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Research 721–750 of 1000+
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- The hair shaft: normality, abnormality, and genetics
- Decorin promotes proliferation and migration of ORS keratinocytes and maintains hair anagen in mice
- Expression of an Olfactomedin-Related Gene in Rat Hair Follicular Papilla Cells
- Comparison of mitochondrial transplantation by using a stamp-type multineedle injector and platelet-rich plasma therapy for hair aging in naturally aging mice
- The E6/E7 oncogenes of human papilloma virus and estradiol regulate hedgehog signaling activity in a murine model of cervical cancer
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Multiple Roles of Integrin-Linked Kinase in Epidermal Development, Maturation and Pigmentation Revealed by Molecular Profiling
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- Common Baldness in Women
- Flightless I Expression Enhances Murine Claw Regeneration Following Digit Amputation
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Spironolactone May Reduce the Risk of Incident Rosacea
- Increased androgen receptor messenger RNA in frontal-parietal hair follicles of women with androgenetic alopecia
- Incidence of adverse cutaneous drug reactions in a Mexican sample: an exploratory study on their association to tumour necrosis factor alpha TNF2 allele
- Protein kinase C is a key target for attenuation of Leigh syndrome by rapamycin
- Acne in Dark Skin
- Association of a polymorphism in the ornithine decarboxylase gene with male androgenetic alopecia
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- SNP Markers: Analysis of Genetic Diversity and Identification of Genomic Regions in Pantaneiro Sheep and Texel Sheep Under Natural Selection
- Abstracts
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- Nanofibers: An Effective Biomedical Tool for Burn Management
- Progeroide Syndrome
- The urine as a diagnostic key for a homozygous EGFR mutation
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child