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Research 571–600 of 1000+
- Two-ligand priming mechanism for potentiated phosphoinositide synthesis is an evolutionarily conserved feature of Sec14-like phosphatidylinositol and phosphatidylcholine exchange proteins
- Autoimmune Diseases and Acquired Von Willebrand Disease in Two Cases of Progeria
- Epigenetics of Colorectal Cancer
- Quaternary ammonium iminofullerenes improve root growth of oxidative-stress maize through ASA-GSH cycle modulating redox homeostasis of roots and ROS-mediated root-hair elongation
- Merkel cell carcinoma: updates in tumor biology, emerging therapies, and preclinical models
- A Simple In Vivo System for Studying Epithelialization, Hair Follicle Formation, and Invasion Using Primary Epidermal Cells from Wild-Type and Transgenic Ornithine Decarboxylase-Overexpressing Mouse Skin
- Genetics of Wool and Cashmere Fibre: Progress, Challenges, and Future Research
- Therapeutic Values of Exosomes in Cosmetics, Skin Care, Tissue Regeneration, and Dermatological Diseases
- Neural, adipocyte and hepatic differentiation potential of primary and secondary hair follicle stem cells isolated from Arbas Cashmere goats
- Combined Molecular Hydrogen and Vitamin C Treatment in Irradiated Normal and Cancer Cell Models: An Exploratory In Vitro Study and Case Reports
- 802 Molecular effect of brepocitinib in hidradenitis suppurativa (HS)
- Finasteride delays atherosclerosis progression in mice and is associated with a reduction in plasma cholesterol in men
- Author response: Loss of Dnmt3a and Dnmt3b does not affect epidermal homeostasis but promotes squamous transformation through PPAR-γ
- The role of reactive oxygen species in cell growth: lessons from root hairs
- The Krüppel-like Factor Epiprofin Is Expressed by Epithelium of Developing Teeth, Hair Follicles, and Limb Buds and Promotes Cell Proliferation
- Expression of COUP-TF-interacting protein 2 (CTIP2) in mouse skin during development and in adulthood
- Roles for Msx and Dlx homeoproteins in vertebrate development
- Conditional knock out of N-WASP in keratinocytes causes skin barrier defects and atopic dermatitis-like inflammation
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Predominant expression of 5 alpha-reductase type 1 in pubic skin from normal subjects and hirsute patients.
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- Hair Growth Defects of Diabetic and Hypercholesterolemic Wistar Albino Rats and Amelioration of Fish Oil-Treatment
- 412 High amphiregulin expression is a high-risk feature of acute graft-versus-host disease of the skin
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Vestibular Hair Cell Regeneration and Restoration of Balance Function Induced by Math1 Gene Transfer
- Keratin disorders: from gene to therapy
- Differential expression and functionality of ATP-binding cassette transporters in the human hair follicle
- Expression of AKT1 along with AKT2 in granulosa-lutein cells of hyperandrogenic PCOS patients
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- CD4 expression controls epidermal stem cell balance