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Mostrati risultati da 1 a 20 di 37
Titolo Data di pubblicazione Autori File
A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta 1-gen-2014 MORGAN, ANNAGASPARINI, PAOLO +
A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss 1-gen-2013 GIROTTO, GIORGIAD'ADAMO, ADAMO PIOVOZZI, DIEGOMORGAN, ANNAGASPARINI, PAOLO +
A novel procedure for quantitative polymerase chain reaction by coamplification of competitive templates. 1-gen-1992 GIACCA, MAURO +
Are key cytokines genetic and serum levels variations related to rheumatoid arthritis clinical severity? 1-gen-2020 Crovella S. +
CCR5 genotype and pre-treatment CD4+ T-cell count influence immunological recovery of HIV-positive patients during antiretroviral therapy 1-gen-2020 Crovella, Sergio +
Changes in the expression of COI1, TIR1, and ERF1 genes and respective MiRNAs in Fusarium basal Rot-Stressed onion 1-gen-2024 Buratti, EmanueleRomano, Maurizio +
Characterization of a highly repeated DNA sequence family in five species of the genus Eulemur. 1-gen-2001 CROVELLA, SERGIO +
Cloning of the murine nonmuscle heavy chain myosin IIA gene, ortholog of human MYH9 responsible for May-Hegglin, Sebastian, Fechtner, and Epstein syndromes 1-gen-2002 SAVOIA, ANNA +
Cloning, chromosome mapping and functional characterization of a human homologue of murine Gtse-1 (B99) gene 1-gen-2000 COLLAVIN, LICIO +
Co-inheritance of two ABCC8 mutations causing an unresponsive congenital hyperinsulinism: Clinical and functional characterization of two novel ABCC8 mutations 1-gen-2013 ATHANASAKIS, EMMANOUILGASPARINI, PAOLOVENTURA, ALESSANDRO +
Comment to Santos et. al., "Hyper-IgD and periodic fever syndrome: a new MVK mutation (p.R277G) associated with a severe phenotype" 1-gen-2015 CROVELLA, SERGIO +
Congenital hyperinsulinism: clinical and molecular analysis of a large Italian cohort. 1-gen-2013 ATHANASAKIS, EMMANOUILMORGAN, ANNAVENTURA, ALESSANDROGASPARINI, PAOLO +
Contribution of SNP arrays in diagnosis of deletion 2p11.2-p12 1-gen-2012 Fabretto, AntonellaFaletra, FlavioSkabar, AldoGasparini, PaoloPecile, Vanna +
Engineering mammalian cell factories with SINEUP noncoding RNAs to improve translation of secreted proteins 1-gen-2015 SBLATTERO, DANIELE +
Extending filamentous phage host range by the grafting of a heterologous receptor binding domain 1-gen-1997 MARZARI, ROBERTOSBLATTERO, DANIELE +
The eyestalk transcriptome of red swamp crayfish Procambarus clarkii 1-gen-2015 MANFRIN, CHIARADE MORO, GIANLUCAGERDOL, MARCOGIULIANINI, PIERO GIULIOPALLAVICINI, Alberto +
Genetic profile of patients with early onset inflammatory bowel disease 1-gen-2018 Girardelli, MartinaPaolera, Sara DellaVuch, JosefTommasini, AlbertoMartelossi, StefanoCrovella, SergioBianco, Anna Monica +
Gonad inhibiting hormone (GIH) of the Norway lobster (Nephrops norvegicus): cDNA cloning, expression, recombinant protein production, and immunolocalization 1-gen-2002 EDOMI, PAOLOAZZONI E.GIULIANINI, PIERO GIULIO +
Gonad-inhibiting hormone of the Norway lobster (Nephrops norvegicus): cDNA cloning, expression, recombinant protein production, and immunolocalization 1-gen-2002 AZZONI E.FERRERO, ENRICOGIULIANINI, PIERO GIULIO +
Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients 1-gen-2014 VOZZI, DIEGOMORGAN, ANNAVUCKOVIC, DRAGANAGASPARINI, PAOLOGIROTTO, GIORGIA +
Mostrati risultati da 1 a 20 di 37
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