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Research 691–720 of 1000+
- A homozygous missense mutation in the fibroblast growth factor 5 gene is associated with the long-hair trait in Angora rabbits
- 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
- 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
- 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
- Does Complement Have a Role in the Pathogenesis of Alopecia Areata?
- 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
- Precision Dermatology: A Review of Molecular Biomarkers and Personalized Therapies
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- <i>BUZZ</i>: an essential gene for postinitiation root hair growth and a mediator of root architecture in <i>Brachypodium distachyon</i>
- Association between Family History and Male Androgenetic Alopecia with Female Pattern Hair Loss
- 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
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Pathology of Mouse Models of Accelerated Aging
- 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>)
- Advancements in Bioactive Compounds and Therapeutic Agents for Alopecia: Trends and Future Perspectives
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- High-throughput T cell receptor sequencing identifies clonally expanded CD8+ T cell populations in alopecia areata
- Alleviation of Multidrug Resistance by Flavonoid and Non-Flavonoid Compounds in Breast, Lung, Colorectal and Prostate Cancer
- The nude gene and the skin
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions