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Research 841–870 of 1000+
- Lack of association between Vitamin D receptor FokI polymorphism and alopecia areata.
- Malignant Melanoma and Its Stromal Nonimmune Microecosystem
- Establishment of Tsc2-deficient rat embryonic stem cells
- Genetic Tools for Cell Lineage Tracing and Profiling Developmental Trajectories in the Skin
- Severe metabolic disorders coexisting with Werner syndrome: a case report
- Cultured Human Foreskin as a Model System for Evaluating Ionizing Radiation-Induced Skin Injury
- Combining multiomics to analyze the molecular mechanism of hair follicle cycle change in cashmere goats from Inner Mongolia
- Human hair production by scalp samples grafted onto nude mice. Biochemical data on normal human hair and the genetic defect trichothiodystrophy
- Synopsis: 2005 Annual Meeting of the American Society of Andrology
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Study on the expression patterns of inner root sheath-specific genes in Tan sheep hair follicle during different developmental stages
- Chemically induced skin tumors arise from long-lived stem cells of the upper hair follicle
- Mimicking Senescence Factors to Characterize the Mechanisms Responsible for Hair Regression and Hair Loss: An In Vitro Study
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- Regulation of Hair Follicle Growth and Development by Different Alternative Spliceosomes of FGF5 in Rabbits
- CRISPR/Cas9: A Promising Approach for Alopecia
- mRNA Levels of Aromatase, 5α-Reductase Isozymes, and Prostate Cancer-Related Genes in Plucked Hair from Young Men with Androgenic Alopecia
- Advantages of Incomplete Digestion in Human Hair Shaft Proteomics, a Focus on Cuticular Keratins
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- 712 Using scanning electron microscopy to elucidate the role of hair shaft malformation in the pathogenesis of Central Centrifugal Cicatricial Alopecia
- Divergent neuroactive steroid responses to stress and ethanol in rat and mouse strains: relevance for human studies
- Are sex hormones promising candidates to explain sex disparities in the COVID-19 pandemic?
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Genetic Basis of Male Pattern Baldness
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Agouti and Agouti-related Protein: Analogies and Contrasts
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71