Jamie L. Lohr, M.D.

Affiliations: 
University of Minnesota, Twin Cities, Minneapolis, MN 
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"Jamie Lohr"
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Publications

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Hamline MY, Corcoran CM, Wamstad JA, et al. (2020) OFCD syndrome and extraembryonic defects are revealed by conditional mutation of the polycomb-group repressive complex 1.1 (PRC1.1) gene BCOR. Developmental Biology
Jimenez E, Zaban N, Sharma N, et al. (2020) His Bundle and Left Bundle Pacing in Pediatrics and Congenital Heart Disease: A Single Center Experience. Pediatric Cardiology
Gerardin JF, Menk JS, Pyles LA, et al. (2015) Compliance with Adult Congenital Heart Disease Guidelines: Are We Following the Recommendations? Congenital Heart Disease
Duffy EA, Pretorius PR, Lerach S, et al. (2015) Mosaic partial deletion of PTPN12 in a child with interrupted aortic arch type A. American Journal of Medical Genetics. Part A. 167: 2674-83
Doyle MJ, Lohr JL, Chapman CS, et al. (2015) Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes as a Model for Heart Development and Congenital Heart Disease. Stem Cell Reviews
Behrens AN, Iacovino M, Lohr JL, et al. (2013) Nkx2-5 mediates differential cardiac differentiation through interaction with Hoxa10. Stem Cells and Development. 22: 2211-20
Kamdar F, Doyle M, Chapman C, et al. (2013) In Vitro Modeling of Duchenne Muscular Dystrophy (DMD) Cardiomyopathy Using Human Induced Pluripotent Stem Cells (hiPSC) The Journal of Heart and Lung Transplantation. 32: S245
Lohr JL, Martin CM, Garry DJ. (2012) Cardiac development and congenital heart disease Coronary Heart Disease: Clinical, Pathological, Imaging, and Molecular Profiles. 2147483647: 19-42
Schleiffarth JR, Person AD, Martinsen BJ, et al. (2007) Wnt5a is required for cardiac outflow tract septation in mice. Pediatric Research. 61: 386-91
Hyatt BA, Resnik ER, Johnson NS, et al. (2007) Lung specific developmental expression of the Xenopus laevis surfactant protein C and B genes. Gene Expression Patterns : Gep. 7: 8-14
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