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Research 841–870 of 1000+
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- "Preparation and Physicochemical Characterization of Topical Niosomal Formulation of Minoxidil and Tretinoin"
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Immunofluorescent localization of collagen types I, III and IV, fibronectin, laminin, and basement membrane proteoglycan in developing mouse skin
- Induction of the hair growth phase in postnatal mice by localized transient expression of Sonic hedgehog
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth
- The Proteins of Hair and Other Hard α-Keratins
- Specific morphogenetic events in mouse external genitalia sex differentiation are responsive/dependent upon androgens and/or estrogens
- Madarosis: A marker of many Maladies
- Prevalence, comorbidities, and treatment patterns of Japanese patients with alopecia areata: A descriptive study using Japan medical data center claims database
- Minoxidil downregulates Interleukin-1 alpha gene expression in HaCaT cells
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Ossifying pilomatrixoma with marrow formation of the left cheek region – Case report with review of literature
- Alopecia areata
- Ancient lineages of the keratin-associated protein (KRTAP) genes and their co-option in the evolution of the hair follicle
- Alterations in Corneal Sensitivity, Staining and Biomechanics of Alopecia Areata Patients: Novel Findings in a Case-Control Study
- TONGUE, RED
- Development, Structure, and Keratin Expression in <i>C57BL/6J</i> Mouse Eccrine Glands
- The Study on Biological Function of Keratin 26, a Novel Member of Liaoning Cashmere Goat Keratin Gene Family
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- Skin Manifestations Associated with Autoimmune Liver Diseases: a Systematic Review
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Diphenylcyclopropenone-Induced Vitiligo in a Patient with Alopecia Universalis
- Dermatology Patient Support Groups
- Correlation Analysis of CXCL10, FOS, HOXC13, and WNT4 Gene Polymorphisms with Key Economic Traits—Initial Population Screening for Jiangnan Cashmere Goats