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Research 181–210 of 1000+
- Nanotechnology in Cosmetics: An Overview
- Neuroendocrine Controls of Keratin Expression in Human Skin
- WHAT OTHER JOURNALS ARE SAYING
- A Novel Point Mutation in the Ligand-Binding Domain (LBD) of the Human Glucocorticoid Receptor (hGR) Causing Generalized Glucocorticoid Resistance: The Importance of the C Terminus of hGR LBD in Conferring Transactivational Activity
- Altered autonomic neural control of the cardiovascular system in patients with polycystic ovary syndrome
- The Mesenchymal Niche of the Hair Follicle Induces Regeneration by Releasing Primed Progenitors from Inhibitory Effects of Quiescent Stem Cells
- Anaemia and skin disease
- Cronkhite-Canada syndrome associated with colon cancer metastatic to liver
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- Hair, Cutaneous Homeostasis and Stem Cell Functions
- Wound Healing Mechanisms
- CERTAIN PHASES OF SULFUR METABOLISM OF THE SKIN
- Stimulation of ectodermal organ development by Ectodysplasin-A1
- Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report
- Pax9 is required for filiform papilla development and suppresses skin-specific differentiation of the mammalian tongue epithelium
- Lamellar ichthyosis, dwarfism, mental retardation, and hair shaft abnormalities
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Whn and mHa3 are components of the genetic hierarchy controlling hair follicle differentiation
- Comprehensive treatment of Cronkhite-Canada syndrome: A case report and literature review
- An Overview of Growth Factors as the Potential Link between Psoriasis and Metabolic Syndrome
- RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS
- Dysfunction of keratinocyte adhesion
- Short anagen hair syndrome is caused by mutations in the <i>WNT10A</i> gene and has a genetic overlap with male pattern hair loss
- A Very Unusual Cause of Diarrhea in a 60-Year-Old Man
- p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Bone Morphogenetic Protein Antagonist Noggin Promotes Skin Tumorigenesis via Stimulation of the Wnt and Shh Signaling Pathways
- Activated Kras Alters Epidermal Homeostasis of Mouse Skin, Resulting in Redundant Skin and Defective Hair Cycling
- Cosmetics for the elderly
- Micronutrients in hair loss