Recent advances in the molecular basis of inherited skin diseases

[21] Corrective transduction of human epidermal stem cells in laminin-5-dependent junctional epidermolysis bullosa [J]. HUMAN GENE THERAPY, 1998, 9 (09) : 1359 - 1370

[22] Sustainable cutaneous gene delivery [J]. NATURE BIOTECHNOLOGY, 1997, 15 (13) : 1388 - 1391

[23] deViragh PA, 1997, J INVEST DERMATOL, V108, P103

[24] CLINICAL HETEROGENEITY IN EPIDERMOLYTIC HYPERKERATOSIS [J]. ARCHIVES OF DERMATOLOGY, 1994, 130 (08) : 1026 - 1035

[25] Clinicopathological correlations of compound heterozygous COL7A1 mutations recessive dystrophic epidermolysis bullosa [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1996, 107 (02) : 171 - 177

[26] EADY RA, 1999, FETAL MED, P545

[27] Revised classification system for inherited epidermolysis bullosa: Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa [J]. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2000, 42 (06) : 1051 - 1066

[28] Mapping of Papillon-Lefevre syndrome to the chromosome 11q14 region [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 1997, 5 (03) : 156 - 160

[29] TRANSGENIC MICE EXPRESSING A MUTANT KERATIN-10 GENE REVEAL THE LIKELY GENETIC-BASIS FOR EPIDERMOLYTIC HYPERKERATOSIS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (15) : 6906 - 6910

[30] Functional re-expression of laminin-5 in laminin-gamma 2-deficient human keratinocytes modifies cell morphology, motility, and adhesion [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (31) : 18437 - 18444

[21] Corrective transduction of human epidermal stem cells in laminin-5-dependent junctional epidermolysis bullosa [J]. HUMAN GENE THERAPY, 1998, 9 (09) : 1359 - 1370

[22] Sustainable cutaneous gene delivery [J]. NATURE BIOTECHNOLOGY, 1997, 15 (13) : 1388 - 1391

[23] deViragh PA, 1997, J INVEST DERMATOL, V108, P103

[24] CLINICAL HETEROGENEITY IN EPIDERMOLYTIC HYPERKERATOSIS [J]. ARCHIVES OF DERMATOLOGY, 1994, 130 (08) : 1026 - 1035

[25] Clinicopathological correlations of compound heterozygous COL7A1 mutations recessive dystrophic epidermolysis bullosa [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1996, 107 (02) : 171 - 177

[26] EADY RA, 1999, FETAL MED, P545

[27] Revised classification system for inherited epidermolysis bullosa: Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa [J]. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2000, 42 (06) : 1051 - 1066

[28] Mapping of Papillon-Lefevre syndrome to the chromosome 11q14 region [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 1997, 5 (03) : 156 - 160

[29] TRANSGENIC MICE EXPRESSING A MUTANT KERATIN-10 GENE REVEAL THE LIKELY GENETIC-BASIS FOR EPIDERMOLYTIC HYPERKERATOSIS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (15) : 6906 - 6910

[30] Functional re-expression of laminin-5 in laminin-gamma 2-deficient human keratinocytes modifies cell morphology, motility, and adhesion [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (31) : 18437 - 18444