CNR Institutional Research Information System

DEIANA, MANILA
 Distribuzione geografica
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Continente #
AS - Asia 46
NA - Nord America 20
EU - Europa 7
Totale 73
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Nazione #
SG - Singapore 35
US - Stati Uniti d'America 20
KR - Corea 9
IT - Italia 7
CN - Cina 2
Totale 73
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Città #
Singapore 29
Seoul 9
Santa Clara 7
Assemini 3
Guangzhou 2
Benevento 1
Catania 1
Florence 1
Forest City 1
Totale 54
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Nome #
Novel action of FOXL2 as mediator of Col1a2 gene autoregulation 5
Wilson disease mutations associated with uncommon haplotypes in Mediterranean patients 5
BCL11A is associated with persistent HbF and ameliorates the ²-thalassemia phenotype. 4
Crisponi Syndrome and Cold-induced Sweating Type 1: two syndromes, but one genetic entity 4
Overexpression of the Cytokine BAFF and Autoimmunity Risk 4
Molecular pathology and haplotype analysis of Wilson disease in Mediterranean populations 3
Heritability of cardiovascular and personality traits in 6,148 Sardinians. 3
Microarray and functional analyses of primordial follicles formation and the etiology of premature ovarian failure. 3
FOXL2 modulates cartilage, skeletal development and IGF1-dependent growth in mice 3
Dissection of the BAFF pathway in Multiple Sclerosis with a view toward more specific and effective therapies 3
Differential secretion of the mutated protein is a major component affecting phenotypic severity in CRLF1-associated disorders. 3
Improvement of prenatal diagnosis of Wilson disease using microsatellite markers. 3
Differential secretion of the mutated protein is a major component affecting phenotypic severity in CRLF1-associated disorders 3
Sindrome di Crisponi e Sindrome della sudorazione indotta dal freddo tipo I: due sindromi un entità genetica. 3
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome 2
Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development. 2
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 2
The forkhead transcription factor Foxl2 is sumoylated in both human and mouse: sumoylation affects its stability, localization, and activity. 2
Crisponi Syndrome and Cold-Induced Sweating Type 1: Two Syndromes - One Genetic Entity 2
ROLE OF THE BLEPHAROPHIMOSIS/PTOSIS/EPICANTHUS INVERSUS SYNDROME (BPES) GENE FOXL2 IN OVARIAN AND EYE DEVELOPMENT 2
Erratum: Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa (The American Journal of Human Genetics (2016) 99(1) (236-245) (S0002929716301616) (10.1016/j.ajhg.2016.05.026)) 2
FOXL2 inactivation by a translocation 171 kb away: Analysis of 500 kb of chromosome 3 for candidate long-range regulatory sequences 2
Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa 2
Role of the Blepharophimosis/Ptosis/Epicanthus Inversus syndrome (BPES) gene FOXL2 in ovarian and eye development. 1
FOXL2: Forkhead transcription factor and Blepharophimosis/Ptosis/Epicanthus inversus syndrome (BPES) 1
FOXL2 inactivation by a translocation 171 kb away: analysis of 500 kb of chromosome 3 for candidate long-range regulatory sequences. 1
Overgrowth of a mouse model of the Simpson - Golabi - Behmel syndrome is independent of IGF signaling 1
Studio delle basi genetiche delle tireopatie autoimmuni nella popolazione sarda 1
Sindrome di Crisponi e Sindrome della sudorazione indotta dal freddo tipo I: due sindromi un entità genetica 1
Totale 73
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Categoria #
all - tutte 543
article - articoli 345
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 888
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202417 0 0 0 0 0 0 0 0 0 0 11 6
2024/202556 3 1 47 5 0 0 0 0 0 0 0 0
Totale 73