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Research 421–450 of 1000+
- The role of mutations on gene AR, in androgenetic alopecia syndrome
- Alopecia Areata
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Nonclassic adrenal hyperplasia
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- Asian Hair: A Review of Structures, Properties, and Distinctive Disorders
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Variation in the ovine keratin-associated protein 15-1 gene affects wool yield
- Genetic basis of polycystic ovary syndrome
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Antiandrogen therapy for androgenetic alopecia
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- ACE1 rs1799752 polymorphism is not associated with long-COVID symptomatology in previously hospitalized COVID-19 survivors
- Increased androgen receptor messenger RNA in frontal-parietal hair follicles of women with androgenetic alopecia
- Skipping of Exons by Premature Termination of Transcription and Alternative Splicing within Intron-5 of the Sheep SCF Gene: A Novel Splice Variant
- Early-onset baldness and the risk of aggressive prostate cancer: findings from a case–control study
- Le gène<i>hairless</i>de la souris
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Grey, curly and short-haired Swiss Holstein cattle show genetic traces of the Simmental breed
- Identification of llama KRTAP7-1 and KRTAP8-1 fiber genes and polymorphism screening