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Research 541–570 of 1000+
- Partial biotinidase deficiency: Clinical and biochemical features
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- The protective role of the immunomodulator AS101 against chemotherapy-induced alopecia studies on human and animal models
- Patterns of epithelial expression of Fos protein suggest important role in the transition from viable to cornified cell during keratinization
- Permeation of topically applied caffeine through human skin – a comparison of <i>in vivo</i> and <i>in vitro</i> data
- Androgenetic Alopecia in the Female
- Potassium Channel Conductance: A Mechanism Affecting Hair Growth both In Vitro and In Vivo
- Endogenous neurosteroids modulate epileptogenesis in a model of temporal lobe epilepsy
- Neural Potential of a Stem Cell Population in the Hair Follicle
- Scarless wound healing: Transitioning from fetal research to regenerative healing
- Case Series Of Selenium Toxicity From A Nutritional Supplement
- Corticosterone inhibits GAS6 to govern hair follicle stem-cell quiescence
- Large Scale Gene Expression Profiles of Regenerating Inner Ear Sensory Epithelia
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Liver transplantation for propionic acidemia in children
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Zinc deficiency and its management in the pediatric population: A literature review and proposed etiologic classification
- Therapeutic strategy for hair regeneration: hair cycle activation, niche environment modulation, wound-induced follicle neogenesis, and stem cell engineering
- Female Gonadal Function before and after Treatment of Acromegaly
- Activation of Cutaneous Protein Kinase Cα Induces Keratinocyte Apoptosis and Intraepidermal Inflammation by Independent Signaling Pathways
- Characterization of a 190-Kilobase Pair Domain of Human Type I Hair Keratin Genes
- Tyrosinase inhibition due to interaction of homocyst(e)ine with copper: the mechanism for reversible hypopigmentation in homocystinuria due to cystathionine beta-synthase deficiency.
- Progressive Alopecia Reveals Decreasing Stem Cell Activation Probability during Aging of Mice with Epidermal Deletion of DNA Methyltransferase 1
- Analysis of the sheep trichohyalin gene: potential structural and calcium-binding roles of trichohyalin in the hair follicle.
- Edar Signaling in the Control of Hair Follicle Development
- Metabolism of Freshly Isolated Human Hair Follicles Capable of Hair Elongation: A Glutaminolytic, Aerobic Glycolytic Tissue
- Natural progression of male pattern baldness in young men
- Drug discovery for alopecia: gone today, hair tomorrow
- Novel Type I Hair Keratins K39 and K40 Are the Last to be Expressed in Differentiation of the Hair: Completion of the Human Hair Keratin Catalog
- The human type I keratin gene family: Characterization of new hair follicle specific members and evaluation of the chromosome 17q21.2 gene domain