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Research 571–600 of 1000+
- Endogenous Skin Fluorescence is a Good Marker for Objective Evaluation of Comedolysis
- Hairlines through history: Frontal fibrosing alopecia over 500 years?
- Relationship of Hypothyroidism with Alopecia Areata and Androgenetic Alopecia: Insights from a Two-Sample Mendelian Randomization Study
- Sebaceous gland loss and inflammation in scarring alopecia: Apotential role in pathogenesis
- Cutaneous manifestations associated with immune checkpoint inhibitors
- Case report: NUDT15 polymorphism and severe azathioprine-induced myelosuppression in a young Chinese female with systematic lupus erythematosus: a case analysis and literature review
- Real-world evidence in alopecia areata treatment: A narrative review
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Basal cell carcinomas acquire secondary mutations to overcome dormancy and progress from microscopic to macroscopic disease
- Acute sensitivity of the oral mucosa to oncogenic <i>K‐ras</i>
- Genetic analysis does not confirm non-classical congenital adrenal hyperplasia in more than a third of the women followed with this diagnosis
- In This Issue
- Adipose Tissue-Derived Therapies for Osteoarthritis: Multifaceted Mechanisms and Clinical Prospects
- Titanium dioxide nanoparticles: a promising candidate for wound healing applications
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Narrowband UVB treatment induces expression of WNT7B, WNT10B and TCF7L2 in psoriasis skin
- RETRACTED: Gut microbiota, skin microbiota, and alopecia areata: A Mendelian randomization study
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience