1136/annrheumdis-2018-eular.2440.

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Gunaldi, M., Y. Okuturlar, A. Üstüngüler, C. Akarsu, and A. Kural. "Abstract P4-04-23: Clinical importance of S100A9 and S100A2 in breast cancer." In Abstracts: Thirty-Eighth Annual CTRC-AACR San Antonio Breast Cancer Symposium; December 8-12, 2015; San Antonio, TX. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.sabcs15-p4-04-23.

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Katono, Ken, Yuichi Sato, Shinichiro Ryuge, Ryo Nagashio, Masanori Yokoba, Masato Katagiri, Kazu Shiomi, Yukitoshi Satoh, and Noriyuki Masuda. "Co-expression of S100A14 and S100A16 is a predictive marker for platinum-based adjuvant chemotherapy in resected lung adenocarcinomas." In ERS International Congress 2016 abstracts. European Respiratory Society, 2016. http://dx.doi.org/10.1183/13993003.congress-2016.oa3339.

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Crowe, L. A. N., M. Akbar, K. Patommel, S. M. Kitson, E. Garcia Melchor, D. S. Gilchrist, G. A. Murrell, I. B. McInnes, and N. L. Millar. "AB0068 Alarmins s100a8 and s100a9 modulate the inflammatory microenvironment in early tendinopathy." In Annual European Congress of Rheumatology, EULAR 2018, Amsterdam, 13–16 June 2018. BMJ Publishing Group Ltd and European League Against Rheumatism, 2018. http://dx.doi.org/10.1136/annrheumdis-2018-eular.7019.

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Lee, Eunmi, Maria Ouzounova, Raziye Piranlioglu, Abdeljabar El Andaloussi, Sena Arbag, Gang Zhou, and Hasan Korkaya. "Abstract 2956: Chemical library screen identifies compounds that target S100A8/S100A9 complex and MDSC accumulation." In Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-2956.

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Ghavami, Saeid, Thomas Vogl, Johannes Roth, Helmut Unruh, and Andrew J. Halayko. "S100A8 And S100A9 Homo-, And Hetero-Dimers Affect Extracellular Matrix In Human Smooth Muscle With Different Down Stream Signalling." In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a6682.

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Gemicioglu, Bilun, Ozgur Yasar, and Tulay Akcay. "Significance of serum YKL-40, S100A8, S100A9, calprotectin, periostin and LRG1 levels in patients with newly diagnosed, controlled and uncontrolled asthma." In ERS International Congress 2018 abstracts. European Respiratory Society, 2018. http://dx.doi.org/10.1183/13993003.congress-2018.pa2023.

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Bou Khzam, Lara, Katherine Hajjar, and Nasrin Mesaeli. "Hyperglycemia Regulates Annexin A2-s100a10 Localization In Endothelial Cells." In Qatar Foundation Annual Research Conference Proceedings. Hamad bin Khalifa University Press (HBKU Press), 2014. http://dx.doi.org/10.5339/qfarc.2014.hbpp0712.

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Chiu, David Kung-Chun, Carmen Chak-Lui Wong, Irene Oi-Lin Ng, and Aki Pui-Wah Tse. "Abstract 533: S100A10 as a novel biomarker in hepatocellular carcinoma." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-533.

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Raporty organizacyjne na temat "S100A12"

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Emberley, Ethan D., and Peter Watson. The Role of S100A7/RANBPM Interaction in Human Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, August 2001. http://dx.doi.org/10.21236/ada396984.

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Emberley, Ethan D., and Peter Watson. The Role of S100A7/RANBPM Interaction in Human Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, August 2003. http://dx.doi.org/10.21236/ada418754.

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Emberley, Ethan, and Peter Watson. The Role of S100A7/RANBPM Interaction in Human Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, August 2002. http://dx.doi.org/10.21236/ada412819.

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West, Nathan. Exploring and Exploiting the Protein S100A7 as a New Target for Breast Cancer Therapy. Fort Belvoir, VA: Defense Technical Information Center, January 2010. http://dx.doi.org/10.21236/ada520729.

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Kim, Edward J., and David Helfman. Characterization of Molecular Factors Critical to the S100A4 (A Metastasis-Associated Protein) - Dependent Increase in Motility of Breast Cancer Cells. Fort Belvoir, VA: Defense Technical Information Center, April 2004. http://dx.doi.org/10.21236/ada424207.

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