IRIS
BALDINI, ANTONIO
 Distribuzione geografica
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Continente #
NA - Nord America 1.759
EU - Europa 655
AS - Asia 467
AF - Africa 21
OC - Oceania 3
Totale 2.905
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Nazione #
US - Stati Uniti d'America 1.714
SG - Singapore 275
IT - Italia 193
CN - Cina 169
UA - Ucraina 159
FI - Finlandia 95
DE - Germania 57
CA - Canada 45
GB - Regno Unito 41
SE - Svezia 36
IE - Irlanda 25
CI - Costa d'Avorio 21
BG - Bulgaria 12
NL - Olanda 12
FR - Francia 9
JP - Giappone 9
HK - Hong Kong 5
SI - Slovenia 5
IN - India 4
ES - Italia 3
TR - Turchia 3
AT - Austria 2
AU - Australia 2
CH - Svizzera 2
KR - Corea 2
CZ - Repubblica Ceca 1
GR - Grecia 1
MT - Malta 1
NZ - Nuova Zelanda 1
RU - Federazione Russa 1
Totale 2.905
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Città #
Chandler 298
Singapore 214
Jacksonville 160
Princeton 96
Millbury 86
Boston 73
Ashburn 57
Santa Clara 56
Nanjing 55
Wilmington 54
Ottawa 39
Napoli 38
Norwalk 24
Nanchang 21
Des Moines 19
Naples 19
Rome 18
Jiaxing 15
Lawrence 13
Ann Arbor 12
Boardman 12
Kronberg 12
Shenyang 12
Sofia 12
Fisciano 11
Hebei 11
Falls Church 10
Woodbridge 10
Chiyoda-ku 9
Houston 9
Amsterdam 8
Florence 8
Newcastle upon Tyne 8
Orange 8
Beijing 7
Shanghai 7
Tianjin 7
Changsha 6
Kunming 6
Fairfield 5
Redmond 5
Cambridge 4
Ercolano 4
Guangzhou 4
Hong Kong 4
Dublin 3
Indiana 3
London 3
Piemonte 3
Seattle 3
Verona 3
Albano Laziale 2
Brisbane 2
Caserta 2
Dearborn 2
Formia 2
Hangzhou 2
Hayward 2
Helsinki 2
Jinju 2
Lille 2
Los Angeles 2
Marano di Napoli 2
Miami 2
Montréal 2
Newark 2
Palma De Mallorca 2
Pune 2
Qingdao 2
Salerno 2
Springfield 2
Torre Annunziata 2
Auckland 1
Birzebbuga 1
Brescia 1
Buffalo 1
Campobasso 1
Chicago 1
Council Bluffs 1
Dallas 1
Fort Mitchell 1
Fort Worth 1
Frankfurt am Main 1
Fremont 1
Genzano Di Lucania 1
Gießen 1
Giugliano In Campania 1
Gragnano 1
Grumo Nevano 1
Gurgaon 1
Hanover 1
Jinan 1
Jupiter 1
Massafra 1
Mcallen 1
Milan 1
Mt. Pleasant 1
Munich 1
New York 1
Ningbo 1
Totale 1.654
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Nome #
DiGeorge-like syndrome in a child with a 3p12.3 deletion involving miRNA-4273 born to a diabetic mother 110
Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development. 81
Microarray analysis of the Df1 mouse model of the 22q11 Deletion Syndrome. 78
Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1. 75
Dissecting contiguous gene defects: TBX1. 70
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract. 69
Tbx1 regulation of myogenic differentiation in the limb and cranial mesoderm 54
A genetic link between Tbx1 and Fibroblast Growth Factor Signaling 48
Tbx1 deletion in Islet1-fated cells recapitulates the cardiovascular Tbx1 mutant phenotype 48
Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway? 45
Fgf15 is required for proper morphogenesis of the mouse cardiac outflow tract 44
Tbx1: Transcriptional and Developmental Functions 43
Diagnosis of Genetic and Malignant Diseases Using Chromosome Specific DNA Probes, Multiple Fluorochromes and Optical Imaging Systems 42
Coronary stem development in wild-type and Tbx1 null mouse hearts 42
Congenital Heart Disease in Mice Deficient for the DiGeorge Syndrome Region. 41
Genetic pathways to mammalian heart development: Recent progress from manipulation of the mouse genome. 40
A deficiency in the region homologous to human 17q21.33-q23.2 causes heart defects in mice 39
Cyp26 genes a1, b1 and c1 are down-regulated in Tbx1 null mice and inhibition of Cyp26 enzyme function produces a phenocopy of DiGeorge Syndrome in the chick. 37
PPARδ up-regulates 14-3-3ε in human endothelial cells via C/Ebpβ. 37
Tbx1 represses Mef2c gene expression and is correlated with histone 3 deacetylation of the anterior heart field enhancer 37
The 22q11.2 deletion syndrome: a gene dosage perspective 36
TBX1 and Basal Cell Carcinoma: Expression and Interactions with Gli2 and Dvl2 Signaling 36
Chromatin and Transcriptional Response to Loss of TBX1 in Early Differentiation of Mouse Cells 35
Dissecting DiGeorge syndrome: The interaction between Tbx1 and the retinoic acid pathway 34
Serotonin transporter role in heart development focusing on cardiac valve and conduction system 34
TBX1 Represses Vegfr2 Gene Expression and Enhances the Cardiac Fate of VEGFR2+ Cells 33
In vivo response to high-resolution variation of Tbx1 mRNA dosage. 32
Congenital heart disease in mice deficient for the DiGeorge syndrome region 32
14-3-3? plays a role in cardiac ventricular compaction by regulating the cardiomyocyte cell cycle. 32
Pharmacological Rescue of the Brain Cortex Phenotype of Tbx1 Mouse Mutants: Significance for 22q11.2 Deletion Syndrome 32
Are primary cilia involved in Embryonic Stem Cells differentiation and/or the maintenance of the undifferentiated state? 31
Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia. 30
A Human Alpha-satellite Dna Subset Specific For Chromosome-12 29
A phenotypic rescue approach identifies lineage regionalization defects in a mouse model of DiGeorge syndrome 28
DiGeorge Syndrome: an update 28
Mapping on human and mouse chromosomes of the gene for the beta-galactoside-binding protein, an autocrine-negative growth factor. 28
Transcription factor TBX1 overexpression induces downregulation of proteins involved in retinoic acid metabolism: a comparative proteomic analysis. 28
Genetic and physical mapping of a voltage-dependent chloride channel gene to human 4q32 and to mouse 8. 27
Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants. 27
A 12-Mb complete coverage BAC contig map in human chromosome 16p13.1-p11.2 27
A fate map of Tbx1 expressing cells reveals heterogeneity in the second cardiac field 27
Preliminary steps of fibroblasts reprogramming to develop mTECs from control or FOXN1(-/-) fibroblasts 27
Congenital heart disease and genetic syndromes: new insights into molecular mechanisms 27
DiGeorge Syndrome: A gene at last. 26
Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization. 26
Gene-environment interaction impacts on heart development and embryo survival 26
Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice 26
Recovery from arterial growth delay reduces the penetrance of cardiovascular defects in mice deleted for the DiGeorge Syndrome region 25
Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis. 25
Cloning and chromosome mapping of human and chicken Iroquois (IRX) genes 25
Chromosomal Assignment of Human Yac Clones By Fluorescence Insitu Hybridization - Use of Single-yeast-colony Pcr and Multiple Labeling 25
Cloning and Comparative Mapping of A Chromosome-20-specific Alphoid Dna-sequence 25
A defect in early myogenesis causes Otitis media in two mouse models of 22q11.2 Deletion Syndrome 25
Peroxisome proliferator-activated receptor-δ upregulates 14-3-3ε in human endothelial cells via CCAAT/enhancer binding protein-β 25
Fate map of serotonin transporter-expressing cells in developing mouse heart 24
22q11 deletions and cardiac disease 24
Single cell multi-omic analysis identifies a Tbx1-dependent multilineage primed population in murine cardiopharyngeal mesoderm 24
Effects of individual segmental trisomies of human chromosome 21 syntenic regions on hippocampal long-term potentiation and cognitive behaviors in mice 23
Rebalancing gene haploinsufficiency in vivo by targeting chromatin 23
A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3 23
Fate map of SERT-expressing cells in developing mouse heart. 22
Tbx1 Mutation Causes Multiple Cardiovascular Defects and Disrupts Neural Crest and Cranial Nerve Migratory Pathways 22
Tbx1 is required for inner ear morphogenesis. 22
A Human Alphoid Dna Clone From the Ecori Dimeric Family - Genomic and Internal Organization and Chromosomal Assignment 22
Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice 21
Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway? 21
Manipulation of endogenous regulatory elements and transgenic analyses of the Tbx1 gene 21
A pivotal role for endogenous TGF-beta-activated kinase-1 in the LKB1/AMP-activated protein kinase energy-sensor pathway 21
Conditional and constitutive expression of a Tbx1-GFP fusion protein in mice. 21
Vitamin B12 ameliorates the phenotype of a mouse model of DiGeorge syndrome 21
Tbx1 regulates extracellular matrix-cell interactions in the second heart field 21
Cardiopharyngeal mesoderm origins of musculoskeletal and connective tissues in the mammalian pharynx 21
EZH2 is required for parathyroid and thymic development through differentiation of the third pharyngeal pouch endoderm 21
Mouse models for Down syndrome-associated developmental cognitive disabilities. 20
The Transcriptional Activity of Individual Ribosomal Dna Gene Clusters Is Modulated By Serum Concentration 18
Tbx1 is a negative modulator of Mef2c 18
TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome 17
Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome 17
Subepicardial endothelial cells invade the embryonic ventricle wall to form coronary arteries. 16
In vivo genetic ablation of the periotic mesoderm affects cell proliferation survival and differentiation in the cochlea 15
Schizophrenia and Chromosomal Deletions Within 22q11.2 15
DiGeorge syndrome: complex pathogenesis? Maybe, maybe not 15
Pharyngeal epithelial deletion of Tbx1 causes caudal pharyngeal arch defect but not cardiac conotruncal anomaly 15
Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments 14
Tbx1 Regulates the BMP-Smad1 Pathway in a Transcription Independent Manner 13
DiGeorge's syndrome: a gene at last 13
Significant improvement of cardiac outflow tract septation defects in a DiGeorge syndrome model after minoxidil treatment 12
Dimeric Structure of A Human Apolipoprotein-b Messenger-rna Editing Protein and Cloning and Chromosomal Localization of Its Gene 12
Genetic analysis of Down syndrome-associated heart defects in mice 12
Tbx1 Regulates Proliferation and Differentiation of Multipotent Heart Progenitors 12
Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis 12
Tbx1 regulates population, proliferation and cell fate determination of otic epithelial cells 12
Timed mutation and cell-fate mapping reveal reiterated roles of Tbx1 during embryogenesis, and a crucial function during segmentation of the pharyngeal system via regulation of endoderm expansion 12
Selection of A Human Chromosome-21 Enriched Yac Sub-library Using A Chromosome-specific Composite Probe 12
Structure and chromosomal locations of mouse steroid receptor coactivator gene family 12
Localization of the Human Prostate Transglutaminase (Type IV) Gene (TGM4) to Chromosome 3p21.33-p22 by Fluorescence in Situ Hybridization 12
p53 suppression partially rescues the mutant phenotype in mouse models of DiGeorge syndrome. 12
Endothelial gene regulatory elements associated with cardiopharyngeal lineage differentiation 11
DiGeorge syndrome: the use of model organisms to dissect complex genetics 11
Tbx1 regulates progenitor cell proliferation in the dental epithelium by modulating Pitx2 activation of p21 11
Totale 2.848
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Categoria #
all - tutte 15.057
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 15.057
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020125 0 0 0 0 41 1 3 1 4 2 23 50
2020/2021349 3 35 45 35 34 61 34 22 44 6 28 2
2021/2022446 13 0 4 4 5 16 11 46 43 7 64 233
2022/2023620 118 55 9 72 79 83 2 59 92 10 35 6
2023/2024592 34 64 32 18 27 8 57 41 3 5 279 24
2024/2025353 148 157 4 12 32 0 0 0 0 0 0 0
Totale 3.000