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Splice site mutation in COL7A1 resulting in aberrant in‐frame transcripts identified in a case of recessive dystrophic epidermolysis bullosa, pretibial

Journal of dermatology, 2018-06, Vol.45 (6), p.742-745

2018

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Bidimensional analysis of desmoglein 1 distribution on the outermost corneocytes provides the structural and functional information of the stratum corneum

Journal of dermatological science, 2010-03, Vol.57 (3), p.192-198

2010

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Actual consumption amount of personal care products reflecting Japanese cosmetic habits

The Journal of Toxicological Sciences, 2017/12/01, Vol.42(6), pp.797-814

2017

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Epidermal Basement Membrane: Its Molecular Organization and Blistering Disorders

Connective Tissue Research, 2006, Vol.47 (2), p.55-66

Masunaga, Takuji

2006

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Compound heterozygosity for novel splice site mutations of ITGA6 in lethal junctional epidermolysis bullosa with pyloric atresia

Journal of dermatology, 2017-02, Vol.44 (2), p.160-166

2017

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Japanese recurrent mutation c.6216 + 5G > T in COL7A1 leads to a mild phenotype of dystrophic epidermolysis bullosa

Journal of dermatological science, 2015-12, Vol.80 (3), p.220-223

2015

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Splicing abnormality of integrin β4 gene (ITGB4) due to nucleotide substitutions far from splice site underlies pyloric atresia-junctional epidermolysis bullosa syndrome

Journal of dermatological science, 2015-04, Vol.78 (1), p.61-66

2015

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Lack of skin carcinogenicity of topically applied titanium dioxide nanoparticles in the mouse

Food and chemical toxicology, 2011-04, Vol.49 (4), p.744-749

2011

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Japanese case of Herlitz junctional epidermolysis bullosa that initially showed a few blisters on the limited area

Journal of dermatology, 2014-04, Vol.41 (4), p.351-353

2014

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Nanomaterials in Cosmetics—Present Situation and Future

YAKUGAKU ZASSHI, 2014/01/01, Vol.134(1), pp.39-43

Masunaga, Takuji

2014

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New non-invasive method for evaluation of the stratum corneum structure in diseases with abnormal keratinization by immunofluorescence microscopy of desmoglein 1 distribution in tape-stripped samples

Journal of dermatology, 2010-10, Vol.37 (10), p.873-881

2010

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Genotype–phenotype correlations in six Japanese patients with recessive dystrophic epidermolysis bullosa with the recurrent p.Glu2857X mutation

Journal of dermatological science, 2008-10, Vol.52 (1), p.13-20

2008

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The G2028R glycine substitution mutation in COL7A1 leads to marked inter-familiar clinical heterogeneity in dominant dystrophic epidermolysis bullosa

Journal of dermatological science, 2004-05, Vol.34 (3), p.195-200

2004

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Genotoxic Stress Abrogates Renewal of Melanocyte Stem Cells by Triggering Their Differentiation

Cell, 2009-06, Vol.137 (6), p.1088-1099

2009

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Splice site mutation in COL 7A1 resulting in aberrant in‐frame transcripts identified in a case of recessive dystrophic epidermolysis bullosa, pretibial

Journal of dermatology, 2018-06, Vol.45 (6), p.742-745

2018

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The Extracellular Domain of BPAG2 Localizes to Anchoring Filaments and its Carboxyl Terminus Extends to the Lamina Densa of Normal Human Epidermal Basement Membrane

Journal of investigative dermatology, 1997-08, Vol.109 (2), p.200-206

1997

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Differences in recurrent COL7A1 mutations in dystrophic epidermolysis bullosa: ethnic-specific and worldwide recurrent mutations

Archives of Dermatological Research, 2004-03, Vol.295 (10), p.442-447

2004

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Safety Assessment of Nanomaterials in Cosmetics

Journal of the Japan Society of Colour Material, 2012/09/20, Vol.85(9), pp.384-388

MASUNAGA, Takuji

2012

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Safety Assessment of Nanomaterials in Cosmetics

Shikizai Kyōkai shi, 2012, Vol.85 (9), p.384-388

MASUNAGA, Takuji

2012

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The Extracellular Domain of BPAG2 has a Loop Structure in the Carboxy Terminal Flexible Tail In Vivo

Journal of investigative dermatology, 2000-11, Vol.115 (5), p.889-892

2000

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Equivalence evaluation of moisturizers in atopic dermatitis patients

Journal of cosmetic science, 2015-09, Vol.66 (5), p.295-303

2015

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Predicting in Vitro Skin Irritation: Use of the Reconstructed Human Epidermis Test Method (EpiDermTM SIT) in a 24-h Exposure Test for Skin Irritation

Alternatives to Animal Testing and Experimentation, 2018, Vol.23(1), pp.1-8

2018

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97-kDa Linear IgA Bullous Dermatosis (LAD) Antigen Localizes to the Lamina Lucida of the Epidermal Basement Membrane

Journal of investigative dermatology, 1996-04, Vol.106 (4), p.739-743

1996

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Desmoyokin/AHNAK Protein Localizes to the Non-Desmosomal Keratinocyte Cell Surface of Human Epidermis

Journal of investigative dermatology, 1995-06, Vol.104 (6), p.941-945

1995

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ナノマテリアルと化粧品の現状と将来

YAKUGAKU ZASSHI, 2014/01/01, Vol.134(1), pp.39-43

増永, 卓司

2014

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Splice site mutation in COL7A1 resulting in aberrant in‐frame transcripts identified in a case of recessive dystrophic epidermolysis bullosa, pretibial

Bidimensional analysis of desmoglein 1 distribution on the outermost corneocytes provides the structural and functional information of the stratum corneum

Actual consumption amount of personal care products reflecting Japanese cosmetic habits

Epidermal Basement Membrane: Its Molecular Organization and Blistering Disorders

Compound heterozygosity for novel splice site mutations of ITGA6 in lethal junctional epidermolysis bullosa with pyloric atresia

Japanese recurrent mutation c.6216 + 5G > T in COL7A1 leads to a mild phenotype of dystrophic epidermolysis bullosa

Splicing abnormality of integrin β4 gene (ITGB4) due to nucleotide substitutions far from splice site underlies pyloric atresia-junctional epidermolysis bullosa syndrome

Lack of skin carcinogenicity of topically applied titanium dioxide nanoparticles in the mouse

Japanese case of Herlitz junctional epidermolysis bullosa that initially showed a few blisters on the limited area

Nanomaterials in Cosmetics—Present Situation and Future

New non-invasive method for evaluation of the stratum corneum structure in diseases with abnormal keratinization by immunofluorescence microscopy of desmoglein 1 distribution in tape-stripped samples

Genotype–phenotype correlations in six Japanese patients with recessive dystrophic epidermolysis bullosa with the recurrent p.Glu2857X mutation

The G2028R glycine substitution mutation in COL7A1 leads to marked inter-familiar clinical heterogeneity in dominant dystrophic epidermolysis bullosa

Genotoxic Stress Abrogates Renewal of Melanocyte Stem Cells by Triggering Their Differentiation

Splice site mutation in COL 7A1 resulting in aberrant in‐frame transcripts identified in a case of recessive dystrophic epidermolysis bullosa, pretibial

The Extracellular Domain of BPAG2 Localizes to Anchoring Filaments and its Carboxyl Terminus Extends to the Lamina Densa of Normal Human Epidermal Basement Membrane

Differences in recurrent COL7A1 mutations in dystrophic epidermolysis bullosa: ethnic-specific and worldwide recurrent mutations

Safety Assessment of Nanomaterials in Cosmetics

Safety Assessment of Nanomaterials in Cosmetics

The Extracellular Domain of BPAG2 has a Loop Structure in the Carboxy Terminal Flexible Tail In Vivo

Equivalence evaluation of moisturizers in atopic dermatitis patients

Predicting in Vitro Skin Irritation: Use of the Reconstructed Human Epidermis Test Method (EpiDermTM SIT) in a 24-h Exposure Test for Skin Irritation

97-kDa Linear IgA Bullous Dermatosis (LAD) Antigen Localizes to the Lamina Lucida of the Epidermal Basement Membrane

Desmoyokin/AHNAK Protein Localizes to the Non-Desmosomal Keratinocyte Cell Surface of Human Epidermis

ナノマテリアルと化粧品の現状と将来

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