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Results: 1-25 | 26-43
Results: 1-25/43
THE USE OF SKIN SUBSTRATES DEFICIENT IN BASEMENT-MEMBRANE MOLECULES FOR THE DIAGNOSIS OF SUBEPIDERMAL AUTOIMMUNE BULLOUS DISEASE
Authors: VODEGEL RM KISS M DEJONG MCJM PAS HH ALTMAYER A MOLNAR K HUSZ S VANDERMEER JB JONKMAN MF
Citation: Rm. Vodegel et al., THE USE OF SKIN SUBSTRATES DEFICIENT IN BASEMENT-MEMBRANE MOLECULES FOR THE DIAGNOSIS OF SUBEPIDERMAL AUTOIMMUNE BULLOUS DISEASE, EJD. European journal of dermatology, 8(2), 1998, pp. 83-85
A MUTATION IN HUMAN KERATIN K6B PRODUCES A PHENOCOPY OF THE K17 DISORDER PACHYONYCHIA-CONGENITA TYPE-2
Authors: SMITH FJD JONKMAN MF VANGOOR H COLEMAN CM COVELLO SP UITTO J MCLEAN WHI
Citation: Fjd. Smith et al., A MUTATION IN HUMAN KERATIN K6B PRODUCES A PHENOCOPY OF THE K17 DISORDER PACHYONYCHIA-CONGENITA TYPE-2, Human molecular genetics (Print), 7(7), 1998, pp. 1143-1148
LAMB3 MUTATIONS IN GENERALIZED ATROPHIC BENIGN EPIDERMOLYSIS-BULLOSA - CONSEQUENCES AT THE MESSENGER-RNA AND PROTEIN-LEVELS
Authors: PULKKINEN L JONKMAN MF MCGRATH JA KUIJPERS A PALLER AS UITTO J
Citation: L. Pulkkinen et al., LAMB3 MUTATIONS IN GENERALIZED ATROPHIC BENIGN EPIDERMOLYSIS-BULLOSA - CONSEQUENCES AT THE MESSENGER-RNA AND PROTEIN-LEVELS, Matrix biology, 17(2), 1998, pp. 163-163
LAMBS MUTATIONS IN GENERALIZED ATROPHIC BENIGN EPIDERMOLYSIS-BULLOSA - CONSEQUENCES AT THE MESSENGER-RNA AND PROTEIN-LEVELS
Authors: PULKKINEN L JONKMAN MF MCGRATH JA KUIJPERS A PALLER AS UITTO J
Citation: L. Pulkkinen et al., LAMBS MUTATIONS IN GENERALIZED ATROPHIC BENIGN EPIDERMOLYSIS-BULLOSA - CONSEQUENCES AT THE MESSENGER-RNA AND PROTEIN-LEVELS, Laboratory investigation, 78(7), 1998, pp. 859-867
A NEW GENE FOR PACHYONYCHIA-CONGENITA TYPE-2 - KERATIN K6B IS THE EXPRESSION PARTNER OF K17 IN EPIDERMAL APPENDAGES
Authors: MCLEAN WHI SMITH FJD VANGOOR H COVELLO SP COLEMAN CS UITTO J JONKMAN MF
Citation: Whi. Mclean et al., A NEW GENE FOR PACHYONYCHIA-CONGENITA TYPE-2 - KERATIN K6B IS THE EXPRESSION PARTNER OF K17 IN EPIDERMAL APPENDAGES, Journal of investigative dermatology, 110(4), 1998, pp. 502-502
TEMPERATURE-DEPENDENT DISSOCIATION OF TRIMERIC BP180 AND LAD-1 TO THEIR MONOMERS
Authors: PAS HH KLOOSTERHUIS GJ NIJENHUIS M DEJONG MCJM VANDERMEER JB JONKMAN MF
Citation: Hh. Pas et al., TEMPERATURE-DEPENDENT DISSOCIATION OF TRIMERIC BP180 AND LAD-1 TO THEIR MONOMERS, Journal of investigative dermatology, 110(4), 1998, pp. 507-507
NOVEL AND RECURRENT GLYCINE SUBSTITUTION MUTATIONS IN COL7A1 IN DYSTROPHIC EPIDERMOLYSIS-BULLOSA - GENOTYPE PHENOTYPE CORRELATIONS/
Authors: ROUAN F PULKKINEN L JONKMAN MF UITTO J
Citation: F. Rouan et al., NOVEL AND RECURRENT GLYCINE SUBSTITUTION MUTATIONS IN COL7A1 IN DYSTROPHIC EPIDERMOLYSIS-BULLOSA - GENOTYPE PHENOTYPE CORRELATIONS/, Journal of investigative dermatology, 110(4), 1998, pp. 508-508
UNUSUAL DOMINANT DYSTROPHIC EPIDERMOLYSIS-BULLOSA PHENOTYPE CAUSED BYA NOVEL GLYCINE SUBSTITUTION MUTATION IN THE TYPE-VII COLLAGEN GENE (COL7A1)
Authors: JONKMAN MF MORENO G ORANJE AP PULKKINEN L UITTO J
Citation: Mf. Jonkman et al., UNUSUAL DOMINANT DYSTROPHIC EPIDERMOLYSIS-BULLOSA PHENOTYPE CAUSED BYA NOVEL GLYCINE SUBSTITUTION MUTATION IN THE TYPE-VII COLLAGEN GENE (COL7A1), Journal of investigative dermatology, 110(4), 1998, pp. 511-511
THE USE OF SKIN SUBSTRATES DEFICIENT IN BASEMENT-MEMBRANE (BM) MOLECULES FOR THE DIAGNOSIS OF SUBEPIDERMAL AUTOIMMUNE BULLOUS DISEASES
Authors: VODEGEL RM KISS M DEJONG MCJM PAS HH ALTMAYER A MOLNAR K HUSZ S VANDERMEER JB YANCEY KB JONKMAN MF
Citation: Rm. Vodegel et al., THE USE OF SKIN SUBSTRATES DEFICIENT IN BASEMENT-MEMBRANE (BM) MOLECULES FOR THE DIAGNOSIS OF SUBEPIDERMAL AUTOIMMUNE BULLOUS DISEASES, Journal of investigative dermatology, 110(4), 1998, pp. 514-514
CHIMERIC RNA-DNA OLIGONUCLEOTIDE MEDIATED GENE CORRECTION OF A COLI7A1 MUTATION IN KERATINOCYTES OF A GABEB PATIENT
Authors: VANDERSTEEGE G NIJENHUIS M HEERES K PAS HH BUYS CHCM SCHEFFER H JONKMAN MF
Citation: G. Vandersteege et al., CHIMERIC RNA-DNA OLIGONUCLEOTIDE MEDIATED GENE CORRECTION OF A COLI7A1 MUTATION IN KERATINOCYTES OF A GABEB PATIENT, Journal of investigative dermatology, 110(4), 1998, pp. 617-617
KERATIN-17 MUTATIONS CAUSE EITHER STEATOCYSTOMA MULTIPLEX OR PACHYONYCHIA-CONGENITA TYPE-2
Authors: COVELLO SP SMITH FJD SMITT JHS PALLER AS MUNRO CS JONKMAN MF UITTO J MCLEAN WHI
Citation: Sp. Covello et al., KERATIN-17 MUTATIONS CAUSE EITHER STEATOCYSTOMA MULTIPLEX OR PACHYONYCHIA-CONGENITA TYPE-2, British journal of dermatology, 139(3), 1998, pp. 475-480
MOSAIC EXPRESSION OF UNCEIN, LINEAR IGA BULLOUS DERMATOSIS ANTIGEN AND 180-KDA BULLOUS PEMPHIGOID ANTIGEN IN GENERALIZED ATROPHIC BENIGN EPIDERMOLYSIS-BULLOSA
Authors: JONKMAN MF PAS HH FINE JD
Citation: Mf. Jonkman et al., MOSAIC EXPRESSION OF UNCEIN, LINEAR IGA BULLOUS DERMATOSIS ANTIGEN AND 180-KDA BULLOUS PEMPHIGOID ANTIGEN IN GENERALIZED ATROPHIC BENIGN EPIDERMOLYSIS-BULLOSA, British journal of dermatology, 138(5), 1998, pp. 904-904
EOSINOPHILIC CELLULITIS (WELLS-SYNDROME) - TREATMENT WITH MINOCYCLINE
