IRIS
BALDINI, ANTONIO
 Distribuzione geografica
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Continente #
NA - Nord America 1.422
EU - Europa 618
AS - Asia 187
AF - Africa 21
OC - Oceania 3
Totale 2.251
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Nazione #
US - Stati Uniti d'America 1.377
IT - Italia 167
CN - Cina 159
UA - Ucraina 159
FI - Finlandia 93
DE - Germania 56
CA - Canada 45
GB - Regno Unito 40
SE - Svezia 36
IE - Irlanda 25
CI - Costa d'Avorio 21
BG - Bulgaria 12
NL - Olanda 12
JP - Giappone 9
HK - Hong Kong 5
SG - Singapore 5
SI - Slovenia 5
FR - Francia 4
IN - India 4
ES - Italia 3
TR - Turchia 3
AU - Australia 2
KR - Corea 2
AT - Austria 1
CH - Svizzera 1
CZ - Repubblica Ceca 1
GR - Grecia 1
MT - Malta 1
NZ - Nuova Zelanda 1
RU - Federazione Russa 1
Totale 2.251
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Città #
Chandler 298
Jacksonville 160
Princeton 96
Millbury 86
Boston 73
Ashburn 57
Nanjing 55
Wilmington 54
Ottawa 39
Napoli 38
Norwalk 24
Nanchang 21
Des Moines 19
Rome 18
Jiaxing 15
Lawrence 13
Ann Arbor 12
Boardman 12
Kronberg 12
Shenyang 12
Sofia 12
Hebei 11
Falls Church 10
Woodbridge 10
Chiyoda-ku 9
Houston 9
Amsterdam 8
Florence 8
Newcastle upon Tyne 8
Orange 8
Beijing 7
Naples 7
Tianjin 7
Changsha 6
Kunming 6
Fairfield 5
Redmond 5
Shanghai 5
Cambridge 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
Jinju 2
Marano di Napoli 2
Montréal 2
Newark 2
Palma De Mallorca 2
Pune 2
Salerno 2
Torre Annunziata 2
Auckland 1
Birzebbuga 1
Brescia 1
Campobasso 1
Chicago 1
Council Bluffs 1
Fisciano 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
Munich 1
New York 1
Ningbo 1
Oxelösund 1
Palermo 1
Pescara 1
Pietrasanta 1
Pisa 1
Providence 1
Redwood City 1
Saint John 1
San Cipriano Picentino 1
San Francisco 1
San Giovanni Rotondo 1
Sassari 1
Totale 1.353
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Nome #
DiGeorge-like syndrome in a child with a 3p12.3 deletion involving miRNA-4273 born to a diabetic mother 101
Tbx1 regulation of myogenic differentiation in the limb and cranial mesoderm 52
A genetic link between Tbx1 and Fibroblast Growth Factor Signaling 45
Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway? 43
Tbx1 deletion in Islet1-fated cells recapitulates the cardiovascular Tbx1 mutant phenotype 43
Fgf15 is required for proper morphogenesis of the mouse cardiac outflow tract 42
Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development. 41
Diagnosis of Genetic and Malignant Diseases Using Chromosome Specific DNA Probes, Multiple Fluorochromes and Optical Imaging Systems 41
Coronary stem development in wild-type and Tbx1 null mouse hearts 38
A deficiency in the region homologous to human 17q21.33-q23.2 causes heart defects in mice 37
Genetic pathways to mammalian heart development: Recent progress from manipulation of the mouse genome. 37
Microarray analysis of the Df1 mouse model of the 22q11 Deletion Syndrome. 36
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. 36
Congenital Heart Disease in Mice Deficient for the DiGeorge Syndrome Region. 35
Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1. 34
PPARδ up-regulates 14-3-3ε in human endothelial cells via C/Ebpβ. 34
The 22q11.2 deletion syndrome: a gene dosage perspective 33
Serotonin transporter role in heart development focusing on cardiac valve and conduction system 33
Dissecting contiguous gene defects: TBX1. 32
Dissecting DiGeorge syndrome: The interaction between Tbx1 and the retinoic acid pathway 31
Tbx1: Transcriptional and Developmental Functions 31
Tbx1 represses Mef2c gene expression and is correlated with histone 3 deacetylation of the anterior heart field enhancer 30
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract. 29
In vivo response to high-resolution variation of Tbx1 mRNA dosage. 29
Pharmacological Rescue of the Brain Cortex Phenotype of Tbx1 Mouse Mutants: Significance for 22q11.2 Deletion Syndrome 29
TBX1 Represses Vegfr2 Gene Expression and Enhances the Cardiac Fate of VEGFR2+ Cells 28
TBX1 and Basal Cell Carcinoma: Expression and Interactions with Gli2 and Dvl2 Signaling 28
Chromatin and Transcriptional Response to Loss of TBX1 in Early Differentiation of Mouse Cells 28
Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia. 27
Congenital heart disease in mice deficient for the DiGeorge syndrome region 27
14-3-3? plays a role in cardiac ventricular compaction by regulating the cardiomyocyte cell cycle. 27
DiGeorge Syndrome: an update 26
Are primary cilia involved in Embryonic Stem Cells differentiation and/or the maintenance of the undifferentiated state? 25
A Human Alpha-satellite Dna Subset Specific For Chromosome-12 25
Congenital heart disease and genetic syndromes: new insights into molecular mechanisms 25
Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants. 24
A 12-Mb complete coverage BAC contig map in human chromosome 16p13.1-p11.2 24
DiGeorge Syndrome: A gene at last. 23
Genetic and physical mapping of a voltage-dependent chloride channel gene to human 4q32 and to mouse 8. 23
Cloning and chromosome mapping of human and chicken Iroquois (IRX) genes 23
A fate map of Tbx1 expressing cells reveals heterogeneity in the second cardiac field 23
Cloning and Comparative Mapping of A Chromosome-20-specific Alphoid Dna-sequence 23
Fate map of serotonin transporter-expressing cells in developing mouse heart 22
Mapping on human and mouse chromosomes of the gene for the beta-galactoside-binding protein, an autocrine-negative growth factor. 22
Recovery from arterial growth delay reduces the penetrance of cardiovascular defects in mice deleted for the DiGeorge Syndrome region 21
Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis. 21
Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization. 21
22q11 deletions and cardiac disease 21
Preliminary steps of fibroblasts reprogramming to develop mTECs from control or FOXN1(-/-) fibroblasts 21
Chromosomal Assignment of Human Yac Clones By Fluorescence Insitu Hybridization - Use of Single-yeast-colony Pcr and Multiple Labeling 20
A Human Alphoid Dna Clone From the Ecori Dimeric Family - Genomic and Internal Organization and Chromosomal Assignment 20
Transcription factor TBX1 overexpression induces downregulation of proteins involved in retinoic acid metabolism: a comparative proteomic analysis. 20
Conditional and constitutive expression of a Tbx1-GFP fusion protein in mice. 20
A defect in early myogenesis causes Otitis media in two mouse models of 22q11.2 Deletion Syndrome 20
Gene-environment interaction impacts on heart development and embryo survival 20
Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice 20
Cardiopharyngeal mesoderm origins of musculoskeletal and connective tissues in the mammalian pharynx 20
Fate map of SERT-expressing cells in developing mouse heart. 19
A pivotal role for endogenous TGF-beta-activated kinase-1 in the LKB1/AMP-activated protein kinase energy-sensor pathway 19
Peroxisome proliferator-activated receptor-δ upregulates 14-3-3ε in human endothelial cells via CCAAT/enhancer binding protein-β 19
A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3 19
Single cell multi-omic analysis identifies a Tbx1-dependent multilineage primed population in murine cardiopharyngeal mesoderm 19
Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice 18
Rebalancing gene haploinsufficiency in vivo by targeting chromatin 18
A phenotypic rescue approach identifies lineage regionalization defects in a mouse model of DiGeorge syndrome 17
Tbx1 Mutation Causes Multiple Cardiovascular Defects and Disrupts Neural Crest and Cranial Nerve Migratory Pathways 17
Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway? 17
Effects of individual segmental trisomies of human chromosome 21 syntenic regions on hippocampal long-term potentiation and cognitive behaviors in mice 17
Vitamin B12 ameliorates the phenotype of a mouse model of DiGeorge syndrome 17
Tbx1 regulates extracellular matrix-cell interactions in the second heart field 17
Tbx1 is required for inner ear morphogenesis. 16
EZH2 is required for parathyroid and thymic development through differentiation of the third pharyngeal pouch endoderm 16
The Transcriptional Activity of Individual Ribosomal Dna Gene Clusters Is Modulated By Serum Concentration 15
Tbx1 is a negative modulator of Mef2c 15
Manipulation of endogenous regulatory elements and transgenic analyses of the Tbx1 gene 14
TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome 13
In vivo genetic ablation of the periotic mesoderm affects cell proliferation survival and differentiation in the cochlea 12
Mouse models for Down syndrome-associated developmental cognitive disabilities. 12
Genetic analysis of Down syndrome-associated heart defects in mice 11
DiGeorge's syndrome: a gene at last 11
DiGeorge syndrome: complex pathogenesis? Maybe, maybe not 11
Pharyngeal epithelial deletion of Tbx1 causes caudal pharyngeal arch defect but not cardiac conotruncal anomaly 11
Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome 11
Tbx1 regulates progenitor cell proliferation in the dental epithelium by modulating Pitx2 activation of p21 10
Tbx1 Regulates the BMP-Smad1 Pathway in a Transcription Independent Manner 10
Schizophrenia and Chromosomal Deletions Within 22q11.2 10
Localization of the Human Prostate Transglutaminase (Type IV) Gene (TGM4) to Chromosome 3p21.33-p22 by Fluorescence in Situ Hybridization 10
Subepicardial endothelial cells invade the embryonic ventricle wall to form coronary arteries. 10
p53 suppression partially rescues the mutant phenotype in mouse models of DiGeorge syndrome. 10
Dimeric Structure of A Human Apolipoprotein-b Messenger-rna Editing Protein and Cloning and Chromosomal Localization of Its Gene 9
Tbx1 Regulates Proliferation and Differentiation of Multipotent Heart Progenitors 9
Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis 9
Selection of A Human Chromosome-21 Enriched Yac Sub-library Using A Chromosome-specific Composite Probe 9
Identification and molecular characterization of de novo translocation t(8;14)(q22.3;q13) associated with a vascular and tissue overgrowth syndrome 9
Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments 8
Early thyroid development requires a Tbx1-Fgf8 pathway 8
Tbx1 regulates population, proliferation and cell fate determination of otic epithelial cells 8
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 8
Genetic dissection of the DiGeorge syndrome phenotype 8
Partial rescue of the Tbx1 mutant heart phenotype by Fgf8: Genetic evidence of impaired tissue response to Fgf8 8
Totale 2.264
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Categoria #
all - tutte 10.258
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 10.258
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20195 0 0 0 0 0 0 0 0 0 2 0 3
2019/2020280 114 0 34 7 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
2023/2024287 34 64 32 18 27 8 57 41 3 3 0 0
Totale 2.342