向外
发表于 2025-3-30 08:22:52
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landmark
发表于 2025-3-30 15:57:47
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壕沟
发表于 2025-3-30 20:22:43
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费解
发表于 2025-3-30 21:59:33
Franziska Schmithüsen,Fernand Antondhesions, which serve as supramolecular signalling and actin-anchoring platforms. Together with talin, kindlins directly bind to integrin β subunit cytoplasmic tails and are responsible for integrin activation. Mutations in the kindlin-1 gene cause the Kindler syndrome, a rare genodermatosis charact
Irrepressible
发表于 2025-3-31 03:43:08
Franziska Schmithüsen,Dieter Ferringhe collagen VII gene (COL7A1). Dystrophic epidermolysis bullosa (DEB) is an inherited skin fragility disorder, and blistering occurs in the sub-lamina densa zone at the level of AF. DEB results from different mutations in the type VII collagen gene (.). The nature of mutations in . and their positio
Extort
发表于 2025-3-31 07:46:58
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Ingenuity
发表于 2025-3-31 10:54:26
Lernstile im interkulturellen Kontextalso with regard to genetic and environmental predisposing factors. A strong association with HLA alleles was found in pemphigus, mucous membrane pemphigoid, pemphigoid gestationis and epidermolysis bullosa acquisita, whereas in bullous pemphigoid, this association appeared much less prominent. Rece
breadth
发表于 2025-3-31 13:47:16
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Substitution
发表于 2025-3-31 18:23:54
Lernstile im interkulturellen Kontextppropriate clinical setting with routine histology consistent wtih an AIBD. Diagnostic modalities for epidermolysis bullosa (EB) include immunofluorescence antigenic mapping (IFM), transmission electron microscopy (TEM), and genetic mutational analysis. Of these, the most preferred is IFM. Because a