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Research 61–90 of 116
- Genetics of Structural Hair Disorders
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Genetic Hair Disorders: A Review
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Monilethrix: A case report imaged by trichoscopy, reflectance confocal microscopy and histopathology
- Trichoscopy in Hair Shaft Disorders
- 196 The endocannabinoid tone regulates human sebocyte biology
- 194 An underlying mechanism of hair loss in acrodermatitis enteropathica
- 192 MicroRNAs and their regulatory interactions in the human hair follicle
- Dermatoscopy of hair shaft disorders
- Non-Edg family LPA receptors: the cutting edge of LPA research
- Hair Loss in Children
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Advances in Hair Diseases
- Diagnostic challenges in determining alopecia areata
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Peer Review #2 of "Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis (v0.1)"
- LPA3, a unique G protein-coupled receptor for lysophosphatidic acid
- Group IID, IIE, IIF and III secreted phospholipase A2s
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Molecular Genetics of Human Hair Diseases
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- CRISPR/Cas9-mediated Disruption of Fibroblast Growth Factor 5 in Rabbits Results in a Systemic Long Hair Phenotype by Prolonging Anagen
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan