Zobrazeno 1 - 4
of 4
pro vyhledávání: '"133"'
Autor:
John E. Chimoskey, William J Flanagan
Publikováno v:
Journal of Investigative Dermatology. 63:362-368
133 Xe disappearance rates in dog skin were determined by injection of 100µc 133 Xe dissolved in 0.025ml physiologic saline solution into the skin with a 30-gauge needle and external detection of gamma radiation with a 2-inch sodium iodide crystal,
Autor:
Jan Maarten van Dijl, Goffe S. Elsinga, Herman Groen, Girbe Buist, Hendrik P. J. Bonarius, José C. Duipmans, Gerlinde N. Westerhout-Pluister, Hans Westra, Corinna Glasner, Magdalena M. van der Kooi-Pol, Corné P. de Vogel, Willem J. B. van Wamel, Hajo Grundmann, Marcel F. Jonkman, Yanka K. Veenstra-Kyuchukova
Publikováno v:
Journal of Investigative Dermatology, 133(3), 847-850. ELSEVIER SCIENCE INC
Journal of Investigative Dermatology, 133(3), 847-850. Nature Publishing Group
Journal of Investigative Dermatology, 133(3), 847-850. Nature Publishing Group
Abbreviations: EB, epidermolysis bullosa; ET, exfoliative toxin; HlgB, gamma-hemolysin B; IsaA, immunodominant antigen A; Isd, iron-responsive surface determinant; Luk, leukocidin; LytM, peptidoglycan hydrolase; MFI, median fluorescence intensity; ML
Autor:
Martin Hrabé de Angelis, Helmut Fuchs, Jenny Li-Ying Huang, Mugdha Deo, Catherine D. Van Raamsdonk
Publikováno v:
J. Invest. Dermatol. 133, 49-58 (2013)
Mutations in neurofibromin (NF1) cause the dominant genetic disorder neurofibromatosis type 1. Neurofibromatosis is characterized by Schwann cell-based tumors and skin hyperpigmentation, resulting from both haploinsufficiency and loss of heterozygosi
Autor:
Bertram F. Pontz, Leena Bruckner-Tuderman, Ulrich Kalinke, D. Ulrike Kalinke, Hauke Schumann, Mirjam Zimmermann, Nadja Hammami-Hauasli, Leena Pulkkinen, Jouni Uitto, Ingrun Anton-Lamprecht
Publikováno v:
Journal of Investigative Dermatology. 109:384-389
We describe a patient with severe generalized dystrophic epidermolysis bullosa (EBD) and a novel combination of compound heterozygous mutations in the COL7A1 gene. The maternal mutation was an A-to-G transition (425-A --> G) at position -2 of the don