List of works by Shoumo Bhattacharya

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

scientific article published on 01 December 1991

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

scientific article published on 01 September 1993

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

scientific article published on 11 July 2018

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

scientific article published on 14 April 2012

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

scientific article published on 13 April 2012

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

scientific article

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

scientific article published on 09 March 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

scientific article published on 21 August 2013

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

scientific article published on 6 February 2006

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

scientific article

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

scientific article

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

scientific article

Biowire Model of Interstitial and Focal Cardiac Fibrosis

scientific article published on 04 June 2019

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

scientific article published in October 1995

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

scientific article

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

scientific article published in September 2004

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

scientific article published on 6 July 2006

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

scientific article

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

scientific article

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

scientific article

Clinical role of indium-111 antimyosin imaging

scientific article published on January 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

scientific article published on June 2010

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

scientific article

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

scientific article

Cyclin E ablation in the mouse

scientific journal article

Cytosine nucleoside/nucleotide deaminases and apolipoprotein B mRNA editing.

scientific article

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

scientific article published on 18 March 2013

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

scientific article

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

scientific article published in August 2016

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

scientific article published on 23 July 2020

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

scientific article published on 29 May 2020

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

scientific article published on 25 April 2008

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

scientific article

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

scientific article

ExCITED about HIF

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

scientific article published on 21 May 2015

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

scientific article

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

scientific article published on 17 June 2016

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

scientific article

Functional significance of SRJ domain mutations in CITED2

scientific article (publication date: 2012)

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

scientific article

Genetic mechanisms controlling cardiovascular development

scientific article published on March 2008

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

scientific article

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

scientific article published on 20 April 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.

scientific article published on 26 May 2013

Glucocorticoid receptor is required for foetal heart maturation

scientific article published on 16 April 2013

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

scientific article published on 18 April 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

scientific article published in February 2003

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

scientific article published in February 2003

High-throughput analysis of mouse embryos by magnetic resonance imaging

scientific article published on January 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

scientific article (publication date: 8 March 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

scientific article

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

scientific article published on June 1997

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

scientific article published in July 1998

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

scientific article

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

scientific article published in September 2004

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

scientific article

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

scientific article

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

scientific article

Molecular mechanisms controlling the coupled development of myocardium and coronary vasculature

scientific article published on July 2006

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

scientific article published in August 2004

Mouse embryonic phenotyping by morphometric analysis of MR images.

scientific article

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

scientific article

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

scientific article

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

scientific article published on 21 June 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

scientific article published on 26 April 2017

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

scientific article

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

scientific article

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

scientific article published in February 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

scientific article published on 23 November 2011

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

scientific article published in January 1992

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

scientific article published on 01 August 2013

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

scientific article published in February 2003

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans

scientific article published on 3 March 2016

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.

scientific article published in July 2014

Rare variants in NR2F2 cause congenital heart defects in humans

scientific article published on April 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.

scientific article published on December 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.

scientific article

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

scientific article

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 ⬇️

scientific article published on September 1, 1991

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

scientific article

Tagged mutagenesis by efficient Minos-based germ line transposition

scientific article

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

scientific article published on 9 September 2015

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

scientific article published in Scientific Reports

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

scientific article published on 27 February 2018

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

scientific article

The Retinoid Agonist Tazarotene Promotes Angiogenesis and Wound Healing

scientific article

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

scientific article

Torsade de pointes and long QT syndrome following major blood transfusion

scientific article published on February 1, 1992

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

scientific article published on November 2003

Transcriptional control of left-right patterning in cardiac development

scientific article published on April 2010

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

scientific article

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

scientific article published on 01 November 1988

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

scientific article published on 27 June 2017

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

scientific article published on 28 May 2007

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