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Research 541–570 of 1000+
- Understanding the Secular Decline in Testosterone: Mechanisms, Consequences, and Clinical Perspectives
- Predicting Physical Appearance from Low Template: State of the Art and Future Perspectives
- Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- FORENSIC DNA PHENOTYPING FOR CRIMINAL IDENTIFICATION
- E-Poster
- Whole-Genome Resequencing Reveals Selection Signal Related to Sheep Wool Fineness
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay
- Meeting Report: 68th Montagna Symposium on the Biology of Skin “Decoding Complex Skin Diseases: Integrating Genetics, Genomics, and Disease Biology”
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Establishment of type II 5α-reductase over-expressing cell line as an inhibitor screening model
- Alleviation of Severe Skin Insults Following High-Dose Irradiation with Isolated Human Fetal Placental Stromal Cells
- Finasteride and male infertility: a case for prospective collaborative research databases?
- Gastric cancer; actualities and perspectives of early diagnosis and targeted therapy
- The cDNA-deduced amino acid sequence for trichohyalin, a differentiation marker in the hair follicle, contains a 23 amino acid repeat.
- Lentiviral Arrays for Live-cell Dynamic Monitoring of Gene and Pathway Activity During Stem Cell Differentiation
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- <i>Pseudomonas aeruginosa</i> heme metabolites biliverdin IXβ and IXδ are integral to lifestyle adaptations associated with chronic infection
- Systematic investigation of a potential epidemiological and genetic association between male androgenetic alopecia and COVID‐19
- Finasteride and Dutasteride for the Treatment of Male Androgenetic Alopecia: A Review of Efficacy and Reproductive Adverse Effects
- Abstracts from the 4th Annual Student Medical Summit
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- BJD Editor's Choice
- Gonadal Dysgenesis: Associations between Clinical Features and Sex of Rearing.
- A preliminary study of finasteride in Tourette syndrome
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I