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Research 31–60 of 92
- Prevalence of MMP-1 rs1799750 Polymorphism in Androgenetic Alopecia: A Cross-Sectional Study in an Indonesia Population
- DMBA/TPA Treatment Is Necessary for BCC Formation from Patched Deficient Epidermal Cells in Ptch flox/flox CD4Cre +/− Mice
- Sulphation catalysed by the human cytosolic sulphotransferases - chemical defence or molecular terrorism?
- Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women
- High incidence of severe hand–foot syndrome during capecitabine–docetaxel combination chemotherapy
- Investigation of Vaspin and Visfatin -4689G/T Gene Polymorphisms in Alopecia Areata Patients
- 184 WITHDRAWN
- 185 Infrared and high frequency ultrasound imaging of skin lesions in atopic dermatitis and psoriasis vulgaris
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Acne, the Skin Microbiome, and Antibiotic Treatment
- Vitamin D receptor polymorphisms and the polycystic ovary syndrome: A systematic review
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Androgens and hair: a biological paradox
- The relationship among androgens, insulin resistanceand ghrelin polymorphisms in post-adolescent malepatients with severe acne vulgaris
- Vogt-Koyanagi-Harada Disease: A Narrative Review
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- Encapsulación en ciclodextrinas de compuestos con actividad frente a la alopecia androgénica masculina.
- Peroxisome Proliferator Activated Receptors Gamma Serum levels and Gene Polymorphism in Frontal Fibrosing Alopecia: A Case Control Study
- rs4541843 G > A variant near miR-182 is associated with susceptibility, severity, and increased hsa-miR-182-5p expression in alopecia areata
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Association between VDR Gene Polymorphisms and Melanoma Susceptibility in a Colombian Population
- Forensic DNA phenotyping: a review on SNP panels, genotyping techniques, and prediction models
- Secondary Syphilis in Cali, Colombia: New Concepts in Disease Pathogenesis
- <i>In vivo</i> alteration of the keratin 17 gene in hair follicles by oligonucleotide‐directed gene targeting
- Review of Different DNA Extraction Methods in Hair Shafts
- Evaluation of androgen receptor gene as a candidate gene in female androgenetic alopecia
- Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses