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Research 151–180 of 569
- Transcriptome Dynamics Reveal Stage-Specific and Melatonin-Triggered Gene Expression Patterns During The Cashmere Growth Cycle in Capra Hircus
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Trichotillomania in Children
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Case report: Systemic granulomatous disease with vasculitis in a bull due to hairy vetch (Vicia villosa) toxicosis
- Is dehydroepiandrosterone a hormone?
- Lipedematous scalp and lipedematous alopecia: Report of three cases in white adults
- Clinical markers of androgenicity in acne vulgaris
- Canine alopecia X-Like disorder
- Clinical Management in Psychodermatology
- Whisker hair (acquired progressive kinking of the hair): An indication for finasteride 1 mg?
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- Frequency of Types of Alopecia in a Single-centre Hair Referral Clinic Over a Ten Years Period
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs
- A polymorphism in the matrix metalloproteinase-1 gene promoter is associated with the presence of polycystic ovary syndrome in Caucasian women
- RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS
- Proteome Analysis of Human Hair Shaft
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Diseases of Hair
- Diseases of Hair
- Molecular Genetics of Human Hair Diseases
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- 513 Demonstration of hair health benefits using an oral supplement
- CRISPR/Cas9-mediated Disruption of Fibroblast Growth Factor 5 in Rabbits Results in a Systemic Long Hair Phenotype by Prolonging Anagen
- Screening and expression validation of key proteins for secondary hair follicle growth in cashmere goats based on iTRAQ quantitative proteomics technology
- Intermediate Hair Follicles from Patients with Female Pattern Hair Loss Are Associated with Nutrient Insufficiency and a Quiescent Metabolic Phenotype
- Development of Hair Fibres