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Research 721–750 of 1000+
- Loss of Keratin K2 Expression Causes Aberrant Aggregation of K10, Hyperkeratosis, and Inflammation
- [Dermatophytic disease: exuberant hyperkeratosis with cutaneous horns].
- 738 Cryo-EM and molecular dynamics of TRPV3 channel in activated state reveal structural features implicated in severe itch and hyperkeratosis
- Unilateral nevoid hyperkeratosis of the nipple and areola in a Saudi female
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Systematized Epidermal Nevus with Epidermolytic Hyperkeratosis Improving with Topical Calcipotriol/Betametasone Dipropionate Combination Ointment
- Intracorneal vacuoles in skin diseases with parakeratotic hyperkeratosis in the dog: a retrospective light‐microscopy study of 111 cases (1973–2000)
- A Rare Case of Orthokeratotic Hyperkeratosis in a Kid Induced by Malassezial Dermatitis
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Role of cholesterol sulfate in epidermal structure and function: Lessons from X-linked ichthyosis
- Activation of Nrf2 in keratinocytes causes chloracne (MADISH)‐like skin disease in mice
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function
- A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Trichoscopy
- Ichthyosis with confetti: clinics, molecular genetics and management
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Zinc‐responsive dermatosis in goats suggestive of hereditary malabsorption: two field cases
- Cutaneous Ultrastructural Features of the Flaky Skin (<i>fsn</i>) Mouse Mutation
- Monilethrix treated with oral retinoids
- Topically Applied Tretinoin in the Treatment of Trichostasis Spinulosa
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Symmetrical acrokeratoderma: A peculiar entity in China? Clinicopathologic and immunopathologic study of 34 new cases
- Two familial cases of Olmsted-like syndrome with a G573V mutation of the<i>TRPV3</i>gene
- Biotinidase deficiency characterized by skin and hair findings
- Casts and pseudocasts
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Ichthyosis with confetti: a rare diagnosis and treatment plan