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Research 151–180 of 784
- Updated mutational spectrum and genotype-phenotype correlations in ichthyosis patients with ABCA12 pathogenic variants
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Chronic Ulceration of the Scalp Associated with Genetically Different Types of Congenital Ichthyosis: A Series of Four Cases
- 478 Mutation-specific siRNA Knockdown of GJB2 − Potential gene therapy for Keratitis-ichthyosis-deafness Syndrome
- Overexpression of Hoxc13 in differentiating keratinocytes results in downregulation of a novel hair keratin gene cluster and alopecia
- Noncalcemic actions of 1,25-dihydroxyvitamin D3 and clinical applications
- Cutaneous Syndromes Produced as Side Effects of Triparanol Therapy
- The keratins and their disorders
- Skin diseases in the alpaca (<i>Vicugna pacos</i>): a literature review and retrospective analysis of 68 cases (Cornell University 1997–2006)
- Hair Shaft Videodermoscopy in Netherton Syndrome
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Retinoids and Keratinization
- Chemotherapy of psoriasis and other skin disorders with oral retinoids
- Off-Label Uses of Topical Vitamin D in Dermatology: A Systematic Review
- Trichothiodystrophy with Dysmyelination and Central Osteosclerosis
- Sjogren-Larsson syndrome
- Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice
- Symmetrical acrokeratoderma: A peculiar entity in China? Clinicopathologic and immunopathologic study of 34 new cases
- Banding Pattern on Polarized Hair Microscopic Examination and Unilateral Polymicrogyria in a Patient With Steroid Sulfatase Deficiency
- The Fate of Epidermal Tight Junctions in the stratum corneum: Their Involvement in the Regulation of Desquamation and Phenotypic Expression of Certain Skin Conditions
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Common Dermatologic Disorders in Down Syndrome: Systematic Review
- Dermatological aspects of the S2k guidelines on Down syndrome in childhood and adolescence
- Sjogren-Larsson Syndrome
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Trichothiodystrophy Associated with Urologic Malformation and Primary Hypercalduria
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- Skin Manifestations of Hypothyroidism-A Clinical Study
- Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response