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Research 241–270 of 1000+
- Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Dermatologic care of patients with differences of sex development
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- The role of mutations on gene AR, in androgenetic alopecia syndrome
- Exploring climate adaptation in European Merino sheep: a landscape genomics approach
- Improving human forensics through advances in genetics, genomics and molecular biology
- Mutation of the doublecortin gene in male patients with double cortex syndrome: Somatic mosaicism detected by hair root analysis
- Gene Expression of Mouse S100A3, a Cysteine-Rich Calcium-Binding Protein, in Developing Hair Follicle
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Clinical Case Notes. Tamoxifen optic neuropathy
- Pallister-Killian Syndrome
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- Characterization of Hair Follicles in Hirosaki Hairless Rats with Deletion of Basic Hair Keratin Genes. Enlarged Medulla, Loss of Cuticle and Long Catagen
- Genetics of Diabetes in Childhood
- Hair follicle-specific keratins and their diseases
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- Androgen receptors and their biology
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- Identification and sequence analysis of the keratin-associated protein 24‐1 (KAP24-1) gene homologue in sheep
- Epidermal Differentiation Complex: A Review on Its Epigenetic Regulation and Potential Drug Targets.
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy
- Genetic correlation analysis does not associate male pattern baldness with COVID-19
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Cutaneous signals of immune system disease
- This Month in the Journal