Vaughn, A., DeHoog, R.J., Eberlin, L.S., and Appling, D.R. (2021) "Metabotype analysis of Mthfd1l-null mouse embryos using desorption electrospray ionization mass spectrometry imaging" Anal. Bioanal. Chem. 413, 3573–3582.
Shin, M., Vaughn, A., Momb, J., and Appling, D.R. (2019) “Deletion of neural tube defect-associated gene Mthfd1l causes reduced cranial mesenchyme density” Birth Defects Research 111, 1520-1534 [BDR Online]
Bryant, J.D., Sweeney, S.R., Sentandreu, E., Shin, M., Ipas, H., Xhemalce, B., Momb, J., Tiziani, S., and Appling, D.R. (2018) “Deletion of the neural tube defect-associated gene Mthfd1l disrupts one-carbon and central energy metabolism in mouse embryos” J. Biol. Chem. 293, 5821-5833 [JBC Online]
Shin, M., Momb, J., and Appling, D.R. (2017) "Human Mitochondrial MTHFD2 Is a Dual Redox Cofactor-specific Methylenetetrahydrofolate Dehydrogenase/Methenyltetrahydrofolate Cyclohydrolase". Cancer & Metabolism 5, 11.
Textbooks:
Mathews, C.K., van Holde, K.E., Appling, D.R., and Anthony-Cahill, S. (2013) Biochemistry, 4th edition. Pearson Canada
Appling, D.R., and Anthony-Cahill, S. and Mathews, C.K. (2019) Biochemistry: Concepts and Connections, 2nd Edition. Pearson USA