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Research 661–690 of 1000+
- Hair follicle dystrophy in a litter of domestic cats resembling lanceolate hair mutant mice
- Diffuse hair loss in Addison disease: A reason for X-linked adrenoleukodystrophy screening
- Identification of a Novel Missense Mutation in the Fibroblast Growth Factor 5 Gene Associated with Longhair in the Maine Coon Cat
- Deletion of an Enhancer in FGF5 is Associated With Ectopic Expression in Goat Hair Follicles and the Cashmere Growth Phenotype
- NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
- Granulomatous skin involvement in a patient with an unusual <i>NOD2</i> mutation
- A Novel Androgen Receptor Gene Mutation in a 46,XY Patient: Complete Androgen Insensitivity Syndrome
- A Newborn With Hair Loss
- Efficient Editing of CSLD2 Orthologue by CRISPR/Cas9 Affects Cell Morphogenesis of Root Hair in Spinach
- Hair Cuts Cause Cancer
- Ischemic Stroke in a Young Adult Male During Finasteride Therapy
- Successful Management of Netherton Syndrome Using IVIG and Dupilumab: A Case Report
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- Successful topical minoxidil treatment for hair density and length in trichorhinophalangeal syndrome type 1
- Cholesterol homeostasis in hair follicle keratinocytes is disrupted by impaired ABCA5 activity
- 1440 DNA dioxygenases Tet2/3 regulate gene promoter accessibility and chromatin topology in lineage-specific loci to control keratinocyte differentiation and hair growth
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay
- Hair follicle associated pluripotent (HAP) stem cells jump from transplanted whiskers to pelage follicles and stimulate hair growth
- Papular atrichia
- Plain language summaries
- Cross‐linked features of mouse pelage hair resistant to detergent extraction
- Monilethrix: Beaded hair and hypotrichosis in a child
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Hair Anomalies in a 6-Year-Old Girl
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Human hair melanins: what we have learned and have not learned from mouse coat color pigmentation
- The genetics of hair shaft disorders
- AGD1, a class 1 ARF‐GAP, acts in common signaling pathways with phosphoinositide metabolism and the actin cytoskeleton in controlling Arabidopsis root hair polarity
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- Asian Hair: A Review of Structures, Properties, and Distinctive Disorders