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Research 91–120 of 1000+
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
- Transcription factor-based transdifferentiation of human embryonic to trophoblast stem cells
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- The diversity of sex development: What do conditions affecting sex development teach us about sexual diversity?
- Detection of circular RNA expression and related quantitative trait loci in the human dorsolateral prefrontal cortex
- Androgenetic alopecia: Identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology
- Matriptase: Potent Proteolysis on the Cell Surface
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation
- Sex differences in the hypothalamic–pituitary–adrenal axis’ response to stress: an important role for gonadal hormones
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Molecular Targets in Modern Cosmetic Science
- Skin Pigmentation Types, Causes and Treatment—A Review
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA
- Androgen receptors and their biology
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Zebrafish Model of Hereditary Pigmentary Disorders
- COVID-19: The question of genetic diversity and therapeutic intervention approaches
- Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Chapter 6. Darwinian Health and Other Contradictions
- Thymosin β4 Promotes Dermal Healing
- Alopecia Areata
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- Human Leukocyte Antigen Class II Alleles Are Associated with Risk of Alopecia Areata
- An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin