Gotowe bibliografie tematyczne / Proteins – Identification

Gotowa bibliografia na temat „Proteins – Identification”

Autor: Grafiati
Data publikacji: 4 czerwca 2021
Data aktualizacji: 12 lutego 2022

Utwórz poprawne odniesienie w stylach APA, MLA, Chicago, Harvard i wielu innych

Wybierz rodzaj źródła:

Spis treści

Zobacz listy aktualnych artykułów, książek, rozpraw, streszczeń i innych źródeł naukowych na temat „Proteins – Identification”.

Przycisk „Dodaj do bibliografii” jest dostępny obok każdej pracy w bibliografii. Użyj go – a my automatycznie utworzymy odniesienie bibliograficzne do wybranej pracy w stylu cytowania, którego potrzebujesz: APA, MLA, Harvard, Chicago, Vancouver itp.

Możesz również pobrać pełny tekst publikacji naukowej w formacie „.pdf” i przeczytać adnotację do pracy online, jeśli odpowiednie parametry są dostępne w metadanych.

Artykuły w czasopismach na temat "Proteins – Identification"

1

Paape, M., S. Nell, S. von Bargen i J. W. Kellmann. "Identification and characterization of host proteins interacting with NSm, the Tomato spotted wilt virus movement protein". Plant Protection Science 38, SI 1 - 6th Conf EFPP 2002 (1.01.2002): S108—S111. http://dx.doi.org/10.17221/10331-pps.

Pełny tekst źródła
Streszczenie:
To search for host proteins involved in systemic spreading of Tomato spotted wilt virus (TSWV), the virus-encoded NSm movement protein has been utilized as a bait in yeast two-hybrid interaction trap assays. J-domain chaperones from different host species and a protein denominated At-4/1 from Arabidopsis thaliana showing homologies to myosins and kinesins were identified as NSm-interacting partners. In this communication we illustrate that following TSWV infection, J-domain proteins accumulated in systemically infected leaves of A. thaliana, whereas At-4/1 was constitutively detected in leaves of A. thaliana and Nicotiana rustica.
Style APA, Harvard, Vancouver, ISO itp.
2

Shaw, G. "Rapid identification of proteins." Proceedings of the National Academy of Sciences 90, nr 11 (1.06.1993): 5138–42. http://dx.doi.org/10.1073/pnas.90.11.5138.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
3

Ryšlavá, H., M. Janatová, G. Čalounová, I. Selicharová, J. Barthová i T. Barth. "Separation and identification of carp pituitary proteins and glycoproteins". Czech Journal of Animal Science 50, No. 9 (11.12.2011): 430–37. http://dx.doi.org/10.17221/4232-cjas.

Pełny tekst źródła
Streszczenie:
Carp pituitary proteins and glycoproteins were separated by the combination of immobilized metal affinity chromatography (IMAC) and affinity chromatography on Con A-Sepharose. The protein fractions were analysed by SDS-PAGE. Luteinizing hormone (in the &alpha;<sub>1</sub>&beta; and &alpha;<sub>2</sub>&beta; forms), growth hormone, free &alpha;<sub>1</sub> subunit and &beta;&nbsp;subunit of thyroid-stimulating hormone were identified by N-terminal amino acid sequencing. N-linked oligosaccharide chains of thyroid-stimulating hormone (&beta; TSH) were separated after fluorescent labelling on a GlycoSep N column and treated by exoglycosidases. Among the saccharide components, complex and hybrid structures terminating SO<sub>4</sub>-GalNAc-GlcNAc-Man-, and high mannose structures, with 1 to 8 mannose units attached to the oligosaccharide core (GlcNAc)<sub>2</sub>(Man)<sub>3</sub>, were found. &nbsp;
Style APA, Harvard, Vancouver, ISO itp.
4

Donnini, Martino, Andrea Lapucci, Laura Papucci, Ewa Witort, Alain Jacquier, Gary Brewer, Angelo Nicolin, Sergio Capaccioli i Nicola Schiavone. "Identification of TINO". Journal of Biological Chemistry 279, nr 19 (9.02.2004): 20154–66. http://dx.doi.org/10.1074/jbc.m314071200.

Pełny tekst źródła
Streszczenie:
Modulation of mRNA stability by regulatory cis-acting AU-rich elements (AREs) and ARE-binding proteins is an important posttranscriptional mechanism of gene expression control. We previously demonstrated that the 3′-untranslated region ofBCL-2mRNA contains an ARE that accounts for rapidBCL-2down-regulation in response to apoptotic stimuli. We also demonstrated that theBCL-2ARE core interacts with a number of ARE-binding proteins, one of which is AU-rich factor 1/heterogeneous nuclear ribonucleoprotein D, known for its interaction with mRNA elements of others genes. In an attempt to search for otherBCL-2mRNA-binding proteins, we used the yeast RNA three-hybrid system assay and identified a novel human protein that interacts withBCL-2ARE. We refer to it as TINO. The predicted protein sequence of TINO reveals two amino-terminal heterogeneous nuclear ribonucleoprotein K homology motifs for nucleic acid binding and a carboxyl-terminal RING domain, endowed with a putative E3 ubiquitin-protein ligase activity. In addition the novel protein is evolutionarily conserved; the two following orthologous proteins have been identified with protein-protein BLAST: posterior end mark-3 (PEM-3) ofCiona savignyiand muscle excess protein-3 (MEX-3) ofCaenorhabditis elegans. Upon binding, TINO destabilizes a chimeric reporter construct containing theBCL-2ARE sequence, revealing a negative regulatory action onBCL-2gene expression at the posttranscriptional level.
Style APA, Harvard, Vancouver, ISO itp.
5

Shionyu, M., i M. Go. "Domain identification of large proteins". Seibutsu Butsuri 41, supplement (2001): S76. http://dx.doi.org/10.2142/biophys.41.s76_4.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
6

Roth, Amy F., Junmei Wan, William N. Green, John R. Yates i Nicholas G. Davis. "Proteomic identification of palmitoylated proteins". Methods 40, nr 2 (październik 2006): 135–42. http://dx.doi.org/10.1016/j.ymeth.2006.05.026.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
7

Guo, Dayong, Andrew Keightley, Jill Guthrie, Patricia A. Veno, Stephen E. Harris i Lynda F. Bonewald. "Identification of osteocyte-selective proteins". PROTEOMICS 10, nr 20 (15.09.2010): 3688–98. http://dx.doi.org/10.1002/pmic.201000306.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
8

Wan, Junmei, Amy F. Roth, Aaron O. Bailey i Nicholas G. Davis. "Palmitoylated proteins: purification and identification". Nature Protocols 2, nr 7 (21.06.2007): 1573–84. http://dx.doi.org/10.1038/nprot.2007.225.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
9

Yonezawa, K. "Identification of TOR-interacting Proteins". Molecular Interventions 3, nr 4 (1.06.2003): 189–93. http://dx.doi.org/10.1124/mi.3.4.189.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
10

Mirzaei, Hamid, i Fred Regnier. "Identification of yeast oxidized proteins". Journal of Chromatography A 1141, nr 1 (luty 2007): 22–31. http://dx.doi.org/10.1016/j.chroma.2006.11.009.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
Więcej źródeł

Rozprawy doktorskie na temat "Proteins – Identification"

1

Arbuckle, Janeen Lynnae. "Identification and characterization of domains in non-core RAG1". Oklahoma City : [s.n.], 2007.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
2

Winter, Sherry Lynn. "Identification of BRCA1 interacting proteins". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape2/PQDD_0026/MQ50432.pdf.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
3

Baakdah, Fadi. "Identification of PfCRT interacting proteins". Thesis, McGill University, 2014. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=121534.

Pełny tekst źródła
Streszczenie:
The lethal form of human malaria is caused by the most prominent human protozoan parasite, Plasmodium falciparum, responsible for an estimated ~1 million deaths annually. Malaria treatment and, prevention heavily rely on antimalarial drugs. The synthetic substitute of quinine, chloroquine, was the most effective treatment for this disease. The rise of chloroquine resistant malaria in endemic areas has suppressed control efforts. Chloroquine resistance has been associated with mutations in a transmembrane protein on the digestive vacuole of the parasite, designated PfCRT. Moreover, the normal function(s) and natural substrate(s) of PfCRT remain a matter of speculation as direct evidence for the normal functions or substrates are yet to be determined. The objectives of this thesis are to develop and characterize two antisera to the N- and C termini of PfCRT as tools for the identification of PfCRT interacting proteins in P. falciparum. Although the molecular mass of PfCRT was estimated as 48.67 kDa, immunobiochemical characterizations using different antiserums raised against the N- and C-cytosolic domains of this protein throughout the published literature yielded varying molecular masses of PfCRT on SDS PAGE. In this thesis, we report the generation and biochemical characterization of two antisera raised against the N- and C-cytosolic domains of PfCRT. Our results show PfCRT-C antiserum to detect non-phosphorylated epitopes or sequences in PfCRT. Moreover, our high-resolution epitope mapping results confirm the specificity of PfCRT-C antiserum to a non-phosphorylated form of PfCRT and show that phosphorylation at two sites in PfCRT sequence, Ser411 and Thr416, prevent its binding to the full-length and phosphorylated protein. In addition, we have identified a novel truncated form of PfCRT that is both unphosphorylated, as it is recognized by PfCRT-C antiserum, and likely to represent a differentially spliced product of PfCRT, that is expressed in vivo on the parasite digestive vacuole. Furthermore, our findings confirm the molecular mass of the full-length and phosphorylated PfCRT as a 52 kDa protein band on SDS PAGE. Using PfCRT antisera together with three different methods of protein interactions, we provide the first evidence of proteins interacting with PfCRT. Identification of these proteins which ranges from ~20 kDa to 200 kDa is under active investigation.
La forme létale du paludisme humain est causée par le plus important parasite protozoaire humain, Plasmodium falciparum, responsable d'environ ~1 million de mort annuellement. Le traitement et la prévention du paludisme dépend des médicaments antipaludiques. Le substitut synthétique de la quinine, la chloroquine, était le traitement le plus efficace pour cette maladie. La montée du paludisme résistant à la chloroquine dans les pays endémiques a supprimé les efforts de contrôle. La résistance à la chloroquine a été associée aux mutations dans la protéine transmembranaire présente sur la vacuole digestive du parasite, désigné PfCRT. De plus, la ou les fonctions normales et substrats naturels de la protéine PfCRT restent une affaire de spéculation étant donné qu'une évidence directe des fonctions normales et des substrats de cette protéine sont encore à déterminer. Les objectives de cette thèse sont de développer et de caractériser deux antisérums de l'extrémité N- et C-terminale de PfCRT comme outils d'identification des protéines interagissant avec la protéine PfCRT de P. falciparum. Bien que la masse moléculaire de la protéine PfCRT était estimée à 48.67 kDa, des caractérisations immunobiochimiques utilisant différents antisérums dirigés contre les domaines cytosoliques N- et C-terminal de cette protéine et publiés à travers la littérature ont abouti à des masses moléculaires variable de la protéine PfCRT sur le SDS PAGE. Dans cette thèse, nous reportons la génération et la caractérisation biochimique de deux antisérums dirigés contre les domaines cytosoliques N- et C de PfCRT. Nos résultats montrent que l'antisérum C de PfCRT détecte les épitopes non-phosphorylés ou des séquences dans la protéine PfCRT. En outre, nos résultats de la cartographie à haute résolution de l'épitope confirment la spécificité de l'antisérum C de PfCRT à la forme non-phosphorylé de PfCRT et montrent que la phosphorylation à deux sites au niveau de la séquence de la protéine, Ser411 et Thr416, qui empêche sa fixation à la protéine complète et phosphorylée. De plus, nous avons identifié une nouvelle forme tronquée de PfCRT qui est à la fois phosphorylée puisqu'elle est reconnue par l'antisérum C de PfCRT, et susceptible de représenter un produit différemment épissé de PfCRT, qui est exprimé in vivo sur la vacuole digestive du parasite. En outre, nos résultats confirment la masse moléculaire de la protéine complète et phosphorylée de PfCRT à 52 kDa sur un SDS PAGE. En utilisant les antisérums de PfCRT combiné à trois méthodes différentes d'interactions protéiques, nous fournissons la première preuve de protéines interagissant avec la protéine PfCRT. L'identification de ces protéines dont la masse varie entre ~20 kDa et 200 kDa est sous enquête active.
Style APA, Harvard, Vancouver, ISO itp.
4

Wei, Heng. "Split PH domain identification & redundancy analyses in the classification of PDZ domains /". View abstract or full-text, 2006. http://library.ust.hk/cgi/db/thesis.pl?BICH%202006%20WEI.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
5

Hellborg, Fredrik. "Identification, cloning and characterization of the p53 induced gene human wig-1 /". Stockholm, 2004. http://diss.kib.ki.se/2004/91-7140-190-3/.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
6

Yap, Jessica. "Identification of Plasmodium falciparum protein kinase substrates and interacting proteins". Honors in the Major Thesis, University of Central Florida, 2012. http://digital.library.ucf.edu/cdm/ref/collection/ETH/id/644.

Pełny tekst źródła
Streszczenie:
Characterization of PfPKA and PfPK5 substrates, as well as the proteins they interact with, will help us to develop innovative therapies targeting binding sites.; Malaria is a devastating disease that results in almost one million deaths annually. Most of the victims are children under the age of five in Sub-Saharan Africa. Malaria parasite strains throughout developing countries are continually building resistance to available drugs. Current therapies such as mefloquine, chloroquine, as well as artemisinin are becoming less effective, and this underscores the urgency for therapeutics directed against novel drug targets. In order to identify new drug targets, the molecular biology of the malaria parasite Plasmodium needs to be elucidated. Plasmodium exhibits a unique cell cycle in which it undergoes multiple rounds of DNA synthesis and mitosis without cytokinesis. Thus, cell cycle regulatory proteins are likely to be promising pathogen-specific drug targets. It is expected that fluctuating activity of key proteins, such as protein kinases, play an essential role in regulating the noncanonical life cycle of Plasmodium. Consequently, malarial kinases are a prime target for therapy. One way to better understand the role of malarial kinases in Plasmodium cell cycle regulation is to identify putative protein kinase substrates and interacting proteins. Two malarial kinases that have been implicated in regulating malaria parasite cell cycle stages were investigated in this study: P. falciparum CDK-like Protein Kinase 5 (PfPK5) and cAMP-Dependent Protein Kinase A (PfPKA). A transgenic P. falciparum line was created for the expression of epitope-tagged PfPK5 for pull-down analysis. Phospho-substrate antibodies were used to identify physiological substrates of both PfPK5 and PfPKA. Immunoblotting with these antibodies identified several potential substrates. Identities of the PfPKA physiological substrates were determined from the global P. falciparum phosphoproteome dataset that has recently been generated in our laboratory.
B.S.
Bachelors
Burnett School of Biomedical Sciences
Molecular and Microbiology
Style APA, Harvard, Vancouver, ISO itp.
7

Wadahama, Hiroyuki. "Identification and Characterization of Soybean Protein Disulfide Isomerase Family Proteins as Functional Proteins for Folding of Seed-storage Proteins". Kyoto University, 2010. http://hdl.handle.net/2433/120458.

Pełny tekst źródła
Streszczenie:
Kyoto University (京都大学)
0048
新制・課程博士
博士(農学)
甲第15414号
農博第1799号
新制||農||978(附属図書館)
学位論文||H22||N4513(農学部図書室)
27892
京都大学大学院農学研究科食品生物科学専攻
(主査)教授 河田 照雄, 教授 村田 幸作, 教授 井上 國世
学位規則第4条第1項該当
Style APA, Harvard, Vancouver, ISO itp.
8

McLoughlin, D. M. "Identification of proteins interacting with the Alzheimer's disease amyloid precursor protein". Thesis, King's College London (University of London), 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.343724.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
9

Mac, Partlin Mary. "Identification of proteins interacting with the human mismatch repair protein MLH1". Thesis, University of Glasgow, 2000. http://theses.gla.ac.uk/1111/.

