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au.\*:("WICHE, Gerhard")

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Plectin regulates the organization of glial fibrillary acidic protein in alexander diseaseRUJIN TIAN; GREGOR, Martin; WICHE, Gerhard et al.The American journal of pathology. 2006, Vol 168, Num 3, pp 888-897, issn 0002-9440, 10 p.Article

Plectin Gene Defects Lead to Various Forms of Epidermolysis Bullosa SimplexREZNICZEK, Gunther A; WALKO, Gernot; WICHE, Gerhard et al.Dermatologic clinics. 2010, Vol 28, Num 1, issn 0733-8635, vii, 33-42 [11 p.]Article

Overlap of the gene encoding the novel poly(ADP-ribose) polymerase Parp10 with the plectin 1 gene and common use of exon sequencesLESNIEWICZ, Krzysztof; LÜSCHER-FIRZLAFF, Juliane; POREBA, Elzbieta et al.Genomics (San Diego, Calif.). 2005, Vol 86, Num 1, pp 38-46, issn 0888-7543, 9 p.Article

Plectin-isoform-specific rescue of hemidesmosomal defects in plectin (-/-) keratinocytesANDRÄ, Kerstin; KORNACKER, Iris; JÖRGL, Almut et al.Journal of investigative dermatology. 2003, Vol 120, Num 2, pp 189-197, issn 0022-202X, 9 p.Article

A compound heterozygous one amino-acid insertion/nonsense mutation in the plectin gene causes epidermolysis bullosa simplex with plectin deficiencyBAUER, Johann W; ROUAN, Fatima; WICHE, Gerhard et al.The American journal of pathology. 2001, Vol 158, Num 2, pp 617-625, issn 0002-9440Article

Plectin contributes to mechanical properties of living cellsNA, Sungsoo; CHOWDHURY, Farhan; TAY, Bernard et al.American journal of physiology. Cell physiology. 2009, Vol 65, Num 4, issn 0363-6143, C868-C877Article

5' Trans-Splicing Repair of the PLEC1 Gene. CommentaryHENGGE, Ulrich R; WALLY, Verena; KLAUSEGGER, Alfred et al.Journal of investigative dermatology. 2008, Vol 128, Num 3, issn 0022-202X, 499-500, 568-574 [9 p.]Article

A site-specific plectin mutation causes dominant epidermolysis bullosa simplex Ogna: Two identical de novo mutationsKOSS-HARNES, Dörte; HOYHEIM, Bjorn; ANTON-LAMPRECHT, Ingrun et al.Journal of investigative dermatology. 2002, Vol 118, Num 1, pp 87-93, issn 0022-202XArticle

Disorganization of the desmin cytoskeleton and mitochondrial dysfunction in plectin-related epidermolysis bullosa simplex with muscular dystrophySCHRÖDER, Rolf; KUNZ, Wolfram S; FÜRST, Dieter O et al.Journal of neuropathology and experimental neurology. 2002, Vol 61, Num 6, pp 520-530, issn 0022-3069Article

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