6 results for author:"Fine J.-D." in Literature citations
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| A mouse model of generalized non-Herlitz junctional epidermolysis bullosa. Bubier J.A., Sproule T.J., Alley L.M., Webb C.M., Fine J.D., Roopenian D.C., Sundberg J.P. J. Invest. Dermatol. 130:1819-1828(2010) · Mapped (5) |
| Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome. Siegel D.H., Ashton G.H.S., Penagos H.G., Lee J.V., Feiler H.S., Wilhelmsen K.C., South A.P., Smith F.J.D., Prescott A.R., Wessagowit V. et al. Am. J. Hum. Genet. 73:174-187(2003) · UniProtKB (1) |
| EB simplex superficialis resulting from a mutation in the type VII collagen gene. Martinez-Mir A., Liu J., Gordon D., Weiner M.S., Ahmad W., Fine J.D., Ott J., Gilliam T.C., Christiano A.M. J. Invest. Dermatol. 118:547-549(2002) · UniProtKB (1) |
| The genetic basis of epidermolysis bullosa simplex with mottled pigmentation. Uttam J., Hutton M.E., Coulombe P.A., Anton-Lamprecht I., Yu Q.-C., Gedde-Dahl T. Jr., Fine J.-D., Fuchs E. Proc. Natl. Acad. Sci. U.S.A. 93:9079-9084(1996) · UniProtKB (1) |
| The genetic basis of Weber-Cockayne epidermolysis bullosa simplex. Chan Y.-M., Yu Q.-C., Fine J.-D., Fuchs E. Proc. Natl. Acad. Sci. U.S.A. 90:7414-7418(1993) · UniProtKB (1) |
| Epidermolysis bullosa simplex superficialis. A new variant of epidermolysis bullosa characterized by subcorneal skin cleavage mimicking peeling skin syndrome. Fine J.-D., Johnson L., Wright T. Arch. Dermatol. 125:633-638(1989) · UniProtKB (1) |