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American Journal of Human Genetics|February 1, 1994
Preferential sites in keratin 10 that are mutated in epidermolytic hyperkeratosisC C Chipev, J M Yang, J J DiGiovanna, et al.Cell|September 4, 1992
A leucine----proline mutation in the H1 subdomain of keratin 1 causes epidermolytic hyperkeratosisC C Chipev, B P Korge, N Markova, et al.The Journal of Biological Chemistry|October 7, 2000
Residues in the 1A rod domain segment and the linker L2 are required for stabilizing the A11 molecular alignment mode in keratin intermediate filamentsT Mehrani, K C Wu, M I Morasso, et al.Cell Death and Differentiation|October 8, 1999
Transglutaminase crosslinking and structural studies of the human small proline rich 3 proteinP M Steinert, E Candi, E Tarcsa, et al.The Journal of Investigative Dermatology|April 5, 2001
Evidence for novel functions of the keratin tail emerging from a mutation causing ichthyosis hystrixE Sprecher, A Ishida-Yamamoto, O M Becker, et al.The Journal of Biological Chemistry|July 10, 1984
Synthetic peptides corresponding to keratin subunits elicit highly specific antibodiesD R Roop, C K Cheng, L Titterington, et al.Nature Genetics|March 1, 1995
Mutations in the gene for transglutaminase 1 in autosomal recessive lamellar ichthyosisL J Russell, J J DiGiovanna, G R Rogers, et al.The Journal of Investigative Dermatology|January 1, 1994
Mutations in the H1 and 1A domains in the keratin 1 gene in epidermolytic hyperkeratosisJ M Yang, C C Chipev, J J DiGiovanna, et al.The Journal of Biological Chemistry|February 15, 1990
Structure of the human desmoplakins. Implications for function in the desmosomal plaqueK J Green, D A Parry, P M Steinert, et al.Ultramicroscopy|January 1, 1986
Odd men out: a quantitative objective procedure for identifying anomalous members of a set of noisy images of ostensibly identical specimensM Unser, A C Steven, B L TrusPageof 27