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Research 391–420 of 1000+
- The idiosyncratic genome of Korean long-tailed chicken as a valuable genetic resource
- 8368 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- 9209 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- Meeting Report: 68th Montagna Symposium on the Biology of Skin “Decoding Complex Skin Diseases: Integrating Genetics, Genomics, and Disease Biology”
- Case report: a study of the clinical characteristics and genetic variants of post-finasteride syndrome patients
- Naturally Occurring Hairlines in Orientals of Southeast and East Asian Origin and Their Application in Hair Restoration Surgery
- Maternal androgen excess significantly impairs sexual behavior in male and female mouse offspring: Perspective for a biological origin of sexual dysfunction in PCOS
- FFA Patient Profile Analysis Based on the Authors’ Observations and a Review of the Literature—An Original Survey
- Sex Differences in Reaction to Chronic Unpredictable Stress in the House Mouse (Mus musculus musculus) of Wild Origin
- Sex Differences in Reaction to Chronic Unpredictable Stress in the House Mouse (<em>Mus m. musculus</em>) of Wild Origin
- Recent Updates of the CRISPR/Cas9 Genome Editing System: Novel Approaches to Regulate Its Spatiotemporal Control by Genetic and Physicochemical Strategies
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Progressive Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) from a Young Age Due to a Rare Genetic Disorder, Familial Partial Lipodystrophy: A Case Report and Review of the Literature
- The Prospect and Application Research Progress of Precision Gene Editing Technology Based on CRISPR/Cas9 in Livestock Genetics and Breeding
- Ethnic Hair Considerations for People of African, South Asian, Muslim, and Sikh origins
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Ovarian Morphology Is a Marker of Heritable Biochemical Traits in Sisters with Polycystic Ovaries
- Endocrine Influences on Hair Growth
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- Do Changes in Chromosomes Cause Aging?
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Gene Delivery to the Hair Follicle
- Unravelling the threads of central centrifugal cicatricial alopecia
- A single-cell transcriptomic atlas elucidates the hair cycle and apoptosis mechanisms in goat hair follicles
- Toward understanding scarless skin wound healing and pathological scarring
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Hair follicle and interfollicular epidermal stem cells make varying contributions to wound regeneration
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- A review of genotrichoses and hair pathology associated with inherited skin diseases