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Research 451–480 of 1000+
- The Important Role of Leptin in Modulating the Risk of Dermatological Diseases
- Pathological sequelae of long-haul COVID
- The scope of the dermoscope
- Application of Topical Immunotherapy in the Treatment of Alopecia Areata: A Review and Update
- Current recommendations for the diagnostic evaluation and follow-up of patients presenting with symptomatic polycystic ovary syndrome
- Zinc Oxide Nanoparticles Fortified Biscuits as a Nutritional Supplement for Zinc Deficient Rats
- The mechanical forces that shape our senses
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Scd1 ab-Xyk : a new asebia allele characterized by a CCC trinucleotide insertion in exon 5 of the stearoyl-CoA desaturase 1 gene in mouse
- Viewpoint 4
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Alopecia and Thyroid Disease
- Congenital hypotrichosis due to short anagen
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Scalp whorls
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- [Translated article] Trichoscopy: An Update
- The Investigation of LPA <sub>4</sub> Functions in Zebrafish
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- Novel <i>RNF113A</i> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
- PA05 A rare case of cardiocutaneous syndrome in a young child
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Tissue Repair Mechanisms of Dental Pulp Stem Cells: A Comprehensive Review from Cutaneous Regeneration to Mucosal Healing
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Mandibulofacial dysostosis with alopecia results from ETAR gain-of-function mutations via allosteric effects on ligand binding
- Advancements in Bioactive Compounds and Therapeutic Agents for Alopecia: Trends and Future Perspectives
- Fertility evaluation of infertile women: a committee opinion
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs