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Research 931–960 of 1000+
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Replicative stress, stem cells and aging
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Beauty is skin deep: the fascinating biology of the epidermis and its appendages.
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Lamins in development, tissue maintenance and stress
- Delayed epidermal permeability barrier formation and hair follicle aberrations in Inv-Cldn6 mice
- AGD1, a class 1 ARF‐GAP, acts in common signaling pathways with phosphoinositide metabolism and the actin cytoskeleton in controlling Arabidopsis root hair polarity
- Signature selection analysis reveals candidate genes associated with production traits in Iranian sheep breeds
- 46,XY DSD due to impaired androgen production
- In Vitro Differences Between Keratinocyte Stem Cells and Transit-Amplifying Cells of the Human Hair Follicle
- The prevalence of idiopathic hirsutism and polycystic ovary syndrome in the Tehran Lipid and Glucose Study
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- JunB defines functional and structural integrity of the epidermo-pilosebaceous unit in the skin
- Goat Genomic Resources: The Search for Genes Associated with Its Economic Traits
- Long COVID: Clinical characteristics, proposed pathogenesis and potential therapeutic targets
- Macrophages are necessary for skin regeneration during tissue expansion
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- LHX2 is a direct NF-κB target gene that promotes primary hair follicle placode down-growth
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Myotonic Dystrophy—A Progeroid Disease?
- No Evidence that 2D:4D is Related to the Number of CAG Repeats in the Androgen Receptor Gene
- Comparison of clinical and laboratory characteristics of cases with polycystic ovarian syndrome based on Rotterdam’s criteria and women whose only clinical signs are oligo/anovulation or hirsutism
- Aromatase deficiency in a male patient - Case report and review of the literature.
- The bright side of fibroblasts: molecular signature and regenerative cues in major organs
- Understanding the role of prostaglandin E2 in regulating human platelet activity in health and disease
- Targeted expression of activated erbB-2 to the epidermis of transgenic mice elicits striking developmental abnormalities in the epidermis and hair follicles.
- Polycystic Ovarian Syndrome: Long-Term Health Consequences