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Research 451–480 of 1000+
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Respective Treatment Modalities with the Use of Combined Ingredients to Address Acne Prone Skin
- Spiny Keratoderma
- Hair Casts and Cutaneous Spicules in Multiple Myeloma
- BRAF Inhibitor Dabrafenib in Patients with Metastatic <i>BRAF</i>-Mutant Thyroid Cancer
- Overexpression of insulin-like growth factor-1 induces hyperplasia, dermal abnormalities, and spontaneous tumor formation in transgenic mice
- Suprabasal Desmoglein 3 Expression in the Epidermis of Transgenic Mice Results in Hyperproliferation and Abnormal Differentiation
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Clinical Findings, Cutaneous Pathology, and Response to Therapy in 21 Patients With Keratosis Pilaris Atrophicans
- Cutaneous Syndromes Produced as Side Effects of Triparanol Therapy
- Hidradenitis suppurativa: a review of cause and treatment
- Divergent roles of HDAC1 and HDAC2 in the regulation of epidermal development and tumorigenesis
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation
- Severe follicular hyperplasia and spontaneous papilloma formation in transgenic mice expressing theneu oncogene under the control of the bovine keratin 5 promoter
- Zinc deficiency in sheep and goats: Three field cases
- Keratosis follicularis spinulosa decalvans: a family study of seven male cases and six female carriers.
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- Clinical, histopathological and immunological characteristics of exfoliative cutaneous lupus erythematosus in 25 German short‐haired pointers
- Cutaneous lupus erythematosus: clinico-pathologic correlation
- Gsdma3 is required for hair follicle differentiation in mice
- Severe form of keratitis–ichthyosis–deafness (KID) syndrome associated with septic complications
- Pathological and Biochemical Studies on Experimental Hypothyroidism in Growing Lambs
- Llama Dermatology
- Oestrogen receptor evaluation in Pomeranian dogs with hair cycle arrest (alopecia X) on melatonin supplementation
- Horizontal and vertical sections of scalp biopsy specimens from dermatomyositis patients with scalp involvement
- Cyclic Alopecia and Abnormal Epidermal Cornification in Zdhhc13 -Deficient Mice Reveal the Importance of Palmitoylation in Hair and Skin Differentiation