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Research 421–450 of 1000+
- Gene detection in a family with monilethrix and observation of the treatment effect with 5% topical minoxidil
- Tradescantia-Based Test Systems Can Be Used for the Evaluation of the Toxic Potential of Harmful Algal Blooms
- Lanceolate hair-J (<i>lah<sup>J</sup> </i> ): A mouse model for human hair disorders
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- <i>Hoxc13</i> mutant mice lack external hair
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- FGF5 is a crucial regulator of hair length in humans
- Roles of GasderminA3 in Catagen–Telogen Transition During Hair Cycling
- Upregulation of interfollicular epidermal and hair infundibulum β-catenin expression in Gsdma3 mutant mice
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Therapeutic inhibition of keratinocyte TRPV3 sensory channel by local anesthetic dyclonine
- Deimination in epidermal barrier and hair formation
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Current Progress Regarding Cordyceps militaris, Its Metabolite Function, and Its Production
- Multiple facial atrophic scars in childhood
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Detection of Type IIHair Keratin Gene in a Family with Monilethrix
- 9. Immunology and Genetics
- Main Plenary Sessions: Summaries of Papers
- <i>CCDC47</i> gene and trichohepatoneurodevelopmental syndrome: Report of the fifth and sixth cases from Saudi Arabia
- Clinical Snippets
- Severe Insulin Resistance in a Pediatric Patient: Key Areas to Address in the Screening
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart
- Keratins: the hair shaft's backbone revealed
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- Survival of patchwork melanoblasts is dependent upon their number in the hair follicle at the end of embryogenesis
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz<sup>ica</sup>) mice points to <i>fuzzy</i> as a key element of hair cycle control
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone