LEADER 01826nam 2200577 a 450 001 9910465545403321 005 20200520144314.0 010 $a1-61668-704-5 035 $a(CKB)2560000000071296 035 $a(EBL)3020003 035 $a(SSID)ssj0000467551 035 $a(PQKBManifestationID)12210740 035 $a(PQKBTitleCode)TC0000467551 035 $a(PQKBWorkID)10489626 035 $a(PQKB)10194141 035 $a(MiAaPQ)EBC3020003 035 $a(Au-PeEL)EBL3020003 035 $a(CaPaEBR)ebr10675011 035 $a(OCoLC)923662447 035 $a(EXLCZ)992560000000071296 100 $a20100407d2010 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aCelluose [sic] allomorphs$b[electronic resource] $estructure, accessibility and reactivity /$fDiana Ciolacu and Valentin I. Popa 210 $aNew York $cNova Science Publishers$dc2010 215 $a1 online resource (81 p.) 225 1 $aPolymer science and technology 300 $aDescription based upon print version of record. 311 $a1-61668-323-6 320 $aIncludes bibliographical references (p. [49]-61) and index. 410 0$aPolymer science and technology series (Nova Science Publishers) 606 $aCellulose$xStructure 606 $aCellulose$xChemistry 606 $aSupramolecular chemistry 608 $aElectronic books. 615 0$aCellulose$xStructure. 615 0$aCellulose$xChemistry. 615 0$aSupramolecular chemistry. 676 $a572/.56682 700 $aCiolacu$b Diana$0931070 701 $aPopa$b Valentin I$0846893 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910465545403321 996 $aCelluose allomorphs$92094400 997 $aUNINA LEADER 01316nam 2200385 n 450 001 996388266203316 005 20221107210434.0 035 $a(CKB)1000000000645300 035 $a(EEBO)2240897153 035 $a(UnM)99857589 035 $a(EXLCZ)991000000000645300 100 $a19930106d1510 uy | 101 0 $aeng 135 $aurbn||||a|bb| 200 10$a[Accidence]$b[electronic resource] 210 $a[Enprynted at London $cIn fletestrete at the sygne of the sonne by wynkyn de worde$d[1510?]] 215 $a[32] p 300 $aA revision of the Accidence of John Stanbridge. 300 $aTitle from STC; place of publication and printer's name from colophon; publication date conjectured by STC. 300 $aWith catch titles; on A3, B3: "Acci. stang. [sic]". 300 $aSignatures: A-B⁶ C⁴. 300 $aImperfect; lacks leaves A1,2. 300 $aReproduction of the original in the British Library. 330 $aeebo-0018 606 $aLatin language$xGrammar$vEarly works to 1800 615 0$aLatin language$xGrammar 700 $aStanbridge$b John$f1463-1510.$0196826 801 0$bCu-RivES 801 1$bCu-RivES 801 2$bCStRLIN 801 2$bWaOLN 906 $aBOOK 912 $a996388266203316 996 $aAccidence$92381557 997 $aUNISA LEADER 02931oam 2200469 450 001 9910137092203321 005 20230621141107.0 010 $a9782889196463 (ebook) 035 $a(CKB)3710000000824732 035 $a(oapen)https://directory.doabooks.org/handle/20.500.12854/45580 035 $a(EXLCZ)993710000000824732 100 $a20191103c2015uuuu |u | 101 0 $aeng 135 $aurmn|---annan 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$aDynamics of cyclic nucleotide signaling in neurons$b[electronic resource] /$fedited by Pierre Vincent, Nicholas C. Spitzer 210 $cFrontiers Media SA$d2015 210 1$aFrance :$cb Frontiers Media SA,$d2015 215 $a1 online resource (92 pages) $cillustrations, charts 225 1 $aFrontiers Research Topics 320 $aIncludes bibliographical references. 330 $aCyclic nucleotides control a number of neuronal properties including neuronal differentiation, pathfinding, regulation of excitability and synaptic transmission, and control of gene expression. Signaling events mediated by cAMP or cGMP are transient and take place within the complex 3-dimensional structure of the neuronal cell. Signaling events happen on the time scale of seconds to minutes and the biological significance of the temporal dimension remains poorly understood. Structural features of neurons (dendritic spines and branches, cell body, nucleus, axon?) as well as AKAPs and other scaffolding proteins that keep signaling enzymes together and form "signaling microdomains", are critical spatial determinants of signal integration. Finally, the types of enzymes involved in signal integration, which are expressed as a number of different types and splice variants, yield another dimension that determines signal integration properties. Biosensor imaging provides direct temporal and spatial measurement of intracellular signals. This novel approach, together with more conventional methods such as biochemistry, electrophysiology, and modeling, now provide a better understanding of the spatial and temporal features of cyclic nucleotide signal integration in living neurons. This topic aims at providing a better understanding of how neurons are "making sense" of cyclic nucleotide signaling in living neurons. 606 $aNeurons 610 $arac GTP-Binding Proteins 610 $aDopamine 610 $abiosensor imaging 610 $acompartmentalization 610 $anoradrenalin 610 $aCyclic GMP 610 $aCyclic AMP 610 $aphosphodiesterases 610 $aEndocannabinoids 615 0$aNeurons 700 $aNicholas C. Spitzer$4auth$01367187 702 $aVincent$b Pierre 702 $aSpitzer$b Nicholas C. 801 0$bUkMaJRU 912 $a9910137092203321 996 $aDynamics of cyclic nucleotide signaling in neurons$93389917 997 $aUNINA