Distribuzione geografica
Continente #
NA - Nord America 1066
EU - Europa 553
AS - Asia 161
OC - Oceania 1
Totale 1781
Nazione #
US - Stati Uniti d'America 1021
UA - Ucraina 159
CN - Cina 155
IT - Italia 127
FI - Finlandia 93
CA - Canada 45
DE - Germania 42
GB - Regno Unito 40
SE - Svezia 36
IE - Irlanda 22
BG - Bulgaria 12
SI - Slovenia 5
FR - Francia 4
NL - Olanda 4
ES - Italia 3
TR - Turchia 3
IN - India 2
AT - Austria 1
AU - Australia 1
CH - Svizzera 1
CZ - Repubblica Ceca 1
GR - Grecia 1
MT - Malta 1
RU - Federazione Russa 1
SG - Singapore 1
Totale 1781
Città #
Chandler 296
Jacksonville 160
Princeton 96
Millbury 86
Boston 73
Nanjing 55
Wilmington 54
Ottawa 39
Napoli 38
Norwalk 24
Nanchang 21
Des Moines 19
Jiaxing 15
Lawrence 13
Ann Arbor 12
Boardman 12
Shenyang 12
Sofia 12
Hebei 11
Falls Church 10
Woodbridge 10
Houston 9
Newcastle upon Tyne 8
Orange 8
Beijing 7
Florence 7
Tianjin 7
Changsha 6
Kunming 6
Fairfield 5
Redmond 5
Cambridge 4
Guangzhou 4
Indiana 3
London 3
Piemonte 3
Shanghai 3
Caserta 2
Dearborn 2
Hangzhou 2
Montréal 2
Naples 2
Newark 2
Palma De Mallorca 2
Salerno 2
Torre Annunziata 2
Ashburn 1
Birzebbuga 1
Brescia 1
Brisbane 1
Campobasso 1
Fisciano 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
Massafra 1
Mcallen 1
Milan 1
Munich 1
New York 1
Ningbo 1
Oxelösund 1
Pescara 1
Pietrasanta 1
Pisa 1
Providence 1
Redwood City 1
Rome 1
Saint John 1
San Francisco 1
Simi Valley 1
Spennymoor 1
Sunnyvale 1
Tappahannock 1
Vienna 1
Walnut 1
Wuhan 1
Totale 1212
Nome #
DiGeorge-like syndrome in a child with a 3p12.3 deletion involving miRNA-4273 born to a diabetic mother 86
Tbx1 regulation of myogenic differentiation in the limb and cranial mesoderm 46
A genetic link between Tbx1 and Fibroblast Growth Factor Signaling 39
Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway? 38
Fgf15 is required for proper morphogenesis of the mouse cardiac outflow tract 38
Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development. 37
Tbx1 deletion in Islet1-fated cells recapitulates the cardiovascular Tbx1 mutant phenotype 34
Coronary stem development in wild-type and Tbx1 null mouse hearts 34
A deficiency in the region homologous to human 17q21.33-q23.2 causes heart defects in mice 33
Microarray analysis of the Df1 mouse model of the 22q11 Deletion Syndrome. 32
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. 31
Diagnosis of Genetic and Malignant Diseases Using Chromosome Specific DNA Probes, Multiple Fluorochromes and Optical Imaging Systems 31
Genetic pathways to mammalian heart development: Recent progress from manipulation of the mouse genome. 30
Congenital Heart Disease in Mice Deficient for the DiGeorge Syndrome Region. 29
Serotonin transporter role in heart development focusing on cardiac valve and conduction system 29
The 22q11.2 deletion syndrome: a gene dosage perspective 28
Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1. 27
PPARδ up-regulates 14-3-3ε in human endothelial cells via C/Ebpβ. 27
Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia. 26
Dissecting DiGeorge syndrome: The interaction between Tbx1 and the retinoic acid pathway 25
In vivo response to high-resolution variation of Tbx1 mRNA dosage. 25
TBX1 Represses Vegfr2 Gene Expression and Enhances the Cardiac Fate of VEGFR2+ Cells 25
Tbx1: Transcriptional and Developmental Functions 25
Dissecting contiguous gene defects: TBX1. 24
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract. 24
Congenital heart disease in mice deficient for the DiGeorge syndrome region 24
DiGeorge Syndrome: A gene at last. 22
A 12-Mb complete coverage BAC contig map in human chromosome 16p13.1-p11.2 21
Congenital heart disease and genetic syndromes: new insights into molecular mechanisms 21
Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants. 20
Tbx1 represses Mef2c gene expression and is correlated with histone 3 deacetylation of the anterior heart field enhancer 20
DiGeorge Syndrome: an update 19
Fate map of serotonin transporter-expressing cells in developing mouse heart 19
TBX1 and Basal Cell Carcinoma: Expression and Interactions with Gli2 and Dvl2 Signaling 19
Pharmacological Rescue of the Brain Cortex Phenotype of Tbx1 Mouse Mutants: Significance for 22q11.2 Deletion Syndrome 19
Fate map of SERT-expressing cells in developing mouse heart. 18
Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis. 18
Genetic and physical mapping of a voltage-dependent chloride channel gene to human 4q32 and to mouse 8. 18
A fate map of Tbx1 expressing cells reveals heterogeneity in the second cardiac field 18
22q11 deletions and cardiac disease 18
Tbx1 Mutation Causes Multiple Cardiovascular Defects and Disrupts Neural Crest and Cranial Nerve Migratory Pathways 17
Recovery from arterial growth delay reduces the penetrance of cardiovascular defects in mice deleted for the DiGeorge Syndrome region 17
Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway? 17
Are primary cilia involved in Embryonic Stem Cells differentiation and/or the maintenance of the undifferentiated state? 17
A Human Alpha-satellite Dna Subset Specific For Chromosome-12 17
14-3-3? plays a role in cardiac ventricular compaction by regulating the cardiomyocyte cell cycle. 17
A defect in early myogenesis causes Otitis media in two mouse models of 22q11.2 Deletion Syndrome 17
Vitamin B12 ameliorates the phenotype of a mouse model of DiGeorge syndrome 17
Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice 16
Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization. 16
Cloning and Comparative Mapping of A Chromosome-20-specific Alphoid Dna-sequence 16
Transcription factor TBX1 overexpression induces downregulation of proteins involved in retinoic acid metabolism: a comparative proteomic analysis. 16
Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice 16
Chromatin and Transcriptional Response to Loss of TBX1 in Early Differentiation of Mouse Cells 16
Tbx1 is required for inner ear morphogenesis. 15
Conditional and constitutive expression of a Tbx1-GFP fusion protein in mice. 15
Rebalancing gene haploinsufficiency in vivo by targeting chromatin 15
Gene-environment interaction impacts on heart development and embryo survival 15
Manipulation of endogenous regulatory elements and transgenic analyses of the Tbx1 gene 14
Cloning and chromosome mapping of human and chicken Iroquois (IRX) genes 14
Cardiopharyngeal mesoderm origins of musculoskeletal and connective tissues in the mammalian pharynx 14
Single cell multi-omic analysis identifies a Tbx1-dependent multilineage primed population in murine cardiopharyngeal mesoderm 14
Chromosomal Assignment of Human Yac Clones By Fluorescence Insitu Hybridization - Use of Single-yeast-colony Pcr and Multiple Labeling 13
A pivotal role for endogenous TGF-beta-activated kinase-1 in the LKB1/AMP-activated protein kinase energy-sensor pathway 13
A Human Alphoid Dna Clone From the Ecori Dimeric Family - Genomic and Internal Organization and Chromosomal Assignment 13
Peroxisome proliferator-activated receptor-δ upregulates 14-3-3ε in human endothelial cells via CCAAT/enhancer binding protein-β 13
Effects of individual segmental trisomies of human chromosome 21 syntenic regions on hippocampal long-term potentiation and cognitive behaviors in mice 13
Tbx1 regulates extracellular matrix-cell interactions in the second heart field 13
TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome 12
Mapping on human and mouse chromosomes of the gene for the beta-galactoside-binding protein, an autocrine-negative growth factor. 11
The Transcriptional Activity of Individual Ribosomal Dna Gene Clusters Is Modulated By Serum Concentration 11
Tbx1 is a negative modulator of Mef2c 11
Mouse models for Down syndrome-associated developmental cognitive disabilities. 11
Preliminary steps of fibroblasts reprogramming to develop mTECs from control or FOXN1(-/-) fibroblasts 11
A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3 11
EZH2 is required for parathyroid and thymic development through differentiation of the third pharyngeal pouch endoderm 11
Subepicardial endothelial cells invade the embryonic ventricle wall to form coronary arteries. 10
Tbx1 Regulates the BMP-Smad1 Pathway in a Transcription Independent Manner 9
Tbx1 Regulates Proliferation and Differentiation of Multipotent Heart Progenitors 9
Selection of A Human Chromosome-21 Enriched Yac Sub-library Using A Chromosome-specific Composite Probe 9
p53 suppression partially rescues the mutant phenotype in mouse models of DiGeorge syndrome. 9
Genetic analysis of Down syndrome-associated heart defects in mice 8
Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments 8
Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis 8
In vivo genetic ablation of the periotic mesoderm affects cell proliferation survival and differentiation in the cochlea 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
Schizophrenia and Chromosomal Deletions Within 22q11.2 8
Localization of the Human Prostate Transglutaminase (Type IV) Gene (TGM4) to Chromosome 3p21.33-p22 by Fluorescence in Situ Hybridization 8
DiGeorge syndrome: the use of model organisms to dissect complex genetics 7
Tbx1 regulates progenitor cell proliferation in the dental epithelium by modulating Pitx2 activation of p21 7
Deficiencies in the region syntenic to human 21q22.3 cause cognitive deficits in mice 7
Simultaneous Visualization of 7 Different Dna Probes By Insitu Hybridization Using Combinatorial Fluorescence and Digital Imaging Microscopy 7
Early thyroid development requires a Tbx1-Fgf8 pathway 7
DiGeorge's syndrome: a gene at last 7
Genetic dissection of the DiGeorge syndrome phenotype 7
Identification and molecular characterization of de novo translocation t(8;14)(q22.3;q13) associated with a vascular and tissue overgrowth syndrome 7
DiGeorge syndrome: complex pathogenesis? Maybe, maybe not 7
Partial rescue of the Tbx1 mutant heart phenotype by Fgf8: Genetic evidence of impaired tissue response to Fgf8 7
Pitx2 promotes development of splanchnic mesoderm-derived branchiomeric muscle 6
Totale 1818
Categoria #
all - tutte 4035
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 4035

Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/201837 0000 00 021 10222
2018/2019131 2280 269 303 10203
2019/2020280 1140347 411 31 422350
2020/2021349 3354535 3461 3422 446282
2021/2022446 13044 516 1146 43764233
2022/2023434 11855972 7983 216 0000
Totale 1869