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Research 421–450 of 1000+
- The role of CYP19A1 and ESR2 gene polymorphisms in female androgenetic alopecia in the Polish population
- Hair loss in children.
- Psychometric validation of the Spanish alopecia areata–life impact questionnaire
- Neonatal screening in Sweden and disease-causing variants in phenylketonuria, galactosaemia and biotinidase deficiency
- Application of multi-omics techniques to androgenetic alopecia: Current status and perspectives
- Polycystic ovary syndrome
- <i>Hedychium spicatum</i>: a systematic review on traditional uses, phytochemistry, pharmacology and future prospectus
- Advances in regenerative medicine-based approaches for skin regeneration and rejuvenation
- ANDROGENETIC ALOPECIA
- The laboratory in the multidisciplinary diagnosis of differences or disorders of sex development (DSD)
- Hair Changes Caused by Aging
- Eclipta prostrata (L.) L. (Asteraceae): Ethnomedicinal Uses, Chemical Constituents, and Biological Activities
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- 130 Expression of nidogen1 in basal cell carcinoma
- Research Snippets
- Keratins and skin disease
- Potential Sequels of Undiagnosed Marfan Syndrome: A Case Report
- De novo assembly and characterization of skin transcriptome using RNAseq in sheep (Ovis aries)
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- Editorial: Mechanisms and novel treatments of pigmentary disorders and skin regeneration
- Hair & Cutaneous Development
- Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
- Twenty-Five and Up (25Up) Study: A New Wave of the Brisbane Longitudinal Twin Study
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Selection signatures for fiber production in commercial species: A review
- Increased risk of chronic fatigue and hair loss following COVID-19 in individuals with hypohidrotic ectodermal dysplasia
- Factors affecting the development of alopecia areata in children
- News in brief
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.