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Research 181–210 of 1000+
- Establishing an Evidence-Based System for Cosmetic Safety and Efficacy Evaluation
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- A 4kb Fragment of the Desmocollin 3 Promoter Directs Reporter Gene Expression to Parakeratotic Epidermis and Primary Hair Follicles
- The Genetic Landscape of Androgenetic Alopecia: Current Knowledge and Future Perspectives
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- Sequencing KRT71 as a candidate gene for hair shape variation in dromedary camels
- Melanocytes in regenerative medicine applications and disease modeling
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Ehlers-Danlos syndrome: From bedside to bench
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- The imbalance between Type 17 T-cells and regulatory immune cell subsets in psoriasis vulgaris
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Werner's syndrome: incidental finding during pregnancy
- Exploring the efficacy evaluation model for androgenic alopecia using hair organoids: Transcending conventional hair research
- Research Progress on Construction Technology of 3D Human Skin Models and Its Application Prospects in Dermatology
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Tumor Necrosis Factor-Alpha and Polycystic Ovarian Syndrome: A Clinical, Biochemical, and Molecular Genetic Study
- Comparative study on seasonal hair follicle cycling by analysis of the transcriptomes from cashmere and milk goats
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Birt-Hogg-Dube Syndrome with a Novel Mutation in the <i>FLCN</i> Gene
- Transcriptome-based selection and validation of optimal house-keeping genes for skin research in goats (Capra hircus)
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Gene expression profiling of intestinal regeneration in the sea cucumber
- Increased rate of hair keratin gene loss in the cetacean lineage
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- High-coverage genome of the Tyrolean Iceman reveals unusually high Anatolian farmer ancestry
- Integrated miRNA-mRNA analysis reveals regulatory pathways underlying the curly fleece trait in Chinese tan sheep