Production and characterization of a monoclonal antibody to human Type IV collagen.

Por Sakai, L. Y., Engvall, E., Hollister, D. W., Burgeson, R. E.
Publicado em 1982

Structural studies of human basement-membrane collagen with the use of a monoclonal antibody.

Por Dieringer, H, Hollister, D W, Glanville, R W, Sakai, L Y, Kühn, K
Publicado em 1985

A BamHI polymorphism at the fibrillin (FBN) locus

Por Clark, B.A., Maslen, C.L., Sakai, L.Y., Dhalimi, M.Al., Litt, R., Litt, M.
Publicado em 1991

Abnormal fibrillin metabolism in bovine Marfan syndrome.

Por Potter, K. A., Hoffman, Y., Sakai, L. Y., Byers, P. H., Besser, T. E., Milewicz, D. M.
Publicado em 1993

Isolation and partial characterization of a new human collagen with an extended triple-helical structural domain.

Por Bentz, H, Morris, N P, Murray, L W, Sakai, L Y, Hollister, D W, Burgeson, R E
Publicado em 1983

Type II achondrogenesis-hypochondrogenesis: morphologic and immunohistopathologic studies.

Por Godfrey, M, Keene, D R, Blank, E, Hori, H, Sakai, L Y, Sherwin, L A, Hollister, D W
Publicado em 1988

Two mutations in Marfan syndrome resulting in truncated fibrillin polypeptides.

Por Kainulainen, K, Sakai, L Y, Child, A, Pope, F M, Puhakka, L, Ryhänen, L, Palotie, A, Kaitila, I, Peltonen, L
Publicado em 1992

Marfan phenotype variability in a family segregating a missense mutation in the epidermal growth factor-like motif of the fibrillin gene.

Por Dietz, H C, Pyeritz, R E, Puffenberger, E G, Kendzior, R J, Corson, G M, Maslen, C L, Sakai, L Y, Francomano, C A, Cutting, G R
Publicado em 1992

Mutations in Fibrillin-1 Cause Congenital Scleroderma: Stiff Skin Syndrome

Por Loeys, B.L., Gerber, E.E., Riegert-Johnson, D., Iqbal, S., Whiteman, P., McConnell, V., Chillakuri, C.R., Macaya, D., Coucke, P.J., De Paepe, A., Judge, D.P., Wigley, F., Davis, E.C., Mardon, H.J., Handford, P., Keene, D.R., Sakai, L.Y., Dietz, H.C.
Publicado em 2010