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Research 931–960 of 1000+
- Challenges in treatment of patients with non-classic congenital adrenal hyperplasia
- Hepatitis C virus: host, environmental and viral factors promoting spontaneous clearance
- Immunological and Metabolic Causes of Infertility in Polycystic Ovary Syndrome
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Genetic prediction of male pattern baldness based on large independent datasets
- Azathioprine‐induced severe myelosuppression accompanied by massive hair loss and painful oral ulcer in an autoimmune hepatitis patient with <i>NUDT15</i> minor variant: A case report
- Capsaicin: an in-depth review of its chemical properties, health benefits, and challenges in food applications
- Differential cold stress intensities drive unique morphological and transcriptomic changes in Zea mays root hairs
- Study of the Thyroid Profile of Patients with Alopecia
- Polycystic ovary syndrome and iron overload: biochemical link and underlying mechanisms with potential novel therapeutic avenues
- AIRE Deficiency Leads to the Development of Alopecia Areata‒Like Lesions in Mice
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Localized alopecia and suppression of hypothalamic-pituitary-adrenal (HPA) axis in dogs following treatment with difluprednate 0.05% ophthalmic emulsion (Durezol®)
- Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients
- A Current Diagnostic and Therapeutic Challenge: Tinea Capitis
- Case report: NUDT15 polymorphism and severe azathioprine-induced myelosuppression in a young Chinese female with systematic lupus erythematosus: a case analysis and literature review
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency
- Precision and Personalized Medicine in Transdermal Drug Delivery Systems: Integrating AI Approaches
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Unravelling the threads of central centrifugal cicatricial alopecia
- Signal Peptide-CUB-EGF-like Domain-Containing Protein 3 (SCUBE3): From Molecule to Therapy
- Dissecting the Impact of α-MSH-MC1R-cAMP Signaling on UVA-Induced Stress in Fibroblasts - Implications for Regulation of Cutaneous Photoaging
- Spatiotemporal regulation of acute wound healing by the NLRP3 inflammasome: dual roles in macrophage-fibroblast chemotaxis and phenotype during wound repair
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- Understanding the Impact of the Skin Microbiome on Dermatological Assessments and Therapeutic Innovation
- Immortality Reconsidered: Clinical Challenges at the Frontier of Plastic Surgery
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review