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Research 481–510 of 1000+
- Alopecia areata
- Role of Aire and Notch4 Allelic Mutations in Alopecia Areata in C3H/HeJ Mice
- Androgenetic alopecia
- Detection of a Second KAP22 Family Member in Sheep and Analysis of Its Genetic Variation and Associations with Selected Wool Fibre Traits
- Characterisation of Four New Genes in the Ovine KAP19 Family
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- Immune and Non-immune Interactions in the Pathogenesis of Androgenetic Alopecia
- Relationship of Hypothyroidism with Alopecia Areata and Androgenetic Alopecia: Insights from a Two-Sample Mendelian Randomization Study
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- ST14 interacts with TMEFF1 and is a predictor of poor prognosis in ovarian cancer
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Divergent progression pathways in male androgenetic alopecia and female pattern hair loss: Trichoscopic perspectives
- A missense mutation in Lama3 causes androgen alopecia
- Ovine KRTAP36-2: A New Keratin-Associated Protein Gene Related to Variation in Wool Yield
- Androgenetic alopecia: An update
- Cells to Surgery Quiz: April 2020
- Acne-Associated Syndromes
- Cyberspace Chat
- Enzymes
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- COVID-19 and Sex Differences
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- New insights into the role of Runx1 in epithelial stem cell biology and pathology
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Optimal Management of Hair Loss (Alopecia) in Children
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Against the Rules: Human Keratin K80
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review