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Research 31–60 of 1000+
- Somatic mutations distinguish melanocyte subpopulations in human skin
- Activation of the integrated stress response in human hair follicles
- Surface modification and endothelialization of biomaterials as potential scaffolds for vascular tissue engineering applications
- Melatonin-Loaded Nanocarriers: New Horizons for Therapeutic Applications
- Stem Cells Therapies in Basic Science and Translational Medicine: Current Status and Treatment Monitoring Strategies
- γδ17 T cell-stromal networks modulate matrix composition and vascularity in foreign body response
- Natural products and their derivatives as candidate treatments for hair greying: from drug discovery to molecular mechanisms
- Physiopathological role of the enzymatic complex 5α-reductase and 3α/β-hydroxysteroid oxidoreductase in the generation of progesterone and testosterone neuroactive metabolites
- LncRNA-000133 from secondary hair follicle of Cashmere goat: identification, regulatory network and its effects on inductive property of dermal papilla cells
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- Temporal Layering of Signaling Effectors Drives Chromatin Remodeling during Hair Follicle Stem Cell Lineage Progression
- Venus trap in the mouse embryo reveals distinct molecular dynamics underlying specification of first embryonic lineages
- Non-viral delivery of the CRISPR/Cas system: DNA<i>versus</i>RNA<i>versus</i>RNP
- Skin regional specification and higher-order <i>HoxC</i> regulation
- Regulatory T cells in dominant immunologic tolerance
- Targeting the Hippo/YAP/TAZ signalling pathway: Novel opportunities for therapeutic interventions into skin cancers
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- A Novel Marker of Tissue Junctions, Collagen XXII
- Transcriptional Characteristics Showed That miR-144-y/FOXO3 Participates in Embryonic Skin and Feather Follicle Development in Zhedong White Goose
- Neuregulin3 alters cell fate in the epidermis and mammary gland
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- A functional role of S100A4/non-muscle myosin IIA axis for pro-tumorigenic vascular functions in glioblastoma
- Chirality Effect on Physical and Biological Properties of Peptide-Based Hydrogels
- Steroid Sulfatase Deficiency and Androgen Activation Before and After Puberty
- Loss of the Y Chromosome: A Review of Molecular Mechanisms, Age Inference, and Implications for Men’s Health
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Genetic Variation in CYP2B6, UGT1A4 and Sulfotransferases Is Associated with Disease-Free Survival in South African Breast Cancer Patients Treated with Tamoxifen
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation