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Research 451–480 of 1000+
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Genome-Wide Association Studies of Hair Whorl in Pigs
- Genomic Markers and Personalized Medicine in Androgenetic Alopecia: A Comprehensive Review
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- <i>BUZZ</i>: an essential gene for postinitiation root hair growth and a mediator of root architecture in <i>Brachypodium distachyon</i>
- Insight into the pathogensis of polycystic ovarian syndrome
- Childhood Alopecia Areata: An Overview of Treatment and Recent Patents
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- 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
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Role of polymorphism of the androgen receptor gene andnon-random x chromosome inactivation in the pathogenesisof androgenic alopecia
- Causal relationship between gut microbiota and androgenetic alopecia: A Mendelian randomization study
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Ichthyosis
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Androgens and hair loss
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- Alopecia Areata: Updates from the Mouse Perspective
- Trichothiodystrophy: Current Concepts
- Two-Stage Machine Learning-Based GWAS for Wool Traits in Central Anatolian Merino Sheep
- Gene-Environment Interaction Between <i>CYP1B1</i> and Oral Contraception on Frontal Fibrosing Alopecia
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy