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Research 30 of 37
- Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia
- Spanlastic Nano-Vesicles: A Novel Approach to Improve the Dissolution, Bioavailability, and Pharmacokinetic Behavior of Famotidine
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Clinicopathologic and molecular characterization of a series of sporadic trichoblastic neoplasms
- Genetic Prediction of Eye, Hair, and Skin Color: Forensic Applications and Challenges in Latin American Populations
- FGF5 is a crucial regulator of hair length in humans
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Human Hair Graying Revisited: Principles, Misconceptions, and Key Research Frontiers
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- The molecular pathogenesis of Trichilemmal carcinoma
- Basal cell carcinomas acquire secondary mutations to overcome dormancy and progress from microscopic to macroscopic disease
- Loss of the Y Chromosome: A Review of Molecular Mechanisms, Age Inference, and Implications for Men’s Health
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- Developing Patient-Derived 3D-Bioprinting models of pancreatic cancer
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Genetic Variants and Protective Immunity against SARS-CoV-2
- GWASs Identify Genetic Loci Associated with Human Scalp Hair Whorl Direction
- Exome analysis for Cronkhite-Canada syndrome: A case report
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Spectrophotometric and Stability Indicating RP-HPLC-PDA method for Simultaneous Determination of Finasteride and Tamsulosin in Combined Tablet Dosage form
- Aberrant Activation of the Hedgehog Pathway in Cutaneous Melanoma: Therapeutic Potential of Pharmacological Inhibitors
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review