Site-specific cell proliferation in renal tubular cells by the renal tubular carcinogen tris(2,3-dibromopropyl)phosphate.

Por Cunningham, M L, Elwell, M R, Matthews, H B
Publicado em 1993

Distinction of mutagenic carcinogens from a mutagenic noncarcinogen in the big blue transgenic mouse.

Por Cunningham, M L, Hayward, J J, Shane, B S, Tindall, K R
Publicado em 1996

Phosphorylation by protein kinase C decreases catalytic activity of avian phospholipase C-beta.

Por Filtz, T M, Cunningham, M L, Stanig, K J, Paterson, A, Harden, T K
Publicado em 1999

Structure of MurA (UDP-N-acetylglucosamine enolpyruvyl transferase) from Vibrio fischeri in complex with substrate UDP-N-acetylglucosamine and the drug fosfomycin

Por Bensen, D. C., Rodriguez, S., Nix, J., Cunningham, M. L., Tari, L. W.
Publicado em 2012

The crystal structure of trypanothione reductase from the human pathogen Trypanosoma cruzi at 2.3 A resolution.

Por Zhang, Y., Bond, C. S., Bailey, S., Cunningham, M. L., Fairlamb, A. H., Hunter, W. N.
Publicado em 1996

Disruption of the trypanothione reductase gene of Leishmania decreases its ability to survive oxidative stress in macrophages.

Por Dumas, C, Ouellette, M, Tovar, J, Cunningham, M L, Fairlamb, A H, Tamar, S, Olivier, M, Papadopoulou, B
Publicado em 1997

3D Head Shape Quantification for Infants with and without Deformational Plagiocephaly

Por Atmosukarto, I., Shapiro, L. G., Starr, J. R., Heike, C. L., Collett, B., Cunningham, M. L., Speltz, M. L.
Publicado em 2010

Craniosynostosis and Risk Factors Related to Thyroid Dysfunction

Por Carmichael, S. L., Ma, C., Rasmussen, S. A., Cunningham, M. L., Browne, M. L., Dosiou, C., Lammer, E. J., Shaw, G. M.
Publicado no Am J Med Genet A (2015)

Transcriptome correlation analysis identifies two unique craniosynostosis subtypes associated with IRS1 activation

Por Stamper, B. D., Mecham, B., Park, S. S., Wilkerson, H., Farin, F. M., Beyer, R. P., Bammler, T. K., Mangravite, L. M., Cunningham, M. L.
Publicado em 2012

Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutations.

Por Paznekas, W A, Cunningham, M L, Howard, T D, Korf, B R, Lipson, M H, Grix, A W, Feingold, M, Goldberg, R, Borochowitz, Z, Aleck, K, Mulliken, J, Yin, M, Jabs, E W
Publicado em 1998