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Research 571–600 of 1000+
- 836 Applying FACS-based single cell RNA-seq to study neonatal mouse skin
- Immune signatures of psoriasis: Comparison of genetic expression profiles in psoriasis patients after therapy with biologic agents
- Faculty Opinions recommendation of Lrig1 expression defines a distinct multipotent stem cell population in mammalian epidermis.
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- MLL histone methylases in estrogen‐mediated regulation of HOX genes involved in hair follicle development and leukemia
- Necrosulfonamide promotes hair growth and ameliorates DHT-induced hair growth inhibition
- Tracing the cellular origin of cancer
- 176 Myeloid cell-specific deletion of mTOR suppresses psoriasis-like skin inflammation in C57BL/6 mice
- Genetically determined metabolites in allergic conjunctivitis: A Mendelian randomization study
- POLYCOMB REPRESSIVE COMPLEX 1 IS REQUIRED TO MAINTAIN STEM CELL IDENTITY AND TO PRESERVE ADULT TISSUE HOMEOSTASIS.
- Population and Individual Stem Cell Dynamics in the Olfactory Epithelium
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- Clinical and molecular genetic studies in hereditary hair loss
- c-Myc activation in transgenic mouse epidermis results in mobilization of stem cells and differentiation of their progeny
- Transcriptome and proteome characterization of surface ectoderm cells differentiated from human iPSCs
- ILK modulates epithelial polarity and matrix formation in hair follicles
- Loss of ‘Epidermal Melanin Unit’ Integrity in Human Skin During Melanoma-Genesis
- Hair Protein Polymorphism and Its Application to Forensic Science Hair Comparison.
- Molecular and spatial design of early skin development
- Dermal Adnexal Neoplasms: Exploring Rare Variants and Their Clinical Behavior
- Single-Cell Transcriptomics to Map Cellular Heterogeneity in Tissue Regeneration Models
- BEYOND HAIR LOSS: EXPLORING THE EVOLUTION OF ANDROGENETIC ALOPECIA RESEARCH BASED ON TEXT MINING AND BIBLIOMETRICS