LEADER 01143nam0 2200277 i 450 001 SUN0022061 005 20100413120000.0 010 $a88-343-8248-X 100 $a20040825d1990 |0itac50 ba 101 $aita 102 $aIT 105 $a|||| ||||| 200 1 $aFaces 3.$euno strumento per la ricerca e l'osservazione clinica della famiglia$fCarlo Galimberti, Marco Farina 205 $aMilano : Vita e pensiero$b[1990] 210 $d135 p. ; 24 cm 215 $aIn testa al front.: Università cattolica del Sacro Cuore, Centro studi e ricerche sulla famiglia. 620 $dMilano$3SUNL000284 700 1$aGalimberti$b, Carlo$3SUNV014330$08961 701 1$aFarina$b, Marco$3SUNV018329$0276032 712 $aVita e pensiero$3SUNV000024$4650 801 $aIT$bSOL$c20181109$gRICA 912 $aSUN0022061 950 $aUFFICIO DI BIBLIOTECA DEL DIPARTIMENTO DI PSICOLOGIA$d16 CONS 1339 $e16 VS 1554 995 $aUFFICIO DI BIBLIOTECA DEL DIPARTIMENTO DI PSICOLOGIA$bIT-CE0119$gVS$h1554$kCONS 1339$oc$qa 996 $aFaces 3$91432698 997 $aUNICAMPANIA LEADER 01087nam a2200217 i 4500 001 991003430099707536 008 171206s1998 it m ||| | ita d 035 $ab14332255-39ule_inst 040 $aBibl. Dip.le Aggr. Matematica e Fisica - Sez. Fisica$beng 100 1 $aElia, Lorella$0785327 245 10$aDeposizione e caratterizzazione di film sottili di nitruro e nitro-carburo di boro. Tesi di laurea in Fisica /$claureanda Lorella Elia ; relatori Armando Luches e Maurizio Martino 260 $aLecce :$bUniversità di Lecce. Facoltà di Scienze. Corso di laurea in Fisica,$ca.a. 1997-98 300 $aiv, 145 p. :$bill. ;$c30 cm 700 1 $aLuches, Armando 700 1 $aMartino, Maurizio 907 $a.b14332255$b06-12-17$c06-12-17 912 $a991003430099707536 945 $aLE006 T1079$g1$i2006000178068$lle006$og$pE0.00$q-$rn$so $t0$u0$v0$w0$x0$y.i15824913$z06-12-17 996 $aDeposizione e caratterizzazione di film sottili di nitruro e nitro-carburo di boro. Tesi di laurea in Fisica$91748408 997 $aUNISALENTO 998 $ale006$b06-12-17$cm$da $e-$fita$git $h0$i0 LEADER 04615nam 2201453z- 450 001 9910557109903321 005 20210501 035 $a(CKB)5400000000040948 035 $a(oapen)https://directory.doabooks.org/handle/20.500.12854/69151 035 $a(oapen)doab69151 035 $a(EXLCZ)995400000000040948 100 $a20202105d2020 |y 0 101 0 $aeng 135 $aurmn|---annan 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 00$aAdvances in Plant Alkaloid Research 210 $aBasel, Switzerland$cMDPI - Multidisciplinary Digital Publishing Institute$d2020 215 $a1 online resource (278 p.) 311 08$a3-03943-172-2 311 08$a3-03943-173-0 330 $aPlant alkaloids are critical components of modern medicine and pharmaceuticals. These compounds are also becoming increasingly important for industrial uses as part of the green chemistry revolution. This Special Issue will focus on the molecular advances being made in understanding how such a large and diverse class of compounds are made by plants and how metabolic engineering advances are increasing the overall yield of crucial precursors. 606 $aBiology, life sciences$2bicssc 606 $aResearch & information: general$2bicssc 610 $a8-oxo-9-dihydromakomakine 610 $aAChE 610 $aacridone alkaloids 610 $aacridones 610 $aalkaloids 610 $aantiplasmodial activity 610 $aAristotelia chilensis Molina Stuntz 610 $aAspergillus flavus 610 $abenzylisoquinoline alkaloids 610 $aBerberidaceae 610 $abiodiscovery 610 $abioprospecting 610 $abiosynthesis 610 $abiotechnological production 610 $aBorago officinalis 610 $aBuChE 610 $aBuxaceae 610 $acalystegine 610 $acambial meristematic cells 610 $acanthin-6-one 610 $acatharanthine 610 $aCatharanthus roseus 610 $achemistry 610 $aChl a fluorescence 610 $acocaine 610 $aCopper-dependent diamine oxidase 610 $aCrassocephalum 610 $acyclopamine 610 $acytochrome P450 monooxygenase 610 $acytotoxicity 610 $adereplication 610 $adichlorocarbene 610 $adimer alkaloids 610 $aDiversinateTM 610 $aendothelium-independent 610 $aepoxidation 610 $aErythroxylaceae 610 $aErythroxylum coca 610 $aGC-MS 610 $aGynura bicolor 610 $ahalogencyclopropane 610 $ahedgehog signaling 610 $aHill reaction inhibitors 610 $aHomospermidine synthase 610 $aHPLC-MS 610 $aindole alkaloid 610 $aisoquinoline alkaloid 610 $alate-stage functionalization 610 $alibrary 610 $aLolium perenne 610 $amahimbrine A 610 $aMahonia imbricata 610 $amedicinal chemistry 610 $amedicinal properties 610 $amethyltransferase 610 $amolecular docking 610 $anatural product 610 $aNecic acids 610 $aNecine bases 610 $aNelumbo nucifera 610 $anext generation sequencing 610 $anorcoclaurine synthase 610 $apapaverine 610 $apharmacology 610 $aphenylacrylamides 610 $aphotosystem II 610 $aPicrolemma huberi 610 $aPyrrolizidine alkaloid biosynthesis 610 $aRhodophiala 610 $aRuta graveolens 610 $asacred lotus 610 $asarchookloides A-C 610 $aSarcococca hookeriana 610 $ascaffold 610 $ascopolamine 610 $aSenecionine 610 $aShh-Light II cells 610 $aSimaroubaceae 610 $astereochemistry 610 $asteroidal alkaloid 610 $asulfinate 610 $aSwinglea glutinosa 610 $aterpenoid indole alkaloids 610 $atraditional medicine 610 $atropane 610 $atropane alkaloids 610 $avascular activity 610 $aVeratrum californicum 610 $avindoline 610 $avindoline trimer 610 $avoltage-dependent calcium channels 615 7$aBiology, life sciences 615 7$aResearch & information: general 700 $aD'Auria$b John C$4edt$01307049 702 $aD'Auria$b John C$4oth 906 $aBOOK 912 $a9910557109903321 996 $aAdvances in Plant Alkaloid Research$93028655 997 $aUNINA