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Research 241–270 of 1000+
- Dermatologic care of patients with differences of sex development
- Improving human forensics through advances in genetics, genomics and molecular biology
- Immune mechanisms associated with sex-based differences in severe COVID-19 clinical outcomes
- Characterisation of an Ovine Keratin Associated Protein (KAP) Gene, Which Would Produce a Protein Rich in Glycine and Tyrosine, but Lacking in Cysteine
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Sex- or Gender-specific Differences in the Clinical Presentation, Outcome, and Treatment of SARS-CoV-2
- Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- The role of mutations on gene AR, in androgenetic alopecia syndrome
- Copy number variation regions in Nellore cattle: Evidences of environment adaptation
- SUN-069 A 14 Year Old Female with Primary Amenorrhea
- Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with <i>MCHR2</i>
- Molecular basis of androgen insensitivity
- Androgens and hair loss
- 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
- Pallister-Killian Syndrome
- Resequencing and Signatures of Selective Scans Point to Candidate Genetic Variants for Hair Length Traits in Long-Haired and Normal-Haired Tianzhu White Yak
- Genetics of Diabetes in Childhood
- Human Hair Keratin‐Associated Proteins (KAPs)
- 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
- Terrestrial vertebrates have two keratin gene clusters; striking differences in teleost fish
- 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
- Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy
- Congenital atrichia with papular lesions
- Fetal alpha 5-reductase Val89Leu mutation is associated with late miscarriage
- Cutaneous signals of immune system disease