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Research 481–510 of 1000+
- 13C-NMR study of 4-azasteroids in solution and solid state
- Fetal Programming of Polycystic Ovary Syndrome by Androgen Excess: Evidence from Experimental, Clinical, and Genetic Association Studies
- Vaccines, adjuvants and autoimmunity
- Genetic Basis of Male Pattern Baldness
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Human Hair Keratin-Associated Proteins
- The emerging role of Janus kinase inhibitors in the treatment of autoimmune and inflammatory diseases
- Androgen receptors and their biology
- Identification and sequence analysis of the keratin-associated protein 24‐1 (KAP24-1) gene homologue in sheep
- Review of Fluconazole Properties and Analytical Methods for Its Determination
- Hepatotoxicity with low- and ultralow-dose flutamide: a surveillance study on 203 hyperandrogenic young females
- Epidemiological study of prostate cancer (EPICAP): a population-based case–control study in France
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Diversity of Trichocyte Keratins and Keratin Associated Proteins
- Molecular basis of androgen action on human sexual desire
- Genome-Wide Association Study for Udder Conformation Traits in Chinese Holstein Cattle
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Alopecia areata. Actualidad y perspectivas
- Review of Fluconazole Properties and Analytical Methods for Its Determination
- Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance?
- Analysis of Genetic Diversity and Construction of a Core Collection of Ginkgo biloba Germplasm Using EST-SSR Markers
- Narrowband UVB treatment induces expression of WNT7B, WNT10B and TCF7L2 in psoriasis skin
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family
- <i>Microsporum gypseum</i> isolated from a feline case of dermatophytosis
- The potential impact of melanosomal pH and metabolism on melanoma
- Intra-host SARS-CoV-2 single-nucleotide variants emerged during the early stage of COVID-19 pandemic forecast population fixing mutations
- Symptomatology of Long COVID Associated with Inherited and Acquired Thrombophilic Conditions: A Systematic Review