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Mostrati risultati da 1.286 a 1.305 di 2.944
Titolo Data di pubblicazione Autori Tipo File Abstract
I giovani, la società, la ricerca scientifica : Cus-Mi-Bio, un progetto-ponte università-scuola per la formazione e la diffusione della cultura scientifica 2008 G. VialeG. PavesiP. PlevaniM.L. Tenchini + Book Part (author) -
Identical fusion transcript associated with different breakpoints in the AML1 gene in simple and variant t(8;21) acute myeloid leukemia 1995 N. Sacchi + Article (author) -
Identification and characterization of 6 novel genetic defects leading to factor V deficiency 2008 I. GuellaS. DugaR. Asselta + Conference Object -
Identification and Characterization of DM1 Patients by a New Diagnostic Certified Assay: Neuromuscular and Cardiac Assessments 2013 V. SansoneG. Meola + Article (author) -
Identification and Characterization of Novel Factors Involved in Interstrand Cross-link Repair 2006 D.M. MuzziniP. PlevaniF. Marini + Conference Object -
IDENTIFICATION AND CHARACTERIZATION OF THE 'GUT VASCULAR BARRIER' 2014 I. Spadoni Doctoral Thesis -
Identification and functional analysis of two U3 binding sites on yeast pre-ribosomal RNA 1992 Beltrame, M + Article (author) -
Identification and spatial distribution of the mRNA encoding an egg envelope component of the Cyprinid zebrafish, Danio rerio, homologous to the mammalian ZP3(ZPC) 2000 L. Del GiaccoF. Cotelli + Article (author) -
Identification and spatial distribution of the mRNA encoding the gp49 component of the gilthead sea bream, Sparus aurata, egg envelope 1997 L. Del GiaccoS. DugaF. Cotelli + Article (author) -
Identification by exome capture and sequencing of two novel mutations in the PRPS1 gene in Italian families with nonsyndromic sensorineural hearing loss 2011 M. RobustoG. SoldàR. AsseltaU. AmbrosettiS. Duga + Conference Object -
Identification by exome sequencing and functional characterization of novel deafness-causing mutations in PRPS1 2012 M. RobustoR. AsseltaS. CacciaU. AmbrosettiS. DugaG. Soldà + Conference Object -
Identification by whole-exome sequencing of two novel LARS2 mutations in an Italian family with Perrault syndrome 2014 G. SoldàM. RobustoU. AmbrosettiR. AsseltaS. Duga + Conference Object -
Identification of a Candidate Gene Set Signature for the Risk of Progression in IgM MGUS to Smoldering/Symptomatic Waldenström Macroglobulinemia (WM) by a Comparative Transcriptome Analysis of B Cells and Plasma Cells 2021 L. LeuzziG. ZamprognaA. Beghini + Article (author) -
Identification of a choroid plexus vascular barrier closing during intestinal inflammation 2021 Carloni S.Bertocchi A.Erreni M.Braga D.Pasini D.Matteoli M. + Article (author) -
Identification of a glucocorticoid response element in the human gamma chain fibrinogen promoter 1998 R. AsseltaS. Duga + Article (author) -
IDENTIFICATION OF A GLYCOPROTEIN INVOLVED IN CELL-CYCLE PROGRESSION IN YEAST 1986 L. POPOLO + Article (author) -
Identification of a labile protein involved in the G1 to S transition in Saccharomyces cerevisiae 1984 L. Popolo + Article (author) -
Identification of a new susceptibility variant for multiple sclerosis in OAS1 by population genetics analysis 2012 D. GalimbertiG.P. ComiE. ScarpiniM. BiasinN. BresolinM. Clerici + Article (author) -
Identification of a novel pathway in sporadic Amyotrophic Lateral Sclerosis mediated by the long non-coding RNA ZEB1-AS1 2023 Rey, FedericaEsposito, LetiziaPandini, CeciliaBordoni, MatteoZuccotti, GianvincenzoCarelli, Stefana + Article (author) -
Identification of a peptidoglycan-lytic enzyme in Bifidobacterium bifidum and study of its immune-stimulatory effect on dendritic cells 2009 S. GuglielmettiS. ArioliI. De NoniM. StuknyteD. Mora + Conference Object -
Mostrati risultati da 1.286 a 1.305 di 2.944
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