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Research 361–390 of 1000+
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Effects of SLC45A2 and GPNMB on Melanin Deposition Based on Transcriptome Sequencing in Chicken Feather Follicles
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Predicting Human Appearance from DNA for Forensic Investigations
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Genome-Wide Association Studies of Hair Whorl in Pigs
- <i>BUZZ</i>: an essential gene for postinitiation root hair growth and a mediator of root architecture in <i>Brachypodium distachyon</i>
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Regulatory T cells in skin mediate immune privilege of the hair follicle stem cell niche
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Lupus erythematosus. What’s new?
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- PCOS in Adolescents—Ongoing Riddles in Diagnosis and Treatment
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Hidradenitis suppurativa and Mediterranean fever gene mutations
- Viewpoint 1
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- A Systematic Scoping Review and Conceptual Analysis of New-Onset Fibromyalgia Manifestations After Non-Hospitalized COVID-19: Empirics, Definitions, Methodologies, Pathophysiology, Mapping of Literature, and Knowledge Gaps
- Two-Stage Machine Learning-Based GWAS for Wool Traits in Central Anatolian Merino Sheep
- Biomarker development for PCOS diagnosis
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Genes and Immune Response in Alopecia Areata: Review of the Alopecia Areata Research Summit First Day Proceedings