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Research 751–780 of 1000+
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Exosomes mediate sensory hair cell protection in the inner ear
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- 17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population.
- A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3
- Intermittent treatment with farnesyltransferase inhibitor and sulforaphane improves cellular homeostasis in Hutchinson-Gilford progeria fibroblasts
- The mouse frizzy (<i>fr</i>) and rat ‘hairless’ (<i>fr</i><sup><i>CR</i></sup>) mutations are natural variants of protease serine S1 family member 8 (<i>Prss8</i>)
- Keratinocyte-derived follistatin regulates epidermal homeostasis and wound repair
- Formation of regulator/target gene relationships during evolution
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Spider joint hair sensilla: adaptation to proprioreceptive stimulation
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Calcium in Root Hair Growth
- Asynchronous telemedicine for isotretinoin management: A direct care pilot
- Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population
- Efficacy of metformin therapy in adolescent girls with androgen excess: relation to sex hormone–binding globulin and androgen receptor polymorphisms
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Characterization of the Promoter Regions of Two Sheep Keratin-Associated Protein Genes for Hair Cortex-Specific Expression
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- An important role of podoplanin in hair follicle growth
- Long noncoding RNA and gene expression analysis of melatonin-exposed Liaoning cashmere goat fibroblasts indicating cashmere growth
- Exosomes derived from umbilical cord mesenchymal stem cells promote healing of complex perianal fistulas in rats
- Electro-optical imaging of F-actin and endoplasmic reticulum in living and fixed plant cells.
- Hairless and the polyamine putrescine form a negative regulatory loop in the epidermis
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies
- Molecular characterization of caprine<i>KRTAP13-3</i>in Liaoning cashmere goat in China
- LGR5 is a conserved marker of hair follicle stem cells in multiple species and is present early and throughout follicle morphogenesis
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Siberian cats help in solving part of the mystery surrounding golden cats