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Journal of Investigative Dermatology, ISSN 0022-202X, 08/2014, Volume 134, Issue 8, pp. 2076 - 2079
Nagashima-type palmoplantar keratosis (NPPK) is an autosomal recessive diffuse non-epidermolytic palmoplantar keratosis caused by mutations in , a member of... 
EPIDERMAL BARRIER FUNCTION | NETHERTON-SYNDROME | EXPRESSION | CAP1/PRSS8 | DERMATOLOGY | Female | Male | Serpins - genetics | Mutation | Keratoderma, Palmoplantar - genetics | Humans | Index Medicus
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2012, Volume 129, Issue 6, pp. 1538 - 1546.e6
Journal Article
Yakugaku Zasshi, ISSN 0031-6903, 2014, Volume 134, Issue 5, pp. 623 - 627
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2013, Volume 132, Issue 5, pp. 1111 - 1120.e4
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2014, Volume 134, Issue 4, pp. 856 - 864
Background The stratum corneum and tight junctions (TJs) form physical barriers in the epidermis. Dendrites of activated Langerhans cells (LCs) extend beyond... 
Allergy and Immunology | stratum corneum | Langerhans cell | atopic dermatitis | FcεRI | langerin | inflammatory dendritic epidermal cell | tight junction | FceRI | FC-EPSILON-RI | BARRIER FUNCTION | OF-FUNCTION MUTATIONS | IMMUNOLOGY | FUNCTION VARIANTS | HIGH-AFFINITY RECEPTOR | PATCH TEST | ALLERGY | REGULATORY T-CELLS | FILAGGRIN GENE | ANTIGEN-PRESENTING CELLS | SKIN | Mannose-Binding Lectins - metabolism | Dendritic Cells - immunology | Humans | Transcriptome | Lectins, C-Type - genetics | Antigens, CD - genetics | Antigens, CD - metabolism | Psoriasis - complications | Lectins, C-Type - metabolism | Antigen Presentation | Dermatitis, Atopic - immunology | Langerhans Cells - immunology | Organ Culture Techniques | Psoriasis - immunology | Tight Junctions - metabolism | Epidermis - pathology | Ichthyosis Vulgaris - complications | Microscopy, Electron, Scanning | Cells, Cultured | Receptors, IgE - genetics | Dermatitis, Atopic - complications | Tight Junctions - ultrastructure | Animals | Mannose-Binding Lectins - genetics | Receptors, IgE - metabolism | Ichthyosis Vulgaris - immunology | Mice | Tight Junctions - pathology | Cell Movement | Medical colleges | Skin | Toiletries industry | Child development | Atopic dermatitis | Skin care products | Antigens | Wound healing | Biopsy | Behavior | Mutation | Allergies | Methods | Asthma | Index Medicus | Abridged Index Medicus
Journal Article
The Journal of Dermatology, ISSN 0385-2407, 03/2016, Volume 43, Issue 3, pp. 264 - 274
Hereditary palmoplantar keratoderma (PPK) is a heterogeneous group of disorders characterized by hyperkeratosis of the palm and the sole skin. Hereditary PPK... 
transgrediens | punctate | diffuse | focal | striate
Journal Article
Pediatric Dermatology, ISSN 0736-8046, 05/2019, Volume 36, Issue 3, pp. 368 - 371
Woolly hair nevus is a rare syndrome that presents as woolly hair in restricted areas of the scalp and may be associated with pigmented macules or epidermal... 
PEDIATRICS | CANCER | COSTELLO-SYNDROME | DERMATOLOGY | Mole (Dermatology) | Genetic aspects | Hair | Case reports | Mutation | Scalp | Pigmentation | Nevus | Case Report | Case Reports
Journal Article
Journal of Experimental Medicine, ISSN 0022-1007, 12/2009, Volume 206, Issue 13, pp. 2937 - 2946
Journal Article
Journal Article
Nature Genetics, ISSN 1061-4036, 05/2009, Volume 41, Issue 5, pp. 602 - 608
Journal Article
The Journal of Dermatology, ISSN 0385-2407, 07/2017, Volume 44, Issue 7, pp. 841 - 843
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 3/2002, Volume 156, Issue 6, pp. 1099 - 1111
Journal Article
The Journal of Dermatology, ISSN 0385-2407, 06/2018, Volume 45, Issue 6, pp. 742 - 745
Dystrophic epidermolysis bullosa ( DEB ), pretibial, a rare subtype of epidermolysis bullosa ( EB ), is characterized by recurrent blisters and erosions... 
basement membrane | VII | collagen | genodermatosis | blistering disease | splice site mutation | type | type VII collagen | GLYCINE SUBSTITUTION | PHENOTYPE | PATIENT | FAMILY | DERMATOLOGY | Epidermolysis bullosa | Genetic aspects | Polymerase chain reaction | Nonsense mutation | Reverse transcription | Heredity | Mutation | Dystrophic epidermolysis bullosa | Index Medicus
Journal Article