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Research 361–390 of 1000+
- Human Hair Graying Revisited: Principles, Misconceptions, and Key Research Frontiers
- Assessment of hair and cashmere properties and their genetic background of several goat breeds in Southwest China
- Spectrum of Phenotypes Associated with Human MC1R Variations
- Genetic Tools for Cell Lineage Tracing and Profiling Developmental Trajectories in the Skin
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Tracking the Path of the Original: A Forensic Genetic, Demographic, and Legal Audit of the Muur Continuity Hypothesis
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Evaluation of the Relationship between Alopecia Areata and Viral Antigen Exposure
- Two-Stage Machine Learning-Based GWAS for Wool Traits in Central Anatolian Merino Sheep
- Evaluation of loci to predict ear morphology using two SNaPshot assays
- Epigenetics of Colorectal Cancer
- Evaluation of noninvasive biospecimens for transcriptome studies
- Data-driven strategies for drug repurposing: insights, recommendations, and case studies
- A Clinical Genetics-Driven Dual Diagnosis of Prader–Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL
- Molecular monitoring of short- and long-term transcriptional effects of hair growth stimulating agents
- Wound repair at a glance
- Identification of reptilian genes encoding hair keratin-like proteins suggests a new scenario for the evolutionary origin of hair
- Genomic Surveillance Reveals the Rapid Expansion of the XBB Lineage among Circulating SARS-CoV-2 Omicron Lineages in Southeastern Wisconsin, USA
- Time-dependent 53BP1 foci kinetics in X-irradiated human hair follicle dermal papilla cells
- Evolution and genetic architecture of sex-limited polymorphism in cuckoos
- Androgenic Alopecia: Cross-Talk Between Cell Signal Transduction Pathways
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Activator Protein-1 Activity Regulates Epithelial Tumor Cell Identity
- Recent Advances in Biopolymeric Composite Materials for Tissue Engineering and Regenerative Medicines: A Review
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- An Integrated Transcriptome Atlas of Embryonic Hair Follicle Progenitors, Their Niche, and the Developing Skin
- Hair follicle gene expression profiling in the SubPopulations and InteRmediate Outcome Measures in COPD Study (SPIROMICS)
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita