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Research 451–480 of 1000+
- Nrf2-Mediated Expansion of Pilosebaceous Cells Accelerates Cutaneous Wound Healing
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Skin disease related to metabolic syndrome in women
- Selection signatures of wool color in Gangba sheep revealed by genome-wide SNP discovery
- Predicting Human Appearance from DNA for Forensic Investigations
- Study of the Thyroid Profile of Patients with Alopecia
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Causal Relationship Between Sleep Characteristics and Alopecia Areata and Other Non-Scarring Alopecia: A Two-Sample Bidirectional Mendelian Randomization Analysis
- Genomic Markers and Personalized Medicine in Androgenetic Alopecia: A Comprehensive Review
- Author response: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Regulatory pathways implicated in male androgenetic alopecia pathogenesis
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Keratin disorders: from gene to therapy
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Regulation of masculinization: androgen signalling for external genitalia development
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- FOXN1 deficient nude severe combined immunodeficiency
- Activation of AR Sensitizes Breast Carcinomas to NVP-BEZ235's Therapeutic Effect Mediated by PTEN and KLLN Upregulation
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- Regulatory pathway analysis of coat color genes in Mongolian horses
- Effects of SLC45A2 and GPNMB on Melanin Deposition Based on Transcriptome Sequencing in Chicken Feather Follicles
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Safety of Whole-Body Abrogation of the TRF1 Shelterin Protein in Wild-Type and Cancer-Prone Mouse Models
- Trichothiodystrophy: Current Concepts
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures