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Research 211–240 of 1000+
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Longitudinal clinical course in patients with 5α-reductase type 2 deficiency treated with testosterone and dihydrotestosterone during infancy and puberty
- Investigation of topical application of procyanidin B-2 from apple to identify its potential use as a hair growing agent
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Effects of Androgen Treatment on Growth in Patients with 5-α-Reductase Type 2 Deficiency
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Linking diet to acne metabolomics, inflammation, and comedogenesis: an update
- Hair Biology and Nutritional Influences
- Health Promotion Potential of Vegetables Cultivated in Northern Thailand: A Preliminary Screening of Tannin and Flavonoid Contents, 5α-Reductase Inhibition, Astringent Activity, and Antioxidant Activities
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Androgen Receptor in Human Health: A Potential Therapeutic Target
- Nutritional Clinical Studies in Dermatology
- Botanicals With Dermatologic Properties Derived From First Nations Healing: Part 1—Trees
- The ITGB6 gene: its role in experimental and clinical biology
- The genetic basis of dermatophytosis skin infection susceptibility
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Polymorphisms in Genes Involved in Steroidogenesis in the Development of Severe Acne
- https://researchopenworld.com/genetics-of-hidradenitis-suppurativa/#
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep