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Research 421–450 of 1000+
- Recent Updates of the CRISPR/Cas9 Genome Editing System: Novel Approaches to Regulate Its Spatiotemporal Control by Genetic and Physicochemical Strategies
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Exploring links with rare variants, COVID-19 and short anagen hair syndrome
- Utilizing functional genomics approaches to characterize risk genes in alopecia areata
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Dissecting Cellulitis of the Scalp
- Quoi de neuf en dermatologie pédiatrique ?
- Androgenetic Alopecia
- Polycystic ovary syndrome
- Aging of the hair follicle pigmentation system
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Molecular characterization of HOXC8 gene and methylation status analysis of its exon 1 associated with the length of cashmere fiber in Liaoning cashmere goat
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Investigation of the association of the MLPH gene with seasonal canine flank alopecia in Rhodesian Ridgeback dogs
- Evaluation of Susceptibility Genes/Loci Associated with Male Androgenetic Alopecia (MAGA) for Female-Pattern Hair Loss in a Chinese Han Population and a Brief Literature Review
- Do Alopecia Areata and Hair Colour Have a Shared Genetic Component?
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- Exploring the Relationship Between Immune Cells and Non-Scarring Hair Loss: A Mendelian Randomization Study
- Editor's evaluation: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Epigenetic and transcriptional profiling of secondary hair follicle stem cells during cashmere growth
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Syndrome of Birt–Hogg–Dubé, a Histopathological Pitfall With Similarities to Tuberous Sclerosis
- Indian Hair
- 5α-Reductase Isoenzymes: From Neurosteroid Biosynthesis to Neuropsychiatric Outcomes
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report