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Molecular pathology of the cutaneous basement membrane zone

Matrix biology, 2006-11, Vol.25, p.S7-S7

Uitto, J.

2006

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Collagenase-3 (matrix metalloproteinase-13) expression is induced in oral mucosal epithelium during chronic inflammation

The American journal of pathology, 1998-06, Vol.152 (6), p.1489-1499

1998

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Compound Heterozygosity for a Recurrent 16.5-kb Alu-Mediated Deletion Mutation and Single-Base-Pair Substitutions in the ABCC6 Gene Results in Pseudoxanthoma Elasticum

American journal of human genetics, 2001-03, Vol.68 (3), p.642-652

2001

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Type 1 segmental manifestation of Hailey-Hailey disease

Journal of the American Academy of Dermatology, 2003-10, Vol.49 (4), p.712-714

2003

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The gene family of ABC transporters – novel mutations, new phenotypes

Trends in molecular medicine, 2005-08, Vol.11 (8), p.341-343

Uitto, Jouni

2005

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Binding interactions of the NC1 domain of collagen VII

Matrix biology, 2006-11, Vol.25, p.S82-S82

2006

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Connective tissue biochemistry of the aging dermis. Age-related alterations in collagen and elastin

Dermatologic clinics, 1986-07, Vol.4 (3), p.433-446

Uitto, J

1986

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Long-term sun exposure alters the collagen of the papillary dermis : Comparison of sun-protected and photoaged skin by Northern analysis, immunohistochemical staining, and confocal laser scanning microscopy

Journal of the American Academy of Dermatology, 1996-02, Vol.34 (2), p.209-218

1996

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Expression of epithelial adhesion proteins and integrins in chronic inflammation

The American journal of pathology, 1995-07, Vol.147 (1), p.193-206

1995

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Molecular organization of the cutaneous basement membrane zone

Clinics in dermatology, 2001-09, Vol.19 (5), p.551-562

2001

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Glycine substitutions in the triple-helical region of type VII collagen result in a spectrum of dystrophic epidermolysis bullosa phenotypes and patterns of inheritance

American journal of human genetics, 1996-04, Vol.58 (4), p.671-681

1996

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Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome

American journal of human genetics, 2002-05, Vol.70 (5), p.1341-1348

2002

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Epidermolysis bullosa simplex associated with muscular dystrophy: Phenotype-genotype correlations and review of the literature

Journal of the American Academy of Dermatology, 1999-12, Vol.41 (6), p.950-956

1999

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High-affinity binding of the NC1 domain of collagen VII to laminin 5 and collagen IV

Biochemical and biophysical research communications, 2006-05, Vol.343 (3), p.692-699

2006

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Progress in epidermolysis bullosa: from eponyms to molecular genetic classification

Clinics in dermatology, 2005, Vol.23 (1), p.33-40

2005

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Structural Organization of the Human Type VII Collagen Gene (COL7A1), Composed of More Exons Than Any Previously Characterized Gene

Genomics (San Diego, Calif.), 1994-05, Vol.21 (1), p.169-179

1994

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Mutation analysis and molecular genetics of epidermolysis bullosa

Matrix biology, 1999-02, Vol.18 (1), p.29-42

1999

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A Deleterious Mutation in SAMD9 Causes Normophosphatemic Familial Tumoral Calcinosis

American journal of human genetics, 2006-10, Vol.79 (4), p.759-764

2006

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Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentition

The American journal of pathology, 1996-06, Vol.148 (6), p.1787-1796

1996

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Matrix Metalloproteinase 2 (Gelatinase A) Is Related to Migration of Keratinocytes

Experimental cell research, 1999-08, Vol.251 (1), p.67-78

1999

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Naegeli-Franceschetti-Jadassohn Syndrome and Dermatopathia Pigmentosa Reticularis: Two Allelic Ectodermal Dysplasias Caused by Dominant Mutations in KRT14

American journal of human genetics, 2006-10, Vol.79 (4), p.724-730

2006

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Achieving global environmental benefits through local development of clean energy? The case of small hilly hydel in India

Energy policy, 2006-12, Vol.34 (18), p.4069-4080

2006

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Premature Termination Codons in the Type VII Collagen Gene (COL7A1) Underlie Severe, Mutilating Recessive Dystrophic Epidermolysis Bullosa

Genomics (San Diego, Calif.), 1994-05, Vol.21 (1), p.160-168

1994

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Molecular pathology of the cutaneous basement membrane zone

Collagenase-3 (matrix metalloproteinase-13) expression is induced in oral mucosal epithelium during chronic inflammation

Compound Heterozygosity for a Recurrent 16.5-kb Alu-Mediated Deletion Mutation and Single-Base-Pair Substitutions in the ABCC6 Gene Results in Pseudoxanthoma Elasticum

Type 1 segmental manifestation of Hailey-Hailey disease

The gene family of ABC transporters – novel mutations, new phenotypes

Binding interactions of the NC1 domain of collagen VII

Connective tissue biochemistry of the aging dermis. Age-related alterations in collagen and elastin

Long-term sun exposure alters the collagen of the papillary dermis : Comparison of sun-protected and photoaged skin by Northern analysis, immunohistochemical staining, and confocal laser scanning microscopy

Expression of epithelial adhesion proteins and integrins in chronic inflammation

Molecular organization of the cutaneous basement membrane zone

Glycine substitutions in the triple-helical region of type VII collagen result in a spectrum of dystrophic epidermolysis bullosa phenotypes and patterns of inheritance

Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome

Epidermolysis bullosa simplex associated with muscular dystrophy: Phenotype-genotype correlations and review of the literature

High-affinity binding of the NC1 domain of collagen VII to laminin 5 and collagen IV

Progress in epidermolysis bullosa: from eponyms to molecular genetic classification

Structural Organization of the Human Type VII Collagen Gene (COL7A1), Composed of More Exons Than Any Previously Characterized Gene

Mutation analysis and molecular genetics of epidermolysis bullosa

A Deleterious Mutation in SAMD9 Causes Normophosphatemic Familial Tumoral Calcinosis

Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentition

Matrix Metalloproteinase 2 (Gelatinase A) Is Related to Migration of Keratinocytes

Naegeli-Franceschetti-Jadassohn Syndrome and Dermatopathia Pigmentosa Reticularis: Two Allelic Ectodermal Dysplasias Caused by Dominant Mutations in KRT14

Achieving global environmental benefits through local development of clean energy? The case of small hilly hydel in India

Desmoglein 4 in Hair Follicle Differentiation and Epidermal Adhesion: Evidence from Inherited Hypotrichosis and Acquired Pemphigus Vulgaris

A simplified laminin nomenclature

Premature Termination Codons in the Type VII Collagen Gene (COL7A1) Underlie Severe, Mutilating Recessive Dystrophic Epidermolysis Bullosa

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