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2. Hemidesmosomal variants of epidermolysis bullosa. Mutations in the alpha6beta4 integrin and the 180-kD bullous pemphigoid antigen/type XVII collagen genes. Pulkkinen L; Uitto J Exp Dermatol; 1998; 7(2-3):46-64. PubMed ID: 9583744 [TBL] [Abstract][Full Text] [Related]
3. Molecular complexity of the cutaneous basement membrane zone. Revelations from the paradigms of epidermolysis bullosa. Christiano AM; Uitto J Exp Dermatol; 1996 Feb; 5(1):1-11. PubMed ID: 8624605 [TBL] [Abstract][Full Text] [Related]
4. Deletion of the cytoplasmatic domain of BP180/collagen XVII causes a phenotype with predominant features of epidermolysis bullosa simplex. Huber M; Floeth M; Borradori L; Schäcke H; Rugg EL; Lane EB; Frenk E; Hohl D; Bruckner-Tuderman L J Invest Dermatol; 2002 Jan; 118(1):185-92. PubMed ID: 11851893 [TBL] [Abstract][Full Text] [Related]
5. Persistent failures in gene repair. van der Steege G; Schuilenga-Hut PH; Buys CH; Scheffer H; Pas HH; Jonkman MF Nat Biotechnol; 2001 Apr; 19(4):305-6. PubMed ID: 11283576 [No Abstract] [Full Text] [Related]
11. Hemizygosity for a glycine substitution in collagen XVII: unfolding and degradation of the ectodomain. Tasanen K; Floeth M; Schumann H; Bruckner-Tuderman L J Invest Dermatol; 2000 Aug; 115(2):207-12. PubMed ID: 10951237 [TBL] [Abstract][Full Text] [Related]
13. Immunohistopathologic diagnosis of epidermolysis bullosa. Bergman R Am J Dermatopathol; 1999 Apr; 21(2):185-92. PubMed ID: 10218683 [TBL] [Abstract][Full Text] [Related]
14. Defining target antigens in linear IgA disease using skin from subjects with inherited epidermolysis bullosa as a substrate for indirect immunofluorescence microscopy. Harman KE; Bhogal BS; Eady RA; McGrath JA; Black MM Br J Dermatol; 1999 Sep; 141(3):475-80. PubMed ID: 10583051 [TBL] [Abstract][Full Text] [Related]
15. The molecular basis for inherited bullous diseases. Korge BP; Krieg T J Mol Med (Berl); 1996 Feb; 74(2):59-70. PubMed ID: 8820401 [TBL] [Abstract][Full Text] [Related]
16. Induced pluripotent stem cells from human revertant keratinocytes for the treatment of epidermolysis bullosa. Umegaki-Arao N; Pasmooij AM; Itoh M; Cerise JE; Guo Z; Levy B; Gostyński A; Rothman LR; Jonkman MF; Christiano AM Sci Transl Med; 2014 Nov; 6(264):264ra164. PubMed ID: 25429057 [TBL] [Abstract][Full Text] [Related]
17. Role of the bullous pemphigoid antigen 180 (BP180) in the assembly of hemidesmosomes and cell adhesion--reexpression of BP180 in generalized atrophic benign epidermolysis bullosa keratinocytes. Borradori L; Chavanas S; Schaapveld RQ; Gagnoux-Palacios L; Calafat J; Meneguzzi G; Sonnenberg A Exp Cell Res; 1998 Mar; 239(2):463-76. PubMed ID: 9521865 [TBL] [Abstract][Full Text] [Related]
18. Ultrastructural findings in epidermolysis bullosa. Smith LT Arch Dermatol; 1993 Dec; 129(12):1578-84. PubMed ID: 7504435 [TBL] [Abstract][Full Text] [Related]
19. Molecular consequences of deletion of the cytoplasmic domain of bullous pemphigoid 180 in a patient with predominant features of epidermolysis bullosa simplex. Fontao L; Tasanen K; Huber M; Hohl D; Koster J; Bruckner-Tuderman L; Sonnenberg A; Borradori L J Invest Dermatol; 2004 Jan; 122(1):65-72. PubMed ID: 14962091 [TBL] [Abstract][Full Text] [Related]
20. A very mild form of non-Herlitz junctional epidermolysis bullosa: BP180 rescue by outsplicing of mutated exon 30 coding for the COL15 domain. Pasmooij AM; van Zalen S; Nijenhuis AM; Kloosterhuis AJ; Zuiderveen J; Jonkman MF; Pas HH Exp Dermatol; 2004 Feb; 13(2):125-8. PubMed ID: 15009107 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]