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Research 451–480 of 1000+
- Regulation of feather follicle development and Msx2 gene SNP degradation in Hungarian white goose
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- A computationally inferred regulatory heart aging model including post-transcriptional regulations
- Woolly Antics between the Sheaths
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- SPT6 maintains epidermal homeostasis by inhibiting an NF-κB-positive feedback loop to prevent excessive inflammation
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Spatiotemporal Expression and Haplotypes Identification of KRT84 Gene and Their Association with Wool Traits in Gansu Alpine Fine-Wool Sheep
- Congenital Atrichia: A Case Report
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- 9. Immunology and Genetics
- Melanocytes: The new Black
- Neuronal plasticity of the “brain–skin connection”: stress-triggered up-regulation of neuropeptides in dorsal root ganglia and skin via nerve growth factor-dependent pathways
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- Alopecia Areata
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- Pediatric Psychocutaneous Disorders
- Improving selective androgen receptor modulator discovery and preclinical evaluation
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Comparison of mitochondrial transplantation by using a stamp-type multineedle injector and platelet-rich plasma therapy for hair aging in naturally aging mice
- Deep phenotyping of skin tissue remodeling in patients with systemic sclerosis treated with CD19-CAR T cells
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- Histological and immunohistochemical examination of the effect of the nonsteroidal antiandrogen {flutamide} on some organs of the male reproductive system in albino rats
- 5-Alpha reductase deficiency
- Dicer- and BSC-dependent miRNAs during murine anagen development