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Research 30 of 258
- Tricotiodistrofia. Reporte de un caso
- Melanogenesis is coupled to murine anagen: Toward new concepts for the role of melanocytes and the regulation of melanogenesis in hair growth
- Lamellar ichthyosis, dwarfism, mental retardation, and hair shaft abnormalities
- A role of melatonin in neuroectodermal‐mesodermal interactions: the hair follicle synthesizes melatonin and expresses functional melatonin receptors
- Trichothiodystrophy without associated neuroectodermal features in two siblings
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Enrichment and Characterization of Human Dermal Stem/Progenitor Cells by Intracellular Granularity
- Feasibility of repairing full-thickness skin defects by iPSC-derived epithelial stem cells seeded on a human acellular amniotic membrane
- Defining the identity of mouse embryonic dermal fibroblasts
- HAIR AND SYSTEMATIC DISEASE
- Hair Loss in Children
- Ppp2r2a Knockout Mice Reveal That Protein Phosphatase 2A Regulatory Subunit, PP2A-B55α, Is an Essential Regulator of Neuronal and Epidermal Embryonic Development
- An overview on congenital alopecia in domestic animals
- TTNPB Promotes Human Pluripotent Stem Cell‐to‐Neural Stem Cell Transition via Modulation of Chromatin Accessibility and the S‐(5′‐adenosyl)‐L‐homocysteine/Choline Metabolic Network
- Biology of melanocytes in mammals
- Disorders of hair
- Diagnosis of an indistinct Leydig cell tumor by positron emission tomography-computed tomography
- Metastatic Melanoma of the Tongue: A Rare Case
- Trichothiodystrophy: Current Concepts
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Trichoscopy in Hair Shaft Disorders
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- New clinico‐genetic classification of trichothiodystrophy
- Lysophospholipid Mediators in Health and Disease
- AN UPDATE OF HAIR SHAFT DISORDERS
- UDP-GlcNAc-1-Phosphotransferase Is a Clinically Important Regulator of Human and Mouse Hair Pigmentation
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Usefulness of Dermoscopy to Provide Accurate Assessment of Skin Cancers
- Scalp Involvement in Primary Cutaneous Lymphomas—An Update on Clinical Presentation, Diagnostics, and Management