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TitoloData di pubblicazioneAutore(i)RivistaEditore
Decreased number of circulating BFU-Es in Paroxysmal Nocturnal Hemoglobinuria1982ROTOLI B; ROBLEDO R; LUZZATTO LBLOOD
Two populations of BFU-Es in Paroxysmal Nocturnal Hemoglobinuria1984ROTOLI B; ROBLEDO R; SCARPATO N; LUZZATTO LBLOOD
In vitro addition of thiamin does not restore BFU-E growth in thiamin-responsive anemia syndrome1986ROTOLI B; POGGI V; DE RENZO A; ROBLEDO RHAEMATOLOGICA
The remarkable specificity of a new transcription termination factor suggests that the mechanisms of termination and antitermination are similar1987ROBERT J; SLOAN S; WEISBERG R; GOTTESMAN M; ROBLEDO R; HARBRECHT DCELL
EcoRI RFLP in the human IGF-II gene1988COCOZZA S; MONTICELLI A; GAROFALO S; ROBLEDO R; CHIARIOTTI L; FRUNZIO R; BRUNI CB; VARRONE SNUCLEIC ACIDS RESEARCH
Lambda nutR mutations convert HK022 Nun protein from a transcription termination factor to a suppressor of termination1990ROBLEDO R; GOTTESMAN M; WEISBERG RJOURNAL OF MOLECULAR BIOLOGY
Escherichia Coli mutations that block transcription termination by phage HK022 Nun protein1991ROBLEDO R; ATKINSON B; GOTTESMAN MJOURNAL OF MOLECULAR BIOLOGY
X-Linked Ichthyosis Without STS Deficiency: Clinical, Genetical, and Molecular Studies1995ROBLEDO R; MELIS P; SCHILLINGER E; CASCIANO I; BALAZS I; RINALDI A; SINISCALCO M; FILIPPI GAMERICAN JOURNAL OF MEDICAL GENETICS
Premutation for the Martin-Bell Syndrome Analyzed in a Large Sardinian Family: III. Molecular Analysis with the StB12.3 Probe1996GRASSO M; PERRONI L; DAGNA BRICARELLI F; RINALDI A; ROBLEDO R; SINISCALCO M; FILIPPI GAMERICAN JOURNAL OF MEDICAL GENETICS
+2.71 LOD Score at Zero Recombination Is Not Sufficient for Establishing Linkage Between X-Linked Mental Retardation and X-Chromosome Markers1996ROBLEDO R; MELIS P; SINISCALCO M; MARCHI J; LAFICARA F; RINALDI A; ROCCHI M; FILIPPI GAMERICAN JOURNAL OF MEDICAL GENETICS
Further Linkage Evidence for Localization of Mutational Sites for Nonsyndromic Types of X-Linked Mental Retardation at the Pericentromeric Region1996ROBLEDO R; MELIS P; LAFICARA F; MARCHI J; RINALDI A; SINISCALCO M; FILIPPI GAMERICAN JOURNAL OF MEDICAL GENETICS
Population genomics in Sardinia: a novel approach to hunt for genomic combinations underlying complex traits and diseases1999SINISCALCO M; ROBLEDO R; BENDER PK; CARCASSI C; CONTU L; BECK JCCYTOGENETICS AND CELL GENETICS
A plea to search for deletion polymorphism through genome scans in populations2000SINISCALCO M; ROBLEDO R; ORRU' S; CONTU L; YADAV P; REN Q; LAI H; ROE BTRENDS IN GENETICS
A novel approach to search for Identity by Descent in small samplings of patients and controls from the same Mendelian Breeding Unit. A pilot study on myopia2001HEATH S; ROBLEDO R; BEGGS W; FEOLA G; PARODO C; RINALDI A; CONTU L; DANA D; STAMBOLIAN D; SINISCA...LCO MHUMAN HEREDITY
A 9.1-kb gap in the genome reference map is shown to be a stable deletion/insertion polymorphism of ancestral origin2002ROBLEDO R; ORRU' S; SIDOTI A; MURESU R; ESPOSITO D; GRIMALDI MC; CARCASSI C; RINALDI A; BERNINI L...; CONTU L; ROMANI M; ROE B; SINISCALCO M.GENOMICS
A 9.1 kb insertion/deletion polymorphism suggests a common pattern of genetic diversity in Island Melanesia2003ROBLEDO R; SCHEINFELDT L; MERRIWETHER DA; THOMPSON F; FRIEDLAENDER JHUMAN BIOLOGY
A simple and cost effective method for rapid genotyping of insertion/deletion polymorphisms2003ROBLEDO R; BEGGS W; BENDER PGENOMICS
The immunoglobulin λ variable light-chain region in Primates has been shaped by multiple, independent, small-scale and large-scale insertion/deletion events2004ROBLEDO R; BENDER P; LEONARD J; ZHU B; OSOEGAWA K; DE JONG P; XU X; YAO Z; ROE BGENOMICS
TaqMan genotyping of insertion/deletion polymorphisms2005ROBLEDO R; BEGGS W; BENDER PMETHODS IN MOLECULAR BIOLOGYInnocenti, F
Further data on a 9.1 kb insertion/deletion polymorphism: A survey on Mediterranean populations2006SIDOTI A; ROBLEDO R; RINALDI A; DANGELO R; RINALDI C; AMATO AHUMAN BIOLOGY
   
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