Relevant bibliographies by topics / TetraNuc

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'TetraNuc'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'TetraNuc.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Journal articles on the topic "TetraNuc"

1

DUDEK, J., D. CURIEN, A. GÓŹDŹ, and K. MAZUREK. "NUCLEAR POINT-GROUP SYMMETRIES AND NEW IDEAS ABOUT NUCLEAR STABILITY: AN OVERVIEW." International Journal of Modern Physics E 18, no. 10 (November 2009): 2155–59. http://dx.doi.org/10.1142/s0218301309014470.

Full text
Abstract:
The nuclear mean-field theory and the group representation theory can be used to optimise the search for strong nuclear shell effects. The two theories allow to correlate the symmetry aspects with the presence of large gaps in the single-particle spectra, facilitate in this way the conditions of search for strong nucleonic- and nuclear-binding and thus for an increased nuclear stability. In this article we give a short overview of the related on-going research, focussing on the results of the TetraNuc Collaboration.
APA, Harvard, Vancouver, ISO, and other styles
2

CURIEN, D., J. DUDEK, H. MOLIQUE, L. SENGELE, A. GÓŹDŹ, and K. MAZUREK. "SEARCH FOR TETRAHEDRAL SYMMETRY IN NUCLEI: A SHORT OVERVIEW." International Journal of Modern Physics E 20, no. 02 (February 2011): 219–27. http://dx.doi.org/10.1142/s0218301311017557.

Full text
Abstract:
Following a series of experiments launched by the TetraNuc collaboration to possibly demonstrate the existence of high-rank symmetries in subatomic physics, the first experimental results on the Rare Earth region appear in publications. Meanwhile an important progress has been made on the theory side strongly suggesting that the original criterion of the static tetrahedral symmetry in the form of vanishing quadrupole moments may need to be revised to include explicitly the vibrational motion. The Actinide region seems of particular interest because of the extra stability provided by the octahedral symmetry. In this article a summary of the current experimental efforts on both the Rare-Earth and Actinide regions is given. Finally the ELMA project addressing the experimental search for the symmetries in the Actinides is briefly discussed.
APA, Harvard, Vancouver, ISO, and other styles
3

Dudek, J., I. Dedes, J. Yang, A. Baran, D. Curien, A. Gaamouci, A. Góźdź, A. Pędrak, and H. L. Wang. "Nuclear High-rank Symmetries: From the Early Theory Predictions via TetraNuc Collaboration to the Final Experimental Discovery." Acta Physica Polonica B Proceedings Supplement 13, no. 3 (2020): 419. http://dx.doi.org/10.5506/aphyspolbsupp.13.419.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Jiang, Minghua, Senhua Chen, Jing Li, and Lan Liu. "The Biological and Chemical Diversity of Tetramic Acid Compounds from Marine-Derived Microorganisms." Marine Drugs 18, no. 2 (February 15, 2020): 114. http://dx.doi.org/10.3390/md18020114.

Full text
Abstract:
Tetramic acid (pyrrolidine-2,4-dione) compounds, isolated from a variety of marine and terrestrial organisms, have attracted considerable attention for their diverse, challenging structural complexity and promising bioactivities. In the past decade, marine-derived microorganisms have become great repositories of novel tetramic acids. Here, we discuss the biological activities of 277 tetramic acids of eight classifications (simple 3-acyl tetramic acids, 3-oligoenoyltetramic acids, 3-decalinoyltetramic acid, 3-spirotetramic acids, macrocyclic tetramic acids, N-acylated tetramic acids, α-cyclopiazonic acid-type tetramic acids, and other tetramic acids) from marine-derived microbes, including fungi, actinobacteria, bacteria, and cyanobacteria, as reported in 195 research studies up to 2019.
APA, Harvard, Vancouver, ISO, and other styles
5

Nagata, Nanae, Sakura Masuko, Rikako Inoue, Tatsuro Nakamura, Kosuke Aritake, and Takahisa Murata. "Development of Monoclonal Antibody-Based EIA for Tetranor-PGDM which Reflects PGD2 Production in the Body." Journal of Immunology Research 2021 (April 26, 2021): 1–6. http://dx.doi.org/10.1155/2021/5591115.

