Lista de obras - Antonio Baldini - Dominio Público Uruguay

14-3-3ε plays a role in cardiac ventricular compaction by regulating the cardiomyocyte cell cycle

artículo científico publicado en 2012

A Genetic Etiology for Interruption of the Aortic Arch Type B ⬇️

artículo científico publicado el 15 de agosto de 1997

A defect in early myogenesis causes Otitis media in two mouse models of 22q11.2 Deletion Syndrome

artículo científico publicado en 2014

A deficiency in the region homologous to human 17q21.33-q23.2 causes heart defects in mice.

artículo científico publicado en 2006

A fate map of Tbx1 expressing cells reveals heterogeneity in the second cardiac field

artículo científico publicado en 2007

A genetic link between Tbx1 and fibroblast growth factor signaling.

artículo científico publicado en 2002

A phenotypic rescue approach identifies lineage regionalization defects in a mouse model of DiGeorge syndrome

artículo científico publicado en 2022

A pivotal role for endogenous TGF-beta-activated kinase-1 in the LKB1/AMP-activated protein kinase energy-sensor pathway

artículo científico publicado en 2006

Canonical Wnt signaling functions in second heart field to promote right ventricular growth

scientific journal article

Conditional and constitutive expression of a Tbx1-GFP fusion protein in mice

artículo científico publicado en 2013

Deficiencies in the region syntenic to human 21q22.3 cause cognitive deficits in mice

artículo científico publicado en 2010

Deletion of chromosome 22q11 and pseudohypoparathyroidism ⬇️

artículo científico publicado el 3 de octubre de 1997

DiGeorge anomaly and chromosome 10p deletions: One or two loci? ⬇️

artículo científico publicado el 28 de noviembre de 1997

DiGeorge syndrome: an update

artículo científico publicado en 2004

DiGeorge syndrome: the use of model organisms to dissect complex genetics

artículo científico publicado en 2002

DiGeorge's syndrome: a gene at last ⬇️

artículo científico publicado el 25 de octubre de 2003

Diagnosis of X-linked Adrenal Hypoplasia Congenita by Mutation Analysis of the DAX1 Gene ⬇️

artículo científico publicado el 26 de julio de 1995

ES2, a gene deleted in DiGeorge syndrome, encodes a nuclear protein and is expressed during early mouse development, where it shares an expression domain with a Goosecoid-like gene ⬇️

artículo científico publicado el 1 de abril de 1998

Early thyroid development requires a Tbx1-Fgf8 pathway

scientific journal article

Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis

scientific journal article

Effects of individual segmental trisomies of human chromosome 21 syntenic regions on hippocampal long-term potentiation and cognitive behaviors in mice.

artículo científico publicado en 2010

Family with 22‐derived marker chromosome and late‐onset dementia of the Alzheimer type: II. Further cytogenetic analysis of the marker and characterization of the high‐level repeat sequences using fluorescence in situ hybridization ⬇️

artículo científico publicado el 1 de agosto de 1993

Fgf15 is required for proper morphogenesis of the mouse cardiac outflow tract

scientific journal article

Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants

scientific journal article

Gain of function of Tbx1 affects pharyngeal and heart development in the mouse

artículo científico publicado en 2009

Gene-environment interaction impacts on heart development and embryo survival

scientific article published on 20 February 2019

Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway?

artículo científico publicado en 2003

Genetic analysis of Down syndrome-associated heart defects in mice.

artículo científico publicado en 2011

Genetic pathways to mammalian heart development: Recent progress from manipulation of the mouse genome

artículo científico publicado en 2006

Goosecoid-Like Sequences and the Smallest Region of Deletion Overlap in DiGeorge and Velocardiofacial Syndromes ⬇️

artículo científico publicado el 1 de diciembre de 1997

In vivo genetic ablation of the periotic mesoderm affects cell proliferation survival and differentiation in the cochlea

artículo científico publicado en 2007

In vivo response to high-resolution variation of Tbx1 mRNA dosage

scientific journal article

Interchromosomal duplications of the adrenoleukodystrophy locus: a phenomenon of pericentromeric plasticity ⬇️

artículo científico publicado el 1 de julio de 1997

Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice

artículo científico publicado en 2019

Localization of BRRN1, the Human Homologue ofDrosophila barr,to 2q11.2 ⬇️

artículo científico publicado el 1 de diciembre de 1997

Mapping segmental imbalances using comparative genomic hybridization and eigenanalysis ⬇️

artículo científico publicado el 1 de enero de 1995

Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development

artículo científico publicado en 2006

Methylation of the 5' flanking sequences of the ribosomal DNA in human cell lines and in a human-hamster hybrid cell line

artículo científico publicado el 1 de diciembre de 1992

Partial rescue of the Tbx1 mutant heart phenotype by Fgf8: genetic evidence of impaired tissue response to Fgf8

scientific journal article

Peroxisome proliferator-activated receptor-delta upregulates 14-3-3 epsilon in human endothelial cells via CCAAT/enhancer binding protein-beta

artículo científico publicado en 2007

Rebalancing gene haploinsufficiency in vivo by targeting chromatin.

artículo científico publicado en 2016

Retracted: Tbx1 Regulates the BMP-Smad1 Pathway in a Transcription Independent Manner

artículo científico publicado en 2009

TBX1 Represses Vegfr2 Gene Expression and Enhances the Cardiac Fate of VEGFR2+ Cells

artículo científico publicado en 2015

TBX1 and Basal Cell Carcinoma: Expression and Interactions with Gli2 and Dvl2 Signaling

scientific article published on 17 January 2020

TBX1 is required for inner ear morphogenesis

scientific journal article

TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome

artículo científico publicado en 2015

Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development

scientific journal article

Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract

scientific journal article

Tbx1 is a negative modulator of Mef2c

artículo científico publicado en 2012

Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways

scientific journal article

Tbx1 regulates Vegfr3 and is required for lymphatic vessel development

scientific journal article

Tbx1 regulates population, proliferation and cell fate determination of otic epithelial cells

scientific journal article

Tbx1 regulates progenitor cell proliferation in the dental epithelium by modulating Pitx2 activation of p21

scientific journal article

Tbx1 regulates proliferation and differentiation of multipotent heart progenitors

scientific journal article

Tbx1 represses Mef2c gene expression and is correlated with histone 3 deacetylation of the anterior heart field enhancer

scientific article published on 30 August 2018

The 22q11.2 deletion syndrome: a gene dosage perspective.

artículo científico publicado en 2006

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

scientific journal article

Transcriptional control in cardiac progenitors: Tbx1 interacts with the BAF chromatin remodeling complex and regulates Wnt5a

artículo científico publicado en 2012

Velo‐cardio‐facial syndrome: Frequency and extent of 22q1l deletions ⬇️

artículo científico publicado el 3 de julio de 1995

p53 Suppression partially rescues the mutant phenotype in mouse models of DiGeorge syndrome

artículo científico publicado en 2014

Lista de obras de Antonio Baldini

14-3-3ε plays a role in cardiac ventricular compaction by regulating the cardiomyocyte cell cycle

A Genetic Etiology for Interruption of the Aortic Arch Type B ⬇️

A defect in early myogenesis causes Otitis media in two mouse models of 22q11.2 Deletion Syndrome

A deficiency in the region homologous to human 17q21.33-q23.2 causes heart defects in mice.

A fate map of Tbx1 expressing cells reveals heterogeneity in the second cardiac field

A genetic link between Tbx1 and fibroblast growth factor signaling.

A phenotypic rescue approach identifies lineage regionalization defects in a mouse model of DiGeorge syndrome

A pivotal role for endogenous TGF-beta-activated kinase-1 in the LKB1/AMP-activated protein kinase energy-sensor pathway

Canonical Wnt signaling functions in second heart field to promote right ventricular growth

Conditional and constitutive expression of a Tbx1-GFP fusion protein in mice

Deficiencies in the region syntenic to human 21q22.3 cause cognitive deficits in mice

Deletion of chromosome 22q11 and pseudohypoparathyroidism ⬇️

DiGeorge anomaly and chromosome 10p deletions: One or two loci? ⬇️

DiGeorge syndrome: an update

DiGeorge syndrome: the use of model organisms to dissect complex genetics

DiGeorge's syndrome: a gene at last ⬇️

Diagnosis of X-linked Adrenal Hypoplasia Congenita by Mutation Analysis of the DAX1 Gene ⬇️

ES2, a gene deleted in DiGeorge syndrome, encodes a nuclear protein and is expressed during early mouse development, where it shares an expression domain with a Goosecoid-like gene ⬇️

Early thyroid development requires a Tbx1-Fgf8 pathway

Ece1 and Tbx1 define distinct pathways to aortic arch morphogenesis

Effects of individual segmental trisomies of human chromosome 21 syntenic regions on hippocampal long-term potentiation and cognitive behaviors in mice.

Family with 22‐derived marker chromosome and late‐onset dementia of the Alzheimer type: II. Further cytogenetic analysis of the marker and characterization of the high‐level repeat sequences using fluorescence in situ hybridization ⬇️

Fgf15 is required for proper morphogenesis of the mouse cardiac outflow tract

Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutants

Gain of function of Tbx1 affects pharyngeal and heart development in the mouse

Gene-environment interaction impacts on heart development and embryo survival

Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway?

Genetic analysis of Down syndrome-associated heart defects in mice.

Genetic pathways to mammalian heart development: Recent progress from manipulation of the mouse genome

Goosecoid-Like Sequences and the Smallest Region of Deletion Overlap in DiGeorge and Velocardiofacial Syndromes ⬇️

In vivo genetic ablation of the periotic mesoderm affects cell proliferation survival and differentiation in the cochlea

In vivo response to high-resolution variation of Tbx1 mRNA dosage

Interchromosomal duplications of the adrenoleukodystrophy locus: a phenomenon of pericentromeric plasticity ⬇️

Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice

Localization of BRRN1, the Human Homologue ofDrosophila barr,to 2q11.2 ⬇️

Mapping segmental imbalances using comparative genomic hybridization and eigenanalysis ⬇️

Mesodermal expression of Tbx1 is necessary and sufficient for pharyngeal arch and cardiac outflow tract development

Methylation of the 5' flanking sequences of the ribosomal DNA in human cell lines and in a human-hamster hybrid cell line

Partial rescue of the Tbx1 mutant heart phenotype by Fgf8: genetic evidence of impaired tissue response to Fgf8

Peroxisome proliferator-activated receptor-delta upregulates 14-3-3 epsilon in human endothelial cells via CCAAT/enhancer binding protein-beta

Rebalancing gene haploinsufficiency in vivo by targeting chromatin.

Retracted: Tbx1 Regulates the BMP-Smad1 Pathway in a Transcription Independent Manner

TBX1 Represses Vegfr2 Gene Expression and Enhances the Cardiac Fate of VEGFR2+ Cells

TBX1 and Basal Cell Carcinoma: Expression and Interactions with Gli2 and Dvl2 Signaling

TBX1 is required for inner ear morphogenesis

TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome

Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development

Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract

Tbx1 is a negative modulator of Mef2c

Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways

Tbx1 regulates Vegfr3 and is required for lymphatic vessel development

Tbx1 regulates population, proliferation and cell fate determination of otic epithelial cells

Tbx1 regulates progenitor cell proliferation in the dental epithelium by modulating Pitx2 activation of p21

Tbx1 regulates proliferation and differentiation of multipotent heart progenitors

Tbx1 represses Mef2c gene expression and is correlated with histone 3 deacetylation of the anterior heart field enhancer

The 22q11.2 deletion syndrome: a gene dosage perspective.

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

Transcriptional control in cardiac progenitors: Tbx1 interacts with the BAF chromatin remodeling complex and regulates Wnt5a

Velo‐cardio‐facial syndrome: Frequency and extent of 22q1l deletions ⬇️

p53 Suppression partially rescues the mutant phenotype in mouse models of DiGeorge syndrome