Lista de obras - Shoumo Bhattacharya - Dominio Público Uruguay

111In antimyosin antibody uptake is related to the age of myocardial infarction

artículo científico publicado en 1991

99mTc-antimyosin antibody imaging for the detection of acute myocardial infarction in human beings

artículo científico publicado en 1993

A Requirement for Zic2 in the Regulation of Nodal Expression Underlies the Establishment of Left-Sided Identity.

artículo científico publicado en 2018

A cell-autonomous role of Cited2 in controlling myocardial and coronary vascular development

artículo científico publicado en 2012

A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot.

artículo científico publicado en 2012

A comparison of exogenous promoter activity at the ROSA26 locus using a ΦiC31 integrase mediated cassette exchange approach in mouse ES cells

artículo científico publicado en 2011

A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.

artículo científico publicado en 2016

A knottin scaffold directs the CXC-chemokine-binding specificity of tick evasins

scientific article published on 05 June 2019

A mutation in the mitochondrial fission gene Dnm1l leads to cardiomyopathy

scientific journal article

A novel role for transcription factor Lmo4 in thymus development through genetic interaction with Cited2

scientific journal article

A pivotal role for tryptophan 447 in enzymatic coupling of human endothelial nitric oxide synthase (eNOS): effects on tetrahydrobiopterin-dependent catalysis and eNOS dimerization

artículo científico publicado en 2013

A protocol for high-throughput phenotyping, suitable for quantitative trait analysis in mice

artículo científico publicado en 2006

Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsomal triglyceride transfer protein

artículo científico publicado en 1993

An essential role for p300/CBP in the cellular response to hypoxia

scientific journal article

Analysis of the asymmetrically expressed Ablim1 locus reveals existence of a lateral plate Nodal-independent left sided signal and an early, left-right independent role for nodal flow

artículo científico publicado en 2010

Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls

scientific article published on 22 July 2013

Biallelic expression of Tbx1 protects the embryo from developmental defects caused by increased receptor tyrosine kinase signaling

artículo científico publicado en 2012

Biowire Model of Interstitial and Focal Cardiac Fibrosis

artículo científico publicado en 2019

Blockade of the human platelet GPIIb/IIIa receptor by a murine monoclonal antibody Fab fragment (7E3): potent dose-dependent inhibition of platelet function

artículo científico publicado en 1995

Bloomsbury report on mouse embryo phenotyping: recommendations from the IMPC workshop on embryonic lethal screening

artículo científico publicado en 2013

Bloomsbury report on mouse embryo phenotyping: recommendations from the IMPC workshop on embryonic lethal screening

CITED4 inhibits hypoxia-activated transcription in cancer cells, and its cytoplasmic location in breast cancer is associated with elevated expression of tumor cell hypoxia-inducible factor 1alpha

artículo científico publicado en 2004

Cardiac malformations and midline skeletal defects in mice lacking filamin A.

artículo científico publicado en 2006

Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator

artículo científico publicado en 2001

Characterization of transcription factor AP-2 β mutations involved in familial isolated patent ductus arteriosus suggests haploinsufficiency

artículo científico publicado en 2014

Cited2 controls left-right patterning and heart development through a Nodal-Pitx2c pathway

scientific journal article

Cited2 is an essential regulator of adult hematopoietic stem cells

artículo científico publicado en 2009

Clinical role of indium-111 antimyosin imaging

artículo científico publicado en 1991

Cloning of mouse Cited4, a member of the CITED family p300/CBP-binding transcriptional coactivators: induced expression in mammary epithelial cells

scientific journal article

Comparative SNR for high-throughput mouse embryo MR microscopy

artículo científico publicado en 2010

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease

artículo científico publicado en 2012

Cooperation of Stat2 and p300/CBP in signalling induced by interferon-alpha

artículo científico publicado en 1996

Cyclin E ablation in the mouse

scientific journal article

Cytosine nucleoside/nucleotide deaminases and apolipoprotein B mRNA editing.

artículo científico publicado en 1994

Deciphering the Mechanisms of Developmental Disorders (DMDD): a new programme for phenotyping embryonic lethal mice

artículo científico publicado en 2013

Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen

artículo científico publicado en 2005

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.

artículo científico publicado en 2016

Early Embryonic Expression of AP-2α Is Critical for Cardiovascular Development

artículo científico publicado en 2020

Engineered anti-inflammatory peptides inspired by mapping an evasin-chemokine interaction

artículo científico publicado en 2020

Epiblastic Cited2 deficiency results in cardiac phenotypic heterogeneity and provides a mechanism for haploinsufficiency

artículo científico publicado en 2008

Escherichia coli cytidine deaminase provides a molecular model for ApoB RNA editing and a mechanism for RNA substrate recognition

artículo científico publicado en 1998

Evolutionary origins of apoB mRNA editing: catalysis by a cytidine deaminase that has acquired a novel RNA-binding motif at its active site

artículo científico publicado en 1995

ExCITED about HIF

Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect.

artículo científico publicado en 2015

FOXA2 controls Pkd1l1 expression in the mouse node during left-right determination

artículo científico publicado en 2015

Functional analysis of AEBP2, a PRC2 Polycomb protein, reveals a Trithorax phenotype in embryonic development and in ESCs.

artículo científico publicado en 2016

Functional role of p35srj, a novel p300/CBP binding protein, during transactivation by HIF-1

artículo científico publicado en 1999

Functional significance of SRJ domain mutations in CITED2

artículo científico publicado en 2012

Furin is the major processing enzyme of the cardiac-specific growth factor bone morphogenetic protein 10.

artículo científico publicado en 2011

Genetic mechanisms controlling cardiovascular development

artículo científico publicado en 2008

Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation

artículo científico publicado en 2009

Genetically engineered two-warhead evasins provide a method to achieve precision targeting of disease-relevant chemokine subsets.

artículo científico publicado en 2018

Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot

scientific journal article

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.

artículo científico publicado en 2013

Glucocorticoid receptor is required for foetal heart maturation

artículo científico publicado en 2013

HIC2 is a novel dosage-dependent regulator of cardiac development located within the distal 22q11 deletion syndrome region

artículo científico publicado en 2014

Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome

scientific journal article

High-resolution imaging of normal anatomy, and neural and adrenal malformations in mouse embryos using magnetic resonance microscopy

artículo científico publicado en 2003

High-resolution, high-throughput magnetic paragraph sign resonance imaging of mouse embryonic paragraph sign anatomy using a fast gradient-echo sequence

artículo científico publicado en 2003

High-throughput analysis of mouse embryos by magnetic resonance imaging

artículo científico publicado en 2012

Human CREB-binding protein/p300-interacting transactivator with ED-rich tail (CITED) 4, a new member of the CITED family, functions as a co-activator for transcription factor AP-2

artículo científico publicado en 2002

Hypoxia-inducible factor (HIF) asparagine hydroxylase is identical to factor inhibiting HIF (FIH) and is related to the cupin structural family

scientific journal article

Identification of cardiac malformations in mice lacking Ptdsr using a novel high-throughput magnetic resonance imaging technique

artículo científico publicado en 2004

JAK2 is required for induction of the murine DUB-1 gene

artículo científico publicado en 1997

Lineage-specific signaling in melanocytes. C-kit stimulation recruits p300/CBP to microphthalmia

artículo científico publicado en 1998

Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of Fallot

artículo científico publicado en 2013

Making the mouse embryo transparent: identifying developmental malformations using magnetic resonance imaging

artículo científico publicado en 2004

Maternal high-fat diet interacts with embryonic Cited2 genotype to reduce Pitx2c expression and enhance penetrance of left-right patterning defects

artículo científico publicado en 2010

Mice carrying a hypomorphic Evi1 allele are embryonic viable but exhibit severe congenital heart defects

artículo científico publicado en 2014

Molecular cloning and chromosomal localization of the human CITED2 gene encoding p35srj/Mrg1.

artículo científico publicado en 1999

Molecular mechanisms controlling the coupled development of myocardium and coronary vasculature

artículo científico publicado en 2006

Mouse development and cell proliferation in the absence of D-cyclins.

artículo científico publicado en 2004

Mouse embryonic phenotyping by morphometric analysis of MR images.

artículo científico publicado en 2010

Mouse mutagenesis identifies novel roles for left-right patterning genes in pulmonary, craniofacial, ocular, and limb development

artículo científico publicado en 2009

NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets

artículo científico publicado en 2015

Negative autoregulation of BMP dependent transcription by SIN3B splicing reveals a role for RBM39.

artículo científico publicado en 2016

Nprl3 is required for normal development of the cardiovascular system

scientific journal article

Pcsk5 is required in the early cranio-cardiac mesoderm for heart development

artículo científico publicado en 2017

Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls

artículo científico publicado en 2012

Physical and functional interactions among AP-2 transcription factors, p300/CREB-binding protein, and CITED2

artículo científico publicado en 2003

Pinch1 is required for normal development of cranial and cardiac neural crest-derived structures.

artículo científico publicado en 2007

Pioneering function of Isl1 in the epigenetic control of cardiomyocyte cell fate

scientific article published on 25 April 2019

Pitx2 confers left morphological, molecular, and functional identity to the sinus venosus myocardium

artículo científico publicado en 2011

Quantitative 111In antimyosin antibody imaging to predict the age of myocardial infarction

artículo científico publicado en 1992

R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease

artículo científico publicado en 2013

Rapid identification and 3D reconstruction of complex cardiac malformations in transgenic mouse embryos using fast gradient echo sequence magnetic resonance imaging

artículo científico publicado en 2003

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

artículo científico publicado en 2016

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.

artículo científico publicado en 2014

Rare variants in NR2F2 cause congenital heart defects in humans

artículo científico publicado en 2014

Rate of change of left ventricular ejection fraction during exercise is superior to the peak ejection fraction for predicting functionally significant coronary artery disease.

artículo científico publicado en 1993

Requirement for integrin-linked kinase in neural crest migration and differentiation and outflow tract morphogenesis

scientific journal article

Role of the transcription factor sox4 in insulin secretion and impaired glucose tolerance

scientific journal article

Semi-automatic segmentation of multiple mouse embryos in MR images.

artículo científico publicado en 2011

Site specific mutation of the Zic2 locus by microinjection of TALEN mRNA in mouse CD1, C3H and C57BL/6J oocytes

artículo científico publicado en 2013

Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes

scientific journal article

Specific binding of 99MTc-antimyosin to necrotic human myocardium: Clinicopathologic correlations ⬇️

artículo científico publicado el 1 de septiembre de 1991

Structure of the DNA-bound T-box domain of human TBX1, a transcription factor associated with the DiGeorge syndrome

artículo científico publicado en 2012

Tagged mutagenesis by efficient Minos-based germ line transposition

artículo científico publicado en 2010

Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability

artículo científico publicado en 2015

Tetrahydrobiopterin modulates ubiquitin conjugation to UBC13/UBE2N and proteasome activity by S-nitrosation

artículo científico publicado en 2018

The N-terminal domain of a tick evasin is critical for chemokine binding and neutralization and confers specific binding activity to other evasins.

artículo científico publicado en 2018

The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype

artículo científico publicado en 2010

The Retinoid Agonist Tazarotene Promotes Angiogenesis and Wound Healing

artículo científico publicado en 2016

The influence of therapeutic blocking of Gp IIb/IIIa on platelet alpha-granular fibrinogen

scientific article published on 01 December 1992

Therapeutic Implications of a Specific Murine Monoclonal Antibody (7E3) to the Platelet Receptor GPIIb/IIIa

artículo científico publicado en 1992

Torsade de pointes and long QT syndrome following major blood transfusion

artículo científico publicado el 1 de febrero de 1992

Transcriptional coactivator Cited2 induces Bmi1 and Mel18 and controls fibroblast proliferation via Ink4a/ARF

artículo científico publicado en 2003

Transcriptional control of left-right patterning in cardiac development

artículo científico publicado en 2010

VACTERL/caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5

artículo científico publicado en 2008

Ventricular tachycardia induced by Valsalva's manoeuvre in a patient with hypertrophic cardiomyopathy

artículo científico publicado en 1988

Yeast surface display identifies a family of evasins from ticks with novel polyvalent CC chemokine-binding activities

artículo científico publicado en 2017

microMRI-HREM pipeline for high-throughput, high-resolution phenotyping of murine embryos

artículo científico publicado en 2007

Lista de obras de Shoumo Bhattacharya

111In antimyosin antibody uptake is related to the age of myocardial infarction

99mTc-antimyosin antibody imaging for the detection of acute myocardial infarction in human beings

A Requirement for Zic2 in the Regulation of Nodal Expression Underlies the Establishment of Left-Sided Identity.

A cell-autonomous role of Cited2 in controlling myocardial and coronary vascular development

A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot.

A comparison of exogenous promoter activity at the ROSA26 locus using a ΦiC31 integrase mediated cassette exchange approach in mouse ES cells

A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.

A knottin scaffold directs the CXC-chemokine-binding specificity of tick evasins

A mutation in the mitochondrial fission gene Dnm1l leads to cardiomyopathy

A novel role for transcription factor Lmo4 in thymus development through genetic interaction with Cited2

A pivotal role for tryptophan 447 in enzymatic coupling of human endothelial nitric oxide synthase (eNOS): effects on tetrahydrobiopterin-dependent catalysis and eNOS dimerization

A protocol for high-throughput phenotyping, suitable for quantitative trait analysis in mice

Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsomal triglyceride transfer protein

An essential role for p300/CBP in the cellular response to hypoxia

Analysis of the asymmetrically expressed Ablim1 locus reveals existence of a lateral plate Nodal-independent left sided signal and an early, left-right independent role for nodal flow

Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls

Biallelic expression of Tbx1 protects the embryo from developmental defects caused by increased receptor tyrosine kinase signaling

Biowire Model of Interstitial and Focal Cardiac Fibrosis

Blockade of the human platelet GPIIb/IIIa receptor by a murine monoclonal antibody Fab fragment (7E3): potent dose-dependent inhibition of platelet function

Bloomsbury report on mouse embryo phenotyping: recommendations from the IMPC workshop on embryonic lethal screening

Bloomsbury report on mouse embryo phenotyping: recommendations from the IMPC workshop on embryonic lethal screening

CITED4 inhibits hypoxia-activated transcription in cancer cells, and its cytoplasmic location in breast cancer is associated with elevated expression of tumor cell hypoxia-inducible factor 1alpha

Cardiac malformations and midline skeletal defects in mice lacking filamin A.

Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator

Characterization of transcription factor AP-2 β mutations involved in familial isolated patent ductus arteriosus suggests haploinsufficiency

Cited2 controls left-right patterning and heart development through a Nodal-Pitx2c pathway

Cited2 is an essential regulator of adult hematopoietic stem cells

Clinical role of indium-111 antimyosin imaging

Cloning of mouse Cited4, a member of the CITED family p300/CBP-binding transcriptional coactivators: induced expression in mammary epithelial cells

Comparative SNR for high-throughput mouse embryo MR microscopy

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease

Cooperation of Stat2 and p300/CBP in signalling induced by interferon-alpha

Cyclin E ablation in the mouse

Cytosine nucleoside/nucleotide deaminases and apolipoprotein B mRNA editing.

Deciphering the Mechanisms of Developmental Disorders (DMDD): a new programme for phenotyping embryonic lethal mice

Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.

Early Embryonic Expression of AP-2α Is Critical for Cardiovascular Development

Engineered anti-inflammatory peptides inspired by mapping an evasin-chemokine interaction

Epiblastic Cited2 deficiency results in cardiac phenotypic heterogeneity and provides a mechanism for haploinsufficiency

Escherichia coli cytidine deaminase provides a molecular model for ApoB RNA editing and a mechanism for RNA substrate recognition

Evolutionary origins of apoB mRNA editing: catalysis by a cytidine deaminase that has acquired a novel RNA-binding motif at its active site

ExCITED about HIF

Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect.

FOXA2 controls Pkd1l1 expression in the mouse node during left-right determination

Functional analysis of AEBP2, a PRC2 Polycomb protein, reveals a Trithorax phenotype in embryonic development and in ESCs.

Functional role of p35srj, a novel p300/CBP binding protein, during transactivation by HIF-1

Functional significance of SRJ domain mutations in CITED2

Furin is the major processing enzyme of the cardiac-specific growth factor bone morphogenetic protein 10.

Genetic mechanisms controlling cardiovascular development

Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation

Genetically engineered two-warhead evasins provide a method to achieve precision targeting of disease-relevant chemokine subsets.

Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.

Glucocorticoid receptor is required for foetal heart maturation

HIC2 is a novel dosage-dependent regulator of cardiac development located within the distal 22q11 deletion syndrome region

Hes1 expression is reduced in Tbx1 null cells and is required for the development of structures affected in 22q11 deletion syndrome

High-resolution imaging of normal anatomy, and neural and adrenal malformations in mouse embryos using magnetic resonance microscopy

High-resolution, high-throughput magnetic paragraph sign resonance imaging of mouse embryonic paragraph sign anatomy using a fast gradient-echo sequence

High-throughput analysis of mouse embryos by magnetic resonance imaging

Human CREB-binding protein/p300-interacting transactivator with ED-rich tail (CITED) 4, a new member of the CITED family, functions as a co-activator for transcription factor AP-2

Hypoxia-inducible factor (HIF) asparagine hydroxylase is identical to factor inhibiting HIF (FIH) and is related to the cupin structural family

Identification of cardiac malformations in mice lacking Ptdsr using a novel high-throughput magnetic resonance imaging technique

JAK2 is required for induction of the murine DUB-1 gene

Lineage-specific signaling in melanocytes. C-kit stimulation recruits p300/CBP to microphthalmia

Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of Fallot

Making the mouse embryo transparent: identifying developmental malformations using magnetic resonance imaging

Maternal high-fat diet interacts with embryonic Cited2 genotype to reduce Pitx2c expression and enhance penetrance of left-right patterning defects

Mice carrying a hypomorphic Evi1 allele are embryonic viable but exhibit severe congenital heart defects

Molecular cloning and chromosomal localization of the human CITED2 gene encoding p35srj/Mrg1.

Molecular mechanisms controlling the coupled development of myocardium and coronary vasculature

Mouse development and cell proliferation in the absence of D-cyclins.

Mouse embryonic phenotyping by morphometric analysis of MR images.

Mouse mutagenesis identifies novel roles for left-right patterning genes in pulmonary, craniofacial, ocular, and limb development

NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets

Negative autoregulation of BMP dependent transcription by SIN3B splicing reveals a role for RBM39.

Nprl3 is required for normal development of the cardiovascular system

Pcsk5 is required in the early cranio-cardiac mesoderm for heart development

Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls