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Research 181–210 of 1000+
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- Enhanced Insights into Frontal Fibrosing Alopecia: Advancements in Pathogenesis Understanding and Management Strategies
- Androgen receptor gene polymorphism and biological age markers in men
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Psychometric validation of the Spanish alopecia areata–life impact questionnaire
- <i>BUZZ</i>: an essential gene for postinitiation root hair growth and a mediator of root architecture in <i>Brachypodium distachyon</i>
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Author response: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Genome-Wide Association Study for Body Conformation Traits in Kazakh Fat-Tailed Coarse-Wool Sheep
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Novel genes and variants associated with longevity in Bulgarian centenarians revealed by whole exome sequencing DNA pools: a pilot study
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- The evaluation of IL-4 VNTR intron 3 and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with alopecia areata: a case–control study
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Human skin color: Origin, variation and significance
- Regulatory T cells in skin mediate immune privilege of the hair follicle stem cell niche
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- The Lived Experience of Women with Alopecia: A Qualitative Study Investigating the Psychological, Social and Emotional Impact of Alopecia in a Sample of Greek Women
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- Alopecia Areata is associated with MICA and an extended HLA haplotype
- Two-Stage Machine Learning-Based GWAS for Wool Traits in Central Anatolian Merino Sheep
- Androgenetic alopecia: An update