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Research 451–480 of 1000+
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
- Depletion of <i>Gsdma1/2/3</i> alleviates PMA-induced epidermal hyperplasia by inhibiting the EGFR–Stat3/Akt pathway
- Genetic Control/Involvement in Hair Fiber Traits
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Mechanisms of aluminium toxicity, tolerance and amelioration in wheat
- Distinct Phenotypic and Genomic Signatures Underlie Contrasting Pathogenic Potential of Staphylococcus epidermidis Clonal Lineages
- Relevance of the Axis Spermidine/eIF5A for Plant Growth and Development
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Vitamin D receptor is essential for normal keratinocyte stem cell function
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- The Vitamin D Receptor Is a Wnt Effector that Controls Hair Follicle Differentiation and Specifies Tumor Type in Adult Epidermis
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Syndecan-1 Is Required to Maintain Intradermal Fat and Prevent Cold Stress
- Epidermal patterning and induction of different hair types during mouse embryonic development
- Whn and mHa3 are components of the genetic hierarchy controlling hair follicle differentiation
- ROOT HAIR DEFECTIVE SIX‐LIKE4 (RSL4) promotes root hair elongation by transcriptionally regulating the expression of genes required for cell growth
- Two distinct signaling pathways in hair cycle induction: Stat3-dependent and -independent pathways
- Notch Signaling Regulates Late-Stage Epidermal Differentiation and Maintains Postnatal Hair Cycle Homeostasis
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- Delayed Cutaneous Wound Healing and Aberrant Expression of Hair Follicle Stem Cell Markers in Mice Selectively Lacking Ctip2 in Epidermis
- Morphologic and molecular characterization of two novel Krt71 (Krt2-6g) mutations: Krt71 rco12 and Krt71 rco13
- Do Changes in Chromosomes Cause Aging?
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- Dynamic expression of Runx1 in skin affects hair structure
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- ERULUS Is a Plasma Membrane-Localized Receptor-Like Kinase That Specifies Root Hair Growth by Maintaining Tip-Focused Cytoplasmic Calcium Oscillations
- Cutaneous Retinoic Acid Levels Determine Hair Follicle Development and Downgrowth
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament