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Research 181–210 of 1000+
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Past, Present and Future Perspectives of Forensic Genetics
- Mitochondrial DNA Variation in Human Hair Shafts Influenced by Physical Characteristics: A Massively Parallel Sequencing Analysis
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- Agouti and Agouti-related Protein: Analogies and Contrasts
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review
- Myotonic Dystrophy—A Progeroid Disease?
- High-coverage genome of the Tyrolean Iceman reveals unusually high Anatolian farmer ancestry
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- The immune response to COVID‐19: Does sex matter?
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women
- Genetic Control/Involvement in Hair Fiber Traits
- Dyslipidaemia in women with polycystic ovary syndrome referred to a teaching hospital in Cape Town, South Africa
- Regulation and dysregulation of hair regeneration: aiming for clinical application
- Human Pigmentation: A Review of Molecular Mechanisms, Genetic Architecture, Evolution, Forensic DNA Phenotyping and Health Implications
- Role of Aire and Notch4 Allelic Mutations in Alopecia Areata in C3H/HeJ Mice
- Exosome-based Therapies for Androgenetic Alopecia: Mechanisms, MicroRNAs, and Clinical Prospects
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- Genetic architecture of thermotolerance traits in beef cattle: a novel integration of SNP and breed-of-origin effects
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- Recent Updates of the CRISPR/Cas9 Genome Editing System: Novel Approaches to Regulate Its Spatiotemporal Control by Genetic and Physicochemical Strategies
- Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study
- A missense mutation in Lama3 causes androgen alopecia
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Loss of the Y Chromosome: A Review of Molecular Mechanisms, Age Inference, and Implications for Men’s Health
- Sex-limited chromosomes and non-reproductive traits