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Research 661–690 of 1000+
- Evaluation of the serum level of regulation upon activation of normal T-cell expressed and secreted protein in different types of alopecia areata
- Cómo hacer que dos más dos sumen cinco
- Implementation and Evaluation of a Platelet-Rich Plasma Multimedia Patient Education Tool for Patients With Androgenetic Alopecia
- Anatomy and Physiology of the Skin
- Skin wound healing in humans and mice: Challenges in translational research
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Lichen Planopilaris and Frontal Fibrosing Alopecia as Model Epithelial Stem Cell Diseases
- Genetic predictors of testosterone and their associations with cardiovascular disease and risk factors: A Mendelian randomization investigation
- The evolutionary impact of androgen levels on prostate cancer in a multi-scale mathematical model
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Identification of the keratin-associated protein 13-3 (KAP13-3) gene in sheep
- Formation of regulator/target gene relationships during evolution
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- Genetic Tools for Cell Lineage Tracing and Profiling Developmental Trajectories in the Skin
- Polycystic ovarian syndrome: current understanding of pathogenesis, diagnosis and treatment
- Genetic and biochemical aspects of the synthesis of keratin by hair follicles
- Progeroide Syndrome
- Beyond “Ethnicity” in Dermatology
- PSS34 THE IMPACT OF POTENTIAL PILL SPLITTING ON GENERIC AND BRANDED FINASTERIDE UPTAKE
- Genetic Polymorphisms of the 3'-Untranslated Regions (3'-UTR) of the HSP 70 Gene in Moa Buffalo (Bubalus bubalis)
- Genetic Association Between Polycystic Ovary Syndrome and the <i>APOA5</i> rs662799 and <i>PLIN1</i> rs894160 Metabolic Variants in the Western Saudi Population: A Case-Control Study
- Congenital Atrichia: A Case Report
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- Moniletrix. Observación de esta infrecuente displasia pilosa en dos hermanos. Reporte clínico y dermatoscópico
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Nociceptive and Nonnociceptive Roles of TRPV3 and Its “Druggability”
- Commentary
- Comparative histomorphometric and transcriptomic analysis reveals potential genetic determinants of pelage variation between hairy and coarse-woolly sheep
- Genetics of infertility and “assisted fertilization” in the Bible: The case of Abraham and his family