Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndrome

מאת Hart, T., Hart, P, Bowden, D., Michalec, M., Callison, S., Walker, S., Zhang, Y., Firatli, E.
יצא לאור 1999

Phenotype of ENAM Mutations is Dosage-dependent

מאת Ozdemir, D., Hart, P.S., Firatli, E., Aren, G., Ryu, O.H., Hart, T.C.
יצא לאור 2005

Apoptosis in Gingival Overgrowth Tissues

מאת Kantarci, A., Augustin, P., Firatli, E., Sheff, M.C., Hasturk, H., Graves, D.T., Trackman, P.C.
יצא לאור 2007

Evidence of a founder effect for four cathepsin C gene mutations in Papillon-Lefèvre syndrome patients

מאת Zhang, Y, Lundgren, T, Renvert, S, Tatakis, D, Firatli, E, Uygur, C, Hart, P, Gorry, M, Marks, J, Hart, T
יצא לאור 2001

Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects

מאת Hart, T, Hart, P, Gorry, M, Michalec, M, Ryu, O, Uygur, C, Ozdemir, D, Firatli, S, Aren, G, Firatli, E
יצא לאור 2003

Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta

מאת Hart, PS, Becerik, S, Cogulu, D, Emingil, G, Ozdemir-Ozenen, D, Han, ST, Sulima, PP, Firatli, E, Hart, TC
הוצא לאור ב Clin Genet (2009)

Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin C

מאת Hart, T, Hart, P, Michalec, M, Zhang, Y, Firatli, E, Van Dyke, T E, Stabholz, A, Zlorogorski, A, Shapira, L, Soskolne, W
יצא לאור 2000

MMP20 Active-site Mutation in Hypomaturation Amelogenesis Imperfecta

מאת Ozdemir, D., Hart, P.S., Ryu, O.H., Choi, S.J., Ozdemir-Karatas, M., Firatli, E., Piesco, N., Hart, T.C.
יצא לאור 2005

Identification of cathepsin C mutations in ethnically diverse Papillon-Lefèvre syndrome patients

מאת Hart, P, Zhang, Y, Firatli, E, Uygur, C, Lotfazar, M, Michalec, M, Marks, J, Lu, X, Coates, B, Seow, W, Marshall, R, Williams, D, Reed, J, Wright, J, Hart, T
יצא לאור 2000