Full text
Abstract:
Tetranor-PGDM is a metabolite of PGD2. Urinary tetranor-PGDM levels were reported to be increased in some diseases, including food allergy, Duchenne muscular dystrophy, and aspirin-intolerant asthma. In this study, we developed a monoclonal antibody (MAb) and a competitive enzyme immunoassay (EIA) for measuring tetranor-PGDM. Spleen cells isolated from mice immunized with tetranor-PGDM were utilized to generate Ab-producing hybridomas. We chose hybridomas and purified MAb against tetranor-PGDM to develop competitive EIA. The assay evaluated the optimal ionic strength, pH, precision, and reliability. Specificity was determined by cross-reactivity to tetranor-PGEM, tetranor-PGFM, and tetranor-PGAM. Recovery was determined by spiking experiments on artificial urine. Optimal ionic strength was 150 mM NaCl, and optimal pH was pH 7.5. Metabolites other than tetranor-PGDM did not show any significant cross-reactivity in the EIA. The assay exhibited a half-maximal inhibition concentration (IC50) of 1.79 ng/mL, limit of detection (LOD) of 0.0498 ng/mL, and range of quantitation (ROQ) value of 0.252 to 20.2 ng/mL. The intra- and inter-assay variation for tetranor-PGDM was 3.9–6.0% and 5.7–10.4%, respectively. The linearity-dilution effect showed excellent linearity under dilution when artificial urine samples were applied to solid-phase extraction (SPE). After SPE, recovery of tetranor-PGDM in artificial urine averaged from 82.3% to 113.5% and was within acceptable limits (80%–120%). We successfully generated one monoclonal antibody and developed a sensitive competitive EIA. The established EIA would be useful for routine detection and monitoring of tetranor-PGDM in research or diagnostic body fluids.
APA, Harvard, Vancouver, ISO, and other styles
6

Ueda, Chihiro, Kazuhiro Tateda, Manabu Horikawa, Soichiro Kimura, Yoshikazu Ishii, Kaoru Nomura, Kanako Yamada, et al. "Anti-Clostridium difficile Potential of Tetramic Acid Derivatives from Pseudomonas aeruginosa Quorum-Sensing Autoinducers." Antimicrobial Agents and Chemotherapy 54, no. 2 (November 16, 2009): 683–88. http://dx.doi.org/10.1128/aac.00702-09.

Full text
Abstract:
ABSTRACT We have examined the potential bactericidal activities of several tetramic acids derived from Pseudomonas autoinducers against Clostridium difficile, a cause of antibiotic-associated pseudomembranous colitis. Clinical isolates of C. difficile (n = 4) were incubated in broth with a chemically synthesized Pseudomonas autoinducer and its tetramic acid derivatives. The structure-activity relationship and the mechanisms of action were examined by a time-killing assay and by determination of the morphological/staining characteristics. The use of some tetramic acids derived from N-3-oxododecanoyl l-homoserine lactone resulted in more than 3-log reductions in the viability of C. difficile within 30 min at 30 μM. The outer membrane was suggested to be one of the targets for the bactericidal activity of tetramic acid, because disturbance of the bacterial outer surface was demonstrated by alteration of the Gram-staining characteristic and electron microscopy. The data for the tetramic acid derivatives demonstrate that the keto-enol structure and the length of the acyl side chain of tetramic acid may be essential for the antibacterial activity of this molecule. These results suggest the potential for tetramic acid derivatives to be novel agents with activity against C. difficile.
APA, Harvard, Vancouver, ISO, and other styles
7

Neumann, Kerstin, Stefan Kehraus, Michael Gütschow, and Gabriele M. König. "Cytotoxic and HLE-Inhibitory Tetramic Acid Derivatives from Marine-Derived Fungi." Natural Product Communications 4, no. 3 (March 2009): 1934578X0900400. http://dx.doi.org/10.1177/1934578x0900400308.

Full text
Abstract:
Tetramic acid derivatives are an important class of nitrogen heterocycles with a pyrrolidine-2,4-dione core as a key structural motif. From the sponge-derived fungus Beauveria bassiana, a new equisetin-like tetramic acid derivative, beauversetin (1), was isolated. The sea weed-derived fungus Microdiplodia sp. produced the tetramic acid derivative 2 (Sch210972) which was shown to inhibit human leucocyte elastase (HLE) with an IC50 of 1.04 μg mL−1.
APA, Harvard, Vancouver, ISO, and other styles
8

Li, Yong, Zheng Huang, Jia Xu, Yong Ding, Dian-Yong Tang, Jie Lei, Hong-yu Li, Zhong-Zhu Chen, and Zhi-Gang Xu. "Microwave-assisted efficient and facile synthesis of tetramic acid derivatives via a one-pot post-Ugi cascade reaction." Beilstein Journal of Organic Chemistry 16 (April 9, 2020): 663–69. http://dx.doi.org/10.3762/bjoc.16.63.

Full text
Abstract:
A facile microwave-assisted method for the synthesis of tetramic acid derivatives has been developed through an Ugi/Dieckmann cyclization strategy with DBU. This two-step one-pot procedure afforded the targeted tetramic acid analogues in good yields. With commercially available Ugi starting materials, microwave irradiation, a simple operation, excellent yields, and a broad scope, this reaction has the potential to produce a large number of tetramic acid analogues, which cannot be easily accessed by the classic synthetic methods.
APA, Harvard, Vancouver, ISO, and other styles
9

Yalcin, M., E. Dyskin, L. Lansing, D. J. Bharali, S. S. Mousa, A. Bridoux, A. H. Hercbergs, et al. "Tetraiodothyroacetic Acid (Tetrac) and Nanoparticulate Tetrac Arrest Growth of Medullary Carcinoma of the Thyroid." Journal of Clinical Endocrinology & Metabolism 95, no. 4 (April 1, 2010): 1972–80. http://dx.doi.org/10.1210/jc.2009-1926.

Full text
Abstract:
Abstract Context: Tetraiodothyroacetic acid (tetrac) blocks angiogenic and tumor cell proliferation actions of thyroid hormone initiated at the cell surface hormone receptor on integrin αvβ3. Tetrac also inhibits angiogenesis initiated by vascular endothelial growth factor and basic fibroblast growth factor. Objective: We tested antiangiogenic and antiproliferative efficacy of tetrac and tetrac nanoparticles (tetrac NP) against human medullary thyroid carcinoma (h-MTC) implants in the chick chorioallantoic membrane (CAM) and h-MTC xenografts in the nude mouse. Design: h-MTC cells were implanted in the CAM model (n = 8 per group); effects of tetrac and tetrac NP at 1 μg/CAM were determined on tumor angiogenesis and tumor growth after 8 d. h-MTC cells were also implanted sc in nude mice (n = 6 animals per group), and actions on established tumor growth of unmodified tetrac and tetrac NP ip were determined. Results: In the CAM, tetrac and tetrac NP inhibited tumor growth and tumor-associated angiogenesis. In the nude mouse xenograft model, established 450–500 mm3 h-MTC tumors were reduced in size over 21 d by both tetrac formulations to less than the initial cell mass (100 mm3). Tumor tissue hemoglobin content of xenografts decreased by 66% over the course of administration of each drug. RNA microarray and quantitative real-time PCR of tumor cell mRNAs revealed that both tetrac formulations significantly induced antiangiogenic thrombospondin 1 and apoptosis activator gene expression. Conclusions: Acting via a cell surface receptor, tetrac and tetrac NP inhibit growth of h-MTC cells and associated angiogenesis in CAM and mouse xenograft models.
APA, Harvard, Vancouver, ISO, and other styles
10

Achilli, Silvia, João T. Monteiro, Sonia Serna, Sabine Mayer-Lambertz, Michel Thépaut, Aline Le Roy, Christine Ebel, et al. "TETRALEC, Artificial Tetrameric Lectins: A Tool to Screen Ligand and Pathogen Interactions." International Journal of Molecular Sciences 21, no. 15 (July 25, 2020): 5290. http://dx.doi.org/10.3390/ijms21155290.

Full text
Abstract:
C-type lectin receptor (CLR)/carbohydrate recognition occurs through low affinity interactions. Nature compensates that weakness by multivalent display of the lectin carbohydrate recognition domain (CRD) at the cell surface. Mimicking these low affinity interactions in vitro is essential to better understand CLR/glycan interactions. Here, we present a strategy to create a generic construct with a tetrameric presentation of the CRD for any CLR, termed TETRALEC. We applied our strategy to a naturally occurring tetrameric CRD, DC-SIGNR, and compared the TETRALEC ligand binding capacity by synthetic N- and O-glycans microarray using three different DC-SIGNR constructs i) its natural tetrameric counterpart, ii) the monomeric CRD and iii) a dimeric Fc-CRD fusion. DC-SIGNR TETRALEC construct showed a similar binding profile to that of its natural tetrameric counterpart. However, differences observed in recognition of low affinity ligands underlined the importance of the CRD spatial arrangement. Moreover, we further extended the applications of DC-SIGNR TETRALEC to evaluate CLR/pathogens interactions. This construct was able to recognize heat-killed Candida albicans by flow cytometry and confocal microscopy, a so far unreported specificity of DC-SIGNR. In summary, the newly developed DC-SIGNR TETRALEC tool proved to be useful to unravel novel CLR/glycan interactions, an approach which could be applied to other CLRs.
APA, Harvard, Vancouver, ISO, and other styles
More sources

Dissertations / Theses on the topic "TetraNuc"

1

Vancraeyenest, Aurélie. "Résultats et simulation en spectroscopie γ des noyaux déformés : cas des noyaux isomériques et tétraédriques." Phd thesis, Université Claude Bernard - Lyon I, 2010. http://tel.archives-ouvertes.fr/tel-00639798.

Full text
Abstract:
Le travail présenté dans ce manuscrit regroupe deux études de spectroscopie γ. La première concerne les isomères des noyaux de néodyme autour de N=82. Ces noyaux, lorsqu'ils sont étudiés par des modèles de type Cranked-Nilsson-Strutinsky, présentent des états énergétiquement favorisés. Ils sont autant de candidats pour la recherche d'isomères de spin. Expérimentalement, un certain nombre d'états isomériques ont déjà été observés dans les noyaux de 138,139,140Nd sur lesquels porte cette étude. Afin de mieux caractériser ces états, une expérience a été menée en août 2009 à Jyväskylä auprès de l'ensemble de détection JUROGAM-RITU-GREAT. La réaction de fusion-évaporation 48Ca + 76Zr 144Nd* réalisée avec une cible mince a permis de produire majoritairement les noyaux 139,140Nd. Les noyaux produits, transportés au plan focal par le spectromètre RITU, sont implantés et le rayonnement émis par la décroissance des isomères est ensuite recueilli par l'ensemble de détection GREAT. Nous développerons l'analyse complète de cette expérience et nous montrerons les résultats émergents. Nous avons, par exemple, pu montrer l'alimentation du niveau 20+ de 140Nd ainsi que le placement énergétique du niveau isomérique du noyau 139Nd. La deuxième partie de ce travail s'articule autour de la recherche de la symétrie tétraédrique dans le noyau 156Gd. Cela a consisté à la fois en un travail de spectroscopie γ des bandes de parité positive de ce noyau, laquelle a fait émerger un certain nombre de nouvelles transitions. Le deuxième volet de cette étude consistait à simuler dans l'environnement ROOT - GEANT4 le seuil d'observation des signaux faibles avec le détecteur de rayonnements γ de nouvelle génération AGATA
APA, Harvard, Vancouver, ISO, and other styles
2

Doan, Quang Tuyen. "Recherche de la symétrie tétraédrique dans le noyau 156Gd par spectroscopie γ." Phd thesis, Université Claude Bernard - Lyon I, 2009. http://tel.archives-ouvertes.fr/tel-00561660.

Full text
Abstract:
Des calculs théoriques utilisant la méthode de champ moyen ont suggérée l'existence des formes du noyau avec la symétrie tétraédrique et/ou octraédrique dans la région des terres rares au voisinage des noyaux 156Gd et 160Yb. Dans les noyaux avec une symétrie tétraédrique pure, des transitions intra-bande E2 à bas spin dans des bandes de parité négative disparaissent ou sont très faibles. Ce travail est dédié à une recherche expérimentale de la symétrie tétraédrique dans le noyau 156Gd. Une expérience a été faite à Jyväskylä avec le multi-détecteur JUROGAM, sur la réaction de fusion - évaporation 154Sm(, 2n)156Gd. L'analyse des données, a établi les rapports d'embranchement de deux bandes de parité négative et a permis, par distribution angulaire, de connaître la nature d'une nouvelle transition. Les rapports d'embranchement obtenus sont comparables avec ceux des expériences précédentes et quelques limites supérieures ont été déterminées. L'absence de transitions à bas spin (I$^{pi}<9$) dans la bande de parité négative à spin impair a été confirmée. Ces résultats ont renforcé l'hypothèse d'une symétrie tétraédrique dans le noyau 156Gd. La spectroscopie gamma est l'outil majeure utilisé dans ce travail. Les principes ainsi qu'une étude de simulation réaliste sont détaillés dans ce manuscrit. La simulation avec des événements réalistes a été faite pour comparer la fonction de réponse de deux types de multidétecteurs EUROBALL et AGATA. Les résultats montrent que sous certain conditions la phase démonstrateur d'AGATA peut être utilisée pour la recherche d'événements rares.
APA, Harvard, Vancouver, ISO, and other styles
3

Doan, Quang Tuyen. "Recherche de la symétrie tétraédrique dans le noyau $^{156}$Gd par spectroscopie gamma." Phd thesis, Université Claude Bernard - Lyon I, 2009. http://tel.archives-ouvertes.fr/tel-00467280.

Full text
Abstract:
Des calculs théoriques utilisant la méthode de champ moyen ont suggérée l'existence des formes du noyau avec la symétrie tétraédrique et/ou octraédrique dans la région des terres rares au voisinage des noyaux 156Gd et 160Yb. Dans les noyaux avec une symétrie tétraédrique pure, des transitions intra-bande E2 à bas spin dans des bandes de parité négative disparaissent ou sont très faibles. Ce travail est dédié à une recherche expérimentale de la symétrie tétraédrique dans le noyau 156Gd. Une expérience a été faite à Jyväskylä avec le multi-détecteur JUROGAM, sur la réaction de fusion - évaporation 154Sm(, 2n)156Gd. L'analyse des données, a établi les rapports d'embranchement de deux bandes de parité négative et a permis, par distribution angulaire, de connaître la nature d'une nouvelle transition. Les rapports d'embranchement obtenus sont comparables avec ceux des expériences précédentes et quelques limites supérieures ont été déterminées. L'absence de transitions à bas spin (I$^{pi}<9$) dans la bande de parité négative à spin impair a été confirmée. Ces résultats ont renforcé l'hypothèse d'une symétrie tétraédrique dans le noyau 156Gd. La spectroscopie gamma est l'outil majeure utilisé dans ce travail. Les principes ainsi qu'une étude de simulation réaliste sont détaillés dans ce manuscrit. La simulation avec des événements réalistes a été faite pour comparer la fonction de réponse de deux types de multidétecteurs EUROBALL et AGATA. Les résultats montrent que sous certain conditions la phase démonstrateur d'AGATA peut être utilisée pour la recherche d'événements rares.
APA, Harvard, Vancouver, ISO, and other styles
4

Patience, J. M. "Routes to substituted tetramic acids." Thesis, University of Nottingham, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.235998.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Bates, Andrew D. "New reactions in tetramic acid synthesis." Thesis, University of Nottingham, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.252629.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Pillainayagam, Terence Anthony. "New methods in tetramic acid synthesis." Thesis, Loughborough University, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.416685.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Law, Ching-Man (Carole). "Novel tetramic acids via 1,3-dipolar cycloaddition." Thesis, Loughborough University, 2008. https://dspace.lboro.ac.uk/2134/34454.

Full text
Abstract:
This Ph.D. thesis has been concerned with the reinvestigation and improvement of the intermolecular 1,3-dipolar cycloaddition strategy using isoxazoles, towards the 3-acyltetramic acids (3-acylpyrrrolidine-2,4-diones) and also the investigation and development of the corresponding intramolecular strategy. A second generation of the intermolecular route was developed previously within our group and we have synthesised a variety of pyrroloisoxazoles, the 'masked' tetramic acids. We have modified and improved both the isoxazole formations and the peptide coupling reactions; we have further developed the chain extension at the isoxazole C-5 (tetramic acid C-3) substituent, testing the aldol-type reaction with some aromatic aldehydes and extending it to aliphatic aldehydes. We have demonstrated the condensation method using a strong base and hydroxyl adducts were obtained. Dehydration has been undertaken to yield the alkenyl C-5 side-chain. Development of the desmethyllaccarin, a derivative of the natural product laccarin, has also been attempted via the intermolecular route. A potential intramolecular route has the reversed sequence from the intermolecular route, by using the N-acylation product produced from an amino acid for the formation of a nitrile oxide and hence our building block pyrroloisoxazole by intramolecular dipolar cycloaddition. We have generated a nitro ketoester compound from the amino acid and investigation on the synthesis of the pyrroloisoxazole has been undertaken.
APA, Harvard, Vancouver, ISO, and other styles
8

Wilson, Jason B. "Synthesis and evaluation of tetramic acids as antimicrobial agents." View the abstract Download the full-text PDF version, 2008. http://etd.utmem.edu/ABSTRACTS/2008-055-Wilson-Index.htm.

Full text
Abstract:
Thesis (M.S.)--University of Tennessee Health Science Center, 2008.
Title from title page screen (viewed on February 27, 2009). Research advisor: Richard E. Lee, Ph.D. Document formatted into pages (viii, 40 p. : ill.). Vita. Abstract. Includes bibliographical references (p. 36-40).
APA, Harvard, Vancouver, ISO, and other styles
9

Lewis, Ian. "Studies in the synthesis of polyene tetramic acid antibiotics." Thesis, University of Edinburgh, 1988. http://hdl.handle.net/1842/12412.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Duller, Kathryn April Marion. "A cycloaddition route to heterocyclic tricarbonyl natural products." Thesis, University of Nottingham, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.307821.

Full text
APA, Harvard, Vancouver, ISO, and other styles
More sources

Books on the topic "TetraNuc"

1

Manny by Tetrarc for Coupechoux. Nantes: Éditions Joca Seria, 2011.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
2

Nauen, Ralf. Aphid toxicology and plant systemic properties of an isecticidal tetramic acid derivative. Portsmouth: University of Portsmouth, School of Biological Sciences, 2002.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
3

Wiebes, J. T. The New World Agaoninae: Pollinators of figs. Amsterdam: North-Holland, 1995.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
4

Saha, Jayanta Kumar. Total synthesis of (±)-bostrycin, synthesis of a chiral catechol-based C b2 s-symmetric ligand and studies directed towards the synthesis of dienoyl tetramic acid section of tirandamycin. 1986.

Find full text
APA, Harvard, Vancouver, ISO, and other styles

Book chapters on the topic "TetraNuc"

1

Bährle-Rapp, Marina. "Stephania Tetranda Extract." In Springer Lexikon Kosmetik und Körperpflege, 531. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_10072.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Gossauer, Albert. "Monopyrrolic Natural Compounds Including Tetramic Acid Derivatives." In Progress in the Chemistry of Organic Natural Products, 1–188. Vienna: Springer Vienna, 2003. http://dx.doi.org/10.1007/978-3-7091-6029-9_1.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Winkelmann, J. "Diffusion of oxygen (1); tetradec-1-ene (2)." In Gases in Gases, Liquids and their Mixtures, 2119. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_1636.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Davis, Paul J., Faith B. Davis, Mary K. Luidens, Hung-Yun Lin, and Shaker A. Mousa. "Tetraiodothyroacetic Acid (Tetrac), Nanotetrac and Anti-angiogenesis." In Angiogenesis Modulations in Health and Disease, 107–17. Dordrecht: Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-6467-5_10.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Cox, Russell J. "The Biosynthesis of Polyketides, Tetramic Acids, and Pyridones in Fungi." In ACS Symposium Series, 33–47. Washington, DC: American Chemical Society, 2007. http://dx.doi.org/10.1021/bk-2007-0955.ch003.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Winkelmann, Jochen. "Diffusion coefficient of tetradec-1-ene in 2,6,10,15,19,23-hexamethyl-tetracosane." In Diffusion in Gases, Liquids and Electrolytes, 1061. Berlin, Heidelberg: Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-540-73735-3_837.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Winkelmann, Jochen. "Diffusion coefficient of tetradec-1-ene in ethane at infinite dilution." In Diffusion in Gases, Liquids and Electrolytes, 2952–53. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_2343.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Winkelmann, Jochen. "Diffusion coefficient of tetradec-1-ene in propane at infinite dilution." In Diffusion in Gases, Liquids and Electrolytes, 2954. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-54089-3_2344.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Lowery, Colin A., Gunnar F. Kaufmann, and Kim D. Janda. "Determination of Acyl Homoserine Lactone and Tetramic Acid Concentrations in Biological Samples." In Methods in Molecular Biology, 101–11. Totowa, NJ: Humana Press, 2010. http://dx.doi.org/10.1007/978-1-60761-971-0_8.

Full text
APA, Harvard, Vancouver, ISO, and other styles
10

Butler, Philip. "A Black Tetratic Future: Blackness and the Age of Hyper-Exponentiation (Hyper-4)." In Critical Black Futures, 37–60. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-7880-9_3.

Full text
APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "TetraNuc"

1

Shishanin, A. O. "The tetradic approach and BF-gravity." In Twelfth Asia-Pacific International Conference on Gravitation, Astrophysics, and Cosmology. WORLD SCIENTIFIC, 2016. http://dx.doi.org/10.1142/9789814759816_0045.

Full text
APA, Harvard, Vancouver, ISO, and other styles
2

Baghai-Wadji, A. R. "The Path from Monadic to Tetradic Green’s Functions." In 2018 International Conference on Electromagnetics in Advanced Applications (ICEAA). IEEE, 2018. http://dx.doi.org/10.1109/iceaa.2018.8520504.

Full text
APA, Harvard, Vancouver, ISO, and other styles
3

Wang, Xiaofang, Xiuyang Zhao, Jin Zhou, and Ming Xu. "A unified framework for flickr group recommendation based on tetradic decomposition." In 2017 4th International Conference on Information, Cybernetics and Computational Social Systems (ICCSS). IEEE, 2017. http://dx.doi.org/10.1109/iccss.2017.8091429.

Full text
APA, Harvard, Vancouver, ISO, and other styles
4

Chin, Yu-Tang, Hsuan-Yu Lai, Heng-Yuan Tang, Hung-Yun Lin, Shaker A. Mousa, and Paul J. Davis. "Abstract B37: Anti-PD-L1 activity of Nano-diamino-tetrac (Nanotetrac) on cancer cells." In Abstracts: Fourth AACR International Conference on Frontiers in Basic Cancer Research; October 23-26, 2015; Philadelphia, PA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.fbcr15-b37.

Full text
APA, Harvard, Vancouver, ISO, and other styles
5

Sudha, Thangirala, Dhruba J. Bharali, Noureldien HE Darwish, Melis Debreli-Coskun, Qishan Lin, Paul J. Davis, and Shaker A. Mousa. "Abstract 2166: Targeted delivery of chemotherapeutic agents to solid tumors via systemic Nano-diamino-tetrac." In Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-2166.

Full text
APA, Harvard, Vancouver, ISO, and other styles
6

Chin, Yu-Tang, Chi-Yu Lin, Ya-Jung Shih, Shin-Ying Lin, YiRu Chen, Shaker A. Mousa, Heng-Yun Tang, Hung-Yun Lin, and Paul J. Davis. "Abstract A196: Nano-diamino-tetrac (NDAT) enhances resveratrol-induced antiproliferation by reducing RRM2 expression in colorectal cancer cells." In Abstracts: AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics; October 26-30, 2017; Philadelphia, PA. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1535-7163.targ-17-a196.

Full text
APA, Harvard, Vancouver, ISO, and other styles
7

Davis, Paul J., Sudha Thangirala, Stewart Sell, Aleck Hercbergs, and Shaker A. Mousa. "Abstract LB-129: NDAT and P-bi-TAT formulations of tetraiodothyroacetic acid (tetrac) induce devascularization, necrosis and apoptosis in glioblastoma xenografts." 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-lb-129.

Full text
APA, Harvard, Vancouver, ISO, and other styles
8

Hercbergs, Aleck A., Faith B. Davis, Paul J. Davis, and John T. Leith. "Abstract 3447: Tetrac (tetraiidothyroacetic acid) decreases in vitro x-ray survival of a human medullary thyroid cancer cell line under oxic and hypoxic conditions." 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.am2012-3447.

Full text
APA, Harvard, Vancouver, ISO, and other styles
9

Hercbergs, Aleck A., Hung-Yun Lin, Faith B. Davis, Paul J. Davis, and John T. Leith. "Abstract 2673: Tetraiodothyroacetic acid (tetrac) produces an increase in the unirradiated steady-state levels of DNA double strand breaks (DSBs) and inhibition of repair of DSBs after x-irradiation in human U87MG brain tumor cells." 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.am2011-2673.

Full text
APA, Harvard, Vancouver, ISO, and other styles
You might also be interested in the extended bibliographies on the topic 'TetraNuc' for particular source types:
Journal articles Dissertations / Theses
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography