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Research 91–120 of 387
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Molecular Genetics of Human Hair Diseases
- Hairless down-regulates expression of Msx2 and its related target genes in hair follicles
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Lack of the Vitamin D Receptor is Associated with Reduced Epidermal Differentiation and Hair Follicle Growth
- Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/Spermine N1-Acetyltransferase Overexpression
- The emerging role of cellular senescence in amyotrophic lateral sclerosis
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Ceramide Synthase 4 Regulates Stem Cell Homeostasis and Hair Follicle Cycling
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Mechanical forces across compartments coordinate cell shape and fate transitions to generate tissue architecture
- CD34 <sup>+</sup> cell–derived fibroblast-macrophage cross-talk drives limb ischemia recovery through the OSM-ANGPTL signaling axis
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth
- The Enrichment of Specific Hair Follicle-Associated Cell Populations in Plucked Hairs Offers an Opportunity to Study Gene Expression Underlying Hair Traits
- Current Genetics in Hair Diseases
- Animal and in vitro Models for the Study of Hair Follicles
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Genetic Hair Disorders: A Review
- A Scarless Healing Tale: Comparing Homeostasis and Wound Healing of Oral Mucosa With Skin and Oesophagus
- Resistance to the Insulin and Elevated Level of Androgen: A Major Cause of Polycystic Ovary Syndrome
- Impaired Hair Growth and Wound Healing in Mice Lacking Thyroid Hormone Receptors
- Mice lacking the epidermal retinol dehydrogenases SDR16C5 and SDR16C6 display accelerated hair growth and enlarged meibomian glands
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- The anti‐apoptotic Bcl‐2 protein regulates hair follicle stem cell function
- Frontiers in Topical Photoprotection
- Retinoic acid exerts sexually dimorphic effects on muscle energy metabolism and function
- Epithelial expression of the hormone leptin by bovine skin
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.