LEADER 01245nam--2200385---450- 001 990002763230203316 005 20060620110428.0 035 $a000276323 035 $aUSA01000276323 035 $a(ALEPH)000276323USA01 035 $a000276323 100 $a20060620d1998----km-y0itay50------ba 101 $aita 102 $aIT 105 $aa---||||001yy 200 1 $a<> antefisse dipinte di Gela$econtributo allo studio della pittura siceliota arcaica$escavi a Gela, campagne 1951-1961; 1973-75$fMarina Castoldi 210 $aMilano$cEdizioni Et$d1998 215 $a111 p.$cill.$d28 cm 300 $aIn testa al front. : Comune di Milano, Settore Cultura e Musei, Raccolte Archeologiche e Numismatiche 410 0$12001 454 1$12001 461 1$1001-------$12001 606 0 $aScavi archeologici$yGela$z1951-1975 676 $a937.8 700 1$aCASTOLDI,$bMarina$0156274 801 0$aIT$bsalbc$gISBD 912 $a990002763230203316 951 $aI A U CAS 1$b5189 DBC$cI A U 959 $aBK 969 $aDBC 979 $aDBC$b90$c20060620$lUSA01$h1102 979 $aDBC$b90$c20060620$lUSA01$h1103 979 $aDBC$b90$c20060620$lUSA01$h1104 996 $aAntefisse dipinte di Gela$9997924 997 $aUNISA LEADER 01620nam a22003131i 4500 001 991002242549707536 005 20040220093404.0 008 040407s2000 it a||||||||||||||||fre 035 $ab12892750-39ule_inst 035 $aARCHE-087237$9ExL 040 $aDip.to Filologia Class. e Scienze Filosofiche$bita$cA.t.i. Arché s.c.r.l. Pandora Sicilia s.r.l. 082 04$a691.4 245 03$aLa brique antique et médiévale :$bproduction et commercialisation d'un matériau : actes du colloque international organisé par le Centre d'histoire urbaine de l'École superieure de Fontenay-Saint Cloud et l'École française de Rome : Saint-Cloud, 16-18 novembre 1995 /$cédités par Patrick Boucheron, Henri Broise et Yvon Thébert 260 $aRoma :$bÉcole française de Rome,$c2000 300 $aVIII, 486 p. :$bill. ;$c28 cm 440 0$aCollection de l'École française de Rome ;$v272 650 4$aMattoni$xCommercio$yAntichità-Sec. 15. 650 4$aMattoni$xProduzione$yAntichità-Sec. 15. 700 1 $aBoucheron, Patrick$eauthor$4http://id.loc.gov/vocabulary/relators/aut$0140238 700 1 $aBroise, Henri$eauthor$4http://id.loc.gov/vocabulary/relators/aut$0284135 700 1 $aThébert, Yvon 710 2 $aCentre d'histoire urbaine 710 2 $aEcole française de Rome 907 $a.b12892750$b02-04-14$c16-04-04 912 $a991002242549707536 945 $aLE007 330 BOU 01.01$g1$i2007000066713$lle007$o-$pE0.00$q-$rl$s- $t0$u1$v0$w1$x0$y.i13456908$z16-04-04 996 $aBrique antique et médiévale$91448808 997 $aUNISALENTO 998 $ale007$b16-04-04$cm$da $e-$ffre$git $h3$i1 LEADER 03057nam 2200457z- 450 001 9910220036503321 005 20210212 035 $a(CKB)3800000000216412 035 $a(oapen)https://directory.doabooks.org/handle/20.500.12854/57927 035 $a(oapen)doab57927 035 $a(EXLCZ)993800000000216412 100 $a20202102d2017 |y 0 101 0 $aeng 135 $aurmn|---annan 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 00$aReelin-Related Neurological Disorders and Animal Models 210 $cFrontiers Media SA$d2017 215 $a1 online resource (179 p.) 225 1 $aFrontiers Research Topics 311 08$a2-88945-111-9 330 $aThe Reeler mutation was so named because of the alterations in gait that characterize homozygous mice. Several decades after the description of the Reeler phenotype, the mutated protein was discovered and named Reelin (Reln). Reln controls a number of fundamental steps in embryonic and postnatal brain development. A prominent embryonic function is the control of radial neuronal migration. As a consequence, homozygous Reeler mutants show disrupted cell layering in cortical brain structures. Reln also promotes postnatal neuronal maturation. Heterozygous mutants exhibit defects in dendrite extension and synapse formation, correlating with behavioral and cognitive deficits that are detectable at adult ages. The Reln-encoding gene is highly conserved between mice and humans. In humans, homozygous RELN mutations cause lissencephaly with cerebellar hypoplasia, a severe neuronal migration disorder that is reminiscent of the Reeler phenotype. In addition, RELN deficiency or dysfunction is also correlated with psychiatric and cognitive disorders, such as schizophrenia, bipolar disorder and autism, as well as some forms of epilepsy and Alzheimer's disease. Despite the wealth of anatomical studies of the Reeler mouse brain, and the molecular dissection of Reln signaling mechanisms, the consequences of Reln deficiency on the development and function of the human brain are not yet completely understood. This Research Topic include reviews that summarize our current knowledge of the molecular aspects of Reln function, original articles that advance our understanding of its expression and function in different brain regions, and reviews that critically assess the potential role of Reln in human psychiatric and cognitive disorders. 606 $aNeurosciences$2bicssc 610 $aautism 610 $aDepression 610 $aintracellular pathways 610 $aNeuronal Death 610 $aneuronal migration 610 $aNeurons 610 $aReeler 610 $aSchizophrenia 610 $aSynapses 615 7$aNeurosciences 700 $aLaura Lossi$4auth$01331046 702 $aAdalberto Merighi$4auth 702 $aGabriella D'Arcangelo$4auth 906 $aBOOK 912 $a9910220036503321 996 $aReelin-Related Neurological Disorders and Animal Models$93040068 997 $aUNINA