Relevant bibliographies by topics / Tyroxin

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

Academic literature on the topic 'Tyroxin'

Author: Grafiati
Published: 4 June 2021
Last updated: 15 February 2022

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Journal articles on the topic "Tyroxin"

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., Pinandoyo, Dicky Harwanto, Seto Windarto, and Vivi Endar Herawati. "The effects of addition Tyroxin hormone on growth and the survival rate of giant prawn Macrobrachium rosenbergii." International Journal of Fisheries and Aquatic Studies 8, no. 6 (2020): 84–87. http://dx.doi.org/10.22271/fish.2020.v8.i6b.2363.

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Pavlík, Aleš, Pavel Jelínek, Martin Matějíček, and Josef Illek. "Blood Plasma Metabolic Profile of Aberdeen Angus Bulls during Postnatal Ontogenesis." Acta Veterinaria Brno 79, no. 3 (2010): 419–29. http://dx.doi.org/10.2754/avb201079030419.

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Selected indicators for the metabolic profile of blood plasma in 22 Aberdeen Angus bulls reared by the extensive method were monitored during postnatal development (from 4 to 564 days of age), including total proteins, albumin, urea, creatinine, glucose, cholesterol, triacylglycerols, bilirubin, alkaline phosphatase, alanine transaminase, aspartate transaminase, tyroxin, triiodothyronine, calcium, inorganic phosphorus, magnesium, potassium, sodium, chlorides, copper, zinc and iron. In assessing the relationship of age to the indicators of the internal environment, values of correlation coefficients for total proteins (r = –0.70;p< 0.01), albumin (r = –0.56;p< 0.01), urea (r = –0.73;p< 0.01), glucose (r = –0.38;p< 0.01) and triiodothyronine (r = –0.82;p< 0.01) were established. Significant relationships were shown between the temperature of the external environment and the amount of total proteins (r = –0.38;p< 0.01), urea concentration (r = –0.41;p< 0.01), ALP (r = 0.58;p< 0.01) and ALT (r = 0.45;p< 0.01) activity. Temperature also showed a significant impact on the concentration of P (r = 0.57;p< 0.01), K (r = –0.69;p< 0.01) and Zn (r = 0.33;p< 0.01). The work yields important information on changes in the indicators of the metabolic profile of the blood plasma of bulls during postnatal development under defined nutritional and temperature conditions that can be used as reference values for evaluating health status as well as nutrition level.
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Adamiec, J., K. Cejpek, J. Rössner, and J. Velíšek. "Novel Strecker degradation products of tyrosine and dihydroxyphenylalanine." Czech Journal of Food Sciences 19, No. 1 (2013): 13–18. http://dx.doi.org/10.17221/6568-cjfs.

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Tyrosine was oxidised with either potassium peroxodisulphate or glyoxal. Volatile reaction products were isolated and analysed by GC/FID and GC/MS, derivatised with diazomethane and analysed by the same methods. Eight reaction products were identified. The major products were the expected Strecker aldehyde (4-hydroxyphenylacetaldehyde) and its lower homologue 4-hydroxybenzaldehyde. They were followed by 1-(4-hydroxyphenyl)-3-propionaldehyde, phenylacetaldehyde, benzaldehyde, phenol, 4-hydroxybenzoic, and benzoic acid. Analogously, the oxidation of 3,4-dihydroxyphenylalanine yielded the corresponding Strecker aldehyde (3,4-dihydroxyphenylacetaldehyde), its lower homologue 3,4-dihydroxybenzaldehyde, 3,4-dihydroxybenzoic, 3,4-dihydroxyphenylacetic, and caffeic acid. An identification of these oxidation products of tyrosine and 3,4-dihydroxyphenylalanine assumes homolytic cleavage of the Strecker aldehydes and a recombination of free radicals formed by this cleavage. As minor products, six O- and N-heterocyclic compounds arose in systems containing glyoxal (pyrazine, methyl- and ethylpyrazine, 3-furancarbaldehyde, 5-methyl-2-furancarbaldehyde, 2-pyrrolcarbaldehyde).
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Bae, Sun-Sik, Jang-Hyun Choi, Sung-Ji Yun, et al. "Direct tyrosine phosphorylation of Akt/PKB by epidermal growth factor receptor." Journal of Life Science 17, no. 2 (2007): 185–91. http://dx.doi.org/10.5352/jls.2007.17.2.185.

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Palangat, M., and D. Roy. "Phosphorylation of Tyrosine Residues of RNA Polymerase II and Other Nuclear Proteins by Active Chromatin Tyrosin Kinase(s)." Biochemical and Biophysical Research Communications 209, no. 1 (1995): 356–64. http://dx.doi.org/10.1006/bbrc.1995.1511.

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Rybalchenko I.V., Krylov V. I. "Synthesis of O-tyrosine Phosphorylated Adducts of Methylphosphonic and Phosphoric Acid Derivatives as Reference Compounds for the Analysis of Biomedical Samples." Journal of NBC Protection Corps 3, no. 2 (2019): 103–10. http://dx.doi.org/10.35825/2587-5728-2019-3-2-103-110.

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Organophosphorus chemical agents are included in the 1st List of the Annex on Chemicals of the Convention on the Prohibition of the Development, Production, Stockpiling and Use of Chemical Weapons and on Their Destruction (Chemical Weapons Convention, CWC). For the purposes of verification of compliance with the provisions of the CWC, special methods, which are considered the most informative at determining the retrospective effects of organophosphorus toxicants on the body, are necessary. Typical long-lived biomarkers of organophosphate toxic agents are tyrosine phosphorylation products, the presence of which in biomedical samples clearly indicates the exposure to sarin, soman, tabun and V-series agents. We have elaborated methods for the synthesis and isolation of tyrosine adducts derivatives of methylphosphonic and phosphoric acids, used as reference samples. The synthesis scheme included the consecutive protection of carboxyl and amino groups of tyrosine, its O-phosphorylation by the corresponding alkylphosphonates and phosphates, the removal of protective groups with the release of corresponding O-phosphorylated tyrosine adducts. Their purification from im purities was carried out, using column chromatography (SiO2, eluent: dichloromethane/ethyl acetate 1:1). The purity of the obtained products was more than 90 %, so it was possible to involve them in further transformations with the use of catalyst without the threat of its «poisoning». Benzyl and carboxybenzyl protection of phosphorylated L-tyrosines (12–17) was removed by means of catalytic hydrogenation by molecular hydrogen under atmospheric pressure. Target adducts of phosphorylated reagents and L-tyrosin were obtained (63–82 %) in form of crystal white substances, readily soluble in water and ethanol, and poorly – in dichloromethane and acetonitrile
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Kobzar, O. L., V. V. Trush, V. Yu Tanchuk, and A. I. Vovk. "Inhibitory potential of polyhydroxylated fullerenes against protein tyrosine phosphatase 1B." Ukrainian Biochemical Journal 87, no. 4 (2015): 24–31. http://dx.doi.org/10.15407/ubj87.04.024.

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Nirmala, N. Baby, and P. Vani P. Vani. "Oxidation of L-Tyrosine by Tetrachloroaurate(III) – a Kinetic Study." International Journal of Scientific Research 2, no. 4 (2012): 25–27. http://dx.doi.org/10.15373/22778179/apr2013/11.

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Oviedo-Silva, Claudia, Mhartyn Elso-Freudenberg, and Mario Aranda-Bustos. "L-DOPA Trends in Different Tissues at Early Stages of Vicia faba Growth: Effect of Tyrosine Treatment." Applied Sciences 8, no. 12 (2018): 2431. http://dx.doi.org/10.3390/app8122431.

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The nonprotein amino acid Levo-3,4-dihydroxyphenylalanine (L-DOPA) has insecticidal, allelochemical, and antiparkinsonian effects. The aim of this research was to assess L-DOPA content in different tissues of Vicia faba (cv. Super Agua Dulce), and to verify if treatment with the phenolic amino acid L-4-hydroxyphenylalanine (tyrosine) had an effect on such content. Under light germination, control and tyrosine-treated early seedling stages of V. faba were studied and L-DOPA was quantified spectrophotometrically (Arnow’s method) and by high-performance thin-layer chromatography (HPTLC), as well. Additionally, tyrosinase (TYROX) and guaiacol peroxidase (GPX) activities (considered markers of a phenolic compounds metabolism) were quantified as germination proceeded. Different organs (roots, sprouts, and seeds) and different developmental stages were considered. Steady high L-DOPA concentrations were found in untreated sprouts and roots compared to seeds, as time progressed. While TYROX activity was not detected in these experiments, GPX had diverse trends. In control tissues, GPX increased in seed tissue as germination progressed, whereas in roots and sprouts, a decreasing GPX activity was observed. Tyrosine exposure decreased L-DOPA content, and decreased or did not change GPX activity (depending on the organ). Both Arnow’s and HPTLC methods were consistent in terms of tendencies, except for the scarce contents found in seeds, in which HPTLC was more sensitive. The richest source of L-DOPA was found in shoots (untreated), reaching as high as 125 mg g−1 DW (12% in DW) (the highest content reported in fava bean seedlings until now), whereas the smallest L-DOPA content was found in seeds. The importance of light germination conditions is discussed in terms of L-DOPA yield and from a physiological perspective. It is concluded that V. faba (cv. Super Agua Dulce) shoots are a good source of L-DOPA and that tyrosine addition (0.55 mM) decreases L-DOPA content in actively growing tissues (shoots and roots).
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M.Kh., Shamsutdinova, Kurbanov Yu.A., Tepsurkaeva I.R. та Khasayeva A.I. "ИССЛЕДОВАНИЕ КООРДИНАЦИОННЫХ СОЕДИНЕНИЙ ЕВРОПИЯ(III) C ТИРОЗИНОМ И β-ЦИКЛОДЕКСТРИНОМ". "Medical & pharmaceutical journal "Pulse" 21, № 8 (2019): 26–31. http://dx.doi.org/10.26787/nydha-2686-6838-2019-21-8-26-31.

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Dissertations / Theses on the topic "Tyroxin"

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Mustafa, Lorin. "Är kombinationsbehandling med levotyroxin och liotyronin ett bättre alternativ än behandling med enbart levotyroxin vid primär hypotyreos?" Thesis, Linnéuniversitetet, Institutionen för kemi och biomedicin (KOB), 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:lnu:diva-95812.

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Bakgrund: Kroppens ämnesomsättning regleras av den endokrina körteln glandula thyreoidea som sitter på framsidan av halsen. Körtelvävnaden består av ett stort antal mikroskopiska hålrum; folliklar. I follikelcellerna produceras två viktiga hormoner; tyroxin och trijodtyronin. Dessa hormon styr många funktioner i kroppen bland annat upprätthåller de en normal ämnesomsättningen i varje cell i kroppen. Tillståndet då produktionen av dess hormoner inte möter kroppens behov kallas för hypotyreos. Vid denna underfunktion i thyreoidea går kroppen på lågvarv, cellaktiviteten och ämnesomsättningshastigheten i kroppen sjunker. Idag är levotyroxin den rekommenderade förstahandsbehandlingen mot hypotyreos. En andel patienter blir inte hjälpta av standardbehandlingen trots välinställda doser av levotyroxin och tillfredsställande koncentrationer i blodprover. Därför kan det vara motiverat för dessa patienter att pröva en kombinationsbehandling med tillägg av liothyronin. Kombinationsbehandlingen tros kunna uppnå en mer fysiologisk effekt, eftersom behandlingen då efterliknar den normala thyreoideautsöndringen. Syfte: att undersöka om behandlingen av primär hypotyreos blir mer effektiv om liothyronin ges som ett komplement till nuvarande standardbehandling med enbart levotyroxin. Metod: En litteraturstudie av fem vetenskapliga artiklar gjordes i databasen PubMed. Sökorden som användes var ”hypothyroidism”, ”levothyroxine”, ”liothyronine” och ”combination”. Artiklar granskades och användes som underlag för detta examensarbete. Resultat: I samtliga fem undersökta studier sjönk tyroxinkoncentrationen i kombinationsbehandlingen jämfört med monobehandlingen. I studie ett var preferens för studiebehandling störst i kombinationsbehandlingen. Resultaten från studie två visade gynnsamma effekter på 7 av 11 QOL och depression-parametrar vid kombinationsbehandlingen. I samma studie sågs även en placeboeffekt på 10 av 11 parametrar vid monobehandlingen. Studie tre och fem påvisade inga större skillnader mellan behandlingarna. I studie fyra var det totala- och LDLkolesterolnivåer signifikant lägre i kombinationsbehandlingen jämfört med monobehandlingen. Slutsats: Resultaten från studierna var varierande gällande fördelarna av kombinationsbehandling jämfört med monobehandlingen. Inga tydliga mönster avseende på fördelar med kombinationsbehandling observerades eller var tillräckligt starka genom studierna. Variationen kan bero på flera faktorer, det kan troligen bero på att patienterna var olika sjuk i studierna samt att studierna använde sig av olika mätningssystem för att mäta resultaten. Det krävs fler och större studier med längre uppföljningstid som kan fastställa styrkan av kombinationsbehandlingen gentemot monobehandlingen för att kunna dra generella slutsatser om att det finns en fördel med kombinationsbehandlingen framför monobehandlingen.
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Franck, Dominic. "Radiofluorinated cyclobutyl group for increased metabolic stability using tyrosine derivatives as model system." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2012. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-99003.

