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Research 151–180 of 548
- A case of monilethrix caused by novel compound heterozygous mutations in the desmoglein 4 (DSG4) gene
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Genetics of Structural Hair Disorders
- PA05 A rare case of cardiocutaneous syndrome in a young child
- Transcriptome Profiling of Pilosebaceous Units in Male Androgenetic Alopecia Reveals Altered Junctional Networks
- Structural and biochemical changes underlying a keratoderma-like phenotype in mice lacking suprabasal AP1 transcription factor function
- 441 RPGRIP1L facilitates desmosomal adhesion through suppressing PKCβII-mediated desmoglein endocytosis: Implication in pemphigus
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Novel compound heterozygous mutations in the<i>desmoplakin</i>gene cause hair shaft abnormalities and culminate in lethal cardiomyopathy
- Increased expression of keratin 16 causes anomalies in cytoarchitecture and keratinization in transgenic mouse skin.
- Pseudo Pemphigus Phenotypes in Mice with Inactivated Desmoglein 3
- 14-3-3σ Is Required for Club Hair Retention
- LB1076 Using the frog embryonic epidermis as a model to study desmosome function during development
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Newborn infant skin gene expression: Remarkable differences versus adults
- Meta-Analysis of Gene Expression Reveals the Core Transcriptomic Profile of Lesional Scalp in Alopecia Areata
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- An Intrinsic Oscillation of Gene Networks Inside Hair Follicle Stem Cells: An Additional Layer That Can Modulate Hair Stem Cell Activities
- MOF-mediated histone H4 Lysine 16 acetylation governs mitochondrial and ciliary functions by controlling gene promoters
- LB1081 Three-dimensional imaging of tight junction-network across multiple layers of human epidermis by array tomography using backscattered electron-mode scanning electron microscopy
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Learning from nudity: lessons from the nude phenotype
- Regulation of Hair Shedding by the Type 3 IP3 Receptor
- Desmosomes in Developing Human Epidermis
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- A desmosomal cadherin controls multipotent hair follicle stem cell quiescence and orchestrates regeneration through adhesion signaling
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Planar cell polarity effector gene Intu regulates cell fate-specific differentiation of keratinocytes through the primary cilia
- Defining stem cell dynamics and migration during wound healing in mouse skin epidermis