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Early intra-amniotic gene transfer using lentiviral vector improves skin blistering phenotype in a murine model of Herlitz junctional epidermolysis bullosa

Gene therapy, 2012-05, Vol.19 (5), p.561-569

2012

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Early intra-amniotic gene transfer using lentiviral vector improves skin blistering phenotype in a murine model of Herlitz junctional epidermolysis bullosa.(CORRIGENDUM)(Correction notice)

Gene therapy, 2012-11, Vol.19 (11), p.1122

2012

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Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy

Nature genetics, 1997-06, Vol.16 (2), p.184-187

1997

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Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

Nature genetics, 1996-08, Vol.13 (4), p.450-457

1996

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Smad3/AP-1 interactions control transcriptional responses to TGF-β in a promoter-specific manner

Oncogene, 2001-06, Vol.20 (26), p.3332-3340

2001

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Treponema denticola chymotrypsin-like proteinase may contribute to orodigestive carcinogenesis through immunomodulation

British journal of cancer, 2018-02, Vol.118 (3), p.428-434

2018

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Differential expression of the versican and decorin genes in photoaged and sun-protected skin. Comparison by immunohistochemical and northern analyses

Laboratory investigation, 1995-06, Vol.72 (6), p.662

1995

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Cell-cell and cell-matrix interactions in the skin

Laboratory investigation, 1993-08, Vol.69 (2), p.133

Uitto, J

1993

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Transforming growth factor-beta up-regulates elastin gene expression in human skin fibroblasts. Evidence for post-transcriptional modulation

Laboratory investigation, 1992-05, Vol.66 (5), p.580

1992

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Molecular Mechanisms of Cutaneous Aging: Connective Tissue Alterations in the Dermis

The Journal of investigative dermatology symposium proceedings, 1998-08, Vol.3 (1), p.41-44

1998

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Mutations in the 180-kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosa

Nature genetics, 1995-09, Vol.11 (1), p.83-86

1995

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Erratum: Early intra-amniotic gene transfer using lentiviral vector improves skin blistering phenotype in a murine model of Herlitz junctional epidermolysis bullosa

Gene therapy, 2012-11, Vol.19 (11), p.1122-1122

2012

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Cellular differentiation and expression of matrix genes in type 1 neurofibromatosis

Laboratory investigation, 1988-12, Vol.59 (6), p.760

1988

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Integrin β4 mutations associated with junctional epidermolysis bullosa with pyloric atresia

Nature genetics, 1995-06, Vol.10 (2), p.229-234

1995

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A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome

Nature genetics, 1996-05, Vol.13 (1), p.70-77

1996

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Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the γ2 subunit of nicein/kalinin (LAMININ-5)

Nature genetics, 1994-03, Vol.6 (3), p.299-304

1994

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Integrin beta 4 mutations associated with junctional epidermolysis bullosa with pyloric atresia

Nature genetics, 1995-06, Vol.10 (2), p.229-234

1995

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Epidermolysis bullosa with congenital pyloric atresia: Novel mutations in the β4 integrin gene (ITGB4) and genotype/phenotype correlations

Pediatric research, 2001-05, Vol.49 (5), p.618-626

2001

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Mutations in the γ2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosa

Nature genetics, 1994-03, Vol.6 (3), p.293-298

1994

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Mutations in the gamma 2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosa

Nature genetics, 1994-03, Vol.6 (3), p.293-298

1994

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Expression of laminin isoforms by peripheral nerve-derived connective tissue cells in culture. Comparison with epitope distribution in normal human nerve and neural tumors in vivo

Laboratory investigation, 1993-01, Vol.68 (1), p.100

1993

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Isolation and characterization of human elastin cDNAs, and age-associated variation in elastin gene expression in cultured skin fibroblasts

Laboratory investigation, 1988-03, Vol.58 (3), p.270

1988

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Epidermolysis bullosa with congenital pyloric atresia: novel mutations in the beta 4 integrin gene (ITGB4) and genotype/phenotype correlations

Pediatric research, 2001-05, Vol.49 (5), p.618-626

2001

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Cooperation between SMAD and NF-κB in growth factor regulated type VII collagen gene expression

Oncogene, 1999-03, Vol.18 (10), p.1837-1844

1999

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Type VI collagen. In situ hybridizations and immunohistochemistry reveal abundant mRNA and protein levels in human neurofibroma, schwannoma and normal peripheral nerve tissues

Laboratory investigation, 1990-04, Vol.62 (4), p.487

1990

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Early intra-amniotic gene transfer using lentiviral vector improves skin blistering phenotype in a murine model of Herlitz junctional epidermolysis bullosa

Early intra-amniotic gene transfer using lentiviral vector improves skin blistering phenotype in a murine model of Herlitz junctional epidermolysis bullosa.(CORRIGENDUM)(Correction notice)

Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy

Plectin deficiency results in muscular dystrophy with epidermolysis bullosa

Smad3/AP-1 interactions control transcriptional responses to TGF-β in a promoter-specific manner

Treponema denticola chymotrypsin-like proteinase may contribute to orodigestive carcinogenesis through immunomodulation

Differential expression of the versican and decorin genes in photoaged and sun-protected skin. Comparison by immunohistochemical and northern analyses

Cell-cell and cell-matrix interactions in the skin

Transforming growth factor-beta up-regulates elastin gene expression in human skin fibroblasts. Evidence for post-transcriptional modulation

Molecular Mechanisms of Cutaneous Aging: Connective Tissue Alterations in the Dermis

Mutations in the 180-kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosa

Erratum: Early intra-amniotic gene transfer using lentiviral vector improves skin blistering phenotype in a murine model of Herlitz junctional epidermolysis bullosa

Cellular differentiation and expression of matrix genes in type 1 neurofibromatosis

Integrin β4 mutations associated with junctional epidermolysis bullosa with pyloric atresia

A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome

Herlitz's junctional epidermolysis bullosa is linked to mutations in the gene (LAMC2) for the γ2 subunit of nicein/kalinin (LAMININ-5)

Integrin beta 4 mutations associated with junctional epidermolysis bullosa with pyloric atresia

Epidermolysis bullosa with congenital pyloric atresia: Novel mutations in the β4 integrin gene (ITGB4) and genotype/phenotype correlations

Mutations in the γ2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosa

Mutations in the gamma 2 chain gene (LAMC2) of kalinin/laminin 5 in the junctional forms of epidermolysis bullosa

Expression of laminin isoforms by peripheral nerve-derived connective tissue cells in culture. Comparison with epitope distribution in normal human nerve and neural tumors in vivo

Isolation and characterization of human elastin cDNAs, and age-associated variation in elastin gene expression in cultured skin fibroblasts

Epidermolysis bullosa with congenital pyloric atresia: novel mutations in the beta 4 integrin gene (ITGB4) and genotype/phenotype correlations

Cooperation between SMAD and NF-κB in growth factor regulated type VII collagen gene expression

Type VI collagen. In situ hybridizations and immunohistochemistry reveal abundant mRNA and protein levels in human neurofibroma, schwannoma and normal peripheral nerve tissues

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