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Research 451–480 of 1000+
- 0441 Systemic autoimmune comorbidity in alopecia totalis and universalis compared with patchy alopecia areata: A retrospective cohort study
- Unraveling the Molecular Mechanism of Bider Marking Formation in Dun Mongolian Horses Through Transcriptome Sequencing
- Genetic Variation in CYP2B6, UGT1A4 and Sulfotransferases Is Associated with Disease-Free Survival in South African Breast Cancer Patients Treated with Tamoxifen
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Genetic Prediction of Eye, Hair, and Skin Color: Forensic Applications and Challenges in Latin American Populations
- A missense mutation in Lama3 causes androgen alopecia
- Bioinformatic analysis of gene expression data reveals Src family protein tyrosine kinases as key players in androgenetic alopecia
- Comparative histomorphometric and transcriptomic analysis reveals potential genetic determinants of pelage variation between hairy and coarse-woolly sheep
- Microneedles as a Promising Technology for Disease Monitoring and Drug Delivery: A Review
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Analysis of Genetic Diversity and Construction of a Core Collection of Ginkgo biloba Germplasm Using EST-SSR Markers
- Uncharted waters
- Regulatory T cell dysfunction and immunotherapeutic breakthroughs in type 1 diabetes
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Detection of a Second KAP22 Family Member in Sheep and Analysis of Its Genetic Variation and Associations with Selected Wool Fibre Traits
- Pharmacogenomic variation and chemotherapy-related toxicity profiles in pediatric patients with cancer in Tanzania: a cross-sectional study
- The Impact of Vitamin D Receptor Gene Polymorphisms (FokI, ApaI, TaqI) in Correlation with Oxidative Stress and Hormonal and Dermatologic Manifestations in Polycystic Ovary Syndrome
- FGF5 is a crucial regulator of hair length in humans
- Recent advances in Forensic DNA Phenotyping of appearance, ancestry and age
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Integrated analysis of lncRNAs and mRNAs by RNA-Seq in secondary hair follicle development and cycling (anagen, catagen and telogen) of Jiangnan cashmere goat (Capra hircus)
- Human Hair Graying Revisited: Principles, Misconceptions, and Key Research Frontiers
- Altered FGF expression profile in human scalp-derived fibroblasts upon WNT activation: implication of their role to provide folliculogenetic microenvironment
- Evo Devo of the Vertebrates Integument
- Hair Growth Regulation by Fibroblast Growth Factor 12 (FGF12)
- The Historical Studies Underpinning the Concept of Hair Follicle Neogenesis
- Assessment of hair and cashmere properties and their genetic background of several goat breeds in Southwest China
- The Rotterdam Study: objectives and design update
- 2022 Update on Prostate Cancer Epidemiology and Risk Factors—A Systematic Review
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities