Frameshift mutation near the 3' end of the COL1A1 gene of type I collagen predicts an elongated Pro alpha 1(I) chain and results in osteogenesis imperfecta type I.

Yazar: Willing, M C, Cohn, D H, Byers, P H
Baskı/Yayın Bilgisi 1990

Osteogenesis imperfecta: translation of mutation to phenotype.

Yazar: Byers, P H, Wallis, G A, Willing, M C
Baskı/Yayın Bilgisi 1991

Absence of mutations in the promoter of the COL1A1 gene of type I collagen in patients with osteogenesis imperfecta type I.

Yazar: Willing, M C, Slayton, R L, Pitts, S H, Deschenes, S P
Baskı/Yayın Bilgisi 1995

Osteogenesis imperfecta type I is commonly due to a COL1A1 null allele of type I collagen.

Yazar: Willing, M C, Pruchno, C J, Atkinson, M, Byers, P H
Baskı/Yayın Bilgisi 1992

Premature chain termination is a unifying mechanism for COL1A1 null alleles in osteogenesis imperfecta type I cell strains.

Yazar: Willing, M. C., Deschenes, S. P., Slayton, R. L., Roberts, E. J.
Baskı/Yayın Bilgisi 1996

Distinct biochemical phenotypes predict clinical severity in nonlethal variants of osteogenesis imperfecta.

Yazar: Wenstrup, R J, Willing, M C, Starman, B J, Byers, P H
Baskı/Yayın Bilgisi 1990

COL5A1 haploinsufficiency is a common molecular mechanism underlying the classical form of EDS.

Yazar: Wenstrup, R J, Florer, J B, Willing, M C, Giunta, C, Steinmann, B, Young, F, Susic, M, Cole, W G
Baskı/Yayın Bilgisi 2000

Osteogenesis imperfecta type I: molecular heterogeneity for COL1A1 null alleles of type I collagen.

Yazar: Willing, M. C., Deschenes, S. P., Scott, D. A., Byers, P. H., Slayton, R. L., Pitts, S. H., Arikat, H., Roberts, E. J.
Baskı/Yayın Bilgisi 1994

Genetic Association of MMP10, MMP14, and MMP16 with Dental Caries

Yazar: Lewis, D. D., Shaffer, J. R., Feingold, E., Cooper, M., Vanyukov, M. M., Maher, B. S., Slayton, R. L., Willing, M. C., Reis, S. E., McNeil, D. W., Crout, R. J., Weyant, R. J., Levy, S. M., Vieira, A. R., Marazita, M. L.
Yayımlandı Int J Dent (2017)

Genetic Association of MPPED2 and ACTN2 with Dental Caries

Yazar: Stanley, B.O.C., Feingold, E., Cooper, M., Vanyukov, M.M., Maher, B.S., Slayton, R.L., Willing, M.C., Reis, S.E., McNeil, D.W., Crout, R.J., Weyant, R.J., Levy, S.M., Vieira, A.R., Marazita, M.L., Shaffer, J.R.
Baskı/Yayın Bilgisi 2014

Genome-wide Association Scan for Childhood Caries Implicates Novel Genes

Yazar: Shaffer, J.R., Wang, X., Feingold, E., Lee, M., Begum, F., Weeks, D.E., Cuenco, K.T., Barmada, M.M., Wendell, S.K., Crosslin, D.R., Laurie, C.C., Doheny, K.F., Pugh, E.W., Zhang, Q., Feenstra, B., Geller, F., Boyd, H.A., Zhang, H., Melbye, M., Murray, J.C., Weyant, R.J., Crout, R., McNeil, D.W., Levy, S.M., Slayton, R.L., Willing, M.C., Broffitt, B., Vieira, A.R., Marazita, M.L.
Baskı/Yayın Bilgisi 2011