Relevant bibliographies by topics / C-Fos

Academic literature on the topic 'C-Fos'

Author: Grafiati
Published: 4 June 2021
Last updated: 22 February 2023

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Journal articles on the topic "C-Fos"

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Portal, M. M., G. O. Ferrero, and B. L. Caputto. "N-Terminal c-Fos tyrosine phosphorylation regulates c-Fos/ER association and c-Fos-dependent phospholipid synthesis activation." Oncogene 26, no. 24 (December 11, 2006): 3551–58. http://dx.doi.org/10.1038/sj.onc.1210137.

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Lee, Sung-Ho. "Effect of Swimming Exercise of c-fos, c-jun Expression in Rat Hippocampus." Journal of the Korea Contents Association 11, no. 1 (January 28, 2011): 245–53. http://dx.doi.org/10.5392/jkca.2011.11.1.245.

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Ferguson, Mark W. J. "Death and c-fos." Nature 366, no. 6453 (December 1993): 308. http://dx.doi.org/10.1038/366308b0.

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Morgan, J. M., and J. Curran. "Death and c-fos." Nature 366, no. 6453 (December 1993): 308. http://dx.doi.org/10.1038/366308c0.

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Cahill, Michael A. "c-Fos transrepression revisited." FEBS Letters 400, no. 1 (January 2, 1997): 9–10. http://dx.doi.org/10.1016/s0014-5793(96)01349-x.

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Kang, Sang-Min, Seri Lim, Seung-Jae Won, Ye-Jin Shin, Yun-Sook Lim, Byung-Yoon Ahn, and Soon B. Hwang. "c-Fos regulates hepatitis C virus propagation." FEBS Letters 585, no. 20 (September 8, 2011): 3236–44. http://dx.doi.org/10.1016/j.febslet.2011.08.041.

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Копаева, М. Ю., А. М. Азиева, А. Б. Черепов, М. В. Нестеренко, and И. Ю. Зарайская. "Human lactoferrin enhances the expression of transcription factor c-Fos in neuronal cultures under stimulated conditions." Nauchno-prakticheskii zhurnal «Patogenez», no. 1 (March 31, 2021): 74–78. http://dx.doi.org/10.25557/2310-0435.2021.01.74-78.

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Целью настоящей работы стало исследование влияния лактоферрина (Лф) человека на экспрессию транскрипционного фактора c-Fos в первичных нейрональных культурах после физиологической стимуляции, определение клеточной локализации Лф человека и возможной колокализации экзогенного белка с индуцированной экспрессией c-Fos. Методы. Первичные диссоциированные клеточные культуры получали из гиппокампа головного мозга новорожденных мышей (Р0-Р1) линии С57Вl/6. Индукцию экспрессии белка c-Fos в клетках осуществляли путем трехкратного добавления 50 мМ KСl в культуральную среду на 8-й день культивирования in vitro. Анализ содержания c-Fos проводили иммунофлюоресцентным методом через 2 часа после стимуляции. Результаты. Лф детектировался как в цитоплазме, так и в ядрах отдельных клеток культуры после стимуляции KСl. В ядрах некоторых клеток была выявлена колокализация включения Лф и экспрессии c-Fos. Было обнаружено, что предварительное введение Лф в культуральную среду увеличивало количество клеток, экспрессирующих c-Fos после добавления 50 мМ KСl. The aims of this research were 1) to study the effect of human lactoferrin (Lf) on the expression of the c-Fos transcription factor in primary neuronal cultures after physiological stimulation; 2) to determine the cellular localization of human Lf and possible colocalization of an exogenous protein with induced c-Fos expression. Methods. Primary dissociated cell cultures were obtained from the hippocampus of newborn C57Bl/6 mice (P0-P1). The expression of c-Fos was induced by addition of 50 mM KCl to the culture medium at 8 day in vitro. c-Fos content was analyzed by immunofluorescence 2 hrs after stimulation. Results. Lf was detected in cytoplasm and in nuclei after stimulation KCl. Lf inclusion and c-Fos expression were colocalized in the nuclei of some cells. Thus, results showed that pretreatment with Lf led to increase in the number of cells expressing c-Fos after exposure to 50 mM KCl.
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Coronella-Wood, June, Jerome Terrand, Haipeng Sun, and Qin M. Chen. "c-Fos Phosphorylation Induced by H2O2Prevents Proteasomal Degradation of c-Fos in Cardiomyocytes." Journal of Biological Chemistry 279, no. 32 (May 10, 2004): 33567–74. http://dx.doi.org/10.1074/jbc.m404013200.

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Yuan, Zhongmin, Shoufang Gong, Jingyan Luo, Zhihao Zheng, Bin Song, Shanshan Ma, Jiaoli Guo, et al. "Opposing Roles for ATF2 and c-Fos in c-Jun-Mediated Neuronal Apoptosis." Molecular and Cellular Biology 29, no. 9 (March 2, 2009): 2431–42. http://dx.doi.org/10.1128/mcb.01344-08.

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ABSTRACT The activator protein 1 (AP-1) transcription factor c-Jun is crucial for neuronal apoptosis. However, c-Jun dimerization partners and the regulation of these proteins in neuronal apoptosis remain unknown. Here we report that c-Jun-mediated neuronal apoptosis requires the concomitant activation of activating transcription factor-2 (ATF2) and downregulation of c-Fos. Furthermore, we have observed that c-Jun predominantly heterodimerizes with ATF2 and that the c-Jun/ATF2 complex promotes apoptosis by triggering ATF activity. Inhibition of c-Jun/ATF2 heterodimerization using dominant negative mutants, small hairpin RNAs, or decoy oligonucleotides was able to rescue neurons from apoptosis, whereas constitutively active ATF2 and c-Jun mutants were found to synergistically stimulate apoptosis. Bimolecular fluorescence complementation analysis confirmed that, in living neurons, c-Fos downregulation facilitates c-Jun/ATF2 heterodimerization. A chromatin immunoprecipitation assay also revealed that c-Fos expression prevents the binding of c-Jun/ATF2 heterodimers to conserved ATF sites. Moreover, the presence of c-Fos is able to suppress the expression of c-Jun/ATF2-mediated target genes and, therefore, apoptosis. Taken together, our findings provide evidence that potassium deprivation-induced neuronal apoptosis is mediated by concurrent upregulation of c-Jun/ATF2 heterodimerization and downregulation of c-Fos expression. This paradigm demonstrates opposing roles for ATF2 and c-Fos in c-Jun-mediated neuronal apoptosis.
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Velazquez, Fabiola N., Beatriz L. Caputto, and François D. Boussin. "c-Fos importance for brain development." Aging 7, no. 12 (December 17, 2015): 1028–29. http://dx.doi.org/10.18632/aging.100862.

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Dissertations / Theses on the topic "C-Fos"

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Fleser, Angelica. "Resténose et expression des proto-oncogènes, c-myc, c-fos et c-jun." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1997. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp03/NQ35590.pdf.

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Ferrari, Ana Luiza. "Expressão dos protooncogenes c-fos, c-myc e c-jun em miométrio e mioma humanos." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2006. http://hdl.handle.net/10183/6629.

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Dalgleish, Gillian Denise. "Localisation signals within the c-myc and c-fos 3'untranslated regions." Thesis, University of Aberdeen, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.481826.

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Pariat, Magali. "Dégradation des protéines c-fos, c-jun et p53 par les calpai͏̈nes." Montpellier 2, 1997. http://www.theses.fr/1997MON20092.

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Les genes des familles fos et jun codent pour des facteurs de transcription instables qui interagissent au sein du complexe transcriptionnel ap-1. La proteine p53 est aussi un facteur de transcription que l'on retrouve inactive par mutation dans 50% des tumeurs. Nous nous sommes interesses au catabolisme de ces proteines dans la mesure ou (i) il constitue un niveau cle de la repression de l'expression de ces genes, (ii) il est affecte dans le cas des formes virales mutees des proteines fos et jun vehiculees par des retrovirus oncogenes, (iii) la proteine p53 est stabilisee dans de nombreuses tumeurs. Nous avons mis en evidence une des voies proteolytiques agissant sur ces proteines : les calpaines, qui sont des cysteines proteases cytoplasmiques. Nous avons pu montrer que les differents membres des familles fos et jun etaient differentiellement sensibles aux calpaines. Par ailleurs, nous avons pu montrer que v-fosfbr, une des formes virales de c-fos etait resistant aux calpaines. Au cours de la caracterisation des motifs peptidiques impliques dans la reconnaissance de c-fos et c-jun par les calpaines, nous avons montre que les sequences pest n'etaient ni necessaires, ni suffisantes a la proteolyse par les calpaines, mais que les motifs impliques recouvraient plusieurs dizaines d'acides amines. L'etude de la degradation de p53 par les calpaines nous a permis de montrer que cette proteine est un substrat tres sensible de ces proteases in vitro et que cette sensibilite est conferee par des determinants d'ordre tertiaire. Certaines formes mutantes de p53 retrouvees dans des tumeurs se sont trouvees etre resistantes aux calpaines. Enfin, un certain nombre d'arguments experimentaux suggerent que les calpaines pourraient participer a la degradation de p53 in vivo.
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Brown, Helen Jane. "Regulation of HOB1 activation domains in c-Fos." Thesis, University of Cambridge, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.390267.

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Sariban, Eric. "Régulation des proto-oncogènes c-fms, c-fos et c-sis lors de la différenciation monocytaire." Doctoral thesis, Universite Libre de Bruxelles, 1988. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/213396.

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Wilson, Timothy Craig. "The role of mRNA stability and Fos protein in transient c-fos mRNA accumulation." Thesis, University of Cambridge, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.304567.

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MATSUI, NOBUO, HIROSHI TAKAGI, HIROOMI FUNAHASHI, YASUYUKI SATOH, NORIHIRO MIYAMOTO, YOSHIHARU MURATA, TSUNEO IMAI, HISAO SEO, and MOTOTSUGU OHNO. "ACTH Increases Expression of c-fos, c-jun and β-actin Genes in the Dexamethasone-treated Rat Adrenals." Thesis, The Japan Endocrine Society, 1992. http://hdl.handle.net/2237/16720.

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Soster, Paula Rigon da Luz. "Imunorreatividade à proteína C-FOS após estimulação periférica nociva e tratamento com morfina no sistema nervoso central do caracol terrestre Megalobulimus abbreviatus." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2005. http://hdl.handle.net/10183/4935.

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Utilizando as técnicas de imunoistoquímica e densitometria óptica, foi investigada a localização e a expressão da proteína c-Fos no SNC do caracol Megalobulimus abbreviatus. Neurônios imunorreativos foram encontrados nos gânglios cerebrais, pedais, parietal direito e visceral de caracóis submetidos ao estímulo térmico aversivo (50oC), e sacrificados em diferentes tempos (3, 6, 12, 18 e 24 h) após a estimulação. A análise da imunorreatividade à c-Fos através do método de medida da densidade óptica (DO) revelou uma diferença significativa no sentido de apresentar uma maior expressão (p<0,05) na área do lobo pedal do pós-cérebro do gânglio cerebral em relação às outras regiões analisadas no mesmo gânglio (mesocérebro, pró-cérebro e lobo pleural do pós-cérebro). Além disso, também houve expressão significativamente maior (p<0,05) quando comparada a densitometria da região do mesocérebro em relação ao lobo pleural do pós-cérebro nos grupos controle, 3h e 18h. O lobo pleural do pós-cérebro apresentou uma expressão significativamente menor (p<0,05) na imunorreatividade da proteína c-Fos quando comparado ao pró-cérebro em animais sacrificados 12h e 24h após e estímulo aversivo. Em relação ao grupo controle, a DO da proteína c-Fos não variou nos diferentes tempos de sacrifício quando comparada a mesma região do gânglio (cerebral, pedal, parietal direito ou visceral) ao longo do tempo na maioria das regiões. A única diferença estatisticamente significativa (p<0,05) foi encontrada no mesocérebro do gânglio de animais sacrificados 12 h após o estímulo térmico aversivo, mostrando uma diminuição da imunorreatividade. Nos animais tratados com salina (1ml) ou morfina (20mg/kg) 15 min antes do estímulo térmico aversivo, os mesmos grupos neuronais nos gânglios do SNC de M. abbreviatus mostraram imunomarcação à proteína c-Fos. Em relação ao grupo controle, observou-se uma expressão significativamente menor (p<0,01) na DO da imunorreatividade da proteína c-Fos nos neurônios anteriores do gânglio pedal nos animais sacrificados 3 h e 6 h após o estímulo térmico aversivo. No momento em que a comparação foi feita entre os grupos salina e morfina de animais sacrificados ao mesmo tempo, na grande maioria dos grupos observou-se uma diminuição na imunorreatividade da proteína c-Fos. Esta diferença, porém, mostrou-se significativa (p<0,01) no mesocérebro de animais do grupo 3h, no lobo pedal do pós cérebro de animais dos grupos 3 h, 6 h e 18 h, nos neurônios anteriores do gânglio pedal nos grupos 6 h e 12 h, nos neurônios mediais do gânglio pedal do grupo 3 h, nos neurônios posteriores do gânglio pedal do grupo 6 h, nos neurônios da região anterior do gânglio parietal direito no grupo 12 h e nos neurônios do gânglio visceral no grupo experimental 12 h. A diferença na DO da proteína c-Fos apresentou uma diminuição extremamente significativa (p<0,001) nos neurônios mediais do gânglio pedal de animais sacrificados 12 h após o estímulo térmico aversivo, nos neurônios posteriores do gânglio pedal dos animais sacrificados 12 h após o estímulo e nos neurônios do gânglio visceral dos animais do grupo experimental 6 h. A partir destes dados e da correlação com estudos realizados em M. abbreviatus para detecção de mediadores químicos envolvidos na nocicepção, podemos concluir que as áreas imunorreativas que apresentaram estas variações na densidade óptica da imunorreatividade à proteína c-Fos em diferentes tempos de sacrifício e tratamento com morfina estão envolvidas no processo nociceptivo neste caracol.
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TEYSSIER, MAGALI. "Expression des oncogenes c-fos et c-myc et immunomodulation de la lignee monocytaire." Paris 11, 1992. http://www.theses.fr/1992PA112239.

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The p388d1 murine macrophage cell line has been chosen to study events resulting from the transduction of immunomodulatory signals. Owing to the frequent implication of the c-myc gene in the tumorigenicity of hematopoietic cells, the normal c-myc status in this cell line is demonstrated by southern analysis. The early modulation of the c-fos and c-myc proto-oncogene expression has been studied by northern analysis and the dna synthesis by #3h-thymidine incorporation after treatment of p388d1 cells by tpa, calcium ionophore a23187, mdp and csf-1. No correlation could be evidenced in this cell line between the mitogenic effect and the c-fos and c-myc modulation induced by these immunomodifiers. The impact of lps, tpa and dibutyryl-cyclic amp on mhc class ii antigen (ia) has been revealed by radio-immuno-assay. These compounds inhibited constitutive or induced by interferon-gamma ia expression. This inhibition seemed to be in relation with c-fos expression. The ia expression was therefore analysed either after c-fos translation blockage by a dna antisense either after overexpression of c-fos by transfection of p388d1 cells with a plasmid containing the c-fos gene. The first results seemed to confirm an inverse correlation between the c-fos induction and the inhibition of ia expression
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Books on the topic "C-Fos"

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Moggy, Susan E. Adhesion-dependent regulation of the c-fos SRE. Sudbury, Ont: Laurentian University, 2000.

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Piersanti, Monique. Gestational and hormonal association of c-Jun, c-Fos and connexin-43 mRNA. Ottawa: National Library of Canada, 1994.

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E, Angel Peter, and Herrlich Peter 1940-, eds. The fos and jun families of transcription factors. Boca Raton: CRC Press, 1994.

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Wei, Ding. Induction of c-fos and activation of parallel MAPK cascades by cadmium. Ottawa: National Library of Canada, 2000.

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Gonzalez, Andrea. Artificial rearing alters c-Fos expression in the brain of juvenile female rats. Ottawa: National Library of Canada, 2001.

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O'Brien, Lee. Expression of c-fos mRNA within rat skeletal muscle in response to nerve-mediated activation. Sudbury, Ont: Laurentian University, 1998.

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Pohl, Ira. C++ for C programmers. Redwood City, Calif: Benjamin/Cummings Pub., 1989.

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Pohl, Ira. C++ for C programmers. 3rd ed. Reading, Mass: Addison-Wesley, 1999.

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Pohl, Ira. C++ for C programmers. 2nd ed. Redwood City, Calif: Benjamin/Cummings Pub. Co., 1994.

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Ranade, Jay. C₊₊ primer for C programmers. 2nd ed. New York: McGraw-Hill, 1995.

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Book chapters on the topic "C-Fos"

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Müller, R., and R. Bravo. "c-fos and Growth Control." In Cell Cycle and Oncogenes, 69–74. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-71686-7_8.

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Shaw, P. E., R. A. Hipskind, H. Schröter, and A. Nordheim. "Transcriptional Regulation of Proto-Oncogene c-fos." In Nucleic Acids and Molecular Biology, 120–32. Berlin, Heidelberg: Springer Berlin Heidelberg, 1989. http://dx.doi.org/10.1007/978-3-642-83709-8_8.

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Van Beveren, Charles, Richard L. Mitchell, Cynthia Henning-Chubb, Eliezer Huberman, and Inder M. Verma. "Expression of the C-Fos Gene During Differentiation." In Mechanisms of Lymphocyte Activation and Immune Regulation, 263–74. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4684-5323-2_26.

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Ringertz, Nils, Magnus Rahm, Anna Hultgardh-Nilsson, Pei Jin, and Thomas Sejersen. "Expression of C-MYC, C-FOS and C-JUN Proto-Oncogenes During Muscle Differentiation in Vitro." In Molecular Basis of Human Cancer, 115–26. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4899-2563-3_5.

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Cutry, Anthony F., Alan J. Kinniburgh, Kirk J. Leister, and C. E. Wenner. "Modulation of c-fos and c-myc Expression by Effectors of Ion Movements." In Cell Calcium Metabolism, 293–303. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4684-5598-4_32.

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Rouiller, E. M. "Mapping Activity in the Auditory Pathway with C-Fos." In Acoustical Signal Processing in the Central Auditory System, 33–48. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4419-8712-9_3.

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Belasco, Joel G., Ann-Bin Shyu, and Michael E. Greenberg. "Rapid Degradation of the c-FOS Proto-Oncogene Transcript." In Post-Transcriptional Control of Gene Expression, 65–71. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990. http://dx.doi.org/10.1007/978-3-642-75139-4_7.

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Cahill, Michael A., Ralf Janknecht, and Alfred Nordheim. "Signal uptake by the c-fos serum response element." In Inducible Gene Expression, Volume 2, 39–72. Boston, MA: Birkhäuser Boston, 1995. http://dx.doi.org/10.1007/978-1-4684-6837-3_2.

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Morgan, James I., and Tom Curran. "Regulation of c-fos Expression by Voltage-Dependent Calcium Channels." In Cell Calcium Metabolism, 305–12. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4684-5598-4_33.

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Jiao, L., T. Funato, W. Wang, T. Tone, M. Kashani-Sabet, and K. J. Scanlon. "The Role of the c-fos Oncogene in Cisplatin Resistance." In Platinum and Other Metal Coordination Compounds in Cancer Chemotherapy, 303–13. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4899-0738-7_28.

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Conference papers on the topic "C-Fos"

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Leahy, R., A. Chambellan, W. Xu, P. Cruickshank, K. Asosingh, SA Comhair, and SC Erzurum. "Survival of Lung Cancer Cells with of c-Fos Knockdown." In American Thoracic Society 2009 International Conference, May 15-20, 2009 • San Diego, California. American Thoracic Society, 2009. http://dx.doi.org/10.1164/ajrccm-conference.2009.179.1_meetingabstracts.a5030.

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Alhendi, Ahmad M. N., Leonel Prado-Lourenço, and Noel Whitaker. "Abstract 2114: Targeting c-Jun and c-Fos using microRNA's has a potential in contesting melanoma." 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.am2015-2114.

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Linder, Markus, Elisabeth Glitzner, Sriram Srivatsa, Parastoo Shahrouzi, Latifa Bakiri, Monika Dumanic, Markus Mitterhauser, Erwin F. Wagner, and Maria Sibilia. "Abstract 530: The role of EGFR in c-fos-dependent osteosarcoma formation." 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.am2017-530.

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Li Jie, Zhang Ming, and Zhu Ying. "Ischemic preconditioning mediate NMDA receptors through downregulation of c-Jun activation and up-regulation of c-fos in hippocampus CA1." In 2014 IEEE Workshop on Electronics, Computer and Applications (IWECA). IEEE, 2014. http://dx.doi.org/10.1109/iweca.2014.6845784.

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Amable, Lauren, Elaine Gavin, Wesley Denny, Erhong Meng, Rodney P. Rocconi, and Eddie Reed. "Abstract 5613: A specific isoform of Gli1 binds the Gli-binding site of the c-jun and c-fos promoters." In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-5613.

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Freire, Marco Aurelio M., Jean Faber, Jose Ronaldo Santos, Nelson A. M. Lemos, Maria Adelia Aratanha, Pedro F. Cavalcanti, and Edgard Morya. "c-Fos immunoreactivity and variation of neuronal units in rat's motor cortex after chronic implants." In 2014 IEEE 16th International Conference on e-Health Networking, Applications and Services (Healthcom 2014). IEEE, 2014. http://dx.doi.org/10.1109/healthcom.2014.7001807.

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Toropova, Ksenia, Olga Ivashkina, Dmitry Sukhinin, Nikita Pospelov, Anna Ivanova, Elena Konovalova, and Konstantin Anokhin. "Resting state networks in the conscious mouse brain: a large-scale c- Fos mapping study." In 2022 Fourth International Conference Neurotechnologies and Neurointerfaces (CNN). IEEE, 2022. http://dx.doi.org/10.1109/cnn56452.2022.9912533.

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Fan, Ping, Fadeke Agboke, Obi L. Griffith, Russell E. McDaniel, Xiaojun Zou, Karen Creswell, Joe W. Gray, and Virgil Craig Jordan. "Abstract 830: Transcriptional modulation of estrogen-induced apoptosis through activation of c-Fos/c-Jun in long-term estrogen deprived breast cancer cells." In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-830.

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Ge, Rongbin, Zongwei Wang, Qing Zeng, Xiaoyin Xu, and Aria Olumi. "Abstract 4099: F-box protein 10, an NF-κB-dependent anti-apoptotic protein, regulates TRAIL-induced apoptosis through modulating c-Fos/c-FLIP pathway." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-4099.

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Cao, En-Hua, Ju-jun Wang, Wenjian Ma, and Jingfen Qin. "Sequence-specific photoinduced c-fos gene damage mediated by triple stranded-forming oligonucleotide conjugated to psoralen." In International Symposium on Biomedical Optics, edited by Qingming Luo, Britton Chance, Lihong V. Wang, and Steven L. Jacques. SPIE, 1999. http://dx.doi.org/10.1117/12.364427.

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Reports on the topic "C-Fos"

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Wuosmaa, A. H., R. R. Betts, and M. Freer. Angular correlation measurements for {sup 12}C{sup 12}C,{sup 12}C{sup 12}C 3{sup -} scattering. Office of Scientific and Technical Information (OSTI), August 1995. http://dx.doi.org/10.2172/166299.

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Gillis, Jessica McDonnel, and Jeffrey Jay Whicker. Dose Assessment of LANL-Derived Residual Radionuclides in Soils within C Tracts (C-2, C-3, and C-4) for Land Transfer Decisions. Office of Scientific and Technical Information (OSTI), June 2015. http://dx.doi.org/10.2172/1186033.

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Flater, David. Configuration of profiling tools for C/C++ applications under 64-bit Linux. National Institute of Standards and Technology, March 2013. http://dx.doi.org/10.6028/nist.tn.1790.

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Gillis, Jessica M., and Jeffrey J. Whicker. Dose Assessment of Los Alamos National Laboratory-Derived Residual Radionuclides in Soils within C Tracts (C-2, C-3, and C-4) for Land Transfer Decisions. Office of Scientific and Technical Information (OSTI), January 2016. http://dx.doi.org/10.2172/1237215.

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Sathyanarayana, K. Evaluation of the 296-C-006 HVAC system for tank 241-C-106. Office of Scientific and Technical Information (OSTI), September 1998. http://dx.doi.org/10.2172/350900.

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Green, M. A. Generation of the J/sub c/, H/sub c/, T/sub c/ surface for commercial superconductor using reduced-state parameters. Office of Scientific and Technical Information (OSTI), April 1988. http://dx.doi.org/10.2172/6979712.

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Krawczyk, Frank L. LANL Accelerator Activities for C-band. Office of Scientific and Technical Information (OSTI), February 2019. http://dx.doi.org/10.2172/1494457.

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Ossorio, P. G., and L. S. Schneider. Knowledge Representation for C(3)I. Fort Belvoir, VA: Defense Technical Information Center, May 1988. http://dx.doi.org/10.21236/ada203710.

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Malitsky N. and R. Talman. User Guide for UAL (C++ Interface). Office of Scientific and Technical Information (OSTI), September 2008. http://dx.doi.org/10.2172/1061913.

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Mora, Claudia I., Zhenghua Li, and Zachary Vance. Bio-Carbon Accounting for Bio-Oil Co-Processing: 14C and 13C/12C. Office of Scientific and Technical Information (OSTI), June 2016. http://dx.doi.org/10.2172/1258359.

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