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Research 121–150 of 1000+
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Hair loss in infancy and childhood
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- Teratogenic effect of isotretinoin in both fertile females and males (Review)
- Presentations of Cutaneous Disease in Various Skin Pigmentations: Keratosis Pilaris
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Collodion baby case series: the success of oral retinoic acid
- AN UPDATE OF HAIR SHAFT DISORDERS
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation
- Porokeratotic adnexal ostial nevus: a paradigm of cutaneous mosaicism
- Disorders of Keratinization
- Keratins and skin disease
- Efficient In Vitro Transfection of Human Keratinocytes with an Adenovirus-Enhanced Receptor-Mediated System
- Hair follicles modulate skin barrier function
- Keratin gene mutations in disorders of human skin and its appendages
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Acne Syndromes and Mosaicism
- Skin, Genetic Defects, and Aging
- Noncalcemic actions of 1,25-dihydroxyvitamin D3 and clinical applications
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- Netherton Syndrome – Responding to Oral Retinoids
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Trichothiodystrophy without associated neuroectodermal features in two siblings