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Research 61–90 of 113
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- Interpretation of the Yak Skin Single-Cell Transcriptome Landscape
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- 192 MicroRNAs and their regulatory interactions in the human hair follicle
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Whole-transcriptome analysis reveals the profiles and roles of coding and non-coding RNAs during hair follicle cycling in Rex rabbits
- Analyses of histological and transcriptome differences in the skin of short-hair and long-hair rabbits
- CRISPR/Cas9-mediated Disruption of Fibroblast Growth Factor 5 in Rabbits Results in a Systemic Long Hair Phenotype by Prolonging Anagen
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Genetic Hair Disorders: A Review
- Hair shaft disorders in children – An update
- Trichoscopy in Hair Shaft Disorders
- 196 The endocannabinoid tone regulates human sebocyte biology
- Dermatoscopy of hair shaft disorders
- Advances in Hair Diseases
- Peer Review #2 of "Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis (v0.1)"
- Diagnostic challenges in determining alopecia areata
- Group IID, IIE, IIF and III secreted phospholipase A2s
- LPA3, a unique G protein-coupled receptor for lysophosphatidic acid
- Hair Loss in Children
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Molecular Genetics of Human Hair Diseases
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia