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Molecular basis and inheritance patterns of amyloidosis cutis dyschromica

Clinical and experimental dermatology, 2020-07, Vol.45 (5), p.650-653

2020

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A novel mutation in the VDR gene in hereditary vitamin D-resistant rickets

British journal of dermatology (1951), 2008-01, Vol.158 (1), p.168-171

2008

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Transient bullous dermolysis of the newborn in three generations

British journal of dermatology (1951), 2005-11, Vol.153 (5), p.1058-1063

2005

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Unusual molecular findings in Kindler syndrome

British journal of dermatology (1951), 2007-12, Vol.157 (6), p.1252-1256

2007

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Transient bullous dermolysis of the newborn in three generations

British journal of dermatology (1951), 2005-11, Vol.153 (5), p.1058-1063

2005

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Molecular abnormalities of the desmosomal protein desmoplakin in human disease

Clinical and experimental dermatology, 2005-05, Vol.30 (3), p.261-266

2005

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Target proteins in inherited and acquired blistering skin disorders

Clinical and experimental dermatology, 2006-03, Vol.31 (2), p.252-259

2006

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Functional redundancy of extracellular matrix protein 1 in epidermal differentiation

British journal of dermatology (1951), 2007-10, Vol.157 (4), p.771-775

2007

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Complete paternal uniparental isodisomy of chromosome 1 resulting in Herlitz junctional epidermolysis bullosa

Clinical and experimental dermatology, 2005-01, Vol.30 (1), p.71-74

2005

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Heterozygous germline missense mutation in the p63 gene underlying EEC syndrome

Clinical and experimental dermatology, 2000, Vol.25 (5), p.441-443

2000

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Globalization of DNA-based prenatal diagnosis for recessive dystrophic epidermolysis bullosa

Clinical and experimental dermatology, 2007-11, Vol.32 (6), p.687-689

2007

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Altered expression of l-arginine metabolism pathway genes in chronic wounds in recessive dystrophic epidermolysis bullosa

Clinical and experimental dermatology, 2004-11, Vol.29 (6), p.664-668

2004

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Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63

Human molecular genetics, 2001-02, Vol.10 (3), p.221-229

2001

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Dermatological applications of DNA array technology

Clinical and experimental dermatology, 2002-09, Vol.27 (6), p.485-492

2002

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EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome: heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis

British journal of dermatology (1951), 2002-02, Vol.146 (2), p.216-220

2002

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Heterozygous germline missense mutation in the p63 gene underlying EEC syndrome

Clinical and experimental dermatology, 2000-07, Vol.25 (5), p.441-443

2000

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Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1)

Human molecular genetics, 2002-04, Vol.11 (7), p.833-840

2002

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Three cases of de novo dominant dystrophic epidermolysis bullosa associated with the mutation G2043R in COL7A1

Clinical and experimental dermatology, 2001-01, Vol.26 (1), p.97-99

2001

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Five New Homozygous Mutations in the KIND1 Gene in Kindler Syndrome

Journal of investigative dermatology, 2007-09, Vol.127 (9), p.2268-2270

2007

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association of skin diseases with human herpesvirus 8 infection in HIV carriers

Archives of virology, 1998-01, Vol.143 (10), p.1881-1892

1998

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Mutations in the p63 gene and genotype-phenotype correlation in ectodermal dysplasia syndromes

British journal of dermatology (1951), 2004-07, Vol.151, p.13

2004

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Complete paternal uniparental isodisomy of chromosome 1 resulting in Herlitz junctional epidermolysis bullosa

British journal of dermatology (1951), 2004-07, Vol.151, p.70

2004

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Clinical effect of dynorphin on heroin addicts

Journal of the Medical Association of Thailand, 1995-10, Vol.78 (10), p.509-516

1995

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Experimental dermatology times Review article: Molecular abnormalities of the desmosomal protein desmoplakin in human disease

Clinical and experimental dermatology, 2005-05, Vol.30 (3), p.261-266

2005

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Keratinocyte gene expression profile in recessive dystrophic epidermolysis bullosa wounds

Wessagowit, V

2004

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Molecular basis and inheritance patterns of amyloidosis cutis dyschromica

A novel mutation in the VDR gene in hereditary vitamin D-resistant rickets

Transient bullous dermolysis of the newborn in three generations

Unusual molecular findings in Kindler syndrome

Transient bullous dermolysis of the newborn in three generations

Molecular abnormalities of the desmosomal protein desmoplakin in human disease

Target proteins in inherited and acquired blistering skin disorders

Functional redundancy of extracellular matrix protein 1 in epidermal differentiation

Complete paternal uniparental isodisomy of chromosome 1 resulting in Herlitz junctional epidermolysis bullosa

Heterozygous germline missense mutation in the p63 gene underlying EEC syndrome

Globalization of DNA-based prenatal diagnosis for recessive dystrophic epidermolysis bullosa

Altered expression of l-arginine metabolism pathway genes in chronic wounds in recessive dystrophic epidermolysis bullosa

Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63

Dermatological applications of DNA array technology

EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome: heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis

Heterozygous germline missense mutation in the p63 gene underlying EEC syndrome

Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1)

Three cases of de novo dominant dystrophic epidermolysis bullosa associated with the mutation G2043R in COL7A1

Five New Homozygous Mutations in the KIND1 Gene in Kindler Syndrome

association of skin diseases with human herpesvirus 8 infection in HIV carriers

Mutations in the p63 gene and genotype-phenotype correlation in ectodermal dysplasia syndromes

Complete paternal uniparental isodisomy of chromosome 1 resulting in Herlitz junctional epidermolysis bullosa

Clinical effect of dynorphin on heroin addicts

Experimental dermatology times Review article: Molecular abnormalities of the desmosomal protein desmoplakin in human disease

Keratinocyte gene expression profile in recessive dystrophic epidermolysis bullosa wounds

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