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Research 931–960 of 1000+
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Sebaceous adenitis in Swedish dogs, a retrospective study of 104 cases
- Isolation and Characterization of a Putative Keratin-Associated Protein Gene Expressed in Embryonic Skin of Mice
- New developments in the molecular treatment of ichthyosis: review of the literature
- Alopecia Diffusa while Using Interleukin-17 Inhibitors against Psoriasis Vulgaris
- Nilotinib-Induced Keratosis Pilaris
- Skin Barrier Dysfunction in Acne Vulgaris: Pathogenesis and Therapeutic Approaches
- A phase 2a trial of brepocitinib for cicatricial alopecia
- Alopécie frontale fibrosante : à propos de trois cas pédiatriques
- Seborrheic keratosis
- Hidradenitis Suppurativa and Comorbid Disorder Biomarkers, Druggable Genes, New Drugs and Drug Repurposing—A Molecular Meta-Analysis
- Frontal Fibrosing Alopecia and Increased Scalp Sweating: Is Neurogenic Inflammation the Common Link
- Prevalence and pathology of mite infestation in street dogs at Dinajpur municipality area
- Vitamin A in Skin and Hair: An Update
- Beard involvement in a man with frontal fibrosing alopecia
- Severe Ulceronecrotic Dermatitis Associated with Mite Infestation in the Critically Endangered Amargosa Vole (<i>Microtus californicus scirpensis</i>)
- Re-investigating the Basement Membrane Zone of Psoriatic Epidermal Lesions: Is Laminin-511 a New Player in Psoriasis Pathogenesis?
- A retrospective analysis of efficacy and safety of intralesional triamcinolone injections in the treatment of frontal fibrosing alopecia either as monotherapy or as a concomitant therapy
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Expression of keratins K6 and K16 in regenerating mouse epidermis is less restricted by cell replication than the expression of K1 and K10.
- Anti-programmed cell death protein 1-induced lichenoid changes of the nail unit: Histopathologic description
- Frontal fibrosing alopecia and lichen planopilaris in HLA-identical mother and daughter
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Adenohypophysitis Associated with Sebaceous Gland Atrophy in a Dog
- Severe onycholysis in a card illusionist with alopecia areata universalis
- Hair follicles modulate skin barrier function
- Scabicidal Potential of Coconut Seed Extract in Rabbits via Downregulating Inflammatory/Immune Cross Talk: A Comprehensive Phytochemical/GC-MS and In Silico Proof
- Epidermal PPARγ Is a Key Homeostatic Regulator of Cutaneous Inflammation and Barrier Function in Mouse Skin