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Research 751–780 of 1000+
- The evaluation of IL-4 VNTR intron 3 and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with alopecia areata: a case–control study
- Identifying causal genes in alopecia areata using integrative analysis of differential expression and Mendelian randomization
- Actinic Keratosis: Risk Factors, Clinical, Diagnosis and Therapeutics Aspects. Part I
- Human and animal cells under influence of different lighting and stimulus
- Noval advance of histone modification in inflammatory skin diseases and related treatment methods
- Baghnakh (Martynia annua): Prehistory to contemporary medicinal value
- Polymorphisms of OCT1 and metformin effects in Iraqi women with polycystic ovary syndrome in Karbala city
- The evaluation of IL-4 intron 3 VNTR and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with Alopecia Areata: a case-control study
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Androgenetic Alopecia: Therapy Update
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Correlation between sebum level and severity of male androgenetic alopecia
- Genetic Single Nucleotide Polymorphisms of IL-16 and its Concentration of Patients Infected with Alopecia Areata in Diyala Province, Iraq
- Hair Loss and Androgen’s Role in the Era of COVID-19
- Exploring the effects of wetting and free fatty acid deposition on an atomistic hair fiber surface model incorporating Keratin Associated Protein 5-1
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women
- Serum IL-21 Level and Its Relation to Activity and Severity of Alopecia Areata
- KIF18B is a cell-type specific regulator of spindle orientation in the epidermis
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- Two females with hair loss
- Autoimmune polyglandular syndrome type 4 – case report
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Hair Loss in Children
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Androgenetska alopecija u žena
- Vaccines, Infections, and Alopecia Areata
- Comparative study of efficacy of excimer light therapy vs. intralesional triamcinolone vs. topical 5% minoxidil for alopecia areata: an observational study