Associate Professor, Pediatrics, Pathology, and Human Genetics The University of Chicago, Pritzker School of Medicine
Pathology
Dr. Ivan P. Moskowitz, MD
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Ivan Moskowitz works in the field of Pathology. He went to medical school at University of Wisconsin School of Medicine and Public Health. Ivan Moskowitz is a published doctor. He has 38 publications published. The most current publication "lin-12 and glp-1 are required zygotically for early embryonic cellular interactions and are regulated by maternal GLP-1 signaling in Caenorhabditis elegans." He is registered with Medicare.
Publications
- The Cardiac TBX5 Interactome Reveals a Chromatin Remodeling Network Essential for Cardiac Septation.
- Foxf genes integrate tbx5 and hedgehog pathways in the second heart field for cardiac septation.
- Tbx5-hedgehog molecular networks are essential in the second heart field for atrial septation.
- Enhanced desumoylation in murine hearts by overexpressed SENP2 leads to congenital heart defects and cardiac dysfunction.
- A novel murine allele of Intraflagellar Transport Protein 172 causes a syndrome including VACTERL-like features with hydrocephalus.
- Defective sumoylation pathway directs congenital heart disease.
- The emerging genetic landscape underlying cardiac conduction system function.
- Inducible recombination in the cardiac conduction system of mink:CreERT(2) BAC transgenic mice.
- Transcription factor genes Smad4 and Gata4 cooperatively regulate cardiac valve development. [corrected]
- Expression of sumoylation deficient nkx2.5 mutant in nkx2.5 haploinsufficient mice leads to congenital heart defects.
- DNMT3B7, a truncated DNMT3B isoform expressed in human tumors, disrupts embryonic development and accelerates lymphomagenesis.
- The role of cardiac troponin T quantity and function in cardiac development and dilated cardiomyopathy.
- Filamin A (FLNA) is required for cell-cell contact in vascular development and cardiac morphogenesis.
- Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy.
- Tetralogy of Fallot with congenital aortic valvar stenosis: the tetralogy-truncus interrelationship.
- Ventricular arrhythmia vulnerability in cardiomyopathic mice with homozygous mutant Myosin-binding protein C gene.
- Comparison of two murine models of familial hypertrophic cardiomyopathy.
- Low-dose cyclosporin A therapy in children with refractory immune thrombocytopenic purpura.
- lin-12 and glp-1 are required zygotically for early embryonic cellular interactions and are regulated by maternal GLP-1 signaling in Caenorhabditis elegans.
- The potential to differentiate epidermis is unequally distributed in the AB lineage during early embryonic development in C. elegans.
- Combinatorial specification of blastomere identity by glp-1-dependent cellular interactions in the nematode Caenorhabditis elegans.
- Characterization of sinoatrial node in four conduction system marker mice.
- Complex interactions between genes controlling trafficking in primary cilia.
- Ventricular fibrillation following autologous intramyocardial cell therapy for inherited cardiomyopathy.
- A mouse chromosome 4 balancer ENU-mutagenesis screen isolates eleven lethal lines.
- Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation.
- Genome-wide identification of mouse congenital heart disease loci.
- Somatic events modify hypertrophic cardiomyopathy pathology and link hypertrophy to arrhythmia.
- Repression of cell-cell fusion by components of the C. elegans vacuolar ATPase complex.
- The T-Box transcription factor Tbx5 is required for the patterning and maturation of the murine cardiac conduction system.
- Cardiac electrophysiological phenotypes in postnatal expression of Nkx2.5 transgenic mice.
- Electrophysiologic characterization and postnatal development of ventricular pre-excitation in a mouse model of cardiac hypertrophy and Wolff-Parkinson-White syndrome.
- Complex genomic rearrangement in CCS-LacZ transgenic mice.
- sonic hedgehog is required in pulmonary endoderm for atrial septation.
- E2F3 plays an essential role in cardiac development and function.
- A molecular pathway including Id2, Tbx5, and Nkx2-5 required for cardiac conduction system development.
- Giant cell myocarditis in a 12-year-old girl with common variable immunodeficiency.
Schools
Univ Of Wi Med Sch
Doctors Specialties
- Anatomic Pathology
- Pathology
Accepted Insurances
Education
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Boston Children's Hospital -
Brigham and Women's Hospital -
University of Wisconsin School of Medicine and Public Health
Hospital
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University of Chicago Medical Center
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1215946488 |
| Last Name Of The Provider | MOSKOWITZ |
| First Name Of The Provider | IVAN |
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