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Research 481–510 of 1000+
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Gomez?Lopez?Hernandez syndrome: another consideration in focal congenital alopecia
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Roles of steroid sulfatase in brain and other tissues
- Steroid Sulfatase: Molecular Biology, Regulation, and Inhibition
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- 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
- The feasibility and utility of hair follicle sampling to measure FMRP and FMR1 mRNA in children with or without fragile X syndrome: a pilot study
- Sperm aneuploidy in infertile male patients: a systematic review of the literature
- Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
- Time-dependent 53BP1 foci kinetics in X-irradiated human hair follicle dermal papilla cells
- Protective Effect of Conditioned Medium of Immortalized Human Stem Cells from Exfoliated Deciduous Teeth Against Hair Graying Caused by X-Ray Irradiation via Its Antioxidative Activity
- Irradiation-induced hair graying in mice: an experimental model to evaluate the effectiveness of interventions targeting oxidative stress, DNA damage prevention, and cellular senescence
- Sex-Chromosome-Related Dimorphism in Steroidogenic Enzymes and Androgen Receptor in Response to Testosterone Treatment: An In Vitro Study on Human Primary Skeletal Muscle Cells
- Ultrastructural evaluation of the radioprotective effects of melatonin against X‐ray‐induced skin damage in Albino rats
- Do Changes in Chromosomes Cause Aging?
- Sex-limited chromosomes and non-reproductive traits
- Childhood‐onset systemic lupus erythematosus with trisomy X and the increased risk for bone complications: a case report
- Les hormones sexuelles et la peau : questionnaire à l'attention des vétérinaires praticiens. Mise à jour bibliographique et synthèse
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Suppression of Vitamin D Receptor and Induction of Retinoid X Receptor α Expression During Squamous Differentiation of Cultured Keratinocytes
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- Human Adipose-Derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Genome Report: chromosome-scale genome assembly of the African spiny mouse (<i>Acomys cahirinus</i>)
- Marie-unna hereditary hypotrichosis
- Pinkie, the First Viable Germline Hypomorph Allele of Retinoid X Receptor Alpha, Reveals an Important Role for RXRa in Th2 Development.
- British Hair and Nail Society
- Congenital Atrichia: A Case Report