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The metabolic stability of these tracers is, in addition to its affinity and selectivity, an important factor for a successful disease diagnosis. PET tracers and all other drugs are subject to biotransformation which can form metabolites as a part of the inactivation or detoxification process of the human body. These metabolites may result in a higher background which has a detrimental influence on the PET image quality or can even make imaging impossible. The aim of this work was to investigate whether [18F]fluorocyclobutyl rings can be introduced into biologically active small molecules to improve metabolic stability of the PET tracer while maintaining or improving the binding affinity and lipophilicity. To test this hypothesis, the tyrosine model compound, O-(3-[18F]fluorocyclobutyl)-L-tyrosine (L-3-[18F]FCBT), was chosen to be investigated. Precursors for the indirect and direct radiolabeling as well as the non-radioactive L- and D-3-FCBT were successfully synthesized. The radiolabeled of L-3-[18F]FCBT were produced via the indirect and direct method in sufficient yield and activity for the biological evaluation. In the biological characterization, L-3-[18F]FCBT showed good tumor uptake in human lung carcinoma cell lines (A549) and was able to be blocked by both non-radioactive L-3-FCBT and non-radioactive FET. In the biodistribution study, the tracer demonstrated tumor uptake and high metabolic stability due to non accumulation of activity in bone. These results were consistent with the animal-PET imaging where L-3-[18F]FCBT showed good tumor uptake and no accumulation of activity in the bone. The D-isomer in comparison with the L-isomer was found to give lower tumor uptake and very low accumulation in the pancreas. The in vitro stability of the L-3[18F]FCBT in human and rat plasma was excellent over 120 minutes. In vivo stability in mice showed very little metabolites and L-3-[18F]FCBT is considered to be stable in vivo. These results have shown that the new [18F]fluorocyclobutyl group has the potential for the preparation of metabolically stable radiotracers and the application looks very promising.
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Duraphe, Prashant S. [Verfasser], and Antje [Akademischer Betreuer] Gohla. "Identifizierung und Charakterisierung von AUM, einer neuen humanen Tyrosin-Phosphatase = Identification and characterization of AUM, a novel human tyrosine phosphatase / Prashant Duraphe. Betreuer: Antje Gohla." Würzburg : Universitätsbibliothek der Universität Würzburg, 2012. http://d-nb.info/101861284X/34.

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Lee, Joseph Moon-Hee 1967. "Characterization of tyrosine phosphorylation in the protein tyrosine phosphatase CD45." Thesis, McGill University, 2001. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=37758.

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The enzymatic activity of the protein tyrosine phosphatase, CD45 has been demonstrated to play an absolutely required role in the regulation of Src family protein tyrosine kinases in T lymphocytes. CD45 function during early events of antigen receptor signaling has been well established, however, the role of CD45 during later stages of T cell activation is only beginning to emerge. Transient tyrosine phosphorylation of CD45 has previously been demonstrated. We show this phosphorylation can be sustained through treatment of a T cell hybridoma cell line with the PTPase inhibitor, pervanadate. Tyrosine phosphorylation of CD45 is significantly increased in the presence of an activated form of Lck. Tyrosine phosphorylated CD45 is correlated with the association of a subset of signaling molecules containing SH2 domains. These molecules include p56Lck, p59Fyn, rasGAP, Grb2 and Csk. Although CD45 becomes abundantly tyrosine phosphorylated upon pervanadate treatment, no other SH2-containing molecules that we had tested demonstrated association with CD45. The interaction between CD45 and Grb2 in particular was found to be dependent upon CD45 tyrosine phosphorylation and mediated through the SH2 domain of Grb2. Interestingly, both Grb2 and a close homolog, Grap are able to bind CD45 in in vitro binding assays. Grap does not, however, associate with CD45 in vivo as was observed for Grb2.<br>CD45 contains two Grb2 consensus binding sequences. Deletion of both results in a greatly diminished capacity for CD45- Grb2 association. However, interaction between the two is not completely abolished and appears to result from an unconventional peptide sequence as observed by 2-dimensional phosphopeptide mapping studies. In the process of mapping the phosphotyrosine sequences required for CD45-Grb2 interaction, many tyrosine-phosphorylated peptides have been identified and assigned to tyrosine residues in CD45.
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Lu, Wei. "Regulation of protein tyrosine phosphatase SHP-2 by tyrosine phosphorylation." Available to US Hopkins community, 2002. http://wwwlib.umi.com/dissertations/dlnow/3080719.

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Eickhoff, Jan. "Untersuchungen zur Funktion der Protein-Tyrosin-Phosphatase PTPRR." [S.l.] : [s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=968671373.

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Hardwick, James S. "Regulation of the Lck tyrosine protein kinase by oxidant-induced tyrosine phosphorylation /." Diss., Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC campuses, 1997. http://wwwlib.umi.com/cr/ucsd/fullcit?p9814544.

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Chen, Shirley Chun-Jyue. "The regulation and function of protein tyrosine phosphatase alpha (PTPα) tyrosine phosphorylation". Thesis, University of British Columbia, 2007. http://hdl.handle.net/2429/31583.

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Protein tyrosine phosphatase alpha (PTPα) is a ubiquitously expressed receptor protein tyrosine phosphatase that functions as an early upstream regulator in the integrin signaling pathway. The integrins, by interacting with extracellular matrix components, regulate cell growth, migration, and survival, and are functionally linked to multiple aspects of cancer biology such as invasion and metastasis. PTPα plays a major role in the integrin signaling cascade by activating Src family kinases (SFKs), which are required for the full activation of the central signaling molecule focal adhesion kinase (FAK). The importance of PTPα in integrin signaling is demonstrated by defects observed in integrin-mediated cytoskeletal rearrangement and focal adhesion formation in PTPα-deficient fibroblasts. PTPα contains a tyrosine phosphorylation site, Tyr-789, located in the intracellular C-terminal tail. Tyr-789 phosphorylation is shown to not affect PTPα catalytic activity, but allows binding of Src and the adaptor protein Grb2. Little is known about the regulation and function of PTPα Tyr-789 phosphorylation. Recent work from our laboratory has discovered that PTPα Tyr-789 phosphorylation is positively regulated upon integrin engagement and is functionally required for integrin-induced cytoskeletal reorganization events, suggesting the importance of the phospho-Tyr-789 motif in PTPα-mediated signaling events. In a search for other regulators of PTPα Tyr-789 phosphorylation, IGF-1, and potentially aFGF, LPA, and PMA, were found to positively regulate PTPα Tyr-789 phosphorylation. These inductions occurred in a Src/Fyn/Yes-independent manner, indicating an involvement of likely non-SFK cellular kinases distinct from those involved in integrin-induced PTPα phosphorylation. Although PTPα Tyr-789 phosphorylation mediates integrin-induced cytoskeletal remodeling, this phosphorylation event did not appear to act upstream of the Rho family of small GTPases that are key regulators of cellular actin structures. To further understand the precise action of PTPα Tyr-789 phosphorylation in integrin (and other) signaling pathway, the interaction between the PTPα phospho-Tyr-789 motif and other cellular proteins was investigated. Integrin-induced PTPα Tyr-789 phosphorylation was accompanied by increased Grb2 recruitment to phospho-PTPα which provides for a mechanism by which Grb2-interacting signaling proteins are recruited to PTPα to mediate downstream integrin signaling events. In addition, several proteins representing potential PTPα phospho-Y789 interacting proteins were isolated by (phospho)peptide affinity purification. The identification of these proteins and validation of their interactions with PTPα may reveal the precise signaling role of PTPα Tyr-789 phosphorylation.<br>Medicine, Faculty of<br>Pathology and Laboratory Medicine, Department of<br>Graduate
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Sun, Guobin. "The role of protein tyrosine phosphatase alpha tyrosine 789 phosphorylation in integrin signaling." Thesis, University of British Columbia, 2013. http://hdl.handle.net/2429/43924.

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Focal adhesions (FA) form interfaces between the extracellular matrix and the cytoskeleton to regulate cell responses such as cell proliferation, survival, and migration. The functions and dynamic interactions of many of the ~180 molecules in this integrin-initiated FA complex network are far from fully understood. Among these is the receptor-like protein tyrosine phosphatase PTPα. In addition to the integrin-proximal action of PTPα to catalyze activation of Src family kinases, subsequent phosphorylation of PTPα at its C-terminal Tyr789 site is essential and acts in an unknown manner to promote cell spreading and migration. We used reconstitution assays in PTPα-null cells to identify and distinguish integrin signaling events that were PTPα-dependent and PTPα-Tyr789-dependent. Results show that PTPα-Tyr789 mediates the localization of PTPα and the scaffolding protein Cas to FAs where Cas interacts with and gets phosphorylated by Src to initiate Cas/Crk-Rac/Cdc42-PAK signaling. Linking these events, this study identifies the Cas-binding protein BCAR3 as a molecular connector of PTPα and Cas, with phosphoTyr789-PTPα interacting with the BCAR3 SH2 domain to recruit BCAR3-Cas to newly forming adhesion sites. These findings identify phospho-Tyr789-PTPα as the first cellular ligand for the SH2 domain of BCAR3, and reveal a role of PTPα in integrin-induced adhesion complex assembly that enables Src-mediated activation of the pivotal function of Cas in cell migration. Furthermore I extended this study into a cancer cell model by showing that the disruption of this PTPα-BCAR3-Cas-Src signaling module inhibits the invasive motility in a rhabdomyosarcoma cell line. In summary, my results in this thesis elucidate the molecular mechanism underlying the PTPα-Tyr789-dependent cell spreading and migration, and support that the PTPα-BCAR3-Cas complex is a critical regulator of cell migration as well as cancer cell invasion and metastasis.
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Müller, Jonathan Wolf. "Zelluläre und biophysikalische Studien an DYRK 3 der N-Terminus als Schlüssel zum Verständnis dieser Protein-Kinase /." [S.l. : s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=973405007.

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Books on the topic "Tyroxin"

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Kellie, Stuart. Tyrosine kinases and neoplastic transformation. R.G. Landes, 1994.

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Goldstein, Barry J. Tyrosine phosphoprotein phosphatases. 2nd ed. Oxford University Press, 1998.

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Pulido, Rafael, ed. Protein Tyrosine Phosphatases. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3746-2.

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Germano, Serena, ed. Receptor Tyrosine Kinases. Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4939-1789-1.

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Fabbro, Doriano, and Frank McCormick, eds. Protein Tyrosine Kinases. Humana Press, 2006. http://dx.doi.org/10.1385/1592599621.

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Barker, Iain F. Studies on tyrosine metabolism. typescript, 1987.

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Goldstein, Barry J. Phosphoprotein phosphatases 1: tyrosine phosphatases. Academic Press, 1995.

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Neel, Benjamin G., and Nicholas K. Tonks, eds. Protein Tyrosine Phosphatases in Cancer. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3649-6.

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Focosi, Daniele, ed. Resistance to Tyrosine Kinase Inhibitors. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-46091-8.

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Daëron, Marc, and Eric Vivier, eds. Immunoreceptor Tyrosine-based Inhibition Motifs. Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-58537-1.

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Book chapters on the topic "Tyroxin"

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Sewell, A. C. "Tyrosin." In Lexikon der Medizinischen Laboratoriumsdiagnostik. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49054-9_3147-1.

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Sewell, A. C. "Tyrosin." In Springer Reference Medizin. Springer Berlin Heidelberg, 2019. http://dx.doi.org/10.1007/978-3-662-48986-4_3147.

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Kobayashi, Kensei. "Tyrosine." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-11274-4_1624.

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Colzato, Lorenza S. "Tyrosine." In Theory-Driven Approaches to Cognitive Enhancement. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-57505-6_1.

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Kvittingen, E. A., P. T. Clayton, and J. V. Leonard. "Tyrosine." In Inborn Metabolic Diseases. Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-662-03147-6_13.

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Kobayashi, Kensei. "Tyrosine." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-27833-4_1624-5.

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Kobayashi, Kensei. "Tyrosine." In Encyclopedia of Astrobiology. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-662-44185-5_1624.

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Bährle-Rapp, Marina. "Tyrosine." In Springer Lexikon Kosmetik und Körperpflege. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_10824.

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Pearson, Mark, Carlos García-Echeverría, and Doriano Fabbro. "Protein Tyrosine Kinases as Targets for Cancer and Other Indications." In Protein Tyrosine Kinases. Humana Press, 2006. http://dx.doi.org/10.1385/1-59259-962-1:001.

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García-Echeverría, Carlos. "Inhibitors of Signaling Interfaces." In Protein Tyrosine Kinases. Humana Press, 2006. http://dx.doi.org/10.1385/1-59259-962-1:031.

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Conference papers on the topic "Tyroxin"

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Pakhomov, V. I., D. V. Rudoy, T. A. Maltseva, N. A. Kulikova, and N. T. Ugrekhelidze. "ANALYSIS OF THE INFLUENCE OF MICROWAVE PROCESSING ON THE CONTENT OF NON-REPLACEABLE AMINO ACIDS IN COMBINE FEEDS." In INNOVATIVE TECHNOLOGIES IN SCIENCE AND EDUCATION. DSTU-Print, 2020. http://dx.doi.org/10.23947/itno.2020.34-37.

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The article presents the results of a study of the effect of micronization of feed samples on proteinogenic amino acids, such as: arginine, lysine, tyrosine, phenylalanine, histidine, leucine-isoleucine, methionine, valine, proline, tyrosine, serine, alanine. The optimal parameters of the micronization of compound feeds are substantiated in order to increase the digestibility of compound feeds and disinfection.
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Tichý, Tomáš, Karel Pomeisl, Marcela Krečmerová, and Charles E. McKenna. "Tyrosine-based prodrugs of acyclic nucleoside phosphonates." In XVIth Symposium on Chemistry of Nucleic Acid Components. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2014. http://dx.doi.org/10.1135/css201414126.

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Wang, Binghua, Minghui Wang, Yujie Jiang, Dongdong Sun, and Xiaoyi Xu. "Predicting tyrosine phosphorylation from site-modification network." In 2015 34th Chinese Control Conference (CCC). IEEE, 2015. http://dx.doi.org/10.1109/chicc.2015.7260996.

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Abid, H., N. Siddiqui, and V. Thirukonda. "Tyrosine Kinase Inhibitor Induced Interstitial Lung Disease." In American Thoracic Society 2020 International Conference, May 15-20, 2020 - Philadelphia, PA. American Thoracic Society, 2020. http://dx.doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a3137.

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Nasir, M. N., E. Bergmann, E. Benichou, et al. "Second harmonic generation from tyrosine containing peptides." In SPIE NanoScience + Engineering, edited by Norihisa Kobayashi, Fahima Ouchen, and Ileana Rau. SPIE, 2013. http://dx.doi.org/10.1117/12.2026866.

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Gueron, Geraldine, Nicolás Anselmino, Paula Chiarella, et al. "Abstract 4717: Clinical implications for m-tyrosine, an isomer of p-tyrosine, for the treatment of aggressive prostate tumors." 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.am2016-4717.

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Kim, Brian, Shilpi Goenka, Srikara V. Peelukhana, Keith F. Stringer, Jay H. Kim, and Rupak K. Banerjee. "Dependence of Higher Frequency Components on Bone Tissue Alterations in the Rat-Tail Model." In ASME 2013 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/sbc2013-14538.

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Through a recently conducted rat-tail vibration experiment, we have been able to determine that the tested frequencies of vibration have a significant effect on biochemical damage signified by nitro-tyrosine (NT) staining on trabecular bone, while structural damage quantified through a Hematoxylin and Eosin (H&amp;E) stain on cortical bone exhibited statistical significance only for the 250 Hz group compared to the control group. These results seem to indicate a relationship between the growing quantities of biochemical damage when increasing the excitation frequency, thus further experimentation for frequencies between 250 Hz and 400 Hz is recommended.
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Yunhai Wang, Yunjing Luo, and Rugang Zhong. "Investigation on insulin tyrosine modification mediated by peroxynitrite." In 2007 IEEE/ICME International Conference on Complex Medical Engineering. IEEE, 2007. http://dx.doi.org/10.1109/iccme.2007.4382060.

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Yang, Hui, Xue Xiao, Xuesong Zhao, and Yan Wu. "Intrinsic Fluorescence Spectra of Tryptophan, Tyrosine and Phenyloalanine." In 5th International Conference on Advanced Design and Manufacturing Engineering. Atlantis Press, 2015. http://dx.doi.org/10.2991/icadme-15.2015.46.

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Oudin, Madeleine J., Shannon K. Hughes-Alford, Miles Miller, et al. "Abstract C41: MenaINVdysregulation of receptor tyrosine kinase signaling." In Abstracts: AACR Special Conference on Tumor Invasion and Metastasis - January 20-23, 2013; San Diego, CA. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.tim2013-c41.

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Reports on the topic "Tyroxin"

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Wirtman, Richard J. Tyrosine, Tryptophan and Performance. Defense Technical Information Center, 1992. http://dx.doi.org/10.21236/ada266278.

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Weier, Heinz-Ulrich. Expression Profiling of Tyrosine Kinase Genes. Defense Technical Information Center, 2003. http://dx.doi.org/10.21236/ada423672.

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Weier, Heinz U. Expression Profiling of Tyrosine Kinase Genes. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada391061.

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Miller, Tod. Peptide-Bassed Inhibitors of Neu Tyrosine Kinase. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada375133.

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Miller, W. T. Peptide-Based Inhibitors of Neu Tyrosine Kinase. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada392289.

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Riese, David J. Functional Analysis of the ErbB4 Receptor Tyrosine Kinase. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada396642.

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Riese, David J. Functional Analysis of the ErbB4 Receptor Tyrosine Kinase. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada396717.

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Tyner, Angela. A Novel Tyrosine Kinase Expressed in Breast Tumors. Defense Technical Information Center, 1997. http://dx.doi.org/10.21236/ada334915.

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Riese, David J. Functional Analysis of the ErbB4 Receptor Tyrosine Kinase. Defense Technical Information Center, 2003. http://dx.doi.org/10.21236/ada418035.

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Riese, David J., and II. Functional Analysis of the ErbB4 Receptor Tyrosine Kinase. Defense Technical Information Center, 2003. http://dx.doi.org/10.21236/ada418740.

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