Authors: STAMWESTERVELD EB DAENEN S VANDERMEER JB JONKMAN MF
Citation: Eb. Stamwesterveld et al., EOSINOPHILIC CELLULITIS (WELLS-SYNDROME) - TREATMENT WITH MINOCYCLINE, Acta dermato-venereologica, 78(2), 1998, pp. 157-157
IMPLICATIONS OF INTRAGENIC MARKER HOMOZYGOSITY AND HAPLOTYPE SHARING IN A RARE AUTOSOMAL RECESSIVE DISORDER - THE EXAMPLE OF THE COLLAGEN TYPE-XVII (COL17A1) LOCUS IN GENERALIZED ATROPHIC BENIGN EPIDERMOLYSIS-BULLOSA
Authors: SCHEFFER H STULP RP VERLIND E VANDERMEULEN M BRUCKNERTUDERMAN L GEDDEDAHL T TEMEERMAN GJ SONNENBERG A BUYS CHCM JONKMAN MF
Citation: H. Scheffer et al., IMPLICATIONS OF INTRAGENIC MARKER HOMOZYGOSITY AND HAPLOTYPE SHARING IN A RARE AUTOSOMAL RECESSIVE DISORDER - THE EXAMPLE OF THE COLLAGEN TYPE-XVII (COL17A1) LOCUS IN GENERALIZED ATROPHIC BENIGN EPIDERMOLYSIS-BULLOSA, Human genetics, 100(2), 1997, pp. 230-235
TOPICAL TETRACYCLINE IN CICATRICIAL PEMPHIGOID
Authors: VANDERWAL VB JONKMAN MF
Citation: Vb. Vanderwal et Mf. Jonkman, TOPICAL TETRACYCLINE IN CICATRICIAL PEMPHIGOID, Journal of the American Academy of Dermatology, 36(3), 1997, pp. 492-493
REVERTANT MOSAICISM IN EPIDERMOLYSIS-BULLOSA CAUSED BY MITOTIC GENE CONVERSION
Authors: JONKMAN MF SCHEFFER H STULP R PAS HH NIJENHUIS M HEERES K OWARIBE K PULKKINEN L UITTO J
Citation: Mf. Jonkman et al., REVERTANT MOSAICISM IN EPIDERMOLYSIS-BULLOSA CAUSED BY MITOTIC GENE CONVERSION, Cell, 88(4), 1997, pp. 543-551
LAD-1 IS ABSENT IN A SUBSET OF JUNCTIONAL EPIDERMOLYSIS-BULLOSA PATIENTS
Authors: MARINKOVICH MP TRAN HH RAO SK GIUDICE GJ BALDING S JONKMAN MF PAS HH MCGUIRE JS HERRON GS BRUCKNERTUDERMAN L
Citation: Mp. Marinkovich et al., LAD-1 IS ABSENT IN A SUBSET OF JUNCTIONAL EPIDERMOLYSIS-BULLOSA PATIENTS, Journal of investigative dermatology, 109(3), 1997, pp. 356-359
TEMPERATURE-DEPENDENT DISSOCIATION OF THE BP180 HOMOTRIMER TO THE MONOMER
Authors: PAS HH KLOOSTERHUIS GJ NIJENHUIS M DEJONG MCJM VANDERMEER JB JONKMAN MF
Citation: Hh. Pas et al., TEMPERATURE-DEPENDENT DISSOCIATION OF THE BP180 HOMOTRIMER TO THE MONOMER, Journal of investigative dermatology, 109(3), 1997, pp. 419-419
IMPLICATIONS OF INTRAGENIC MARKER HOMOZYGOSITY AND HAPLOTYPE SHARING IN GENERALIZED ATROPHIC BENIGN EPIDERMOLYSIS-BULLOSA (GABEB)
Authors: SCHEFFER H STULP RP VERLIND E BRUCKNERTUDERMAN L GEDDEDAHL T TEMEERMAH GJ SONNENBERG A BUYS CHCM JONKMAN MF
Citation: H. Scheffer et al., IMPLICATIONS OF INTRAGENIC MARKER HOMOZYGOSITY AND HAPLOTYPE SHARING IN GENERALIZED ATROPHIC BENIGN EPIDERMOLYSIS-BULLOSA (GABEB), Journal of investigative dermatology, 109(3), 1997, pp. 419-419
BULLOUS PEMPHIGOID AND LINEAR IGA DERMATOSIS SERA RECOGNIZE A SIMILAR120-KDA KERATINOCYTE COLLAGENOUS GLYCOPROTEIN WITH ANTIGENIC CROSS-REACTIVITY TO BP180
Authors: PAS HH KLOOSTERHUIS GJ HEERES K VANDERMEER JB JONKMAN MF
Citation: Hh. Pas et al., BULLOUS PEMPHIGOID AND LINEAR IGA DERMATOSIS SERA RECOGNIZE A SIMILAR120-KDA KERATINOCYTE COLLAGENOUS GLYCOPROTEIN WITH ANTIGENIC CROSS-REACTIVITY TO BP180, Journal of investigative dermatology, 108(4), 1997, pp. 423-429
ANALYSIS OF THE CLINICAL AND CELLULAR PHENOTYPE RESULTING FROM ABLATION OF KERATIN-14 IN RECESSIVE EPIDERMOLYSIS-BULLOSA SIMPLEX
Authors: JONKMAN MF SMITH FJD MCLEAN WHI SCHEFFER H
Citation: Mf. Jonkman et al., ANALYSIS OF THE CLINICAL AND CELLULAR PHENOTYPE RESULTING FROM ABLATION OF KERATIN-14 IN RECESSIVE EPIDERMOLYSIS-BULLOSA SIMPLEX, Journal of investigative dermatology, 107(5), 1996, pp. 3-3
EFFECTS OF KERATIN-14 ABLATION ON THE CLINICAL AND CELLULAR PHENOTYPEIN A KINDRED WITH RECESSIVE EPIDERMOLYSIS-BULLOSA SIMPLEX
Authors: JONKMAN MF HEERES K PAS HH VANLUYN MJ ELEMA JD CORDEN LD SMITH FJD MCLEAN WHI RAMAEKERS FCS BURTON M SCHEFFER H
Citation: Mf. Jonkman et al., EFFECTS OF KERATIN-14 ABLATION ON THE CLINICAL AND CELLULAR PHENOTYPEIN A KINDRED WITH RECESSIVE EPIDERMOLYSIS-BULLOSA SIMPLEX, Journal of investigative dermatology, 107(5), 1996, pp. 764-769
HUMAN SOMATIC GENE CONVERSION ACTING AS REVERSE MUTATION IN A PATIENTWITH NONLETHAL JUNCTIONAL EB
Authors: JONKMAN MF NIJENHUIS M HEERES K PAS HH STULP R PULKKINEN L SCHEFFER H UITTO J
Citation: Mf. Jonkman et al., HUMAN SOMATIC GENE CONVERSION ACTING AS REVERSE MUTATION IN A PATIENTWITH NONLETHAL JUNCTIONAL EB, Journal of investigative dermatology, 107(3), 1996, pp. 192-192
SPLICE-SITE MUTATION IN THE GENE FOR KERATIN-14 IN AUTOSOMAL RECESSIVE EPIDERMOLYSIS-BULLOSA SIMPLEX WITH K14 KNOCKOUT
Authors: JONKMAN MF HEERES K PAS HH BURTON M SCHEFFER H
Citation: Mf. Jonkman et al., SPLICE-SITE MUTATION IN THE GENE FOR KERATIN-14 IN AUTOSOMAL RECESSIVE EPIDERMOLYSIS-BULLOSA SIMPLEX WITH K14 KNOCKOUT, Journal of investigative dermatology, 106(4), 1996, pp. 250-250
BULLOUS PEMPHIGOID AND LINEAR IGA DERMATOSIS SERA RECOGNIZE A SIMILAR120 KD KERATINOCYTE ANTIGEN WITH HOMOLOGY TO BP180
Authors: PAS HH KLOOSTERHUIS GJ HEERES K VANDERMEER JB JONKMAN MF
Citation: Hh. Pas et al., BULLOUS PEMPHIGOID AND LINEAR IGA DERMATOSIS SERA RECOGNIZE A SIMILAR120 KD KERATINOCYTE ANTIGEN WITH HOMOLOGY TO BP180, Journal of investigative dermatology, 106(4), 1996, pp. 278-278
Risultati: 1-25 | 26-43