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Research 811–840 of 1000+
- The fatty acids and the skin: a focus on the n-6 family of unsaturated fatty acids
- Comparative evaluation of potential phytopharmacological and nutritional properties of some Indigenous rhizomes of Zingiberaceae family (Alpinia calcarata, Alpinia galanga, Alpinia zerumbet) localized in Southeast Asia
- A cross-sectional study for alopecia patterns, family history, and diet, reveals early-onset hair loss in residents of Saudi Arabia and a lack of awareness about available treatments
- Hair steroid before and after COVID-19 in preschoolers: the moderation of family characteristics
- Autosomal dominant monilethrix with incomplete penetrance due to a novel KRT86 mutation in a Chinese family
- The fatty acids and the skin: a focus on the n-6 family of unsaturated fatty acids
- Chi-miR-130b-3p regulates Inner Mongolia cashmere goat skin hair follicles in fetuses by targeting<i>Wnt family member 10A</i>
- m6A Methylation Analysis Reveals Networks and Key Genes Underlying the Coarse and Fine Wool Traits in a Full-sib Merino Family
- Expression Patterns of Gli-1, Pleckstrin Homology-Like Domain, Family A, Member 1, Transforming Growth Factor-β1/β2, and p63 in Sebaceous and Follicular Tumors
- Relationship between diet, atopy, family history, and premature hair graying
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Genome-wide identification, characterization, and expression analysis of keratin genes (KRTs) family in yak (Bos grunniens)
- Identification of novel mutation in the<i>HR</i>gene responsible for atrichia with papular lesions in a Pakistani family
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Prevalence of post–COVID syndrome in a cohort of faculty of a medical institute and their family members
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Post-Exposure Syndromes as State-Space Trapping: A set-theoretic perspective on PSSD and the post-exposure family.
- Post-Exposure Syndromes as State-Space Trapping: A set-theoretic perspective on PSSD and the post-exposure family.
- Coexisting trichorrhexis nodosa and pili annulati: a case report of hair shaft abnormalities in a syrian family
- The problem of excessive hair loss as a signal for the diagnosis of coeliac disease – A family case
- - Hair steroid concentration before and after the beginning of the COVID-19 pandemic in preschoolers: the moderating effect of family characteristics
- Structural & functional studies of L-PGDS and SMPDL3A enzymes in lipid signaling family
- Size Polymorphisms in the Human Ultrahigh Sulfur Hair Keratin-Associated Protein 4, KAP4, Gene Family
- <i>Mrp4</i>, A New Mitogen-Regulated Protein/Proliferin Gene; Unique in this Gene Family for its Expression in the Adult Mouse Tail and Ear<sup>1</sup>
- The Study on Biological Function of Keratin 26, a Novel Member of Liaoning Cashmere Goat Keratin Gene Family
- Evolution, classification, structure, and functional diversification of steroid 5α-reductase family in eukaryotes
- Quality of life in Romanian patients with schizophrenia based on gender, type of schizophrenia, therapeutic approach, and family history
- Chemical Principles, Bioactivity, and Pharmacology of Hedychium spicatum Sm. (Family: Zingiberaceae)
- Evaluation of Prevalence of PCOS and Associated Depression, Nutrition, and Family History: A Questionnaire-based Assessment.
- Profile of 513 patients with alopecia areata: associations of disease subtypes with atopy, autoimmune disease and positive family history