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Huber, M., Scaletta, C., Benathan, M., Frenk, E., Greenhalgh, D. A., Rothnagel, J. A., Roop, D. R. and Hohl, D. (1994) Abnormal keratin 1 and 10 cytoskeleton in cultured keratinocytes from epidermolytic hyperkeratosis caused by keratin 10 mutations. Journal of Investigative Dermatology, 102 5: 691-694. doi:10.1111/1523-1747.ep12374270 62   12 Cited 10 times in Scopus10 3
Rothnagel, J. A., Fisher, M. P., Axtell, S. M., Pittelkow, M. R., Antonlamprecht, I., Huber, M., Hohl, D. and Roop, D. R. (1993) A mutational hot spot in keratin 10 (KRT 10) in patients with epidermolytic hyperkeratosis. Human Molecular Genetics, 2 12: 2147-2150. doi:10.1093/hmg/2.12.2147 27   37 Cited 32 times in Scopus32 3
Huber, M. R., Steele, R. W. and Mushatt, D. M. (1999) An AIDS patient with aseptic meningitis. Infections in Medicine, 16 9: 558-+. 32   0 Cited 0 times in Scopus0
Arin, M. J., Longley, M. A., Kuster, W., Huber, M., Hohl, D., Rothnagel, J. A. and Roop, D. R. (1999) An aspatagine to threonine substitution in the 1A domain of keratin 1: A novel mutation that causes epidermolytic hyperkeratosis. Experimental Dermatology, 8 2: 124-127. doi:10.1111/j.1600-0625.1999.tb00359.x 46   11 0
Joh, G. Y., Traupe, H., Metze, D., Nashan, D., Huber, M., Hohl, D., Longley, M. A., Rothnagel, J. A. and Roop, D. R. (1997) A novel dinucleotide mutation in keratin 10 in the annular epidermolytic ichthyosis variant of bullous congenital ichthyosiform erythroderma. Journal of Investigative Dermatology, 108 3: 357-361. doi:10.1111/1523-1747.ep12286491 31   27 Cited 32 times in Scopus32 0
Arin, M. J., Longley, M. A., Anton-Lamprecht, I., Kurze, G., Huber, M., Hohl, D., Rothnagel, J. A. and Roop, D. R. (1999) A novel substitution in keratin 10 in epidermolytic hyperkeratosis. Journal of Investigative Dermatology, 112 4: 506-508. doi:10.1046/j.1523-1747.1999.00557.x 42   12 Cited 15 times in Scopus15 0
Rothnagel, J. A., Wojcik, S., Liefer, K. M., Dominey, A. M., Huber, M., Hohl, D. and Roop, D. R. (1995) Mutations in the 1A domain of keratin 9 in patients with epidermolytic palmoplantar keratoderma. Journal of Investigative Dermatology, 104 3: 430-433. doi:10.1111/1523-1747.ep12666018 20   48 Cited 54 times in Scopus54 0
Rothnagel, J. A., Traupe, H., Wojcik, S., Huber, M., Hohl, D., Pittelkow, M. R., Saeki, H., Ishibashi, Y. and Roop, D. R. (1994) Mutations in the Rod Domain of Keratin 2E in Patients with Ichthyosis Bullosa of Siemens. Nature Genetics, 7 4: 485-490. doi:10.1038/ng0894-485 33   108 Cited 103 times in Scopus103 3
Rothnagel, J. A., Dominey, A. M., Dempsey, L. D., Longley, M. A., Greenhalgh, D. A., Gagne, T. A., Huber, M., Frenk, E., Hohl, D. and Roop, D. R. (1992) Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosis. Science, 257 5073: 1128-1130. doi:10.1126/science.257.5073.1128 20   290 Cited 211 times in Scopus211 3