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Research 181–210 of 1000+
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Novel anti-Mullerian hormone receptor 2 binding peptide prevents chemotherapy-related ovarian follicle loss in a mouse model
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- Glucocorticoid Receptor Mutants Demonstrate Increased Motility Inside the Nucleus of Living Cells: Time of Fluorescence Recovery After Photobleaching (FRAP) Is an Integrated Measure of Receptor Function
- NAD⁺ Biology in Ageing and Chronic Disease: Mechanisms and Evidence across Skin, Fertility, Osteoarthritis, Hearing and Vision Loss, Gut Health, Cardiovascular–Hepatic Metabolism, Neurological Disorders, and Muscle
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- TRP Channels in Skin Biology and Pathophysiology
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- 316 Specialized ribosomes in human dermal fibroblast senescence
- Retinol Esterification by DGAT1 Is Essential for Retinoid Homeostasis in Murine Skin
- KLHL24-Mediated Hair Follicle Stem Cells Structural Disruption Causes Alopecia
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Animal and in vitro Models for the Study of Hair Follicles
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Biochemical and Structural Characteristics, Gene Regulation, Physiological, Pathological and Clinical Features of Lipocalin-Type Prostaglandin D2 Synthase as a Multifunctional Lipocalin
- The androgen receptor gene polyglycine repeat polymorphism is associated with memory performance in healthy Chinese individuals
- Observations that suggest a contribution of altered dermal papilla mitochondrial function to androgenetic alopecia
- The Role of T‐Helper 17 Cells and Regulatory T Cells in Acute Diffuse and Total Alopecia: The Increased Function of Regulatory T Cells May Explain the Favorable Prognosis
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- Targeting the Gut Microbiota with Pro- and Postbiotics: Emerging Strategies against Alopecia
- The amazing miniorgan: Hair follicle
- Case report: NUDT15 polymorphism and severe azathioprine-induced myelosuppression in a young Chinese female with systematic lupus erythematosus: a case analysis and literature review
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Alopecia areata - Vitiligo overlap syndrome: An emerging clinical variant
- Store-operated calcium channels in skin
- TRPV3 Ion Channel: From Gene to Pharmacology
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)