D. Mahnke

发表

Human gene copy number spectra analysis in congenital heart malformations.

C. Struble, U. Broeckel, D. Bick, 2012, Physiological genomics.

Calcium activates erythrocyte AMP deaminase [isoform E (AMPD3)] through a protein-protein interaction between calmodulin and the N-terminal domain of the AMPD3 polypeptide.

R. Sabina, D. Mahnke, Donna K. Mahnke, 2005, Biochemistry.

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

P. Simpson, M. Mitchell, D. Newman, 2016, Pediatric Research.

Splicing defective mutants of the COXI gene of yeast mitochondrial DNA: initial definition of the maturase domain of the group II intron aI2.

J. V. Moran, P. Perlman, S. Belcher, 1994, Nucleic acids research.

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

G. Phillips, B. Han, R. Sabina, 2005, Acta crystallographica. Section F, Structural biology and crystallization communications.

Impact of MYH6 variants in hypoplastic left heart syndrome

P. Simpson, J. Tweddell, J. Lough, 2016, Physiological genomics.

Activin-A and Bmp4 Levels Modulate Cell Type Specification during CHIR-Induced Cardiomyogenesis

John Lough, Karl Stamm, Rebekah L. Gundry, 2015, PloS one.

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

R. Bannen, G. Phillips, B. Han, 2006, Journal of Biological Chemistry.

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

P. Simpson, M. A. Baker, K. Stamm, 2020, PloS one.

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

U. Broeckel, W. Grossman, P. Simpson, 2010, Physiological genomics.

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

Michael T. Zimmermann, Nikita R. Dsouza, M. Zimmermann, 2020, Molecular genetics & genomic medicine.

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

A. Alli, O. Palygin, K. Stamm, 2019, Physiological genomics.

Noninvasive Assay for Donor Fraction of Cell-Free DNA in Pediatric Heart Transplant Recipients.

P. Simpson, K. Stamm, M. Mitchell, 2018, Journal of the American College of Cardiology.

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

P. Simpson, K. Stamm, P. North, 2020, The Annals of thoracic surgery.