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Research 931–960 of 1000+
- Oral gabapentin for scalp pruritus in patients with lichen planopilaris: A case series
- Chemically induced skin tumors arise from long-lived stem cells of the upper hair follicle
- Aligning Stem Cell Models and Postmortem Studies to Query Striatal Neurodevelopment in Schizophrenia
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Clinical cases of Darier-White follicular dyskeratosis
- Faculty Opinions recommendation of Nonviral in situ green fluorescent protein labeling and culture of primary, adult human hair follicle epithelial progenitor cells.
- Genetic analysis of the role of androgen metabolism in the pathogenesis of prostate cancer
- Dermal PapillaCell-Derived Exosomes Regulate Hair Follicle Stem Cell Proliferation via LEF1
- p63 regulates <i>Satb1</i> to control tissue-specific chromatin remodeling during development of the epidermis
- Temporal Layering of Signaling Effectors Drives Chromatin Remodeling during Hair Follicle Stem Cell Lineage Progression
- GRHL3 binding and enhancers rearrange as epidermal keratinocytes transition between functional states
- Restoration of Spermatogenesis and Male Fertility Using an Androgen Receptor Transgene
- Developmental and evolutionary comparative analysis of a regulatory landscape in mouse and chicken
- Examination of epigenetic inhibitor zebularine in treatment of skin wounds in healthy and diabetic mice
- H3K9me3 controls epidermis morphogenesis by regulating RNA Pol II dynamics at developmental promoters and enhancers
- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog
- Molecular Mechanisms Regulating Hair Follicle Development
- The Catalog of Human Hair Keratins
- Hyperactivation of sympathetic nerves drives depletion of melanocyte stem cells
- Cell-Type-Specific Chromatin States Differentially Prime Squamous Cell Carcinoma Tumor-Initiating Cells for Epithelial to Mesenchymal Transition
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Expression of hair-related keratins in a soft epithelium: Subpopulations of human and mouse dorsal tongue keratinocytes express keratin markers for hair-, skin- and esophageal-types of differentiation
- The role of fibroblast growth factor receptor 2b in skin homeostasis and cancer development
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- PandaOmics: An AI-Driven Platform for Therapeutic Target and Biomarker Discovery
- Retinol Esterification by DGAT1 Is Essential for Retinoid Homeostasis in Murine Skin
- Human Female Hair Follicles Are a Direct, Nonclassical Target for Thyroid-Stimulating Hormone
- Six Novel Susceptibility Loci for Early-Onset Androgenetic Alopecia and Their Unexpected Association with Common Diseases
- Towards Defining the Pathogenesis of the Hairless Phenotype