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Research 901–930 of 1000+
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Chronic overlapping pain conditions and nociplastic pain
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Nonscarring alopecias
- Characterisation of Four New Genes in the Ovine KAP19 Family
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Dissection of a Complex Enhancer Element: Maintenance of Keratinocyte Specificity but Loss of Differentiation Specificity
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Siberian cats help in solving part of the mystery surrounding golden cats
- The need for African dermatology guidelines—Steps towards equitable care
- Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages
- The molecular pathogenesis of Trichilemmal carcinoma
- 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
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Genome-Wide Association Study for Body Conformation Traits in Kazakh Fat-Tailed Coarse-Wool Sheep
- miR-200a Targets PITX2 to Mediate Goose Fibroblast Proliferation Through the Wnt Pathway
- Molecular mechanisms underlying cashmere quality differences between Jiangnan cashmere goats and Changthangi pashmina goats
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Author response: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Skin precancer.
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Keratin disorders: from gene to therapy