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Research 91–120 of 1000+
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- Modelling androgen synthesis and action during human sexual differentiation
- Atlas of Geriatric Dermatology
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Deciphering the cellular landscape and genetic underpinnings of fiber diameter determined by dermal papilla cells in fine-wool sheep
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- The prevalence and types of androgenetic alopecia in Korean men and women
- Improving translational research in sex-specific effects of comorbidities and risk factors in ischaemic heart disease and cardioprotection: position paper and recommendations of the ESC Working Group on Cellular Biology of the Heart
- Organ Specificity in Autoimmune Diseases: Thyroid and Islet Autoimmunity in Alopecia Areata
- Androgens and hair: a biological paradox
- Lab Quality Management and Methodology
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- The Basic Science of Hair Biology
- Genetic, hormonal and metabolic aspects of PCOS: an update
- Exploring the therapeutic potential of naturally occurring taxifolin, a dietary flavonoid: an updated comprehensive review
- What may be the markers of the male equivalent of polycystic ovary syndrome?
- Exosomes and Their Bioengineering Strategies in the Cutaneous Wound Healing and Related Complications: Current Knowledge and Future Perspectives
- Advanced nanocarrier- and microneedle-based transdermal drug delivery strategies for skin diseases treatment
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population
- <i>In vivo</i> alteration of the keratin 17 gene in hair follicles by oligonucleotide‐directed gene targeting
- Molecular Diagnostics and Control of Zoonotic Dermatophytosis: First Detection of Trichophyton indotineae in a Dog in Africa
- Identification of the Ovine Keratin-Associated Protein 21-1 Gene and Its Association with Variation in Wool Traits
- A kindred with mutant IKAROS and autoimmunity
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Suprabasal Desmoglein 3 Expression in the Epidermis of Transgenic Mice Results in Hyperproliferation and Abnormal Differentiation
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans