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Research 391–420 of 1000+
- Expression, characterization, and structural analysis of human liver delta4-3-ketosteroid 5beta-reductase (AKR1D1) and its disease-related mutant P133R
- Long non-coding RNA Xist contribution in systemic lupus erythematosus and rheumatoid arthritis
- Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss
- Infertility and teratogenicity after paternal exposure to systemic dermatologic medications: A systematic review
- Change in surface chemistry of the cuticle of human hair by chemical and photochemical oxidation
- Diagnosed with primary adrenal insufficiency? search adrenoleukodystrophy-two brothers presented with similar phenotype
- Dissecting the Molecular Mechanisms Involved in Keloid Pathogenesis and Response to Therapy
- Valence-engineered catalysis-selectivity regulation of molybdenum oxide nanozyme for acute kidney injury therapy and post-cure assessment
- Structural Study of Polymorphs and Solvates of Finasteride
- Three-Dimensional-Bioprinted Non-Small Cell Lung Cancer Models in a Mouse Phantom for Radiotherapy Research
- Multiorgan Dysfunction in a 7-Month-Old Boy With Developmental Delay and Poor Growth
- TRANSTORNOS DISSOCIATIVOS EM PACIENTES VÍTIMAS DE ABUSO SEXUAL NA INFÂNCIA
- Big Self-Supervised Models Advance Medical Image Classification
- A Dispute Between the Cavendish and Caltech: The Emergence and Ubiquity of the α-Helix
- Triton modified polyethyleneimine conjugates assembled with growth arrest-specific protein 6 for androgenetic alopecia transdermal gene therapy
- Enzymatic and non-enzymatic sulfation mechanisms in the biological actions of minoxidil
- Evidence for 1,25-Dihydroxyvitamin D3-independent Transactivation by the Vitamin D Receptor
- The Sex-Linked Histocompatibility Antigens
- Further errors in polymorph identification: furosemide and finasteride
- Direct access to novel chromeno-pyrimidine-N-oxides via tandem base catalyzed double nucleophilic addition/dehydration reaction
- Clinical, Microscopic and Ultrastructural Findings in a Case of Short Anagen Syndrome
- Tail Tales: What We Have Learned About Regeneration from Xenopus Laevis Tadpoles
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- The location of the thioglycolic acid molecules in intrafibrillar unordered areas of the human hair keratin structure
- Structural analysis of human hair single fibres by scanning microbeam SAXS
- Molecular basis of androgen insensitivity
- Vitamin D receptor: molecular signaling and actions of nutritional ligands in disease prevention
- Disturbed Epidermal Structure in Mice with Temporally Controlled Fatp4 Deficiency
- Successful etanercept therapy in therapy refractory acrodermatitis continua suppurativa Hallopeau