Pełny tekst źródła
Streszczenie:
Loss of expression of the human DNA mismatch repair (MMR) gene, hMLH1, is seen in a number of tumour cell lines resistant to a variety of cytotoxic drugs. The aim of this study was to identify other proteins that interact with hMLH1 to attempt to further elucidate its role in MMR and the engagement of downstream damage response pathways. A yeast two-hybrid system, an in vivo system for detecting protein-protein interactions was utilised for this purpose. Fifteen known and five unknown genes were identified as encoding proteins interacting with hMLH1. These included three known hMLH1 binding proteins, hMLH3, hPMS1 and MED1. Amongst the other genes identified was the proto-oncogene c-MYC, a gene previously implicated in genetic instability and apoptosis. Using in vitro derived mutants of c-MYC, it has been shown that hMLH1 interacts with the leucine-zipper domain of c-MYC. The effect of elevated c-MYC expression on functional MMR was examined. An inducible c-MYC expression system, Rat-1 fibroblasts expressing c-MYCERTM, a fusion of c-MYC to the hormone binding domain of the oestrogen receptor was utilised. Elevated expression of c-MYC did not effect the mismatch specific binding complex activity in these cells as measured in EMSA experiments. However c-MYC overexpression utilising the Rat-1 cMYCERTM system was shown to result in a mutator phenotype in these cells. The results suggest there may be a link between the mutator phenotype, induced through overexpression of c-MYC, and loss of MMR. Overexpression of c-MYC, which is associated with many cancers, may result in the sequestration of hMLH1 preventing functional MMR. The interaction between hMLH1 and c-MYC is proposed to act in a DNA damage response pathway which is disrupted upon aberrant c-MYC expression.
Style APA, Harvard, Vancouver, ISO itp.
10

Höglund, Pär J. "Identification, Characterization and Evolution of Membrane-bound Proteins /". Uppsala : Acta Universitatis Upsaliensis Acta Universitatis Upsaliensis, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-9329.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
Więcej źródeł

Książki na temat "Proteins – Identification"

1

Winter, Sherry Lynn. Identification of BRCA1 interacting proteins. Ottawa: National Library of Canada, 2000.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
2

1953-, Budowle Bruce, red. Protein staining and identification techniques. [Natick, MA]: BioTechniques Books, 1999.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
3

Yan, Qingyou. Identification of tannin-binding proteins in human saliva. Ottawa: National Library of Canada, 1994.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
4

Yan, Qingyou. Identification of tannin-binding proteins in human saliva. [Toronto: Faculty of Dentistry, University of Toronto], 1995.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
5

Lawson, David Alexander. Identification of immunogenic proteins of litomosoides carinii (Nematoda, Filarioidea). Salford: University of Salford, 1988.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
6

Silverman, Gregory Lindsay. Identification and characterization of proteins binding to the amino-terminus of the human prion protein. Ottawa: National Library of Canada, 1999.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
7

Sun, Frank. Identification of Porphyromonas (Bacteroides) Gingivalis outer membrane proteins that bind to and degrade human matrix proteins. [Toronto: Faculty of Dentistry, University of Toronto, 1992.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
8

Ladak, Rahim Akbarali. Identification of ROM1- and PHR1-interacting proteins in the mammalian photoreceptor. Ottawa: National Library of Canada, 1999.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
9

E, Sherman Nicholas, red. Protein sequencing and identification using tandem mass spectrometry. New York: John Wiley, 2000.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
10

Hearn, Melanie Jane. Identification and characterisation of a binding protein from pollen membranes for the Papaver rhoeas stigmatic self-incompatability [(S-)] proteins. Birmingham: University of Birmingham, 1998.

Znajdź pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
Więcej źródeł

Części książek na temat "Proteins – Identification"

1

Hopp, Thomas P. "Identification of Protein Surfaces and Interaction Sites by Hydrophilicity Analysis". W Proteins, 437–43. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1787-6_43.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
2

Cheng, Heung-Chin, Bruce E. Kemp, Alan J. Smith, Richard B. Pearson, Scott M. Van Patten, Lufti Misconi i Donal A. Walsh. "Identification of Functional Domains of the Inhibitor Protein of Camp-Dependent Protein Kinase". W Proteins, 631–39. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1787-6_63.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
3

Misono, Kunio S. "Atrial Natriuretic Factor Receptor in Adrenal Plasma Membrane: Identification by Photo-Affinity Labeling". W Proteins, 641–48. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1787-6_64.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
4

Lindesmith, Lisa C., Janardan Kumar i Michael P. Sheetz. "Identification of Kinesin-Associated Proteins". W Kinesin Protocols, 205–12. Totowa, NJ: Humana Press, 2001. http://dx.doi.org/10.1385/1-59259-069-1:205.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
5

Dong, Qunfeng, i Volker Brendel. "Computational Identification of Related Proteins". W The Proteomics Protocols Handbook, 555–70. Totowa, NJ: Humana Press, 2005. http://dx.doi.org/10.1007/978-1-59259-890-8_51.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
6

George, David G., Winona C. Barker i Lois T. Hunt. "The Protein Identification Resource (PIR): An On-Line Computer System for the Characterization of Proteins Based on Comparisons with Previously Characterized Protein Sequences". W Proteins, 445–53. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1787-6_44.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
7

Mc Cormick, Daniel J., Benjamin J. Madden i Robert J. Ryan. "Identification of Side-Chain Protected L-Phenylthiohydantoins on Cyano HPLC Columns: An Application to Gas-Phase Microsequencing of Peptides Synthesized on Solid-Phase Supports". W Proteins, 403–13. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1787-6_40.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
8

Li, Dongxia, Grazyna Dobrowolska i Edwin G. Krebs. "Identification of proteins that associate with protein kinase CK2". W A Molecular and Cellular View of Protein Kinase CK2, 223–28. Boston, MA: Springer US, 1999. http://dx.doi.org/10.1007/978-1-4419-8624-5_27.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
9

Treiber, Thomas, Nora Treiber i Gunter Meister. "Identification of microRNA Precursor-Associated Proteins". W Methods in Molecular Biology, 103–14. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-8624-8_9.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
10

Buratti, Emanuele. "Identification of Proteins Bound to RNA". W Alternative pre-mRNA Splicing, 290–97. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2012. http://dx.doi.org/10.1002/9783527636778.ch27.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.

Streszczenia konferencji na temat "Proteins – Identification"

1

Jung, Suk Hoon, Desok Kim i Dong-Soo Han. "Conserved Domain Combination Identification in Human Proteins". W 22nd International Conference on Advanced Information Networking and Applications - Workshops (aina workshops 2008). IEEE, 2008. http://dx.doi.org/10.1109/waina.2008.228.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
2

Shen, Xianjun, Rui Xu, Xiaohui Chen, Jincai Yang i Tingting He. "Identification of essential proteins based on network capital assessment and invalidating protein node". W 2013 IEEE International Conference on Bioinformatics and Biomedicine (BIBM). IEEE, 2013. http://dx.doi.org/10.1109/bibm.2013.6732570.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
3

Dempewolf, Chris, Jacqueline Morris, Meghna Chopra, Srinivas Jayanthi, Thallapuranam K. Suresh Kumar i Wing Ning Li. "Identification of Consensus Glycosaminoglycan Binding Strings in Proteins". W 2013 International Conference on Information Science and Applications (ICISA). IEEE, 2013. http://dx.doi.org/10.1109/icisa.2013.6579411.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
4

Chatterjee, S., i B. S. Sanjeev. "Identification of human proteins vulnerable to multiple organisms". W 2016 International Conference on Bioinformatics and Systems Biology (BSB). IEEE, 2016. http://dx.doi.org/10.1109/bsb.2016.7552164.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
5

Jung, Suk Hoon, Hee-Young Hur, Desok Kim i Dong-Soo Han. "Identification of Conserved Domain Combinations in S.cerevisiae Proteins". W 2007 IEEE 7th International Symposium on BioInformatics and BioEngineering. IEEE, 2007. http://dx.doi.org/10.1109/bibe.2007.4375539.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
6

Huang, Yue, Jun Zhang i Yunying Huang. "Computational identification of proteins sub-network in Parkinson's disease study". W 2012 International Conference on Anti-Counterfeiting, Security and Identification (2012 ASID). IEEE, 2012. http://dx.doi.org/10.1109/icasid.2012.6325320.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
7

Iyuke, Festus O., James R. Green i William G. Willmore. "Active Learning for the Prediction of Asparagine/Aspartate Hydroxylation Sites on Proteins". W Computational Intelligence and Bioinformatics / Modelling, Simulation, and Identification. Calgary,AB,Canada: ACTAPRESS, 2011. http://dx.doi.org/10.2316/p.2011.753-034.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
8

Iyuke, Festus O., James R. Green i William G. Willmore. "Active Learning for the Prediction of Asparagine/Aspartate Hydroxylation Sites on Proteins". W Computational Intelligence and Bioinformatics / Modelling, Simulation, and Identification. Calgary,AB,Canada: ACTAPRESS, 2012. http://dx.doi.org/10.2316/p.2012.753-034.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
9

Boisson, J. C., L. Jourdan, E. G. Talbi i C. Rolando. "A preliminary work on evolutionary identification of protein variants and new proteins on grids". W 20th International Conference on Advanced Information Networking and Applications - Volume 1 (AINA'06). IEEE, 2006. http://dx.doi.org/10.1109/aina.2006.48.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
10

Han, Bing, Ming Du, Weili Xu i Haibo Gao. "Purification and Identification of Acidic Proteins in Bovine Colostrum". W 2010 4th International Conference on Bioinformatics and Biomedical Engineering (iCBBE). IEEE, 2010. http://dx.doi.org/10.1109/icbbe.2010.5515583.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.

Raporty organizacyjne na temat "Proteins – Identification"

1

Branda, Steven S., Todd W. Lane, Victoria A. VanderNoot i Amanda S. Jokerst. Small acid soluble proteins for rapid spore identification. Office of Scientific and Technical Information (OSTI), grudzień 2006. http://dx.doi.org/10.2172/984135.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
2

Rabinovsky, Rosalia. Identification and Validation of PTEN Complex, Associated Proteins. Fort Belvoir, VA: Defense Technical Information Center, listopad 2006. http://dx.doi.org/10.21236/ada463362.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
3

Staiger, C. J. Identification of Actin-Binding Proteins from Maize Pollen. Office of Scientific and Technical Information (OSTI), styczeń 2004. http://dx.doi.org/10.2172/820708.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
4

Fenczik, Csilla A. Identification and Characterization of Proteins Involved in Integrin Signaling. Fort Belvoir, VA: Defense Technical Information Center, wrzesień 2000. http://dx.doi.org/10.21236/ada394209.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
5

Songyang, Zhou. Identification of Signaling Proteins That Modulate Androgen Receptor Activity. Fort Belvoir, VA: Defense Technical Information Center, maj 2003. http://dx.doi.org/10.21236/ada416488.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
6

Songyang, Zhou. Identification of Signaling Proteins the Modulate Androgen Receptor Activity. Fort Belvoir, VA: Defense Technical Information Center, listopad 2004. http://dx.doi.org/10.21236/ada432546.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
7

Fenczik, Csilla A. Identification and Characterization of Proteins Involved in Integrin Signaling. Fort Belvoir, VA: Defense Technical Information Center, wrzesień 1999. http://dx.doi.org/10.21236/ada391337.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
8

Songyang, Zhou. Identification of Signaling Proteins that Modulate Androgen Receptor Activity. Fort Belvoir, VA: Defense Technical Information Center, maj 2002. http://dx.doi.org/10.21236/ada406842.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
9

Du, Guangwei. Identification of Druggable Proteins Regulating Receptor Recycling in Breast Cancer Cells. Fort Belvoir, VA: Defense Technical Information Center, wrzesień 2012. http://dx.doi.org/10.21236/ada568808.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
10

Du, Guangwei, Ping Wu, Yoshiya Yonekubo i Melissa Wilmarth. Identification of Druggable Proteins Regulating Receptor Recycling in Breast Cancer Cells. Fort Belvoir, VA: Defense Technical Information Center, wrzesień 2011. http://dx.doi.org/10.21236/ada554389.

Pełny tekst źródła
Style APA, Harvard, Vancouver, ISO itp.
Możesz być także zainteresowany rozszerzonymi bibliografiami na temat „Proteins – Identification” dla poszczególnych typów źródeł:
Artykuły w czasopismach Rozprawy doktorskie Książki
Oferujemy zniżki na wszystkie plany premium dla autorów, których prace zostały uwzględnione w tematycznych zestawieniach literatury. Skontaktuj się z nami, aby uzyskać unikalny kod promocyjny!

Do bibliografii