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Research 61–90 of 1000+
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Clinical relevance of hair microscopy in alopecia
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Molecular genetics of androgen insensitivity
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia
- British Society for Dermatopathology
- Sex-limited chromosomes and non-reproductive traits
- Trichoscopy in genetic hair shaft abnormalities
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- The X Factor in Immunity: Sex Differences Shaped by the X Chromosome
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Conditional Activin Receptor Type 1B (Acvr1b) Knockout Mice Reveal Hair Loss Abnormality
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- SUN-208 Rare Case of 47XXY/46XX Mosaic Klinefelter Syndrome
- Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature
- Vulvovaginal involvement in Netherton syndrome: A case report
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- Potential Role of the Epidermal Differentiation Complex in the Pathogenesis of Psoriasis
- Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Author response: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- Decision letter: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- Atrichia with papular lesions