FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2140443886> ?p ?o ?g. }

• W2140443886 endingPage "26" @default.
• W2140443886 startingPage "26" @default.
• W2140443886 abstract "Reversible protein phosphorylation is one of the most important forms of cellular regulation. Thus, phosphoproteomic analysis of protein phosphorylation in cells is a powerful tool to evaluate cell functional status. The importance of protein kinase-regulated signal transduction pathways in human cancer has led to the development of drugs that inhibit protein kinases at the apex or intermediary levels of these pathways. Phosphoproteomic analysis of these signalling pathways will provide important insights for operation and connectivity of these pathways to facilitate identification of the best targets for cancer therapies. Enrichment of phosphorylated proteins or peptides from tissue or bodily fluid samples is required. The application of technologies such as phosphoenrichments, mass spectrometry (MS) coupled to bioinformatics tools is crucial for the identification and quantification of protein phosphorylation sites for advancing in such relevant clinical research. A combination of different phosphopeptide enrichments, quantitative techniques and bioinformatic tools is necessary to achieve good phospho-regulation data and good structural analysis of protein studies. The current and most useful proteomics and bioinformatics techniques will be explained with research examples. Our aim in this article is to be helpful for cancer research via detailing proteomics and bioinformatic tools." @default.
• W2140443886 created "2016-06-24" @default.
• W2140443886 creator A5015243475 @default.
• W2140443886 creator A5023949119 @default.
• W2140443886 creator A5061201501 @default.
• W2140443886 creator A5083246007 @default.
• W2140443886 creator A5084350139 @default.
• W2140443886 creator A5088497625 @default.
• W2140443886 date "2011-01-01" @default.
• W2140443886 modified "2023-10-17" @default.
• W2140443886 title "Technical phosphoproteomic and bioinformatic tools useful in cancer research" @default.
• W2140443886 cites W149212085 @default.
• W2140443886 cites W1594750612 @default.
• W2140443886 cites W1964211866 @default.
• W2140443886 cites W1965296166 @default.
• W2140443886 cites W1965807926 @default.
• W2140443886 cites W1972600929 @default.
• W2140443886 cites W1975024278 @default.
• W2140443886 cites W1975558168 @default.
• W2140443886 cites W1979456040 @default.
• W2140443886 cites W1979813950 @default.
• W2140443886 cites W1983086129 @default.
• W2140443886 cites W1983836332 @default.
• W2140443886 cites W1984871500 @default.
• W2140443886 cites W1986568749 @default.
• W2140443886 cites W1989702804 @default.
• W2140443886 cites W1993410470 @default.
• W2140443886 cites W1996693787 @default.
• W2140443886 cites W2004182894 @default.
• W2140443886 cites W2004704197 @default.
• W2140443886 cites W2005126769 @default.
• W2140443886 cites W2005646394 @default.
• W2140443886 cites W2012611489 @default.
• W2140443886 cites W2020459598 @default.
• W2140443886 cites W2023645046 @default.
• W2140443886 cites W2023953164 @default.
• W2140443886 cites W2024923641 @default.
• W2140443886 cites W2029282790 @default.
• W2140443886 cites W2029857102 @default.
• W2140443886 cites W2030157681 @default.
• W2140443886 cites W2032833505 @default.
• W2140443886 cites W2033044042 @default.
• W2140443886 cites W2033889320 @default.
• W2140443886 cites W2042629507 @default.
• W2140443886 cites W2054479115 @default.
• W2140443886 cites W2058280884 @default.
• W2140443886 cites W2060770087 @default.
• W2140443886 cites W2068940814 @default.
• W2140443886 cites W2069547389 @default.
• W2140443886 cites W2078363421 @default.
• W2140443886 cites W2081622316 @default.
• W2140443886 cites W2083577779 @default.
• W2140443886 cites W2089691645 @default.
• W2140443886 cites W2091787667 @default.
• W2140443886 cites W2093348051 @default.
• W2140443886 cites W2095750018 @default.
• W2140443886 cites W2099255819 @default.
• W2140443886 cites W2104726963 @default.
• W2140443886 cites W2105909402 @default.
• W2140443886 cites W2108136469 @default.
• W2140443886 cites W2115298892 @default.
• W2140443886 cites W2115425267 @default.
• W2140443886 cites W2120016245 @default.
• W2140443886 cites W2121732893 @default.
• W2140443886 cites W2128987420 @default.
• W2140443886 cites W2138970997 @default.
• W2140443886 cites W2140946052 @default.
• W2140443886 cites W2140969503 @default.
• W2140443886 cites W2141097619 @default.
• W2140443886 cites W2141376777 @default.
• W2140443886 cites W2142905191 @default.
• W2140443886 cites W2148300747 @default.
• W2140443886 cites W2152521607 @default.
• W2140443886 cites W2155880596 @default.
• W2140443886 cites W2157766441 @default.
• W2140443886 cites W2165526004 @default.
• W2140443886 cites W2166037338 @default.
• W2140443886 cites W2167932805 @default.
• W2140443886 cites W2171064835 @default.
• W2140443886 cites W2318009062 @default.
• W2140443886 cites W2401055558 @default.
• W2140443886 doi "https://doi.org/10.1186/2043-9113-1-26" @default.
• W2140443886 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3195713" @default.
• W2140443886 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/21967744" @default.
• W2140443886 hasPublicationYear "2011" @default.
• W2140443886 type Work @default.
• W2140443886 sameAs 2140443886 @default.
• W2140443886 citedByCount "18" @default.
• W2140443886 countsByYear W21404438862012 @default.
• W2140443886 countsByYear W21404438862013 @default.
• W2140443886 countsByYear W21404438862014 @default.
• W2140443886 countsByYear W21404438862015 @default.
• W2140443886 countsByYear W21404438862023 @default.
• W2140443886 crossrefType "journal-article" @default.
• W2140443886 hasAuthorship W2140443886A5015243475 @default.
• W2140443886 hasAuthorship W2140443886A5023949119 @default.
• W2140443886 hasAuthorship W2140443886A5061201501 @default.
• W2140443886 hasAuthorship W2140443886A5083246007 @default.

• next