CNR Institutional Research Information System

CAO, ANTONIO
 Distribuzione geografica
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Continente #
AS - Asia 26
EU - Europa 15
NA - Nord America 2
Totale 43
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Nazione #
IT - Italia 12
CN - Cina 11
KR - Corea 8
SG - Singapore 7
GB - Regno Unito 2
US - Stati Uniti d'America 2
NL - Olanda 1
Totale 43
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Città #
Assemini 11
Guangzhou 11
Seoul 8
Singapore 4
Bromley 2
Forest City 2
Amsterdam 1
Cagliari 1
Totale 40
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Nome #
A novel mutation in the GLC1A gene causes Juvenile Open Angle Glaucoma in four families from the Italian region of Puglia. 11
Wilson disease mutations associated with uncommon haplotypes in Mediterranean patients 3
First results of a genome-wide association using jointly 10k and 500k Affymetrix chips in a Sardinian cohort 2
Early and severe neurological features in a Wilson disease patient compound heterozygous for two frameshift mutations. 2
Crisponi syndrome is caused by mutations in the CRLF1 gene and is allelic to cold-induced sweating syndrome type 1 2
Neonatal onset of nephrogenic syndrome of inappropriate antidiuresis 1
Haplotype and mutation analysis in Mediterranean patients with Wilson disease 1
Haplotype and mutation analysis in Greek patients with Wilson disease 1
A synonymous mutation in the CFTR gene causes an aberrant splicing in an Italian patient affected by a mild form of cystic fibrosis. 1
Normal delta globin gene sequence in carrier of the silent -101 (C-T) beta talassemia mutation with normal HbA2 level 1
The forkhead transcription factor Foxl2 is sumoylated in both human and mouse: sumoylation affects its stability, localization, and activity. 1
Common variants at ten genomic loci influence hemoglobin A1C levels via glycemic and non-glycemic pathways. 1
Identificazione di IRAK-M come gene di suscettibilità per l asma persistente ad esordio precoce 1
Role of candidate regions for asthma susceptibility on Sardinian population 1
Different switching patterns of beta-thalassaemic mutations at the proximal and distal CACCC box of the human HBB (beta-globin) gene 1
The canine copper toxicosis gene MURR1 is not implicated in the pathogenesis of Wilson disease. 1
Il gene MURR1 responsabile della tossicosi idiopatica canina da rame non è implicato nella patogenesi della malattia di Wilson 1
Individuazione di loci di suscettibilità in un campione di famiglie con asma allergico di origine Sarda 1
Linkage Disequilibrium's extension in Corsica. Looking for genetic isolates. 1
Studies on linkage and association of asthma with the Interleukin 4-Receptor alpha chain gene (IL-4Ra) in Sardinian population 1
Further delineation of the molecular pathology of Wilson disease in the Mediterranean population. 1
Disequilibrium extension analysis on the Xq13 region in Corsica 1
Molecular characterization of Wilson disease in the Sardinian population. Evidence of a founder effect 1
Studio di fattibilità dello screening neonatale per la prevenzione della malattia di Wilson attraverso la ricerca di mutazioni 1
Mutation and functional analysis of the IRAK-M gene in Sardinian asthmatic patients 1
Molecular pathology of congenital anomalies of the kidney and urinary tract 1
IRAK-M Is Involved in the Pathogenesis of Early-Onset Persistent Asthma 1
In vitro expression of the -87 beta thalassemic mutation 1
Totale 43
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Categoria #
all - tutte 1.429
article - articoli 991
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 2.420
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202435 0 0 0 0 0 0 0 0 1 0 19 15
2024/20258 6 2 0 0 0 0 0 0 0 0 0 0
Totale 43