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Research 691–720 of 1000+
- Identification of the Ovine Keratin-Associated Protein 21-1 Gene and Its Association with Variation in Wool Traits
- The Role of MicroRNA, Long Non-Coding RNA and Circular RNA in the Pathogenesis of Polycystic Ovary Syndrome: A Literature Review
- Recent Advances in the Pathogenesis of Autoimmune Hair Loss Disease Alopecia Areata
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- IL-1 Receptor–Knockout Mice Develop Epidermal Cysts and Show an Altered Innate Immune Response after Exposure to UVB Radiation
- The Role of the Slc39a Family of Zinc Transporters in Zinc Homeostasis in Skin
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Analysis of histology and long noncoding RNAs involved in the rabbit hair follicle density using RNA sequencing
- Deferasirox, an oral iron chelator, prevents hepatocarcinogenesis and adverse effects of sorafenib
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- Wounds and the Microbiota: The Healing Interplay Between Host and Microbial Communities
- Transcriptomic analysis of regulatory mechanisms in the telogen-anagen transition of ovine hair follicles
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID‐19
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Seasonal Variability in Transcript Expression of Type I and Type II Keratins in Wool Follicles of Lustrous Fleece-Producing Magra Sheep
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- Gene expression of FOXA1 and CCL2 in different phenotypes of infertile women with polycystic ovarian syndrome
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Divergent progression pathways in male androgenetic alopecia and female pattern hair loss: Trichoscopic perspectives
- Association between Family History and Male Androgenetic Alopecia with Female Pattern Hair Loss
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- 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>)
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Advancements in Bioactive Compounds and Therapeutic Agents for Alopecia: Trends and Future Perspectives