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Research 661–690 of 1000+
- Development of Heritable Melanoma in Transgenic Mice
- Viral-associated trichodysplasia spinulosa: a case with electron microscopic and molecular detection of the trichodysplasia spinulosa-associated human polyomavirus
- Replicative stress, stem cells and aging
- New clinico‐genetic classification of trichothiodystrophy
- Human Hair Follicle Benzo[a]pyrene and Benzo[a]pyrene 7,8-diol Metabolism: Effect of Exposure to a Coal Tar-Containing Shampoo
- The Paradox of p53: What, How, and Why?
- Lamins in development, tissue maintenance and stress
- Suppression of fibroblast proliferation and lysyl hydroxylase activity by minoxidil.
- Direct Effects of Minoxidil on Epidermal Cells in Culture
- Notch Signaling Regulates Late-Stage Epidermal Differentiation and Maintains Postnatal Hair Cycle Homeostasis
- The Majority of Multipotent Epidermal Stem Cells Do Not Protect Their Genome by Asymmetrical Chromosome Segregation
- c-MYC-Induced Sebaceous Gland Differentiation Is Controlled by an Androgen Receptor/p53 Axis
- Murine skin as a target for melatonin bioregulation
- A neuroendocrinological perspective on human hair follicle pigmentation
- Growth of secondary hair follicles of the Cashmere goat in vitro and their response to prolactin and melatonin.
- Clock genes, hair growth and aging
- Modulation of Dermal Cell Activity During Hair Growth in the Rat
- Role of the vitamin D receptor in hair follicle biology
- Human KAP Genes, Only the Half of it? Extensive Size Polymorphisms in Hair Keratin-Associated Protein Genes
- Vitamin D Receptor, UVR, and Skin Cancer: A Potential Protective Mechanism
- Androgen-Dependent Beard Dermal Papilla Cells Secrete Autocrine Growth Factor(s) in Response to Testosterone Unlike Scalp Cells
- Evaluation of hydro-alcoholic extract of Eclipta alba for its anticancer potential: An in vitro study
- Do Changes in Chromosomes Cause Aging?
- Abnormal epigenetic modifications in peripheral blood mononuclear cells from patients with alopecia areata
- Hair Defects and Pup Loss in Mice with Targeted Deletion of the First Cut Repeat Domain of theCux/CDPHomeoprotein Gene
- Myotonic Dystrophy—A Progeroid Disease?
- Integrated Analysis of Methylome and Transcriptome Changes Reveals the Underlying Regulatory Signatures Driving Curly Wool Transformation in Chinese Zhongwei Goats
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- Polarity signaling ensures epidermal homeostasis by coupling cellular mechanics and genomic integrity
- A primer for studying cell cycle dynamics of the human hair follicle