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Research 751–780 of 1000+
- Faculty Opinions recommendation of Conditional telomerase induction causes proliferation of hair follicle stem cells.
- An interview Drs. Felix Brockschmidt and Markus Nöthen about the genetics of androgenetic alopecia
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Drug Repositioning: New Approaches and Future Prospects for Life-Debilitating Diseases and the COVID-19 Pandemic Outbreak
- The Tissue-dependent Keratin 19 Gene Transcription Is Regulated by GKLF/KLF4 and Sp1
- A Nonredundant Human Protein Chip for Antibody Screening and Serum Profiling
- The Krüppel-like Factor Epiprofin Is Expressed by Epithelium of Developing Teeth, Hair Follicles, and Limb Buds and Promotes Cell Proliferation
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Activation of TRPV3 Regulates Inflammatory Actions of Human Epidermal Keratinocytes
- PRC 2 preserves intestinal progenitors and restricts secretory lineage commitment
- Biomarkers of alopecia areata disease activity and response to corticosteroid treatment
- Vitamin D Concentrations are Decreased in Patients with Alopecia Areata
- Acceptance of COVID-19 Vaccine Booster Doses Using the Health Belief Model: A Cross-Sectional Study in Low-Middle- and High-Income Countries of the East Mediterranean Region
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Long and short non-coding RNA and radiation response: a review
- Role of OsPHR2 on phosphorus homoestasis and root hairs development in rice (<i>Oryza sativa</i>L.)
- Establishment and characterization of a canine keratinocyte organoid culture system
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Gene trajectory inference for single-cell data by optimal transport metrics
- Elevated <em>DKK1</em> expression is an independent unfavorable prognostic indicator of survival in head and neck squamous cell carcinoma
- The Genetics of Human Skin Disease
- Profibrotic Subsets of SPP1+ Macrophages and POSTN+ Fibroblasts Contribute to Fibrotic Scarring in Acne Keloidalis
- The Molecular Biology of the Vitamin D Receptor
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene
- Epigenetic age estimation in saliva and in buccal cells
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Variation in the ovine keratin-associated protein 15-1 gene affects wool yield
- Molecular basis of congenital atrichia in humans and mice.