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Cell-free DNA donor fraction analysis in pediatric and adult heart transplant patients by multiplexed allele-specific quantitative PCR: Validation of a rapid and highly sensitive clinical test for stratification of rejection probability

PloS one, 2020-01, Vol.15 (1), p.e0227385-e0227385

2020

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Total Cell-Free DNA Predicts Death and Infection Following Pediatric and Adult Heart Transplantation

The Annals of thoracic surgery, 2021-10, Vol.112 (4), p.1282-1289

2021

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Impact of MYH6 variants in hypoplastic left heart syndrome

Physiological genomics, 2016-12, Vol.48 (12), p.912-921

2016

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Human gene copy number spectra analysis in congenital heart malformations

Physiological genomics, 2012-05, Vol.44 (9), p.518-541

2012

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Novel KLHL26 variant associated with a familial case of Ebstein’s anomaly and left ventricular noncompaction

Molecular genetics & genomic medicine, 2020-04, Vol.8 (4), p.e1152-n/a

2020

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Exploring molecular profiles of calcification in aortic vascular smooth muscle cells and aortic valvular interstitial cells

Journal of molecular and cellular cardiology, 2023-10, Vol.183, p.1-13

2023

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Effect of 22q11.2 deletion on bleeding and transfusion utilization in children with congenital heart disease undergoing cardiac surgery

Pediatric research, 2016-02, Vol.79 (2), p.318-324

2016

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Human genotyping and an experimental model reveal NPR-C as a possible contributor to morbidity in coarctation of the aorta

Physiological genomics, 2019-06, Vol.51 (6), p.177-185

2019

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Membrane Association, Mechanism of Action, and Structure of Arabidopsis Embryonic Factor 1 (FAC1)

The Journal of biological chemistry, 2006-05, Vol.281 (21), p.14939-14947

2006

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Multiplexed quantitative real-time PCR to detect 22q11.2 deletion in patients with congenital heart disease

Physiological genomics, 2010-09, Vol.42A (1), p.52-60

2010

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Calcium Activates Erythrocyte AMP Deaminase [Isoform E (AMPD3)] through a Protein−Protein Interaction between Calmodulin and the N-Terminal Domain of the AMPD3 Polypeptide

Biochemistry (Easton), 2005-04, Vol.44 (14), p.5551-5559

2005

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N-terminal Sequence and Distal Histidine Residues Are Responsible for pH-regulated Cytoplasmic Membrane Binding of Human AMP Deaminase Isoform E

The Journal of biological chemistry, 2002-11, Vol.277 (45), p.42654-42662

2002

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Genetic and other determinants of AMP deaminase activity in healthy adult skeletal muscle

Journal of applied physiology (1985), 1998-10, Vol.85 (4), p.1273-1278

1998

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Novel Aspects of Tetramer Assembly and N-terminal Domain Structure and Function Are Revealed by Recombinant Expression of Human AMP Deaminase Isoforms

The Journal of biological chemistry, 1998-12, Vol.273 (52), p.35118-35125

1998

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Regulation of AMP Deaminase by Phosphoinositides

The Journal of biological chemistry, 1999-09, Vol.274 (36), p.25701-25707

1999

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Towards an understanding of the functional significance of N-terminal domain divergence in human AMP deaminase isoforms

Pharmacology & therapeutics (Oxford), 2000-08, Vol.87 (2), p.279-283

2000

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Cover

Molecular genetics & genomic medicine, 2020-04, Vol.8 (4)

2020

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Crystallization and preliminary X-ray crystallographic analysis of adenosine 5′-monophosphate deaminase (AMPD) from Arabidopsis thaliana in complex with coformycin 5′-phosphate

Acta crystallographica. Section F, Structural biology and crystallization communications, 2005-08, Vol.61 (8), p.740-742

2005

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Abstract 16717: Human Gene Copy Number Spectra Analysis in Congenital Heart Malformations

Circulation (New York, N.Y.), 2011-11, Vol.124 (suppl_21)

2011

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Localization of N-Terminal Sequences in Human AMP Deaminase Isoforms That Influence Contractile Protein Binding

Biochemical and biophysical research communications, 2001-07, Vol.285 (2), p.489-495

2001

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Cloning of human AMP deaminase isoform E cDNAs. Evidence for a third AMPD gene exhibiting alternatively spliced 5'-exons

The Journal of biological chemistry, 1992-10, Vol.267 (29), p.20866-20877

1992

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Molecular cloning of AMP deaminase isoform L. Sequence and bacterial expression of human AMPD2 cDNA

The Journal of biological chemistry, 1992-11, Vol.267 (31), p.22407-22413

1992

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Regulation of rat AMP deaminase 3 (isoform C) by development and skeletal muscle fibre type

Biochemical journal, 1997-09, Vol.326 ( Pt 2) (2), p.521-529

1997

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Cloning, sequence and characterization of the human AMPD2 gene: evidence for transcriptional regulation by two closely spaced promoters

Biochimica et biophysica acta, 1996-08, Vol.1308 (2), p.122-132

1996

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Characterization of the human AMPD3 gene reveals that 5′ exon useage is subject to transcriptional control by three tandem promoters and alternative splicing

Biochimica et biophysica acta. Gene structure and expression, 1996-04, Vol.1306 (1), p.75-92

1996

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Cell-free DNA donor fraction analysis in pediatric and adult heart transplant patients by multiplexed allele-specific quantitative PCR: Validation of a rapid and highly sensitive clinical test for stratification of rejection probability

Total Cell-Free DNA Predicts Death and Infection Following Pediatric and Adult Heart Transplantation

Impact of MYH6 variants in hypoplastic left heart syndrome

Human gene copy number spectra analysis in congenital heart malformations

Novel KLHL26 variant associated with a familial case of Ebstein’s anomaly and left ventricular noncompaction

Exploring molecular profiles of calcification in aortic vascular smooth muscle cells and aortic valvular interstitial cells

Effect of 22q11.2 deletion on bleeding and transfusion utilization in children with congenital heart disease undergoing cardiac surgery

Human genotyping and an experimental model reveal NPR-C as a possible contributor to morbidity in coarctation of the aorta

Membrane Association, Mechanism of Action, and Structure of Arabidopsis Embryonic Factor 1 (FAC1)

Multiplexed quantitative real-time PCR to detect 22q11.2 deletion in patients with congenital heart disease

Calcium Activates Erythrocyte AMP Deaminase [Isoform E (AMPD3)] through a Protein−Protein Interaction between Calmodulin and the N-Terminal Domain of the AMPD3 Polypeptide

N-terminal Sequence and Distal Histidine Residues Are Responsible for pH-regulated Cytoplasmic Membrane Binding of Human AMP Deaminase Isoform E

Genetic and other determinants of AMP deaminase activity in healthy adult skeletal muscle

Novel Aspects of Tetramer Assembly and N-terminal Domain Structure and Function Are Revealed by Recombinant Expression of Human AMP Deaminase Isoforms

Regulation of AMP Deaminase by Phosphoinositides

Towards an understanding of the functional significance of N-terminal domain divergence in human AMP deaminase isoforms

Cover

Crystallization and preliminary X-ray crystallographic analysis of adenosine 5′-monophosphate deaminase (AMPD) from Arabidopsis thaliana in complex with coformycin 5′-phosphate

Abstract 16717: Human Gene Copy Number Spectra Analysis in Congenital Heart Malformations

Localization of N-Terminal Sequences in Human AMP Deaminase Isoforms That Influence Contractile Protein Binding

Cloning of human AMP deaminase isoform E cDNAs. Evidence for a third AMPD gene exhibiting alternatively spliced 5'-exons

Molecular cloning of AMP deaminase isoform L. Sequence and bacterial expression of human AMPD2 cDNA

Regulation of rat AMP deaminase 3 (isoform C) by development and skeletal muscle fibre type

Cloning, sequence and characterization of the human AMPD2 gene: evidence for transcriptional regulation by two closely spaced promoters

Characterization of the human AMPD3 gene reveals that 5′ exon useage is subject to transcriptional control by three tandem promoters and alternative splicing

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