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Research 271–300 of 1000+
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- Characterization of Bsk mice: I. The Bsk mutation does not involve a recombination of cornea-specific keratin 12 and skin-specific hair keratin genes.
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Regulatory T cells in skin regeneration and wound healing
- Report on the 11th National Congress AICPE (Associazione Italiana di Chirurgia Plastica Estetica) Held in Rimini, Italy, 12–14 April 2024
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Screened of long non-coding RNA related to wool development and fineness in Gansu alpine fine-wool sheep
- Activation of Nrf2 in keratinocytes causes chloracne (MADISH)‐like skin disease in mice
- The keratin 19 promoter is potent for cell-specific targeting of genes in transgenic mice
- Comparative Anatomy of Mouse and Human Nail Units
- Natural Sources of Therapeutic Agents Used in Skin Conditions
- Chronic graft versus host disease and skin
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Biology, diagnosis and treatment of <i>Malassezia</i> dermatitis in dogs and cats
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- Single-cell transcriptomics reveals lineage trajectory of human scalp hair follicle and informs mechanisms of hair graying
- Self-consistent field theory for the interactions between keratin intermediate filaments
- Identification of the C-terminal tail domain of AHF/trichohyalin as the critical site for modulation of the keratin filamentous meshwork in the keratinocyte
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- Expression of fox-related genes in the skin follicles of Inner Mongolia cashmere goat
- Unlocking the therapeutic potential of TRPV3: Insights into thermosensation, channel modulation, and skin homeostasis involving TRPV3
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Hidradenitis suppurativa: A folliculotropic disease of innate immune barrier dysfunction?
- Recent advances in understanding of radiation-induced skin tissue reactions with respect to acute tissue injury and late adverse effect
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- A Look Inside—Histopathological Examinations of Different Tail Tip Lesions in Dairy Cows
- Keratin Promotes Differentiation of Keratinocytes Seeded on Collagen/Keratin Hydrogels